Pathogenesis and treatment of multiple myeloma

Abstract

Multiple myeloma (MM) is the second‐ranking malignancy in hematological tumors. The pathogenesis of MM is complex with high heterogeneity, and the development of the disease is a multistep process. Chromosomal translocations, aneuploidy, genetic mutations, and epigenetic aberrations are essential in disease initiation and progression. The correlation between MM cells and the bone marrow microenvironment is associated with the survival, progression, migration, and drug resistance of MM cells. In recent decades, there has been a significant change in the paradigm for the management of MM. With the development of proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, chimeric antigen receptor T‐cell therapies, and novel agents, the survival of MM patients has been significantly improved. In addition, nanotechnology acts as both a nanocarrier and a treatment tool for MM. The properties and responsive conditions of nanomedicine can be tailored to reach different goals. Nanomedicine with a precise targeting property has offered great potential for drug delivery and assisted in tumor immunotherapy. In this review, we summarize the pathogenesis and current treatment options of MM, then overview recent advances in nanomedicine‐based systems, aiming to provide more insights into the treatment of MM.

Multiple myeloma (MM) is the second‐ranking malignancy in hematological tumors. There has been a significant change in the paradigm for the management of MM. In this review, we summarize the pathogenesis and current treatment options of MM, then overview recent advances in nanomedicine‐based systems, aiming to provide more insights into the treatment of MM.

1. INTRODUCTION

As the second‐ranking hematological malignancy, multiple myeloma (MM) is a disease characterized by clonal expansion of malignant plasma cells that accumulate in the bone marrow (BM). ¹ The latest cancer statistics indicated that in 2021, there were 34,920 estimated new cases of MM in the United States, with an estimated 12,410 deaths. ² The disease is prevalent in people over 65 years old, and more than half of the patients are men. In 2019, there were 155,688 MM patients worldwide, with an increased global burden (Figure 1). Besides, MM had a higher age‐standardized incidence rate and age‐standardized death rate in more developed countries. ³

FIGURE 1.

Age‐standardized rates of incidence of multiple myeloma worldwide in 2019. ASIR, age‐standardized incidence rate (Copyright 2021, Springer Nature ³ )

The etiology of MM is not clear, while environmental exposures and genetic events may be risk factors. In almost all patients, MM evolves from an asymptomatic premalignant stage termed monoclonal gammopathy of undetermined significance (MGUS). The definition of MGUS is less than 30 g/L of M protein, less than 10% of clonal BM plasma cells, and the absence of symptoms related to MM. ⁴ Another asymptomatic but more advanced stage refers to smoldering MM (SMM). The median time to progression from SMM to active MM is around 5 years. ⁵ The risk of progression relates to the proportion of plasma cells in the BM and the serum monoclonal protein level at diagnosis. The genetic events increase the progression rate from MGUS to SMM and then to MM. ⁶ , ⁷

The proliferation of monoclonal plasma cells in the BM impedes the normal course of blood cells and leads to anemia. In addition, malignant plasma cells secrete monoclonal immunoglobulin, the so‐called paraprotein or M‐protein, and infiltrate other vital organs. Bone pain is one of the symbolized manifestations of MM, including spine, chest, and long bones, due to increased activity of osteoclasts and enhanced bone resorption. ⁸ The lytic lesions and fractures of bones lead to high blood calcium levels. The MM defining events, hypercalcemia, renal insufficiency, anemia, and bone lesions, are commonly referred to as the “CRAB” feature. ⁹ Besides, myeloma is always associated with hyperviscosity, amyloidosis, fatigue, and recurrent infections. ¹⁰ And the presence of extramedullary foci indicates a more aggressive situation.

Over the last decades, there has been increased attention on disease evolution and pathogenesis. Significant changes have also been made in the paradigm for the management of MM. A good variety of agents can be offered to MM patients at different phases. In this review, we summarize the pathogenesis and current treatment options of MM, then overview recent advances in nanomedicine‐based systems, aiming to provide more insights into the treatment of MM (Figure 2).

FIGURE 2.

Schematic illustration of treatment options and nanomedicine‐based strategies for multiple myeloma. ADC, antibody‐drug conjugate; CAR‐T, chimeric antigen receptor T cell; IMiD, immunomodulatory drug; MGUS, monoclonal gammopathy of undetermined significance; PI, proteasome inhibitor; SMM, smoldering multiple myeloma;

