Bispecific Antibodies for Multiple Myeloma: A Review of Targets, Drugs, Clinical Trials, and Future Directions

Abstract

Multiple myeloma (MM) is a plasma cell malignancy and the second most common hematological neoplasm in adults, comprising 1.8% of all cancers. With an annual incidence of ~30,770 cases in the United States, MM has a high mortality rate, leading to 12,770 deaths per year. MM is a genetically complex, highly heterogeneous malignancy, with significant inter- and intra-patient clonal variability. Recent years have witnessed dramatic improvements in the diagnostics, classification, and treatment of MM. However, patients with high-risk disease have not yet benefited from therapeutic advances. High-risk patients are often primary refractory to treatment or relapse early, ultimately resulting in progression toward aggressive end-stage MM, with associated extramedullary disease or plasma cell leukemia. Therefore, novel treatment modalities are needed to improve the outcomes of these patients. Bispecific antibodies (BsAbs) are immunotherapeutics that simultaneously target and thereby redirect effector immune cells to tumor cells. BsAbs have shown high efficacy in B cell malignancies, including refractory/relapsed acute lymphoblastic leukemia. Various BsAbs targeting MM-specific antigens such as B cell maturation antigen (BCMA), CD38, and CD138 are currently in pre-clinical and clinical development, with promising results. In this review, we outline these advances, focusing on BsAb drugs, their targets, and their potential to improve survival, especially for high-risk MM patients. In combination with current treatment strategies, BsAbs may pave the way toward a cure for MM.

Introduction

Multiple myeloma (MM) is the second most common hematologic malignancy in adults (1). In the United States in 2018, ~30,770 patients were diagnosed with MM and 12,770 died from their disease, representing 2.9% of all cancer deaths (2). MM is characterized by a clonal expansion of malignantly transformed plasma cells in the bone marrow (BM). These cells produce an excess of monoclonal immunoglobulins, which are secreted into the blood and urine. Major complications in MM patients include tumor-induced bone lesions and associated pathological fractures, anemia, renal failure, and immunodeficiency, leading to impaired quality of life and decreased overall survival (3, 4).

Over the last few decades, novel drug classes such as immunomodulators (e.g., lenalidomide), proteasome inhibitors (e.g., bortezomib), histone deacetylase inhibitors (e.g., panobinostat), and monoclonal antibodies (mAbs) (e.g., daratumumab [anti-CD38]) have significantly improved the response rates and overall survival for MM patients (5, 6). Currently, the median overall survival for MM patients is 5 years (7). However, stratification by disease risk, according to the Revised International Staging System (R-ISS), reveals significant variability: 82% of low-risk, stage I patients survive 5 years, compared to only 40% of high-risk, stage III patients (7). While high-risk MM patients only account for 15 to 20% of newly diagnosed cases, these patients are often primary refractory to treatment or relapse early (8). Additionally, the majority of low-risk MM patients ultimately develop drug-resistant clones, become refractory to treatment and transition to high-risk disease (8–10). These findings underscore the need to identify MM patients who have active high-risk disease, as well as those who are likely to progress, and develop novel treatment strategies targeted at this population.

Bispecific antibodies (BsAbs) offer a promising immunotherapeutic approach for numerous malignancies including MM. Immune effector cell redirecting BsAbs commonly bind to a tumor cell antigen and CD3 on a T cell, resulting in T cell binding to the tumor cell, activation, and tumor cell lysis (11, 12). Since BsAbs directly stimulate CD3 and thus bypass the T cell receptor, they activate T cells independently from antigen presentation on major histocompatibility complex (MHC) class I. In addition, they have the ability to activate T cells in the absence of co-stimulation, bypassing the normal dependence on antigen presenting cells or cytokines and reducing the risk of anergy that accompanies TCR stimulation in the absence of a costimulatory signal (12–20).

Here, we review the potential of BsAbs in MM, with an emphasis on high-risk patients, although the benefits of BsAbs can extend to all MM patients. A brief introduction into MM is followed by an overview of current BsAb strategies. Next, novel BsAb developments and clinical trials for different MM targets are discussed. Finally, the future direction of BsAbs as a MM treatment modality is addressed, along with obstacles that need to be overcome.

Origins of MM and Features of High-Risk Disease

MM is a cancer of plasma cells, which are terminally differentiated B cells. Numerous hematologic malignancies result from the malignant transformation of B cells at different stages in their lifecycle. For instance, B cell leukemias usually arise from BM-residing pre-B cells; B cell lymphomas, from mature B cells that have migrated to lymph nodes; and MM, from long-lived, BM-residing plasma cells (Figure 1A). Malignant B cells and malignant plasma cells have key differences in their molecular architecture. Unlike malignant B cells, malignant plasma cells generally do not express the widely targeted cell-surface proteins CD19 and CD20, although up to 20% of patients have CD20⁺ MM clones (23). As such, most MM patients cannot be treated with many of the newly-approved targeted therapies for B cell leukemias and lymphomas. This is in part reflected by the number of new drug approvals/indications, which was 56 for B cell leukemias/lymphomas and only 10 for MM in the past 4 years [(21, 22); Figure 1B].

Figure 1.

Differences in molecular architecture and therapeutic success for hematologic malignancy subtypes. (A) B cell leukemia, B cell lymphoma, and multiple myeloma occur at different stages of the B cell lifecycle. Unlike pre- and mature B-cells, which express CD19 and CD20, plasma cells uniquely express BCMA and CD138. CD38 is expressed at all stages of the B cell lifecycle but is more highly expressed on malignant plasma cells. (B) New drug approvals for leukemia, lymphoma, and multiple myeloma between 2016 and December 2019 (21, 22). The pace of drug development for multiple myeloma has failed to keep pace with that of leukemia and lymphoma.

MM develops from a pre-malignant condition known as monoclonal gammopathy of undetermined significance (MGUS), which progresses to smoldering MM (SMM) and MM at a rate of 1% per year (24). Virtually all known MM cases are preceded by MGUS, but the vast majority of MGUS cases never develop into MM. MGUS is characterized by low levels of serum M-protein (<3 g/dL) and <10% clonal BM plasma cells, whereas these levels are >3 g/dL and >10% for SMM, respectively (24). Importantly, the proliferation of malignant plasma cells in patients with MGUS and SMM is asymptomatic and these patients do not exhibit end-organ damage. MM patients are further staged into risk categories, which predict prognosis and treatment response. The most commonly used risk stratification model is the R-ISS, but several models exist (Table 1). With ongoing disease progression, MM patients ultimately develop aggressive, end-stage MM in the form of extramedullary disease or plasma cell leukemia. Table 2 details emerging factors associated with high-risk MM.

Table 1.

MM classification systems and definitions of high-risk disease.

Classification system	Features	Model	Year introduced	References
Durie-Salmon	Stage III One or more of the following: hemoglobin <8.5 g/dL; serum calcium >12 mg/dL; Advanced lytic bone lesions; high M-component production rates IgG value>7 g/dL, IgA >5 g/dL; urine light chain M-component >12 g/24 h	Tumor Burden/Stage	1975	Durie-Salmon Staging System (25)
International Staging System (ISS)	Stage III Serum β2-microglobulin ≥ 5.5 mg/L (other stages consider serum albumin levels as well)	Tumor Burden/ Stage	2005	Greipp et al. (26)
University of Arkansas for Medical Sciences (UAMS)17-gene model	High Risk Deregulated expression of 17 genes (1q32.1, 21q22.3, 1q21.2, 8q23.1, 10q23.31, 12q22, 1p36.21, 3p21.3, 7p14-p13, 1q22, 1q43, 1q31, 1p13.2, 1p22, 1p13.3, 2p22-p21, 6p21)	Cytogenetics	2007	Shaughnessy et al. (27)
Medical Research Council (MRC) Myeloma IX Trial	Adverse lesions defined as +1q21, del(17p13), del(13q14), or adverse IGH translocations t(4;14), t(14;16), or t(14;20) High Risk Presence of >1 adverse lesion Ultra-high Risk Presence of >1 adverse genetic lesions and ISS II or III	Combined Cytogenetics-ISS	2012	Boyd et al. (28)
mSMART	High Risk Genetic abnormalities on t(14;16), t(14;20), del(17p); GEP high risk signature	Cytogenetics	2013	Mikhael et al. (29)
International Myeloma Working Group (IMWG)	High Risk ISS II/III and t(4;14) or del(17p13)	Combined Cytogenetics-ISS	2014	Chng et al. (30)
Revised International Staging System (R-ISS)	Stage III ISS stage III (Serum β2-microglobulin 5.5 mg/L) and either: high risk CA by iFISH (presence of del(17p) and/or translocation t(4;14) and/or translocation t(14;16), or high lactate dehydrogenase (LDH) (serum LDH > the upper limit of normal)	Combined Cytogenetics-ISS	2015	Palumbo et al. (7)
mSMART 3.0	High Risk Genetic abnormalities: t(4;14), t(14;16), t(14;20), del(17p), p53 mutation, +1q; RISS stage III; High plasma cell s-phase; high GEP risk signature	Combined Genetics-ISS	2018	Treatment Guidelines (31)

CA, cytogenetic abnormality; GEP, gene expression profiling; iFISH, interphase fluorescence in situ hybridization; IGH, immunoglobulin heavy; ISS, International Staging System; LDH, lactate dehydrogenase; mSMART, Mayo stratification of myeloma and risk-adapted therapy; R-ISS, Revised International Staging System.

Table 2.

Emerging high-risk MM factors.

Type	Factors	Year	References
Cytogenetic	t(14;16) (q32;q23); t(14;20) (q32;q23); Del(17p)	2016	Rajkumar (32)
Cytogenetic	FISH: t(4;14), t(14;16), t(14;20), del(17/17p), gain(1q); Non-hyperdiploid karyotype; Karyotype del(13); high-risk GEP70 signature	2016	Sonneveld et al. (33)
Cytogenetic	Primary translocations: t(4;14), t(14;16), t(14;20) Secondary translocations: MYC, jumping translocation 1q Copy change number: Isochromosome formation, hyperhaploidy, gain(1q), del(1p), del(17p) Homozygous inactivation of TSGs: Mutation +/- copy number change Genetic changes associated with DNA repair deficiency: genome-wide loss of heterozygosity	2017	Pawlyn and Morgan (34)
Epigenetic	Epigenetic modifier mutations; histone methylation and acetylation; DNA methylation, measured via mutations in DNA methylation modifiers, e.g., IDH1; microRNA	2017	Pawlyn and Morgan (34)
Bone Lesions	Presence of 3 large focal lesions, with a product of the perpendicular diameters > 5 cm2	2018	Rasche et al. (35)

IDH1, isocitrate dehydrogenase 1; EZH2, enhancer-of-zeste 2 polycomb repressive complex 2 subunit; FISH, fluorescence in situ hybridization; GEP70, 70-gene expression profiling; MM, multiple myeloma; TSG, tumor suppressor gene.