2. PATHOGENESIS OF MULTIPLE MYELOMA

2.1. Genetic alterations

The pathogenesis of MM is complex with high heterogeneity, and the development of the disease is a multistep process. Chromosomal translocations, aneuploidy, genetic mutations, and epigenetic aberrations are essential in disease initiation and progression. ¹¹ The initiating events are thought to occur in the germinal center during the procedure of class switching and somatic hypermutation. ¹² Double‐strand DNA breaks and fuses with other breaks in the genome, leading to aberrant fusions and chromosomal translocations. And translocations involving oncogenes can lead to pathological states including MGUS, SMM, and MM. The identified translocations involve the immunoglobulin heavy chain (IgH) gene loci and a set of recurrent partner genes. A vast majority of chromosomal translocations are related to the IgH chain locus at chromosome 14, resulting in specific oncogenes falling under the control of the IgH enhancer. The t(11;14) translocation results in a high prevalence of CCND1, which encodes cyclin D1 and is essential for cell cycle progress. ¹³ The t(4;14) leads to increased expression of NSD2 and FGFR3, and is identified in 10 to 15% of MM patients. ¹⁴ The overall survival (OS) of patients with t(4;14) was significantly poor, with a reported median OS of 41 months. ¹⁵ Another study showed that among a group of patients, the progression time from SMM to symptomatic MM was 28 months in patients with the t(4;14) compared with 55 months in patients with t(11;14). ¹⁶ Other representative translocations include t(14;16) involving MAF, t(14;20) involving MAFB, and t(6;14) involving CCND3 (Table 1). ¹⁷ , ¹⁸ , ¹⁹ , ²⁰ , ²¹ Another possible driving event is aneuploidy, including hypodiploidy, pseudodiploidy, and the most frequent entity, hyperdiploidy. Chretien et al. conducted a genomic analysis by single‐nucleotide polymorphism array, and a cohort of 965 patients was enrolled. At least one trisomy was found in 61% of patients, with chromosome 9, 15, 19, 5, 3, 11, 7, 21, 18, or 17 trisomy. Most of the trisomies were associated with a protective effect on survival, except trisomy 17, 18, and 21. The patients with trisomy 3 showed a significantly longer time interval between diagnosis and progression than patients without a trisomy of chromosome 3. And patients who had a trisomy 21 showed worse outcomes than patients lacking this trisomy. Besides, patients with hypodiploidy were related to shorter time to progression and shorter OS. ²²

TABLE 1.

Primary chromosomal translocations related to 14q32

Cytogenetic abnormality	Affected genes	Approximate frequency (%)	Refs.
t(11;14)	CCND1	14–21	11, 13, 15
t(4;14)	NSD2, FGFR3	10–15	11, 13, 15
t(14;16)	MAF	3–5	11, 19, 20
t(6;14)	CCND3	1–4	11, 13, 18
t(14;20)	MAFB	1–2	11, 14, 21

The short arm deletion of chromosome 17 (del(17p)) is one of the major abnormalities that impair the survival of patients. The median OS was 22 months in a group of transplant‐eligible patients with del(17p). ¹⁵ In addition, patients with acquired del(17p) after treatment showed shorter median progression‐free survival (PFS) and OS compared with the control group without acquiring del(17p) at a comparable time point. The median PFS and OS were 5.4 and 18.1 months, respectively, after the detection of del(17p). ²³ Recently, scholars conducted a study on a large group of patients with del(17p) presenting in more than 55% of their plasma cells. Next‐generation sequencing targeting on TP53 was performed after homogeneous treatment. The results indicated that a group of patients showed the worst survival with the situation when del(17p) was associated with TP53 mutation. Nevertheless, del(17p) alone was also a very high‐risk feature associated with a poor outcome compared with the control cohort lacking del(17p). ²⁴ Other chromosomal abnormalities observed in MM patients include loss of the short arm of chromosome 1 (del(1p)), deletion of the long arm of chromosome 13 (del(13q)), and gain of the long arm of chromosome 1 (gain(1q)). ²⁵ The amplification of 1q21 exists in a certain portion of MM patients, and this unfavorable cytogenetic abnormality has been associated with poor response to standard treatment. ²⁶

The frequency of somatic mutations varies among patients. One study found that KRAS and NRAS mutated exclusively in MM patients, 21.2 and 19.4% in 463 patients, respectively. ²⁷ Other frequently mutated genes include BRAF, FAM46C, and DIS3. Besides, TRAF3, CYLD, RB1, IRF4, EGR1, and MAX are recurrently mutated genes. ²⁸ Structural variants involving MYC oncogene are common in MM patients. Deregulated MYC expression can promote genome instability and is associated with chromosomal rearrangements, leading to progression from newly diagnosed MM (NDMM) to a refractory state. ²⁹ In addition, epigenetic alterations also play an important role in myeloma. The global DNA methylation levels vary among patients, while levels of hypomethylation are increased in MM compared to precursor stages. ⁴

2.2. Related signaling pathways

These genetic abnormalities affect several signaling pathways. The nuclear factor kappa B (NF‐κB) pathway, mitogen‐activated protein kinase (MAPK) pathway, and cell cycle pathway have been involved. The NF‐κB pathway is a pivotal signaling pathway for the development of lymphocytes, and lymphoid malignancies are always associated with the dysregulation of this pathway. Increased NF‐κB activity can be caused by gene mutations. Positive regulators, such as NF‐κB‐inducing kinase (NIK) and upstream receptor CD40, were overexpressed in MM. ³⁰ Other genetic abnormalities include mutations in NF‐κB2, and loss of function of negative regulators such as TRAF2, TRAF3, and CYLD. ¹¹ Activation of the NF‐κB pathway is mostly via two ways. In the canonical pathway, the activated IκB kinase (IKK) complex phosphorylates IκB proteins, resulting in the accumulation of heterodimers p50/p65 and c‐Rel/p65 in the nucleus. Unlike other B‐cell malignancies, MM is mostly related to the noncanonical NF‐κB pathway. NIK is necessary for the noncanonical pathway and is activated after initial stimulation. IKK‐α homodimers phosphorylate P100, which results in removal of the C‐terminal domain and accumulation of the p52/Rel‐B heterodimers in the nucleus. ³¹ The proteins of the NF‐κB family are essential for nuclear translocation and DNA binding, and aberration of the NF‐κB pathway contributes to the initiation and progression of MM by regulating the expression of several genes associated with the growth, survival, and angiogenesis of MM. ³²

The MAPK pathway is a fundamental mediator of many biological processes involved in cell proliferation, growth, adhesion, and apoptosis. Genetic alterations in MM are associated with pathway activation. For instance, the t(4; 14) translocation leads to overexpression of FGFR3 and then stimulates the signaling cascade. RAS mutations, generally represented by NRAS and KRAS, are associated with the aberration of this pathway in MM. ²⁷ These mutations that activate MAPK signaling have been evidenced in aggressive myeloma cases. In particular, RAS mutation has been found in more advanced clinical scenarios with a shorter time to progression. ³³ RAS activates downstream targets and promotes the recruitment and phosphorylation of RAF, which then phosphorylates MEK. And MEK phosphorylates ERK in turn. ³⁴ Activated ERK can phosphorylate numerous downstream targets in the nucleus and cytoplasm. Moreover, RAS mutations may enhance proteasome capacity and reduce cellular stress, thereby inhibiting the efficacy of proteasome inhibitor (PI) and correlating with PI resistance. ³⁵ A preclinical study proved that with the inhibitory effect of sorafenib, which targets RAF and VEGFR2, apoptosis was induced among a panel of MM cell lines and in vivo models. ³⁶ Increased genome instability, both initiating and secondary genetic events, leads to cell cycle dysregulation in MM. Representative abnormalities include the overexpression of CCND1, CCND2, CCND3, and CKS1B, mutations of TP53 and RB1, leading to cell proliferation and clonal growth. ³⁷ In addition, dysregulation of the apoptotic pathway occurs, with increased expression of antiapoptotic proteins.

2.3. Bone marrow microenvironment

The correlation between MM cells and the BM microenvironment is associated with the pathogenesis of MM, contributing to the activation of signaling pathways and participating in the survival, progression, migration, and drug resistance of MM cells. Both cellular and noncellular components of BM niches play a role in the generation of tumor progression microenvironment. BM stromal cells (BMSCs) play a vital role in MM cell growth. The CXCL12 expressed on the surface of BMSCs binds to CXCR4 expressed on MM cells, mediating the homing and retention of MM cells in the BM. Furthermore, very late antigen‐4 integrin (VLA‐4) on MM cells binds to its ligand, vascular cell adhesion molecule 1, facilitating the trafficking of MM cells into BM niches. ³⁸ Other molecules, including α4β7 integrin, P‐selectin glycoprotein ligand‐1, and CD147, also contribute to cell adhesion and migration. ³⁹ , ⁴⁰

The interaction between MM cells and the BM microenvironment leads to considerable secretion of cytokines and growth factors, including IL‐6, insulin‐like growth factor (IGF‐1), B‐cell activating factor (BAFF), a proliferation‐inducing ligand (APRIL), tumor necrosis factor‐α (TNF‐α), and vascular endothelial growth factor (VEGF). ⁴¹ These soluble factors activate intracellular signals that regulate the growth, proliferation, migration, and drug resistance of malignant cells. The secretion of BAFF, APRIL, and TNF‐α stimulates the NF‐κB signaling pathway. ³² Besides, IGF‐1 has been reported to activate the NF‐κB pathway indirectly and is needed for the survival of MM cells. ⁴² IL‐6 is another growth factor for MM cells and is involved in the NF‐κB pathway. Activation of the NF‐κB signal can also promote the production of several factors, including IL‐6, BAFF, and APRIL, thus, resulting in a positive feedback loop that allows for constitutive activation of NF‐κB and, consequently, the augmented survival and proliferation of MM cells. ³¹ In addition to the NF‐κB pathway, PI3K/Akt/mTOR signaling pathway, JAK/STAT pathway, and MAPK pathway have also been involved in this response. Downstream sequelae include dysregulation of cytokines, cell‐cycle regulatory proteins, and antiapoptotic proteins (Figure 3). ⁴³ , ⁴⁴

FIGURE 3.

Roles of cytokines and signaling pathways in the pathogenesis of multiple myeloma. Cytokines and growth factors have been secreted in the bone marrow microenvironment such as IL‐6, IGF‐1, BAFF, APRIL, TNF‐α, and VEGF. These soluble factors activate signaling pathways, including the NF‐κB pathway, PI3K/Akt/mTOR pathway, JAK/STAT pathway, and MAPK pathway, which regulate the survival, proliferation, apoptosis, migration, adhesion, and drug resistance of myeloma cells

Drug resistance is a crucial issue in tumor treatment. The binding of MM cells to BMSCs causes cell adhesion‐mediated drug resistance. Endothelial cells, macrophages, stromal cells, and other components in the BM microenvironment are involved in the formation of vascular niches that promote the proliferation and survival of MM cells, and protect them from antimyeloma agents. ⁴⁵ In addition, factors in the microenvironment, such as the VEGF family, monocyte chemotactic protein‐1 (MCP‐1), TNF‐α, and IL‐8, are important for enhanced angiogenesis in MM, which is parallel with disease progression. ⁴⁵ The BM microenvironment can mediate immune escape via the immune suppression of regulatory T cells, regulatory B cells, and myeloid‐derived suppressor cells (MDSCs). MDSCs can suppress immune responses, especially driven by the activation of the STAT3 pathway, and inhibit the proliferation of cytotoxic T lymphocytes and nature killer (NK) cells. ⁴⁶ Besides, osteoclasts play a role in the immunosuppressive microenvironment. With the stimulation of signaling pathways, the BM microenvironment acquires antiapoptotic effects via the increase of antiapoptotic regulatory proteins. ⁴⁷ For instance, BCL‐2, BCL‐XL, and MCL‐1 have been significantly upregulated. Increased soluble factors and surface molecules, such as IL‐6, transforming growth factor‐β (TGF‐β), IL‐10, APRIL, ICAM‐1, and CD40, also contribute to immune escape and resistance against immune effector cells.