Genetic and epigenetic events that initiate MM include chromosomal hyperdiploidy, translocations of chromosome 14 (bringing the strong immunoglobulin heavy-chain enhancer into the proximity of oncogenes), the dysregulation of cell cycle genes, abnormalities in signaling pathways, and alteration of DNA methylation (36–38). Further aberrations, including MYC overexpression and mutations in RAS oncogenes, amongst others, are associated with disease progression (34, 36). In contrast to the evolving genetic heterogeneity associated with disease progression, the immune phenotype of MM cells is relatively conserved. For example, the malignant plasma cells in MGUS, SMM, and MM all express the key surface markers B cell maturation antigen (BCMA), CD38, and CD138. While BCMA expression significantly increases with disease progression, changes in CD38 and CD138 levels are less well-characterized (38, 39). In addition to these molecular features, MM cells rely on their BM microenvironment for growth, survival, and the development of therapy-resistant clones. Through cell-cell interactions and the secretion of cytokines, chemokines, and other factors, MM cells proliferate and impair the effector function of neighboring immune cells (38). For instance, in the BM of MM patients, key immunosuppressive cytokines are expressed at high levels (40, 41). These include interleukin-6 (IL-6), which mediates autocrine and paracrine growth of MM cells and inhibits tumor cell apoptosis, as well as TGF-β, which is an immune inhibitory factor that induces IL-6 secretion. Additionally, regulatory T cell (Treg) numbers are increased in MM patients, further suppressing the immune BM milieu (42, 43). The immunosuppressive characteristics of the molecular and cellular constituents of the BM microenvironment aid in disease progression and lead to poor clinical outcomes (37).

Given the immunosuppressive microenvironment of MM, successful therapies must simultaneously destroy malignant plasma cells and restore an effective anti-tumoral immune response (44). Such immunotherapies should (1) target surface molecules that are ideally expressed exclusively or at higher levels in MM cells than normal plasma or other immune cells and (2) bring effector immune cells into contact with MM cells, thereby enhancing effector cell-directed anti-tumor immunity. BsAbs meet these criteria, and therefore represent a next-generation immunotherapy with the potential to provide sustained clinical responses and even a cure for MM patients.

Bispecific Antibodies: Overview, Designs, and Potential for MM

The idea of using BsAbs to redirect immune cells to tumor cells was first demonstrated in the 1980s and led to several clinical trials (45, 46). Catumaxomab (anti-EpCAM × anti-CD3) was the first BsAb to meet clinical approval by the European Union in 2009 (47). Blinatumomab (anti-CD19 × anti-CD3) was the first BsAb approved by the US Food and Drug Administration (FDA) in 2014 (48–50). Since then, one more BsAb—emicizumab, used to treat hemophilia A—has obtained FDA approval, and there are currently more than 60 BsAbs in various stages of preclinical and clinical development (51, 52). To date, no BsAb has been approved for use in MM patients, although there are 13 currently in clinical trials, and a pilot study evaluating the effects of blinatumomab in relapsed/refractory (R/R) MM patients was initiated in May 2017 (Table 3).

Table 3.

Clinical trials of BsAbs targeting MM.

Targets	Drug name	Design	Trial type	Estimated enrollment	Estimated completion	References
BCMA × CD3	PF-06863135	IgG2a Fc region	Phase 1	80	Early 2022	NCT03269136
BCMA × CD3	TNB-383B	IgG4 Fc region	Phase 1	72	Late 2021	NCT03933735
BCMA × CD3	REGN5458	Fc region, Fab arms	Phase 1/2	56	Late 2022	NCT03761108
BCMA × CD3	REGN5459	Fc region, Fab arms	Phase 1/2	56	Late 2023	NCT04083534
BCMA × CD3	CC-93269	Trivalent, Fc region	Phase 1	19	Mid 2022	NCT03486067
BCMA × CD3	JNJ-64007957	IgG1 Fc region	Phase 1	120	Mid 2020	NCT03145181
BCMA × CD3	AMG420	BiTE	Phase 1	120	Early 2025	NCT02514239
BCMA × CD3	AMG701	Half-life extended BiTE (scFvs plus Fc region)	Phase 1	135	Mid 2025	NCT03287908
CD38 × CD3	AMG424	Fc region, scFv x Fab arms	Phase 1	20	Late 2022	NCT03445663
CD38 × CD3	GBR1342	Fc region, scFv x Fab arms	Phase 1	125	Early 2021	NCT03309111
CD19 × CD3	Blinatumomab	BiTE	Phase 1	20	Mid 2020	NCT03173430
FcRL5 × CD3	BFCR4350A	IgG1Fc region	Phase 1	80	Mid 2021	NCT03275103
GPRC5D × CD3	JNJ-64407564	IgG1Fc region	Phase 1	185	Mid 2021	NCT03399799

The majority of BsAbs are effector cell redirecting and most commonly involve αβ T cells via an anti-CD3 arm connected to a tumor antigen binding site. Anti-NKp30 BsAbs, which bind to natural killer (NK) cells, as well as BsAbs engaging CD16A and NKG2D, which bind to NK cells and γδ T cells, also exist in various stages of development (12, 15, 19). Two other types of BsAbs include tumor-targeted immunomodulators and dual immunomodulators. Tumor-targeted immunomodulators direct immune co-stimulation to pre-activated, tumor-infiltrating immune cells (e.g., tumor-specific effector T cells) by binding to a tumor antigen and a costimulatory molecule (e.g., 4-1BB on T cells). By activating a pool of many different tumor-specific T cell clones, rather than harnessing non-specific effector cells to one pre-determined tumor antigen, tumor-targeted immunomodulators may recognize tumor cells with antigen heterogeneity and build immunological memory. Dual immunomodulators bind two separate immunomodulating targets (usually T cell checkpoint pathways such as PD-1, LAG-3, or TIM-3) to block the mechanisms of the immunosuppressive tumor microenvironment (12). Importantly, BsAbs are effective in directing lysis of malignant cells with low antigen expression levels, a significant advantage when targeting surface molecules that are down-regulated as a mode of tumor evasion. Since no immunomodulatory BsAbs are currently in clinical trials for MM, this review will focus on immune cell redirecting BsAbs.

BsAbs can combine multiple functions of individual mAbs (such as direct cancer cell lysis, blocking malignant signaling pathways, independent T cell activation), entailing a comparatively simpler treatment regimen than one requiring the combination of multiple separate agents (12).

BsAbs are classed into ~100 different formats, which fall roughly into two categories: BsAbs that include a fragment crystallizable (Fc) region, and BsAbs that consist of only fragment antigen-binding (Fab) variable regions and linkers. Both designs are being tested in MM. Some BsAbs with an Fc region (especially those that target NK cells rather than T cells) exhibit Fc-mediated effector functions, including antibody-dependent cell-mediated cytotoxicity (ADCC) via Fc receptor (FcR) binding, as well as added stability and a longer half-life (48, 53, 54). Anti-CD3 BsAbs often have an engineered, effector-silenced Fc region that mainly imparts a longer half-life and added stability (55). Fc-containing BsAbs are structurally similar to IgG molecules, with variations on the symmetry of their molecular composition and the number of binding sites (Figure 2A) (54). Increasing the number of binding sites on a BsAb (multivalency) can increase target affinity, especially for targets with low expression on tumor cells.

Figure 2.

Examples of BsAb constructs and designs. (A) (1) Fc domain and peptide linker, which connect antigen-binding sites in IgG-like BsAbs and Fc-less BsAbs, respectively. The Fc domain confers a number of additional features. (2) Effector cell binding sites, usually anti-CD3e for T cells or anti-CD16A for NK cells: single-chain fragment variable (scFv), bivalent binding site (tumor antigen and effector cell binding site), monovalent binding site. (3) Tumor antigen binding sites: scFv, bivalent binding site, monovalent binding site. (B) Simplified BsAb constructs. (1) Bispecific T cell Engager (BiTE) design, comprised of two scFvs and a peptide linker—e.g., blinatumomab. (2) Bivalent IgG-like BsAb design, with an Fc domain and two monovalent binding arms. (3) Trivalent IgG-like 2+1 BsAb design, with an Fc domain, a bivalent anti-tumor antigen and anti-CD3 or CD16A arm, and a monovalent anti-tumor antigen arm. Tetravalent BsAbs have a similar construction, but with two bivalent arms.

BsAbs that lack an Fc region merely consist of the antigen-binding sites of two antibodies, and most commonly follow the single-chain variable fragment (scFv) design. ScFvs only contain the variable regions of the heavy and light chains and are therefore the simplest iterations of the antigen binding site: They are relatively small and commonly connected by a peptide linker (56, 57). The scFv and linker format is utilized in the construction of bispecific T cell engager molecules (BiTEs), of which blinatumomab and AMG420 are examples (Figure 2B). The simplicity and small size of BiTEs and other scFv BsAbs confer both benefits (e.g., relative ease of adding additional scFvs to create trispecific or trivalent molecules) and drawbacks (e.g., short serum half-lives, decreased efficacy and increased cost by requiring repetitive dosing) (58, 59). Independent T cell activation (inducing cytotoxicity without requiring co-stimulation with CD28 or IL-2) has been observed in BsAbs with and without Fc region (12–19). Proposed mechanisms for this include clustering of the TCR-CD3 complexes to induce signaling in the absence of co-stimulation and the predominance of acting on memory T cells that require less stimulation to become activated (13). The wide array of BsAb structural designs and their advantages and disadvantages have been extensively reviewed by Brinkmann and Kontermann (54).

An alternative to exploiting the cytotoxic potential of T cells for tumor destruction is to redirect and activate NK cells. NK cell redirecting BsAb designs, such as Bispecific NK Engagers (BiKEs) (comprised of two scFvs) and BsAbs with modified Fc regions, are currently in clinical trials for hematologic malignancies; their use for MM is a promising future avenue (60, 61). Since NK cells are the first lymphocyte population to reappear after high-dose chemotherapy, NK cell redirecting BsAbs may be used to eradicate minimal residual disease (MRD) after first-line MM treatment (62). Additionally, NK cell redirecting BsAbs have the potential to be used in combination with other treatments, such as adoptive NK cell transfer after autologous stem cell transplantation (autoSCT).

Their mechanism of action makes BsAbs unique candidates for high-risk MM therapy. High-risk MM patients often display a great degree of intra-tumoral genetic heterogeneity (63); therefore, activating the immune system for broad tumor recognition may be more promising than targeting single genetic lesions. The few studies that have investigated the treatment of patients with high-risk disease failed to conclude that intensification of personalized targeted therapy was significantly beneficial (64, 65). Even therapy regimens containing two autoSCTs (“tandem transplants”) only delay disease progression in high-risk patients rather than cure it (66). The need for new therapies that effectively target high-risk and R/R MM is therefore great, and BsAbs have the potential to fulfill this need.