Exosomes establish cell–cell communication and act in the interplay between the BM microenvironment and MM cells. The content inside exosomes has been identified as different between MM patients and healthy donors, which can serve as tumor biomarkers and therapeutic targets. ⁴⁸ BMSC‐derived exosomes were loaded with higher levels of oncogenic proteins, cytokines, and adhesion molecules, including IL‐6 and fibronectin, while expressed a lower level of tumor‐suppressive factors, promoting cell growth and facilitating MM progression. ⁴⁹ MM‐derived exosomes were enriched with amphiregulin, which led to the activation of the epidermal growth factor pathway in preosteoclasts and osteoclastogenesis. ⁵⁰ Furthermore, exosomes in the BM microenvironment have been shown to be related to drug resistance, enhanced angiogenesis, and the generation of the immunosuppressive environment. ⁵¹ , ⁵²

2.4. Myeloma‐related bone disease

The osteolytic bone disease is one of the symbolized manifestations of MM. The aberrant bone formation process is caused by disturbance of the balance between the bone‐repairing osteoblasts and bone‐resorbing osteoclasts (Figure 4). ⁵³ Through the cell contact between MM cells and BMSCs, high levels of osteoclastogenic stimuli have been produced, mainly including receptor activator of NF‐κB ligand (RANKL). RANKL binds to the receptor activator of NF‐κB (RANK) on the surface of osteoclasts, stimulating their differentiation and promoting their activity. Osteoprotegerin (OPG) performs as a decoy RANK receptor to prevent the binding of RANKL and RANK, inhibiting the process of osteoclastogenesis. ⁸ However, the interaction between MM cells with BMSCs and osteoblasts can decrease the level of OPG and increase the expression of RANKL. The serum level of soluble RANKL/OPG ratio is associated with bone resorption and osteolytic lesions. ⁵⁴ Macrophage inflammatory protein‐1α (MIP‐1α) is an osteoclast stimulator secreted by MM cells and is related to bone destruction in MM. MIP‐1α interacts with its receptor and then induces the production of osteoclasts. ⁵⁵ Besides, TNF‐α produced by MM cells is associated with the activation of a number of signaling pathways, not only enhancing the growth of MM cells, but also promoting the differentiation of osteoclasts. ⁵⁶

FIGURE 4.

Disturbance of the balance between the bone‐repairing osteoblasts and bone‐resorbing osteoclasts leads to myeloma‐related bone disease. The interaction between the bone marrow microenvironment and MM cells induces the release of cytokines and pro‐osteoclastogenic factors, increasing osteoclast activity and inhibiting osteoblastogenesis (Copyright 2018, Springer Nature ⁵³ )

In contrast to the increased activity of osteoclasts, differentiation and activity of osteoblasts have been severely impaired and then fail to repair bone destruction. The Wnt/β‐catenin cascade is a conserved signaling pathway and plays a dominant role in regulating the proliferation, survival, and differentiation of osteoblasts, responsible for the balance between bone forming and bone resorbing. ⁵⁷ The secretion of Wnt antagonists can disturb the balance in the BM and lead to the development of osteolytic bone lesions. A high level of dickkopf‐1 (DKK‐1), the canonical Wnt inhibitor, has been found to be related to decreased bone formation and the presence of bone lesions in animal models and patient samples. ⁵⁸ In addition, Wnt signaling also plays a more indirect role in influencing the RANK/RANKL/OPG signaling axis. Other factors, such as sFRP‐2, sclerostin, and activin‐A, impede the production of osteoblasts. Releasing of TGF‐β, IL‐17, IL‐3, and IL‐6 also collaborates to impair the balance of bone formation. ⁵⁹ It is conceivable that through these intensive studies, the pathogenesis and molecular mechanisms have been deciphered, thus, providing more strategies for the treatment of MM.

3. CURRENT TREATMENTS FOR MULTIPLE MYELOMA

With the presence of PIs, immunomodulatory drugs (IMiDs), monoclonal antibodies (mAbs), and novel therapies, the PFS and OS of MM have been significantly improved in recent decades. ⁴ MM has a great variety of genetic abnormalities, and there is a crosstalk between intracellular signaling pathways, making it a complicated network. The primary goals of MM treatment are to control disease progression, suppress malignancy over the long term, mitigate disease‐related complications, and increase survival. Combination therapies are effective strategies to achieve favorable outcomes. The treatment process usually includes induction, consolidation, and maintenance therapy. The eligibility for autologous stem cell transplantation (ASCT) should be evaluated according to age, comorbidities, and risk stratification of patients. The triplet therapy regimen, RVd (lenalidomide, bortezomib [BTZ], and dexamethasone), is currently a standard for initial treatment. ⁶⁰ And the quadruplet regimen with added daratumumab has gained success in high‐risk patients, followed by ASCT and lenalidomide maintenance therapy. ⁶¹ Relapse is inevitable in many MM patients. For the purpose of long‐term disease control, new generation PIs and IMiDs, including ixazomib and pomalidomide, could be preferred options for relapsed patients. ⁶² Besides, isatuximab‐containing regimens have shown promising outcomes. ⁶³ Selinexor, panobinostat, and belantamab mafodotin have been approved for second or higher relapse. And chimeric antigen receptor (CAR) T‐cell therapy has been evidenced to have unprecedented efficacy in relapsed or refractory MM (RRMM) patients as well. The optimal choice of agents can be decided depending on several factors including patient features, previous treatments, and disease characteristics. The primary treatment options and representative regimens are summarized in Table 2.