Several novel treatment approaches like chimeric antigen receptor (CAR) T cell therapies, targeted therapies, and combining mAbs are being implemented for high-risk and R/R MM patients, but BsAb therapies offer numerous advantages. Unlike CAR T cell therapies that have to be individualized by ex vivo manipulation of patient-derived T cells, BsAb therapies are “one size fits all” therapies that can be started immediately. BsAbs can be given in incremental doses and interrupted if necessary, so treatment-related toxicities are easier to manage than in CAR T cell therapies. This simplifies treatment regimens and study design/infrastructure and reduces costs (48, 67, 68). Notably, a recent report by Maruta et al. provides a direct comparison between target-reactivity and cross-reactivity of BsAb and CAR T cell models in MM, which showed similar tumor-killing activity, but a delay in CAR T cells relative to BsAbs (69). Additionally, targeted therapies directed at a particular genetic lesion (e.g., bortezomib, palbociclib, encorafenib, etc.) may only eradicate a certain subclone containing that lesion (e.g., the clone present in the diagnostic random iliac crest biopsy), whereas other clones (including disease-driving clones present in focal lesions) are spared (63). In contrast, BsAbs target antigens that are broadly expressed in all malignant plasma cells, such as BCMA, CD38, and CD138, and increase the chances of thoroughly eradicating all malignant clones. mAbs can similarly target tumor antigens, but are unable to directly harness the potent lytic power of T cells to aid in tumor destruction (70). The ADCC functions of mAbs are dependent on Fc functionality, which can be inhibited by alternative Fc glycosylation or Fc receptor polymorphisms, activation of inhibitory receptors, and competition with circulating IgG. BsAbs ensure effector cell involvement via their specific binding arm, guaranteeing the retargeting of effector cells against the malignant cell (47, 71). Thus, BsAbs present an unprecedented opportunity for all MM patients, and particularly those with high-risk and R/R MM for whom standard and targeted therapies have failed.

Despite the novel and promising features of BsAbs, these immunotherapeutics have faced considerable roadblocks on the path to commercial approval and widespread use. For T cell redirecting BsAbs, the activation of large proportions of non-specific T cells can lead to significant toxicity and treatment-related adverse events (AEs) (12). Cytokine release syndrome (CRS) is among the most important AEs of BsAb treatment, with multiple instances recorded in clinical trials of blinatumomab, PF-0683135, CC-93269, and AMG420 (68, 72–74). CRS can present as a variety of symptoms, ranging from influenza-like symptoms to neurotoxicity and multi-organ failure; the recommended treatment depends on its grade of severity (68, 75). Low-grade CRS can be treated symptomatically with antihistamines, antipyretics, and fluids, while high-grade CRS is treated with corticosteroids. Notably, a prophylactic protocol (consisting of dose adjustment and premedication with dexamethasone) for severe CRS was successfully devised to limit severe CRS during blinatumomab trials (68, 76). An additional study with dexamethasone and tocilizumab (anti-IL-6) has reduced CC-93269-induced CRS (77, 78).

NK cell redirecting BsAbs, which operate via FcR mediated cytotoxicity, present an alternative immunotherapy that may result in reduced general toxicity (12, 79, 80). However, to be successful in MM, NK cell redirecting BsAbs must find antigen epitopes that are not subject to competitive interference by serum IgGs (such as the high levels of M-paraprotein displayed in many MM patients) (79). CD16A, a type III FcγR, may be such an antigen (62). Hallmarks of tumor immune evasion, such as heterogenous expression and down-regulation of antigen levels, present obstacles to both T cell and NK cell redirecting BsAbs (79). New constructs, such as multivalent and tri-specific BsAbs, are under investigation as possible responses to these concerns (81–83). These new designs may also be pivotal in reducing toxicity.

MM Drug Targets for BsAbs

Ideally, BsAb therapeutic targets should be highly expressed on malignant cells and absent or at low levels on other cell types to avoid dose-limiting toxicities (84). Additionally, ideal BsAb targets play an important role in the survival and proliferation of malignant cells, preventing their down-regulation as a mechanism of tumor immune evasion (48). Antigen distribution and content vary both between patients and within a given patient, emphasizing that the success of each drug depends not only on construct but on target expression. So far, there are 24 BsAbs in development against eight MM targets (Table 3). Each MM target and its associated drugs will be discussed below, including ongoing clinical trials and preclinical developments.

BCMA (B Cell Maturation Antigen)

The most important MM drug target for BsAbs is BCMA (also known as TNFRSF17), which currently has eight BsAbs in clinical development (Table 3) and four in preclinical studies (Table 4). BCMA is a type III transmembrane glycoprotein belonging to the tumor necrosis factor receptor (TNFR) superfamily (90–93). BCMA is expressed primarily on B lineage cells and plays an important role in B cell proliferation (90). It is also widely expressed on all plasma cells, up-regulated during plasma cell differentiation, critical for long-term plasma cell survival, and overexpressed on malignant plasma cells and MM cell lines (90, 94–96) (Figure 3). BCMA is absent on most other cell types, except for low expression on plasmacytoid dendritic cells (pDCs) (90, 97). Importantly, and in contrast to other MM targets such as CD38, BCMA is not expressed on CD34⁺ hematopoietic stem/progenitor cells (90).

Table 4.

Preclinical models of BsAbs targeting MM.

Targets	Drug	Design	Model	References
BCMA × CD3	EM801	IgG1 Fc region	MM cell and effector cell co-cultures BMAs of MM patients (autologous T cells) NOG mice with human myeloma allogeneic xenograft Cynomolgus monkeys	Seckinger et al. (85)
BCMA × CD16A	AFM26	Tetravalent, Fc region	NK cell cultures, serum IgG MM cell and primary human NK cell co-cultures MM cell and PBMC co-cultures	Gantke et al. (62)
BCMA × NKp30	CTX-8573	IgG1 Fc region	MM and NK cell co-cultures, in the presence of sBCMA, sBAFF and sAPRIL Humanized mice models engrafted with MM tumors Cynomolgus monkeys	Watkins-Yoon et al. (15)
BCMA × CD3	AP163	Information not available	MM and effector cell co-cultures NSG mice models with human PBMCs and MM or Burkitt lymphoma tumor cells	Li et al. (16)
CD138 × CD3	STL001 or BiTE-hIgFc	scFvs and IgG1 Fc region	MM cell and PBMC co-cultures T cell activation assay NSG mice with human myeloma xenograft	Zou et al. (17)
CD138 × CD3	H-STL002 & M-STL002	scFvs and IgG1 Fc region	MM cell and PBMC co-cultures	Chen et al. (86)
CD38 × CD3	Sorrento CD38/CD3	scFv-Fc region fusion chain and Fab arm	MM cell and PBMC co-cultures NSG mice models with implanted MM or Burkitt lymphoma tumor cells and unstimulated PBMCs	He (87)
CD319 × NKG2D	CS1-NKG2D	BiKE	IL-2 primed NK cultures IL-2 primed PBMC with high, intermediate, low CS1 expression MM cell line co-cultures NSG mice engrafted with human PBMCs and high- and intermediate-CS1 expressing MM cell line xenografts	Chan et al. (19)
GPRC5D × CD3	GPRC5D TRAB	IgG region	MM cell and unstimulated PBMC co-cultures NSG mice model inoculated with human T cells and MM tumor cells NOG mice model engrafted with CD34+ hematopoietic stem cells and MM tumor cells	Kodama et al. (88)
NY-ESO-1 × CD3	ImmTAC-NYE	TCR-like HLA-A2/NY-ESO-1157−165arm, scFv, peptide linker	MM cell and CD8+ cell co-cultures	McCormack et al. (89)
NY-ESO-1 × CD3	A2/NY-ESO-1157 –specific BsAb	anti-HLA-A2/NY-ESO-1157−165 scFv, scFv, peptide linker	Peripheral blood T cells and T2 cells loaded with NY-ESO-1157 peptide co-cultures MM cell and peripheral blood T cell co-cultures Peripheral blood T cells and cells presenting the NY-ESO-1157−165 peptide by HLA-A*02:06 co-cultures NOG mice model engrafted with MM cells and activated T cells	Maruta et al. (69)

Figure 3.

Schematic of key tumor targets and the mechanism of action of BsAbs in multiple myeloma. The superior aspect of the figure highlights the importance of the BCMA/BAFF/APRIL axis and the associated BCMA signaling pathways for malignant plasma cell survival. The inferior aspect of the figure provides a schematic of how BsAbs induce effective T cell-directed MM cell death. A T cell redirecting BsAb binds to BCMA on a MM cell and CD3e on a T cell, coupling these two cells. NK cell redirecting BsAbs bind to CD16A rather than CD3e. Alternative BsAb targets on MM cells include CD38, CD138, FcLR5, CD19, CD319, GPRC5D, and NY-ESO-1. TCR-CD3e cross-linking leads to the activation and proliferation of CD4⁺ and CD8⁺ T cells. Cytokines (i.e., IFN-g, IL-2, IL-6, TNF-a) and cytolytic enzymes (i.e., granzyme B and perforin) are released, resulting in MM cell death.

BCMA has two cognate ligands: (1) B cell activating factor (BAFF, also known as TNFSF13B), which is necessary for B cell development and homeostasis, and (2) a proliferation-inducing ligand (APRIL or TNFSF13A). BAFF and APRIL, either as membranous ligands or in the cleaved, soluble form, bind to BCMA to promote plasma cell growth and survival. Upon ligation by BAFF or APRIL, BCMA activates downstream signaling pathways including the NF-κB, ETS-1 like protein 1 (Elk-1), JNK, ERK, and MAPK pathways (Figure 3) (98–101). This induces pronounced up-regulation of the MCL-1 and BCL-2 anti-apoptotic proteins, preventing dexamethasone-induced cell death. MM patients have up to five times higher soluble BAFF and APRIL serum levels than healthy individuals (102). BCMA also associates with three known TNFR-associated factors (TRAFs)—TRAF1, TRAF2, and TRAF3—which are signal transducers that bind to several members of the TNFR superfamily and facilitate activation of NF-κB, Elk-1, and JNK signaling pathways (101).

Membranous (m)BCMA expression levels per cell increase as healthy plasma cells transform from normal into malignant cells through the disease progression of MGUS to MM (90, 103). Similarly, soluble (s)BCMA levels increase with disease progression, and are found at increased serum levels in MM patients (104). sBCMA levels are also inversely proportional to overall and progression free survival rates (105). sBCMA, which is released from the membrane by spontaneous γ-secretase activity, negatively regulates mBCMA signaling and its associated pathways by competing with mBCMA for BAFF and APRIL (105, 106). Studies suggest that the sequestering of BAFF by sBCMA prevents BAFF from binding to mBCMA and BAFF-R on both healthy and cancer cells. In MM, this blocks the stimulation of normal antibody production, thus contributing to the immunosuppressive MM phenotype by inducing hypogammaglobulinemia (105). Additional studies have shown that high levels of sBCMA may weaken the effectiveness of anti-BCMA type therapies, including BsAbs (104, 107). Additionally, the accumulation of sBCMA in the BM may inhibit BsAb recognition of tumor cells, and reduced mBCMA levels on malignant cells (due to their release as sBCMA by γ-secretase) may further facilitate tumor evasion. These effects may be mitigated by γ-secretase inhibitors (104, 107).

MM patients also display elevated BCMA expression levels on pDCs, which are often in close proximity to MM cells in the BM, and are present in higher numbers in MM patients than in healthy controls (97). pDCs were shown to promote MM progression by secreting factors that enhance MM cell growth (i.e., IL-6), MM chemotaxis (i.e., CXCL-12), and BM angiogenesis (i.e., VEGF), and induce local immunosuppression (i.e., IL-10) (90, 97, 108). Furthermore, pDCs can be resistant to MM therapies, such as bortezomib, lenalidomide, and dexamethasone (97). Given the expression of BCMA on pDCs and their role in MM progression, BCMA-targeting BsAbs have the potential to co-eradicate a key pro-tumorigenic immune cell subset in the BM microenvironment.

Importantly, BCMA seems to be of relatively limited importance to other cell types and tissues. BCMA is not involved in early B cell development or B cell homeostasis, which is in contrast to BAFF receptor (BAFF-R) and Transmembrane Activator and CAML (calcium modulating cyclophilin ligand) Interactor (TACI), which are key to these processes (Figure 3) (102, 109). BCMA-deficient mice develop normally and display healthy physical appearances (110), and only the survival of long-lived BM plasma cells is impaired when compared to wild-type mice (90, 94). In contrast to BCMA, the importance of which to MM is clearly documented, BAFF-R is absent on malignant plasma cells and TACI is expressed at lower levels compared to BCMA (103). Because BCMA's crucial functions in the maintenance and survival of MM cells make its down-regulation unlikely, the likelihood of tumor evasion and drug resistance during treatment is low (85). Collectively, BCMA's plasma cell-specific expression pattern, its overexpression on MM cells and its active involvement in the malignant phenotype make it an ideal BsAb therapeutic target.

Clinical Trials of BCMA-Targeting BsAbs

PF-06863135 (PF-3135)

PF-06863135 is an anti-BCMA x anti-CD3 BsAb that consists of targeting arms within an IgG2a Fc backbone. It has a half-life of 4–6 days in cynomolgus monkeys (111). PF-06863135 is currently under investigation in a dose-escalation phase 1 trial (ClinicalTrials.gov identifier NCT03269136). The study population includes adult patients with R/R MM, who previously received a proteasome inhibitor, an immunomodulatory drug, and/or an anti-CD38 mAb. Patients received escalating doses of PF-06863135 intravenously once a week to determine the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D). Results from 23 patients treated weekly over a median duration of 4 weeks showed one complete response, two minimal responses, and nine stable disease cases. Every patient developed more than one AE; most events were grade 1–2, with 5 patients developing grade 3 events. CRS was the most common treatment-related AE, affecting six patients. CRS primarily occurred after the first dose, was dose-dependent and resolved in all patients in less than 4 days. Dose escalation is ongoing as of early 2020, with plans to continue until the maximum tolerated dose is reached (73).

TNB-383B

TNB-383B is a trivalent anti-BCMA x anti-CD3 BsAb, with a bivalent anti-BCMA arm (112). The BsAb has a silenced human IgG4 Fc region, with a 10-day half-life in cynomolgus monkeys (113). Preclinical studies testing the drug in BM samples from seven R/R MM patients showed that TNB-383B induced MM cell death, dose-dependent T cell activation, and less cytokine secretion than other BsAbs. NOD/SCID/IL-2Rγ-deficient (NSG) xenograft mouse models showed that TNB-383B reduced tumor growth in vivo (114). In June 2019, a phase 1 dose-escalation and expansion trial (NCT03933735) of TNB-383B in patients with R/R MM, who have received at least 3 prior lines of therapy, was initiated. Study arm A will investigate escalating doses of single-agent TNB-383B (25 μg to 40 mg per dose) once every 3 weeks, and arm B will involve an expansion cohort after the recommended dose is established. As of 2019, 12 patients have been enrolled in arm A, with no grade 3 or higher treatment-related AEs (115).

REGN5458

REGN5458 is an anti-BCMA x anti-CD3 BsAb, with an Fc domain and anti-BCMA/anti-CD3 Fab domains (116). In preclinical studies, REGN5458 increased surface levels of BCMA on MM cell lines, in addition to inducing T cell killing of MM cells and cytotoxicity in primary human plasma cells (117). In NSG mice, REGN5458 inhibited xenografted tumor growth at doses of 0.4 mg/kg, and at ten times lower doses in immunocompetent mouse models (117). In cynomolgus monkey studies, REGN5458 depleted BCMA⁺ plasma cells in the BM (117). The REGN5458 treatment induced a mild inflammatory response in the cynomolgus monkeys characterized by transiently increased C-reactive protein and serum cytokines, but was otherwise well-tolerated (117). In a comparative study with CAR T cells, REGN5458 displayed targeted cytotoxicity of MM cells lines and primary plasmablasts. Additionally, administration of REGN5458 to NSG mice led to clearance of systemic OPM-2 myeloma tumors within 4 days (compared with CAR T cells, which required 10–14 days for tumor clearance) (117). A clinical trial (NCT03761108) of a first-in-human study of the drug was initiated in January 2019, in patients with R/R MM. The study involves cohorts of multiple REGN5845 dose levels administered intravenously. Results from seven patients after 4 weeks of treatment showed four responses, of which two were MRD negative. Three responders have ongoing responses after a duration of follow-up ranging from 1 to 5.2 months. Every patient had at least one treatment-related AE, five of which were grade 3 or higher (116).

REGN5459

REGN5459 is an anti-BCMA x anti-CD3 CD3 BsAb, with an Fc domain and with different binding characteristics from REGN5458 (118). A first-in-human clinical trial (NCT04083534) was initiated in September 2019, in patients with R/R MM. The study involves cohorts of multiple REG5845 dose levels administered intravenously and is expected to end in 2023.

CC-93269 (formerly EM901)

CC-93269 is an anti-BCMA × anti-CD3 trivalent BsAb with a bivalent anti-BCMA arm for increased avidity and an IgG1 based Fc region (85, 119, 120). A phase 1 trial (NCT03486067) of a dose-escalation and expansion study of the drug in patients with R/R MM started in April 2018, consisting of intravenous infusion on 28-day cycles (78). As of October 2019, 30 patients had received the drug, with doses ranging from 0.15 to 10 mg. Preliminary results suggest that higher doses (≥3 mg) of CC-93269 result in improved clinical outcomes: overall response rates were 36% in patients treated with 3–6 mg and 89% in patients treated with >6 mg. None of the patients receiving <3 mg responded. The complete response rate was 17% overall, and 44% among the 9 patients treated with 10 mg. The median response rate was 4.1 weeks (range 4.0–13.1), and 92% of responders achieved MRD negativity, often by the end of the first cycle. During follow-up, 29 of the 30 patients experienced at least one treatment-related AE, and 22 patients (73%) experienced a grade 3 or higher AE. The most common treatment-related AEs were neutropenia (43%), anemia (37%), infections (30%), and thrombocytopenia (17%). Twenty-three patients (77%) developed any-grade CRS, including one grade 5 (i.e., death). Most CRS events were successfully managed using dexamethasone and tocilizumab (78).

JNJ-64007957

JNJ-64007957 is an anti-BCMA × anti-CD3 BsAb with an IgG1 Fc region (121, 122). In preclinical pharmacokinetic and tolerability studies conducted on cynomolgus monkeys, JNJ-64007957 was well-tolerated at doses up to 10 mg/kg per week. No toxicologically significant effects were found when administered once a week for a 5-week period. The pharmacokinetic report suggested a low anti-drug antibody response, indicating that this drug can be safely administered multiple times per week (123). A phase 1 trial (NCT03145181) of a dose-escalation and expansion study of JNJ-64007957 in patients with R/R MM started in May 2017. The study is being conducted in two parts: one for intravenous administration and one for subcutaneous administration. Additionally, a phase 1 trial (NCT04108195) of subcutaneous daratumumab in combination with intravenous JNJ-64007957 or JNJ-64407564 (i.e., an anti-GPRC5D BsAb) in patients with MM started in January 2020. This study is being conducted in two parts, beginning with a dose escalation phase consisting of 28-day cycles, followed by a dose expansion part. It is expected to end in 2020.

AMG420 (formerly BI 836909)

AMG420 is an anti-BCMA × anti-CD3 human BiTE antibody comprised of two scFvs (124). In preclinical studies with co-cultures of unstimulated peripheral blood mononuclear cells (PBMCs) and MM cell lines, AMG420 induced redirected lysis of MM cells and target-dependent release of cytokines by T cells. Anti-tumor activity was further examined in two NSG mouse models reconstituted with human T cells and either subcutaneous or intravenous MM cell line xenotransplantations (125). Comparable dose-dependent anti-tumoral activity was observed in both subcutaneous and intravenous administration regimens of AMG420. Toxicity studies in cynomolgus monkeys showed a dose-dependent decrease of healthy plasma cells in the BM (126). A phase 1 first-in-human dose-escalation and expansion study (NCT02514239) of the drug in patients with R/R MM started in July 2015. Results from this study, which enrolled 42 patients, showed 13 responses, including 6 MRD-negative complete responses, 3 complete responses, and 4 partial responses (127). The median response time was 1 month, and 11 patients responded within the first treatment cycle. Of the 7 patients dosed at 400 μg/d, 5 had complete response with no presence of MRD, and 2 had partial responses. No major toxicities were observed. Thus, 400 μg/d was set as the MTD (128). Of the 42 patients enrolled in this trial, 7 discontinued treatment due to AEs, of which 6 were considered serious, including CRS (3 instances), peripheral polyneuropathy (1 instance), edema (1 instance), and pyrexia (1 instance) (128, 129). Nineteen patients (45%) experienced SAEs, of which infection (14 instances) was most commonly reported (74, 127).

AMG701

AMG701 is an anti-BCMA × anti-CD3 human BiTE comprised of two scFvs and an Fc region for extended half-life (~5 days in non-human primates) (14, 130). Preclinical studies of AMG701 in MM cell lines and patient samples showed significant induction of T cell-mediated lysis of MM cells, even at low concentrations and low effector:target cell (E:T) ratios (2:1 and 1:2). This finding was also confirmed in drug-resistant MM cell lines or in the presence of MM-supporting osteoclasts. AMG701 also induced lysis of tumor cells from R/R MM patients in tumor and effector cell co-cultures. Analysis of AMG701-treated MM and effector cell co-cultures revealed that AMG701 induced CD8⁺ and CD4⁺ T cell proliferation (47.5 and 16.7% at 10 ng/ml, respectively) and T cell activation (up-regulation of CD25 and CD69). AMG701 also increased the differentiation of naive CD4⁺ and CD8⁺ T cells toward the central and effector memory phenotype. Additionally, it was postulated that the proliferating T cells potently lysed even those MM cells with reduced BCMA expression. In xenograft MM mouse models, AMG701 blocked tumor growth after 5 days and completely eradicated growth after three injections at all dose levels (0.02, 0.2, and 2 mg/kg); however, with AMG701 treatment alone, mice experienced tumor regrowth by the end of the study. Mice treated with a combination of AMG701 and the immunomodulator and anti-MM agent lenalidomide experienced significant anti-tumor activity 2 days after their first injection, and their tumor volume remained low even after 45+ days of the study. In in vitro MM cell and effector cell co-cultures, the AMG701 lenalidomide combination treatment enhanced MM cell-killing as compared to AMG701 treatment alone, including in the presence of MM-supporting cells from the BM microenvironment [such as osteoclasts and bone marrow stromal cells (14, 131)]. A phase 1 trial (NCT03287908) of a dose-escalation and expansion study of the drug in patients with R/R MM started in November 2017 and is expected to end in 2026.