TABLE 2.

Pharmacological options for multiple myeloma

Categories	Agents	Mechanisms	Representative regimen	ClinicalTrials.gov number
Proteasome Inhibitor	Bortezomib	Inhibition of 20S proteasome; increased stress of the endoplasmic reticulum; inhibition of the NF‐κB pathway	Bortezomib, lenalidomide, and dexamethasone	NCT00644228
	Carfilzomib		Carfilzomib, lenalidomide, and dexamethasone	NCT01863550
	Ixazomib		Ixazomib, lenalidomide, and dexamethasone	NCT01850524
	Marizomib		Marizomib and dexamethasone	NCT00461045
	Oprozomib		Oprozomib and dexamethasone	NCT01832727
Immunomodulatory drug	Thalidomide	Targets cereblon; immunomodulatory effect	Thalidomide, bortezomib, and dexamethasone	NCT01134484
	Lenalidomide		Bortezomib, lenalidomide, and dexamethasone	NCT00644228
	Pomalidomide		Pomalidomide, bortezomib, and dexamethasone	NCT01734928
Monoclonal antibody	Daratumumab	Anti‐CD38 monoclonal antibody	Daratumumab, bortezomib, and dexamethasone	NCT02136134
	Isatuximab		Isatuximab, pomalidomide, and dexamethasone	NCT02990338
	MOR202		MOR202, pomalidomide/lenalidomide, and dexamethasone	NCT01421186
	Elotuzumab	Anti‐SLAMF7 monoclonal antibody	Elotuzumab, pomalidomide, and dexamethasone	NCT02654132
	BHQ880	Anti‐DKK‐1 monoclonal antibody	BHQ880, zoledronic acid, and anti‐myeloma therapy	NCT00741377
CAR T‐cell therapy	Idecabtagene vicleucel	CAR T‐cell therapy targets BCMA	Monotherapy	NCT02658929
	Ciltacabtagene autoleucel		Monotherapy	NCT03548207
Small‐molecule inhibitor	Panobinostat	Inhibition of pan‐deacetylase	Panobinostat, bortezomib, and dexamethasone	NCT01023308
	Ricolinostat	Selectively inhibition of histone deacetylase 6	Ricolinostat, bortezomib, and dexamethasone	NCT01323751
	Venetoclax	Inhibition of BCL‐2	Venetoclax, dexamethasone	NCT01794520
	Selinexor	Inhibition of exportin 1	Selinexor, dexamethasone	NCT02336815
	Filanesib	Inhibition of kinesin spindle	Filanesib, pomalidomide, and dexamethasone	NCT02384083
Other novel therapies	Belantamab mafodotin	Antibody‐drug conjugate targets BCMA	Monotherapy	NCT03525678
	AMG 420	Bispecific T‐cell engager targets BCMA and CD3	Monotherapy	NCT02514239
	Teclistamab	Bispecific antibody binds to BCMA and CD3	Monotherapy	NCT03145181

3.1. Pharmacological therapy

3.1.1. Proteasome inhibitors

The proteasome regulates protein catabolism through the ubiquitin‐proteasome pathway. The 20S proteasome core is the vital catalytic site for degrading deubiquitinated proteins and releasing oligopeptides. ⁶⁴ PIs are one of the most promising agents for NDMM patients and RRMM patients, and several mechanisms of action have been demonstrated. When the proteasome function is inhibited, proteins inside cells accumulate in the cytoplasm, leading to the increased stress of the endoplasmic reticulum, disrupting cell‐cycle signals, and activating apoptotic pathways. ⁶⁵ Another mechanism is the inhibition of NF‐κB activity. PIs can inhibit the degradation of the inhibitor of NF‐κB, thus, blocking the progression of the disease. ³²

BTZ is a first‐in‐class PI that has been approved by the FDA since 2003. ⁶⁶ BTZ‐based regimens have been the first‐line and cornerstone option for MM. BTZ leads to apoptosis directly, inactivates the NF‐κB pathway, inhibits the production of IL‐6 and IGF‐1, and prevents the adherence of myeloma cells to the BM microenvironment. ⁶⁷ In clinical trials, BTZ‐based regimens have achieved a high overall response rate (ORR), and prolonged PFS and OS. ⁶⁸ A phase 3 clinical trial recruited patients at 139 institutions and randomized them into the RVd group or the Rd (lenalidomide and dexamethasone) group. The median PFS was meaningfully longer in the RVd group than that in the Rd group. And the median OS was also greatly improved in the RVd group. ⁶⁹ After longer follow‐up, the updated report included 460 patients for survival endpoints analysis. The PFS in RVd group was 41 months, while in the Rd group, it was 29 months. ⁷⁰ The RVd regimen results in a clinically meaningful improvement and occupies a vital position in treatment approaches for MM. Adverse effects of BTZ include fatigue, gastrointestinal symptoms, thrombocytopenia, and peripheral neuropathy. A study compared the efficacy of subcutaneous and intravenous BTZ in induction therapy for NDMM patients. After long‐term follow‐up, subcutaneous BTZ was not inferior to intravenous BTZ. Moreover, the occurrence of nervous system disorders during maintenance therapy decreased in patients treated with subcutaneous BTZ. ⁷¹