Preclinical Models of BCMA-Targeting BsAbs

EM801

EM801 is an anti-BCMA × anti-CD3 trivalent BsAb with a bivalent anti-BCMA arm for increased avidity and an IgG1 based Fc region (85). Preclinical studies in human MM cell lines showed that EM801 binds T cells and MM cells, leading to TCR/CD3 cross-linking and activating the CD3 downstream signaling pathways. In BM aspirates from MM patients, EM801 induced significant primary myeloma cell death by autologous T cells, reaching 90% reduction in 48 h (85). To further evaluate the anti-tumor activity of EM801, studies were performed in human MM xenografted immunodeficient mice and in cynomolgus monkeys. In mice, EM801 was potent against highly proliferating MM cells. In monkeys, a reduction in BCMA⁺ plasma cells was observed in the BM and peripheral blood (85).

AFM26

AFM26 is an anti-BCMA × anti-CD16A tetravalent BsAb, consisting of a bivalent anti-CD16A arm for increased NK cell avidity connected to a bivalent anti-BCMA arm by an IgG-like backbone (62, 79). AFM26 binds to an epitope of CD16A that is not blocked by serum IgG (e.g., M-protein) binding. A preclinical study conducted on NK cell cultures found that AFM26 exhibits prolonged retention on the surface of NK cells, with receptor retention levels of AFM26 remaining above 60% after 1 h, even in the presence of serum IgG. This is particularly significant for MM because high M-protein levels are characteristic of the disease. In the same preclinical study, AFM26 was applied to primary human NK and MM cell co-cultures (E:T, 5:1), and induced MM cell-specific lysis. In an experiment conducted on multiple MM cell lines with varying BCMA expression levels, AFM26 was found to retain potency even on cells with low BCMA expression. Additionally, unlike mAbs such as daratumumab and elotuzumab (anti-SLAMF7), AFM26 did not induce NK cell lysis. Furthermore, when compared with BiTE incubation on MM and PBMC co-cultures, AFM26 displayed comparable efficacy and markedly reduced cytokine production, suggesting a superior safety profile (62, 132).

CTX-8573

CTX-8573 is an anti-BCMA × anti-NKp30 BsAb, with an IgG1-like afucosylated Fc region to additionally engage CD16A on NK cells and γδ T cells (15). It displays a 16-day half-life in cynomolgus monkeys (133). CTX-8573 was tested on human NK and MM cell co-cultures and displayed potent cytotoxicity toward BCMA⁺ tumor cells, including on low BCMA-expressing cell lines. Significantly, this cytotoxic activity was maintained in the presence of sBCMA, sBAFF, and sAPRIL, all of which are displayed at higher levels in high-risk MM patients. A model of the BsAb with an aglycosylated Fc region (to preclude CD16A engagement) retained ADCC, showing that NKp30 engagement alone can promote innate cell activation and cytotoxicity, although CD16A involvement enhances such activity. A preclinical study conducted on multiple humanized mouse models engrafted with MM tumors showed potent anti-tumor activity. Pharmacokinetic and safety profiling in cynomolgus monkeys showed standard biphasic pharmacokinetics and no evidence of systemic immune activation as measured by C-reactive protein levels (133).

AP163

AP163 is an anti-BCMA × anti-CD3 BsAb with a 9 h half-life in cynomolgus monkeys (16). Preclinical testing on MM cell lines and effector cell co-cultures showed that AP163 induces cross-linking, T cell activation, cytokine production, proliferation, and redirected target cell killing, eradicating tumor cells. AP163 was studied in multiple NSG mice models injected with human PBMCs and subcutaneous MM cell xenografts or BCMA-expressing Burkitt's lymphoma cell xenografts. In all models, AP163 resulted in T cell activation, cytokine production, and cancer cell killing. In the two MM xenografts tested, AP163 eradicated or significantly delayed tumor growth at doses as low as 0.04 mg/kg. Toxicity testing was carried out on cynomolgus monkeys and non-human primates, in which the drug was well-tolerated at doses up to 5 mg/kg. Significantly, AP163 induced minimal cytokine release as compared to conventional BsAbs (16).

CD138 (Syndecan-1)

CD138 is a type I transmembrane protein of the syndecan proteoglycan family (134). CD138 has a wide variety of functions, including cell signaling, cell-cell adhesion, cytoskeletal organization, and tumorigenesis (i.e., proliferation, angiogenesis, and metastasis) (135). It is expressed primarily on epithelial cells, transiently on developing mesenchymal cells and at the terminal plasmacytic differentiation stage of B cells (136, 137). Viable MM cells have high expression of membranous (m)CD138; when cells undergo apoptosis, shedding of mCD138 is triggered (138, 139). Studies have found that CD138 suppresses apoptosis in MM cells by activating the insulin-like growth factor-1 receptor; high mCD138 expression can thus indicate non-apoptotic cells, making it an efficient antigen for targeting viable MM cells (140, 141). CD138 also acts as a co-receptor for TACI and APRIL, promoting the APRIL/TACI-associated pathways that induce survival and proliferation of MM cells (142). Additionally, soluble (s)CD138, which is proteolytically shed by matrix metalloproteases and sheddases, is present at high levels in the serum of MM patients and is heavily implicated in disease progression: it acts as a key mediator between MM cells and the BM microenvironment on which they rely, promoting signaling pathways that lead to tumor cell proliferation, angiogenesis, and metastasis. As such, sCD138 is an independent predictor of poor prognosis in MM (143–145).

Various anti-CD138 mAb and T cell engaging MM therapies have taken advantage of the high expression levels of CD138 on MM cells. One mechanism involves coating tumor cells with anti-CD138 mAbs as a method of enhancing dendritic cell cross-presentation of the tumor antigen and the generation of myeloma specific killer T cells (146). CD138's elevated expression on MM cells and its active role in the disease phenotype make it a promising MM BsAb target. Additionally, mCD138's role in preventing apoptosis likely makes tumor cells addicted to this molecule, although a significant proportion of patients were shown to have CD138-negative MM clones (141, 147). Potential drawbacks of CD138 include its high expression on epithelial cells and the accumulation of sCD138 in the BM. In a first-in-human phase 1 trial of an anti-CD138 DM4 (a derivative of the cytotoxic agent maytansine)-antibody conjugate in R/R MM patients, patients suffered from common epithelial-related AEs (e.g., hand-foot syndrome, xerophthalmia, stomatitis, and blurred vision) (148). Furthermore, the characteristic, accelerated shedding of sCD138 and its accumulation in the BM of MM patients may inhibit BsAb recognition of tumor cells. As of February 2020, CD138-targeting MM BsAbs have not yet entered clinical trials.

Preclinical Models of CD138-Targeting BsAbs

STL001 (also known as BiTE-hIgFc)

STL001 is an anti-CD138 × anti-CD3 BsAb with two scFv arms and an IgG1 Fc region to allow for FcR-mediated NK binding. A preclinical study tested the effects of STL001 on PBMC and MM cell co-cultures (E:T 7:1) and compared the cytotoxicity to that of an anti-CD138 mAb and an anti-CD3 mAb combination and various controls (17). STL001 induced lysis of 90.1% of MM cells after 48 h, compared to 70.5% in the mAb combination and 13.8% and 12.3% in the controls. STL001 was also incubated in a T cell activation assay consisting of PBMCs from healthy donors and IL-2, whereby T cell activation was measured by CD25 and CD69 expression levels. After 24 h, STL001 showed 78.12–85.45% T cell activation efficiency. After 2 weeks of PBMC stimulation and activation, STL001 bound over 96% of the total NK cells. STL001 was also tested at an intravenous dose of 3 mg/kg in an NSG xenograft MM tumor mouse model that had also been injected with unstimulated healthy human PBMCs (E:T, 3:1). Compared to the isotype control, STL001 significantly impaired MM tumor growth, resulting in an ~75% decrease in the mean tumor volume relative to the control (17).

H-STL002 and M-STL002

H-STL002 and M-STL002 are anti-CD138 × anti-CD3 BsAbs with two scFv arms and an IgG1 Fc region. A preclinical study tested the effects of these BsAbs on PBMC and MM cell co-cultures (86). After 20 h of incubation, 74–80% of T cells were activated (measured by CD69 expression), and significant MM cell lysis was observed at E:T ratios as low as 7:1. Furthermore, cytotoxicity activity of 98.4% and 98.3% was measured for M-STL002 and H-STL002, respectively (86).

CD38 (Cyclic ADP Ribose Hydrolase)

CD38 is a type II glycoprotein of the ADP-ribosyl cyclase family, with ectoenzymatic and receptor functionality (149, 150). CD38 plays a regulatory role in calcium homeostasis, nicotinamide adenine dinucleotide (NAD) signaling, and weak adhesion events (151). Originally thought to be a lymphocyte-specific antigen, CD38 was shown to be expressed in nearly every type of tissue, but with elevated expression on hematopoietic cells (151). CD38 is expressed at varying stages of B cell development (i.e., in BM precursor B cells and in terminally differentiated plasma cells) and serves as a marker of T lymphocyte development (149). Additionally, CD38 is uniformly and highly expressed in MM, making it attractive for BsAb targeting. In its role as a receptor, CD38 binds to CD31 (PECAM-1), which is expressed on endothelial cells, lymphoid cells and in the lungs and kidney (152). Interactions between CD38 and CD31 regulate adhesion events between CD38⁺ cells and human umbilical vein endothelial cells. These interactions are also involved in the binding and migration of leukocytes through the endothelial wall, the activation and proliferation of leukocytes, and in B cell development (152, 153). The role of CD38-CD31 interactions is important for MM cell survival in the BM by mediating adhesion to BM endothelial and stromal cells. Clinical studies examining mAb agents that target CD38—such as daratumumab—often lead to down-regulation of CD38 surface expression. Although down-regulation of a target antigen is usually undesirable, in this case it may be beneficial, leading to reduced interaction and support of MM cells by the BM microenvironment (154, 155). A potential obstacle to CD38's use as an MM target is its expression on T cells; however, a preclinical study has shown that T cell fratricide does not preclude the efficacy of anti-CD38 BsAbs as long as tumor cells are lysed at a higher or equal rate to T cells (18).

Clinical Trials of CD38-Targeting BsAbs

AMG424

AMG424 is an anti-CD38 × anti-CD3 BsAb, with an Fc domain, an anti-CD38 scFv, and an anti-CD3 Fab domain (18). In a preclinical study using MM target cells co-cultured with purified human T cells (E:T 10:1), AMG424 induced complete target cell lysis and limited cytokine release, compared to other BsAbs with higher CD3 affinities. In human PBMC and MM cell line co-cultures (E:T 1:1), AMG424 triggered a pronounced depletion of MM cells and normal B cells, induced a 2-fold increase in T cell numbers and triggered robust T cell activation as measured by induction of CD25. Likewise, in cynomolgus monkeys, intravenous injection of AMG424 triggered T cell activation. However, it also triggered depletion of T cells, B cells, lymphocytes, and monocytes. In an orthotopic tumor model in NSG mice reconstituted with human T cells, intravenous injection of AMG424 induced tumor regression and T cell activation (18). While AMG424 also depleted T cell numbers, the E:T ratio remained stable. A phase 1 first-in-human trial (NCT03445663) of the drug in patients with R/R MM started in July 2018. Part 1 of the study aims to assess the safety and tolerability of AMG424 and determine the MTD and/or biologically active dose. Part 2 will further evaluate the safety and tolerability of the MTD. The trial is expected to end in 2022.

GBR1342

GBR1342 is an anti-CD38 × anti-CD3 BsAb, with an Fc domain, an anti-CD38 scFv and an anti-CD3 Fab domain; it has a half-life of ~5 days in rats (156, 157). In human PBMC and MM cell co-cultures (E:T 10:1), GBR1342 demonstrated potent killing of MM cells (157). Additionally, in redirected lysis assays, it demonstrated greater potency than commercial anti-CD38 antibodies, such as daratumumab (157). A phase 1 first-in-human dose-escalation and expansion study (NCT03309111) in patients with previously treated MM began in 2017, with GBR1342 administered by intravenous infusion at an initial dose of 1 ng/kg, with varying dose escalations by cohort (up to 1,000 ng/kg) in 28 day cycles (157). Part 1 of the study is dose evaluating and aimed to assess the safety and tolerability of GBR1342. Part 2 will focus on efficacy exploration. Preliminary results from 19 patients revealed 28 treatment-related AEs in 14 patients, two of which were treatment-related and reversible (i.e., a creatine phosphokinase elevation and an infusion-related reaction, with no neurotoxicity observed to date). Of the 19 patients, 4 were still undergoing treatment with GBR1342 in 2018; as of 2020, the longest duration on the drug has been five cycles, with one patient entering his sixth cycle of dosing at 400 ng/kg (158). In September 2019, GBR1342 was granted orphan drug designation by the FDA (159).

Preclinical Models of CD38-Targeting BsAbs

Sorrento anti-CD38/CD3 BsAb

Sorrento Therapeutics' anti-CD38/CD3 BsAb has an anti-CD38 Fab arm and an anti-CD3 scFv-Fc region fusion chain. The fusion chain has hinge mutations for reduced Fc region affinity/effector function, to decrease antigen-independent T cell toxicity (87). A preclinical study showed that the BsAb induced potent lysing of CD38⁺ MM cell lines, with antigen density positively correlating with cytotoxic potency. In an in vivo follow up, the BsAb construct with the most prolonged anti-tumor activity and best T cell stimulation was the one with a balanced CD38 and CD3 affinity. In a cytotoxicity assay using human PBMCs and MM cell lines, the BsAb showed more potent tumor cell killing than the daratumumab control. In NSG mice models with implanted CD38-expressing Burkitt's lymphoma tumor cells and previously unstimulated human PBMCs, BsAb treatment inhibited tumor growth and prolonged survival. An investigational new drug application is projected to be filed for the BsAb in the first half of 2020 (160).

CD19

CD19 is a type I transmembrane glycoprotein member of the immunoglobulin superfamily (161). CD19 is primarily involved in the immune response, by modulating B cell receptor (BCR)-dependent and independent signaling to establish B cell signaling thresholds (162–164). It works as the lead receptor in a complex with CD21, CD81, and CD225 to decrease the threshold for receptor-dependent signaling, acting as a co-receptor for BCR signal transduction and interacting with various down-stream protein kinases (including the Src family, Ras family, Abl, Bruton's tyrosine kinase, adapter molecules, and PI3K) (161, 165–169). CD19 is expressed on B cells, from the pre-B cell stage and throughout development, with expression decreasing during terminal plasma cell differentiation (161, 162, 168). CD19 expression is further reduced as plasma cells transform into MM cells. It has been proposed that CD19 loss aids MM cell proliferation (170), and this loss precludes MM patients from benefitting from anti-CD19 therapies. However, there have been reports of R/R MM patients responding to anti-CD19 CAR T cell therapies in combination with other treatments (171, 172). Additionally, super-resolution microscopy has shown very low CD19 expression on MM cells, which was undetectable by flow cytometry but may be accessible to antibodies and modified effector cells (173). These findings make CD19 a potentially interesting BsAb target for MM, despite its unconventional expression pattern and unclear role in the disease phenotype.

Clinical Trials of CD19-Targeting BsAbs

Blinatumomab

Blinatumomab is an anti-CD19 × anti-CD3 BiTE made of two scFvs, with a half-life of ~2 h in humans (174). In July 2017, it was approved by the FDA for treatment of R/R B cell precursor acute lymphoblastic leukemia (B-ALL) in adults and children (175). Importantly, blinatumomab is the first FDA-approved BsAb. In the phase III trial, which confirmed the clinical benefit of blinatumomab in B-ALL, the drug increased median survival rate from 4 to 7.7 months and resulted in a higher rate of event-free survival than chemotherapy (31% vs. 12%) (TOWER trial, NCT02013167) (176). SAEs including neurologic events, CRS, administration-site reactions, and procedural complications, were reported in 62% of patients treated with blinatumomab as compared to 45% in the chemotherapy group. Results from a phase II study (BLAST, NCT01207388) evaluating blinatumomab in B-ALL found a median OS of 36.5 months after treatment, and more than 50% of patients who achieved MRD after their first cycle were alive at 5 years (72).

Given the success of blinatumomab in B-ALL, it is currently in clinical trials for numerous other B cell malignancies, including R/R MM (177). A phase 1 clinical trial of blinatumomab in combination with salvage autoSCT for patients with R/R MM began in May 2017 (NCT03173430). The study consists of administering up to two 28-day cycles of blinatumomab to patients who previously received high-dose melphalan and autoSCT for MM, with results pending. A case study of blinatumomab-induced response of R/R MM in the context of a secondary pre-B cell ALL emerged in 2017 (172). The patient, a 70-year-old female, developed pre-B-ALL while undergoing lenalidomide therapy for MM, for which she was in partial remission. She underwent cytoreductive therapy and began blinatumomab induction, which resulted in a complete remission of her ALL and a very good partial response of her MM by International Myeloma Working Group criteria (172). Although this case is promising for the application of blinatumomab to other MM patients, it is important to point out that this patient's MM cells stained positive for CD19, which is atypical for MM tumors (172).

CD319 (SLAMF7 or CS1)

CD319 is a homophilic (self-ligand) surface glycoprotein receptor of the signaling lymphocyte activation molecule (SLAM) family (178). CD319 is a regulatory receptor, with a key role in immune cell function and immune signaling mediation (178, 179). CD319's cytoplasmic tail includes an immunoreceptor tyrosine switch-motif (180). The immunoreceptor tyrosine switch-motif mediates binding to Ewing sarcoma/Friend leukemia integration 1 transcription factor-activated transcript 2 (EAT-2), a member of the SLAM-associated protein (SAP) family of adaptors. CD319/EAT-2 binding determines whether CD319 stimulation will activate or inhibit immune cell functions; in the presence of EAT-2, CD319 plays an activating role, while in the absence of EAT-2, it mediates inhibitory effects (178). CD319 is expressed predominately on NK cells, but also CD8⁺ T cells and B cells, with marked up-regulation during terminal B cell differentiation into plasmablasts and plasma cells (181). It is absent on hematopoietic stem/progenitor cells and blood cancers, except for malignant plasma cells (182, 183). CD319 mRNA has been detected on over 97% of CD138⁺ MM cells, with protein expression confirmed by flow cytometry (184). The function of CD319 in plasma cells and MM cells is not certain: both seemingly lack EAT-2, theoretically suggesting an inhibitory role for CD319 mediation, as is the case in EAT-2-negative NK cells (178, 185). However, a study testing isolated and activated B cells found that stimulation with anti-CD319 mAbs (along with an anti-CD40 mAb and IL-4) increased cell proliferation and induced the expression of growth-supporting cytokines (179). This suggests the possibility of an activating role for CD319 on MM cells, despite their lack of EAT-2. CD319 may also aid in the communication and adhesion between MM cells and the BM microenvironment. A study investigating the effects of an anti-CD319 mAb found that CD319 is localized to the uropod membrane domains of MM cells, regions promoting cell-cell adhesion (183). When CD319 was blocked by the mAb, MM cell adhesion to BM stromal cells was reduced in a dose-dependent manner (183). By supporting adhesion of MM and BM stromal cells, CD319 may promote MM cell proliferation and survival. The ubiquitous and elevated expression of CD319 on MM cells and its possible involvement in disease progression make it a promising BsAb target. As of February 2020, CD319-targeting MM BsAbs have not yet entered clinical trials.

Preclinical Models of CD319-Targeting BsAbs

CS1-NKG2D BsAb

CS1-NKG2D BsAb is an anti-CD319 × anti-NKG2D bispecific T/NK cell engager made of two scFvs (19). NKG2D is expressed on cytolytic immune cells such as NK cells, CD8⁺ T cells, γδ T cells, and NKT cells (with no expression on CD34⁺ hematopoietic stem/progenitor cells). It is one of the major activating NK cell receptors and a co-stimulatory molecule on cytotoxic CD8⁺ T cells and NKT cells (186). A preclinical study incubated IL-2-primed NK cell cultures with NKG2D and found that the CS1-NKG2D BsAb binds to and triggers the activation of NK cells (19). The study then tested the effects of the BsAb on three different co-cultures consisting of IL-2-primed PBMCs with MM cell lines with high, intermediate, and low CD319 expression. Dose-dependent increases in MM cell lysis were observed in the high and intermediate expression co-cultures. The BsAb was then tested in primary MM patient peripheral blood samples treated with allogeneic PBMCs (E:T, 10:1), which reduced MM cells with high CD319 expression. No specific lysis against T, NKT, or NK cells was found. NSG mice engrafted with human PBMCs and CD319 high- and intermediate-expressing MM cell lines were also administered subcutaneous doses of the BsAb. In this context, only mice engrafted with CD319 high-expressing MM cell lines experienced a significant prolonged survival in response to the BsAb (i.e., ~40 days compared to ~30 days in the control group) (19).