Carfilzomib is a second‐generation PI indicated for MM patients who exhibit invalidation or relapse after receiving at least two kinds of drugs. ⁷² The mechanism of carfilzomib is different from that of BTZ, which binds to the chymotrypsin‐like proteasome site irreversibly and exclusively, leading to apoptosis consequently. ⁷³ The single‐agent clinical trial of carfilzomib showed that the ORR was 23.7% in 257 heavily pretreated patients. And the median OS was 15.6 months. ⁷⁴ Adding carfilzomib with lenalidomide and dexamethasone (KRd) demonstrated superior benefits over the control group. The PFS in the carfilzomib group was 26.3 months compared to 17.6 months in the control group. ⁷⁵ Carfilzomib has notably extended the PFS while the rate of adverse events was slightly higher. These results indicated durable responses of carfilzomib in RRMM patients. A large group of NDMM patients were randomized to receive either the RVd regimen or the KRd regimen. The median PFS was 34.6 months in the KRd group and 34.4 months in the RVd group. The KRd group did not show a better outcome in NDMM patients, and the treatment‐related adverse events occurred more frequently in the KRd group. ⁷⁶ In addition, the safety profile of carfilzomib was analyzed from four phase 2 trials. The most common grade 3 or higher adverse events were thrombocytopenia, anemia, lymphopenia, and pneumonia. Aggregated cardiac failure events were reported in 7.2% of patients. Overall, the results indicated a tolerable safety profile of carfilzomib in patients. ⁷⁷

Ixazomib is an orally administrated, reversible PI that acts by inhibiting the chymotrypsin‐like activity of the β5 subunit of the 20S proteasome. ⁷⁸ In a phase 3 randomized clinical trial, the ORR was 78.3% in the IRd (ixazomib, lenalidomide, and dexamethasone) group compared with 72% in the placebo‐Rd group in RRMM patients. The median duration of response and PFS in the IRd group was longer than that in the placebo‐Rd group. Meanwhile, the IRd group showed a substantial benefit in high‐risk patients. Regarding safety, adverse events of grade 3 and higher happened in 74 and 69% of the patients in each group. ⁷⁹ , ⁸⁰ Nevertheless, after longer follow‐up, there was no statistically significant benefit of OS in the IRd group. In a clinical trial that recruited transplant‐ineligible NDMM patients, the median PFS was 35.3 months in the IRd group and 21.8 months in the placebo‐Rd group, with primarily tolerable safety profiles. ⁸¹ This oral combination regimen can be a feasible choice for these patients. Besides, some other compounds are underway. Marizomib is an irreversible PI, and a phase I trial demonstrated its safety and activity in RRMM patients. ⁸² Oprozomib is orally administrated, and antimyeloma activity has been identified in NDMM patients while accompanied by gastrointestinal toxicities. ⁸³

3.1.2. Immunomodulatory drugs

The IMiDs have been reported to target the cereblon ubiquitin ligase and lead to the degradation of Ikaros family zinc finger proteins 1(IKZF1) and 3 (IKZF3), thus, downregulating the downstream targets including the expression of IRF4. ⁸⁴ Besides, IMiDs have been evidenced to reduce the production of IL‐6 and IL‐16, increase IL‐2, interfere with the interaction between BMSCs and MM cells, and exhibit antitumor and immunomodulatory effects. ⁸⁵ , ⁸⁶ Thalidomide is the first IMiD used in MM, and now this drug is still a member of several regimens combined with BTZ, melphalan, and dexamethasone. In a randomized phase 3 study, patients received thalidomide and dexamethasone (Td) regimen, either alone or with BTZ (VTd), followed by ASCT and VTd or Td consolidation therapy. The 10‐year‐PFS was 34% in the VTd group and 17% in the Td group. ⁸⁷ The second‐generation IMiD, lenalidomide, has a potent immunomodulatory effect in the costimulation of T cells. ⁸⁸ This drug was initially approved for RRMM combined with dexamethasone. A complete or partial response in the lenalidomide group was 60.2%, which was significantly better than that in the placebo group. ⁸⁹ Thereafter, the carfilzomib, lenalidomide, and dexamethasone regimen were evidenced to be tolerable and highly effective, demonstrating favorable rates of minimal residual disease (MRD) negativity in NDMM. ⁹⁰ Currently, lenalidomide‐based regimens are fundamental and valuable for MM. The combination of lenalidomide and several PIs, mAbs, or other novel agents has been explored in clinical trials. ⁸¹ , ⁹¹