FcRL5 (Fc Receptor-Like 5)

FcRL5 (CD307) is a membrane protein that is closely related to the Fc receptor family. FcRL5 regulates BCR signaling and binds aggregated IgG (84, 187). It is restricted to B lineage cells, with high expression on mature B cells and plasma cells (187). FcRL5 mRNA is overexpressed in MM cells, and one study found FcRL5 protein expression to be three times higher on MGUS and MM cells than on normal plasma cells (84). Another study found comparable expression levels between normal and malignant plasma cells, but higher expression on plasma cells than on normal B cells (188). Significantly, the FcRL5 gene is located at the chromosomal breakpoint in 1q21, the amplification of which is associated with aggressive MM (189). A study analyzing primary MM biopsies found a significant correlation between FcRL5 mRNA expression and 1q21 gain, suggesting that the 1q21 gain can lead to FcRL5 overexpression in high-risk MM patients (188, 190). Therefore, the development of FcRL5-targeting BsAbs may be especially valuable for high-risk MM patients. One concern about FcRL5 as a BsAb target is its large extra-cellular region: large antigen size (in particular large extracellular regions) and increased distance from the epitope to the target cell membrane can interfere with efficient T cell synapse formation (191). However, constructing an anti-FcRL5 BsAb that targets an epitope on the most membrane-proximal domain of FcRL5's extracellular region is an effective solution to this issue; such a BsAb has displayed promising preclinical results at picomolar concentrations (188).

Clinical Trials of FcRL5-Targeting BsAbs

BFCR4350A (formerly RO7187797)

BFCR4350A is an anti-FcRL5 × anti-CD3 BsAb with an IgG1 Fc region (188, 192). BFCR4350A's anti-FcRL5 arm is constructed to bind to an epitope chosen for its location on the most membrane-proximal extracellular domain, and its ability to achieve efficient synapse formation. In preclinical studies, BFCR4350A was applied to MM cell and CD8⁺ or CD4⁺ T cell co-cultures, resulting in dose-dependent T cell activation and killing of the MM cells. It also induced robust T cell proliferation, with 95% of the CD8⁺ T cells undergoing up to six cell divisions in 5 days (188). BFCR4350A was then tested on co-cultures of patient-derived BM mononuclear cells (BMMCs) with healthy-donor CD8⁺ T cells and healthy BMMCs. BFCR4350A displayed similarly cytotoxic dose-dependent killing of myeloma BMMCs and of normal plasma cells. The preclinical study also examined the activity of BFCR4350A in humanized NSG mice with transplanted CD34⁺-purified human hematopoietic stem cells. The mice were subcutaneously inoculated with MM cells and later given weekly IV doses of 0.5 mg/kg of BFCR4350A, which resulted in tumor regression in all mice. A study consisting of a single intravenous dose with slow infusion of 1–4 mg/kg of BFCR4350A was conducted in cynomolgus monkeys (188). The treatment resulted in T cell activation, transient T cell decrease, complete depletion of B cells in the spleen and BM, robust dose-dependent depletion of B cells in the lymph nodes, a dose-dependent reduction of IgG levels, and mild cytokine release (188). Collectively, plasma cell and IgG depletion suggest effective BFCR4350A activity in the BM. A second preclinical study, testing the efficacy of single host cell construction of BFCR4350A (i.e., in vivo as opposed to in vitro assembly), found comparable results between these construction methods (193). A phase 1 dose escalation and expansion trial (NCT03275103) of the drug in patients with R/R MM started in September 2017 (Table 3). The drug is being administered intravenously in 21-day cycles, up to a maximum of 17 cycles or unacceptable toxicity, and the expected primary completion date is 2021.

GPRC5D (G Protein-Coupled Receptor Class C Group 5 Member D)

GPRC5D is a transmembrane orphan receptor of the G protein-coupled receptor family, whose functions are poorly characterized (194–196). MM patients have high GPRC5D mRNA expression in their BM, with low expression in normal tissues (194). GPRC5D is also highly expressed on the surface of MM cells, with lower expression on B and plasma cells and no expression on other hematopoietic cells (88). Due to this expression pattern, GPRC5D is thought to play a key role in MM tumor cell proliferation (197). GPRC5D mRNA expression has also been associated with the high-risk cytogenetic events del(13q14) and t(4;14), suggesting its possible role as a prognostic marker (194). Therefore, GPRC5D is an interesting and novel target for MM.

Clinical Trials of GPRC5D-Targeting BsAbs

JNJ-64407564

JNJ-64407564 is an anti-GPRC5D × anti-CD3 BsAb with an IgG1 Fc region (198, 199). A preclinical study tested JNJ-64407564 in a co-culture of MM cell lines and healthy human T cells (E:T, 5:1), a co-culture of healthy human whole blood and MM cell lines, and a co-culture of BMMCs from MM patients and exogenous healthy human T cells (200). JNJ-64407564 induced MM cell directed cytotoxicity in all co-cultures and dose-dependent T cell proliferation in the MM cell line and healthy human T cell co-culture. T cell activation was observed in both healthy human T cell co-cultures but not in the blood co-culture. JNJ-64407564 was then tested in two NSG mice models with human MM xenografts and human PBMCs; the drug led to significant anti-tumor activity and 100% complete responses in both groups. Testing of the drug in cynomolgus monkeys showed no adverse effects (200). A phase 1 dose-escalation and expansion trial (NCT03399799) in patients with R/R MM began in 2017, with JNJ-64407564 administered by intravenous or subcutaneous injection. Additionally, a phase 1 trial (NCT04108195) testing combinations of daratumumab with JNJ-64407564 (anti-GPRC5D BsAb) or JNJ-64007957 (anti-BCMA BsAb) in MM patients started in January 2020. This study is being conducted in two parts, beginning with a dose escalation phase consisting of 28-day cycles, followed by a dose expansion part, and is expected to end in 2021.

Preclinical Models of GPRC5D-Targeting BsAbs

GPRC5D TRAB

GPRC5D TRAB (T-cell redirecting antibody) is an anti-GPRC5D × anti-CD3 BsAb with an IgG base. A preclinical study testing four prototypes examined their anti-tumor activity (88). Two prototypes were added to a co-culture of unstimulated human PBMCs and GPRC5D-expressing MM cell lines and to a control of unstimulated human PBMCs and GPRC5D-negative lung cancer cell lines, respectively. Both prototypes induced cytotoxicity against the MM cells but not the lung cancer cells; GPRC5D expression levels on MM cells did not strongly impact cytotoxicity. The effects of two BsAbs were also tested in an NSG mouse model xenografted with human T cells and GPRC5D-expressing MM cell lines and in a NOG mouse model engrafted with human CD34⁺ hematopoietic stem/progenitor cells and xenotransplanted with a MM cell line.

Importantly, these mouse models used MM cell lines that possess t(4;14), a translocation associated with high-risk MM (88, 201). In the NSG model, treatment with 10 mg/kg of the BsAb prototypes led to significant reduction in volume of both tumors as compared to the non-tumor specific control BsAb, curing up to 50% of the mice. In the NOG model, IV treatment with 10 mg/kg of the BsAb prototypes induced tumor regression in 60% of mice. The cytotoxicity of GPRC5D TRAB against these MM models suggest that this molecule may represent a promising treatment candidate for high-risk MM patients.

NY-ESO-1 (New York Esophageal Squamous Cell Carcinoma 1)

NY-ESO-1 (also known as cancer/testis antigen 1B, CTAG1B) is an immunogenic member of the cancer/testis antigen family—a protein family with germ and cancer cell expression patterns—showing nuclear localization in mesenchymal stem cells and predominately cytoplasmic expression in tumor cells (202, 203). Little is known about the biological function of NY-ESO-1, but its structural features and expression patterns have suggested a role in cell cycle progression and growth, apoptosis, germ cell self-renewal and differentiation, and stem and cancer cell proliferation (203–207). Its expression in healthy tissue is limited to testis and placental cells, but it is expressed in a wide range of tumor types, including MM. NY-ESO-1 expression is particularly high in relapsed patients and patients with cytogenetic abnormalities as defined by gene expression profiling (208). In 335 newly diagnosed MM patients, NY-ESO-1 expression was present in 60% of cases in patients with cytogenetic abnormalities vs. 31% of cases with no abnormalities; this number increased to 100% and 61% at relapse, respectively (208). These findings suggest that NY-ESO-1 expression may correlate with MM clonal evolution.

NY-ESO-1 is highly immunogenic, with the ability to elicit simultaneous humoral and cellular immune responses (208, 209). In MM, antibody responses to NY-ESO-1 have been found to correlate with tumor load and disease progression (208, 210). NY-ESO-1-derived peptides are presented on MHC class I molecules, allowing for T cell recognition (69). Spontaneous CD8⁺ T cell responses (recognizing NY-ESO-1 peptides 157–165 presented on HLA-A2) have been exhibited in MM patients, and laboratory expansion of these T cells has resulted in efficient MM cell killing (208). The HLA-A2/NY-ESO-1_157−165 peptide complex is therefore being used as a target antigen in the development of NY-ESO-1-targeting BsAbs for MM (69, 89). The tumor-specific expression of NY-ESO-1 and its elevated prevalence in high-risk patients makes it a promising BsAb target; however, its MHC machinery-dependent presentation may result in loss of expression as a means of immune escape. The combination of HLA-A2/NY-ESO-1_157−165-targeting BsAb therapy with agents that increase the expression of MHC-machinery proteins, such as interferon (IFN)-γ, may be an avenue worth exploring, to reduce the chances of immune escape via HLA-A2 down regulation (211–214). As of February 2020, NYE-ESO-1-targeting MM BsAbs have not yet entered clinical trials.

Preclinical Models of NY-ESO-1-Targeting BsAbs

ImmTAC-NYE

ImmTAC-NYE (immune-mobilizing monoclonal TCR against cancer) is an anti-NY-ESO-1 × anti-CD3 BsAb, consisting of a TCR-like, anti-HLA-A2/NY-ESO-1_157−165 arm fused to an anti-CD3 scFv arm via a peptide linker (89, 215). A preclinical study of the BsAb in a co-culture of MM cells and CD8⁺ effector T cells (E:T, 10:1) showed dose-dependent tumor lysis at 0.1–10 nM (89). ImmTAC-NYE was able to bind to cells with a low-density of HLA-A2/peptide complexes, suggesting maintained functionality despite MHC down-regulation. The study also found that ImmTAC-NYE-activated T cells release cytokines IFN-γ, IL-2, and TNF-α, which, in addition to attracting effector immune cells to the tumor site, may spur long-term anti-tumor activity by promoting components of the death receptor pathway in tumor cells, providing an additional mechanism of tumor cell killing even after the BsAb is metabolized (89, 216).

A2/NY-ESO-1₁₅₇-specific BsAb

A2/NY-ESO-1₁₅₇-specific BsAb is an anti-NY-ESO-1 × anti-CD3 BsAb consisting of an anti-HLA-A2/NY-ESO-1_157−165 scFv connected to an anti-CD3 scFv via a peptide linker (69). A preclinical study testing the BsAb on a co-culture of peripheral blood T cells and antigen presentation-deficient T2 cells loaded with NY-ESO-1₁₅₇ peptide showed that the BsAb triggered T cell production of IFN-γ, IL-2, and TNF-α. The BsAb only released cytokines in the presence of the NY-ESO-1₁₅₇-loaded cells and did not appear to be activated by CD3 binding alone, indicating reduced general toxicity. The BsAb was also tested in a peripheral blood T cell and MM cell co-culture, where it triggered cytokine production and killing of MM cells. A NOG mouse model engrafted with MM cells and activated T cells showed that 10-μg doses of the BsAb significantly suppressed tumor growth. The cross-reactivity of the BsAb with different HLA-A2 alleles was then tested by incubating it in peripheral blood T cell co-cultures with cells presenting the NY-ESO-1_157−165 peptide by HLA-A^*02:06 instead of HLA-A^*02:01. Levels of reactivity between the two different alleles were comparable, suggesting that the BsAb would be successful in patients with either type of HLA-A2. The study, which also directly compared the BsAb to a CAR T cell construct with the same anti-HLA-A2/NY-ESO-1_157−165 scFv, found that the anti-tumor effects of the BsAb were seen earlier than those of the CAR T cell therapy. This may be explained by the fact that the cytolytic synapses induced by the BsAb were more similar to those formed by TCR binding to HLA/peptide complexes than the synapses induced by the CAR T cells were (69).

Future Directions and Conclusions

The development of BsAb treatments for MM has great potential. Preclinical findings in in vitro and in vivo models have shown effective tumor eradication. Additionally, preliminary clinical results of BCMA-targeting BsAbs PF-06863135 and AMG420 have been promising, with an absence of dose-limiting toxicity in PF-06863135 and six MRD-negative complete responses in AMG420 (73, 74). As more study results materialize, BsAbs will continue to be refined to increase efficacy and safety.

Multiple areas of further development are already emerging, with a focus on reducing treatment-related adverse events and on conquering tumor evasion.

Down-regulation of the target antigen is a classic mechanism of tumor resistance, and multivalent BsAb constructs that increase target avidity, as well as trispecific antibodies that target more than one tumor antigen, may be methods to overcome this obstacle (82). Targeting multiple tumor antigens in one antibody may also prove useful in addressing the heterogeneity of target expression on malignant cells. The increased specificity provided by trispecific antibodies may lead to new combinations of MM targets or to novel targets altogether.

Multi-target specificity may also be a crucial development for avoiding B cell aplasia, leukopenia, and the accompanying increased risk of infection, by ensuring that only the cells that express a particular antigen combination are directly targeted, reducing the chance that healthy cells are lysed. Because many target antigens are also expressed on non-transformed B cells and plasma cells (and are thus targeted by effector T cells), the depletion of B and plasma cell compartments poses a risk of AEs like infection. Febrile neutropenia occurs in up to 40% of B-ALL patients treated with blinatumomab (48, 217). In most patients receiving higher doses of blinatumomab, hypogammaglobulinemia has been observed, but there has been no evidence for an increase in long-term infectious complications. A study examining the long-term effects of CD20-expressing B cell depletion in lymphoma and rheumatoid arthritis patients undergoing rituximab therapy was conducted in 2011. It found that multiple courses of drug exposure may result in IgG and IgM levels below the lower limit of normal serum levels, halted plasma cell formation, and higher serious infection risks (218). B cell aplasia resulting from CAR T cell therapy has been addressed by intravenous or subcutaneous immunoglobulin replacement therapy, and it has been suggested that the same response can be used during BsAb treatment until B cells have recovered (48, 219). Emerging BsAb technologies may prevent against unnecessary B and plasma cell depletion by increasing their specificity. A promising example of such technology is the “split” trispecific antibody, which is divided into two scFv halves, both connected to the same anti-CD3 antibody (83). The CD3-binding site only becomes functional when both scFvs have attached to their target antigen, ensuring that effector cell lysis is only directed at cells expressing both antigens. Thus, antigen combinations uniquely expressed by the cancer cells can be targeted, without accompanying B cell and plasma cell depletion (83).

Multi-target specificity is likely to also reduce BsAbs' toxicity profile by limiting the instances of T cell activation. Increasing target avidity may be another way to decrease unwanted cell lysis and the associated risks of aplasia and cytotoxicity. Asymmetric BsAb constructs with bivalent sites for the tumor antigen may not only increase the strength of binding to tumor cells, but also avoid CD3 activation in the absence of sufficient target antigens (e.g., in the case of low antigen expression on healthy cells) (81).

Independent T cell activation, a feature displayed by some but not all BsAbs, is an important area of further development. In some MM cases, inhibition of co-stimulation in the tumor microenvironment via expression of co-inhibitory molecules aids tumor evasion by neutralizing T cell activity (82). BsAb designs that induce biological synergies, resulting in independent T cell activation without the need for costimulatory molecules (e.g., the designs of anti-BCMA BsAb AMG420, anti-CD38 BsAb AMG424, and anti-FcRL5 BsAb BFCR4350A), are thus important for further development (18, 125, 188). Trispecific antibody models designed to stimulate two T cell antigens (rather than only CD3) aim to increase and prolong T cell activation without the need of external co-stimulatory models. One such MM-specific model targets CD38 on the tumor cell, and stimulates both CD3 and CD28 on the T cell (220). CD28, the most important “second signal” on T cells, is also expressed on MM cells at low levels (221, 222). A preclinical study testing the effects of the trispecific antibody was conducted on co-cultures of human PBMCs and MM cell lines and in NSG mouse models xenografted with human CD8⁺ T cells and MM cell lines. The study found that the inclusion of the CD28-binding site not only eliminated the need for external co-stimulation, but also prolonged T cell survival, improved recognition of MM cells, reduced non-specific toxicity, and contributed significantly to anti-tumor efficacy. In the NSG mouse model, tumor growth was completely suppressed in the presence of antibody doses as low as 1 μg/kg (220). These results encourage the further development of trispecific anti-CD28 arm-including antibodies and are particularly promising for MM antibodies, given their increased specificity resulting from MM cell CD28 expression.

Combining BsAbs with immune checkpoint inhibitors (ICIs) may play a key role in the advancement of MM-targeting BsAb therapy by preventing against T cell exhaustion. T cell exhaustion is a feature of MM that may be exacerbated by treatment with BsAbs (223, 224). PD-1/PD-L1 signaling is a hallmark of tumor immunosuppression and T cell exhaustion. Increased PD-1 and PD-L1 expression has been observed in MM patients throughout the course of disease progression, resulting in T cell deactivation and allowing for tumor growth (225). Clinical cases of BsAb-induced T cell exhaustion have been recorded, with a blinatumomab-resistant ALL patient displaying an increase of PD-L1-expressing B-precursor ALL cells (224). Significantly, preclinical findings in MM-targeting BsAbs have also suggested induced T cell exhaustion: increased PD-1 expression in T cells after stimulation by anti-FcRH5/CD3 BsAb in the presence of target-expressing MM cells was observed in cynomolgus monkeys and led to reduced lysis of PD-L1 expressing target-cells (188). However, such mechanisms of T cell exhaustion can be therapeutically countered using ICIs (81). Combinations of anti-PD-1/PD-L1 mAbs with BsAbs have enhanced T cell activation and proliferation and increased cancer cell lysis in vitro in multiple studies (226, 227). In MM, the addition of an anti-PD-L1 mAb to anti-FcRH5/CD3 BsAb therapy significantly increased the efficiency of MM cell killing in vitro and in vivo, restoring T cell activity (188). Such combinations of ICIs with BsAbs may be pivotal in developing treatments that are responsive to immunosuppression.

Combinations of BsAbs with therapeutic Treg depletion may also assist in fighting against immunosuppression. A potential concern about BsAb treatment is that independent T cell activation may also activate unwanted Tregs (82). In MM, Treg numbers are abnormally high, aiding immunosuppression of effector cells in the BM microenvironment (42). Combinations of BsAbs with therapeutic Treg depletion may be helpful or necessary. A preclinical study examining Treg levels in the blood of 42 blinatumomab-treated R/R B-ALL patients confirmed a negative correlation between Treg levels and response to blinatumomab therapy. Importantly, depleting Tregs in vitro restored the blinatumomab-triggered proliferation activity of patient T cells. Therapeutic Treg depletion may be achieved in vivo by treating patients with cyclophosphamide or fludarabine before blinatumomab therapy (228). Co-infusion of ICIs and manipulation of BsAb design to recruit additional cell types may also prove valuable in overcoming immunosuppression (82). An interesting model of BsAb design ingenuity can be seen in “TriKEs,” which are trispecific killer cell engagers. TriKEs are like NK cell redirecting BsAbs (e.g., BiKEs), with the added integration of IL-15 to drive expansion of NK cells for increased anti-tumoral activity. Preclinical studies in AML have shown TriKE activity to be more efficient than BiKE activity (229). Similarly, innovative BsAb designs such as BsAb-armed T cells are also being applied to MM (230). A clinical study (NCT00938626) targeting myeloma precursor cells in standard and high-risk MM patients administered the patients with anti-CD3 × anti-CD2 BsAb-armed activated T cell infusions prior to autoSCT (230). The infusions induced anti-myeloma IFN-γ and anti-SOX-2 IgG responses, which were then boosted in every patient post-autoSCT. Such responses have been shown to be associated with reduced risk of progression from MGUS to MM (231). This finding suggests that BsAb-armed activated T cell infusions can induce cellular and humoral anti-myeloma immunity that can be detected and boosted after autoSCT (230).

Bispecific immunoconjugates, which consist of two tumor-targeting arms linked to a cytotoxic agent, are another frontier of BsAb innovation with the potential to benefit MM patients. A BsAb-cytokine conjugate−20-C2-2b, which targets tumor antigens CD20 and HLA-DR and is fused to two copies of IFN-α2b—has shown potent inhibition of MM cell lines. A preclinical study found that this compound showed potent cytotoxicity against MM cell lines, even those with limited expression of CD20 or HLA-DR individually (232). As the BsAb field continues to grow and the clinical data accumulates, ongoing innovations will be implemented to improve the immunotherapeutic options for patients with MM and numerous other cancers.

Despite recent therapeutic advances, existing treatments remain largely ineffective for high-risk and R/R MM. Novel immunotherapies, especially BsAbs, provide a new treatment approach for these patients. With numerous phase 1 clinical trials of MM-targeting BsAbs currently underway, the prospect of this new immunotherapeutic treatment for MM patients is on the horizon.

Author Contributions

CS conceived of the review. CC drafted the manuscript with help from SK. CC and DP created the figures. CC created the tables. DP, CC, and CS edited the manuscript. CC and CS revised the manuscript, and all authors approved its final version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.