For lenalidomide‐refractory patients, pomalidomide is a suitable option. Pomalidomide can mitigate lytic bone disease, and the anti‐inflammatory effect has also been demonstrated. ⁹² Pomalidomide with low‐dose dexamethasone is efficacious for myeloma patients who have received more than two prior therapies. The median PFS and OS were 4.2 months and 16.5 months, respectively, and ORR was 33%. ⁹³ Scholars assessed the safety and efficacy of cyclophosphamide, pomalidomide, and dexamethasone regimen. The median PFS was 9.5 months, and the ORR was 64.7% in this triplet group. This combination therapy showed a superior efficacy to the pomalidomide and dexamethasone regimen. ⁹⁴ Another triplet regimen containing pomalidomide, BTZ, and dexamethasone (PVd) has been investigated. The ORR among all evaluable patients was 86%, with a stringent complete response of 12%, and the median PFS was 13.7 months. ⁹⁵ In the OPTIMISMM trial, which was a randomized phase 3 multicentre clinical trial, the median PFS was 11.2 months in lenalidomide‐refractory patients when treated with PVd regimen, compared with 7.1 months in the BTZ and dexamethasone group. ⁹⁶ This result indicated that the PVd combination therapy is a manageable and efficacious option for lenalidomide‐refractory patients. Since the synergistic efficacy between PIs and IMiDs, pomalidomide has been studied in combination with carfilzomib and dexamethasone. And the combination therapy showed acceptable safety profiles. ⁹⁷ In addition, once‐weekly carfilzomib, pomalidomide, and dexamethasone were assessed. The median PFS was 10.3 months, and the median OS was not reached, with a median follow‐up of 12.8 months. Any grade adverse events included neutropenia, thrombocytopenia, anemia, infections, and vascular events. ⁹⁸

3.1.3. Monoclonal antibodies

CD38 is a glycoprotein that acts as an extracellular enzyme. ⁹⁹ It is related to cell adhesion and cytokine secretion, and is expressed highly and coincidently on MM cells, making it a potential target. ¹⁰⁰ Daratumumab is an immunoglobulin G1 kappa mAb that binds to CD38. ¹⁰¹ Daratumumab monotherapy has exhibited encouraging efficacy in heavily pretreated patients. The ORR was 29.2%, and the median PFS was 3.7 months. ¹⁰² A study performed a pooled analysis of two daratumumab monotherapy trials, in which 86.5% of patients were double refractory to a PI and an IMiD. This pooled analysis indicated a clinical benefit with deep and durable responses of daratumumab monotherapy. Common adverse events included fatigue, upper respiratory tract infection, nausea, anemia, back pain, and thrombocytopenia. The infusion‐related reactions (IRRs) occurred in 48% of patients, and mostly during the first infusion. ¹⁰³ In addition, daratumumab has shown decisive action when combined with BTZ and dexamethasone. ¹⁰⁴ The PFS in the Dara‐Vd (daratumumab, BTZ, and dexamethasone) group was 16.7 months, while it was only 7.1 months in the BTZ and dexamethasone group. Even in the high cytogenetic risk subgroup, the PFS was greatly prolonged in the Dara‐Vd group. Besides, the rate of MRD negativity was also significantly improved, demonstrating favorable clinical benefit. ¹⁰⁵ , ¹⁰⁶ The POLLUX trial evaluated another triplet regimen, Dara‐Rd (daratumumab, lenalidomide, and dexamethasone). The PFS was 44.5 months in the Dara‐Rd group compared to 17.5 months in the control group, and the ORR in the Dara‐Rd group was 92.9%, accompanied with deep responses. ¹⁰⁷ To relieve IRRs, subcutaneous infusion of daratumumab has been applied, with recombinant human hyaluronidase enzyme. A total of 522 patients were recruited in the COLUMAB trial, and the ORR was 41% in the subcutaneous group compared with 37% in the intravenous group, indicating that the subcutaneous formulation was noninferior to the intravenous formulation with an improved safety profile. ¹⁰⁸ In addition, the four‐drug regimen incorporating daratumumab, BTZ, lenalidomide, and dexamethasone has been adopted for transplantation‐eligible NDMM patients, aiming for more profound disease responses. ⁹¹ These inspiring results support the status of daratumumab‐based regimens for both RRMM and NDMM patients.

Isatuximab is another antibody that binds to CD38 and targets an amino acid sequence different from that of daratumumab. ¹⁰⁹ Isatuximab monotherapy showed an ORR of 23.9% in RRMM patients, and when combined with dexamethasone, the ORR was 43.6%. ¹¹⁰ A multicentre phase 3 clinical trial recruited 307 patients to determine the PFS benefit of isatuximab, pomalidomide, and dexamethasone combinational therapy. This triplet regimen significantly improved the PFS, with a median PFS of 11.5 months. ⁶³ IRRs, upper respiratory tract infections, and diarrhea were the most common adverse events. The combination of isatuximab and PIs has also been assessed. The addition of isatuximab to carfilzomib and dexamethasone regimen showed improved PFS and depth of response in RRMM patients. ¹¹¹ Isatuximab has become an important new treatment option for the management of this population.

Elotuzumab binds to signaling lymphocytic activation molecule family member 7 (SLAMF7), which is expressed in NK cells and myeloma cells. ¹¹² Elotuzumab has been shown to eliminate myeloma cells by downregulating target expression and inducing NK cell‐mediated antibody‐dependent cell cytotoxicity. ¹¹³ The combination of elotuzumab and lenalidomide was reported to enhance NK cell function and myeloma cell killing efficacy, with increased secretion of IL‐2 and production of TNF‐α. ¹¹⁴ In a clinical trial, the elotuzumab, pomalidomide, and dexamethasone regimen showed prolonged PFS. ¹¹⁵ Furthermore, aberration of the Wnt/β‐catenin cascade has been involved in the progression of MM. BHQ880 is a DKK‐1 neutralizing antibody, and Fulciniti et al. reported that BHQ880 could increase osteoblast differentiation and decrease IL‐6 secretion. ¹¹⁶ BHQ880 combined with antimyeloma therapy and zoledronic acid was tolerable and demonstrated potential activity in RRMM patients. ¹¹⁷

3.1.4. Chimeric antigen receptor T‐cell therapies

CAR T‐cell therapy possesses a high status and revolutionizes the treatment of hematological malignancies. Autologous T cells adopted from MM patients have been engineered with CARs to recognize specific antigens and then transfused back into patients. ¹¹⁸ The CARs usually consist of an antigen‐binding domain, followed by a hinge and transmembrane domain. The signaling domains include costimulatory domain and activation domain, which are essential for activating cytokine production and cytolytic capacity. ¹¹⁹ In addition, choosing a proper target is vital, and B‐cell maturation antigen (BCMA), CD38, and CD19 are attractive targets in MM. ¹²⁰ , ¹²¹ A group of patients who received salvageable therapy and ASCT were injected with anti‐CD19 CAR T‐cells, and 2 of 10 patients showed significantly longer PFS. ¹²² BCMA belongs to the TNF receptor superfamily. ¹²³ Besides, BCMA is significantly expressed in malignant cells and a limited portion of nonmalignant cells, including plasma cells and a small subset of B cells, leading to activation of the NF‐κB pathway, and multiple‐step progression in MM patients. ¹²⁴ Idecabtagene vicleucel (Bb2121) is the first anti‐BCMA CAR T‐cell product approved by the FDA in 2021, which consists of an anti‐BCMA single‐chain variable fragment, a 4‐1BB costimulatory motif, and a CD3‐zeta signaling domain. In a phase 1 trial, the ORR was 85%, and 45% of patients achieved a complete response. Hematologic toxic effects were common events, and cytokine release syndrome occurred in 76% of patients. ¹²⁵ In a phase 2 study, 128 patients received Bb2121 with a median follow‐up over 1 year. The ORR was 73%, and 33% of patients had a complete or better response. Besides, the median PFS was 8.8 months, and 33 of 128 patients achieved MRD‐negative status. Toxic effects occurred in almost all patients, and the rate of cytokine release syndrome was 84%. ¹²⁶ In addition to Bb2121, the second anti‐BCMA CAR T‐cell product, Ciltacabtagene autoleucel, has been approved recently, and plenty of CAR T‐cell therapies targeting BCMA or other targets are in active development. ¹²⁷

3.1.5. Small‐molecule inhibitors

Some subgroups of MM patients, including frail elderly, high‐risk, and refractory patients, remain suboptimal in survival outcomes. And novel agents are needed to improve the prognosis further. The histone deacetylase inhibitors (HDACis), such as panobinostat and ricolinostat, have emerged as important choices. ¹²⁸ Histone deacetylase has been evidenced to be overexpressed in neoplasm cells and associated with poor prognosis. ¹²⁹ Furthermore, HDACis have exhibited the ability to induce differentiation and inhibit migration, invasion, and tumor growth in both animal models and patients. ¹³⁰ Panobinostat is an oral pan‐deacetylase inhibitor, the panobinostat, BTZ, and dexamethasone regimen was compared with the BTZ and dexamethasone regimen. The panobinostat group showed a longer PFS and a higher complete or near complete response rate. Nevertheless, serious adverse events were reported more in the panobinostat group, and common adverse events included thrombocytopenia, lymphopenia, diarrhea, asthenia or fatigue, and peripheral neuropathy. ¹³¹ Another study combined oral panobinostat and dexamethasone with subcutaneous BTZ. The ORR in the panobinostat (20 mg), three‐times‐weekly group was 62.2%, and the result indicated a favorable safety profile. ¹³² In addition, the panobinostat and carfilzomib combination therapy resulted as a practical steroid‐sparing choice for RRMM. ¹³³ Ricolinostat is an HDAC6‐selective inhibitor, and the ricolinostat, BTZ, and dexamethasone combination therapy was tolerable at a ricolinostat dose of 160 mg daily, suggesting an acceptable safety profile and efficacy as well. ¹³⁴

The BCL‐2 protein family regulates the apoptosis pathway, and the abnormal expression or dysfunction of the BCL‐2 protein family is associated with carcinogenesis and resistance to anticancer drugs. ¹³⁵ BCL‐2 and MCL‐1, which belong to the prosurvival BCL‐2‐like proteins, represent attractive targets. ¹³⁶ Venetoclax is a highly selective BCL‐2 inhibitor and has demonstrated impressive results in clinical trials by directly provoking apoptosis of tumor cells. ¹³⁷ In a multicentre study, the combination of venetoclax and dexamethasone demonstrated efficacy and safety in heavily pretreated t(11;14) RRMM patients, with an ORR of 60% in phase 1 and 48% in phase 2. ¹³⁸ The venetoclax, BTZ, and dexamethasone regimen showed a median PFS of 22.4 months, notably longer than that in the placebo group. ¹³⁷ However, the rate of adverse events was higher in the venetoclax group, with increased mortality, limiting this treatment option.

Exportin 1 (XPO1) is responsible for the nuclear export of more than 200 proteins, many of which are tumor suppressor proteins, and XPO1 is overexpressed in several tumor cells. ¹³⁹ Selinexor is the first XPO1 inhibitor approved by the FDA for RRMM. ¹⁴⁰ In triple‐class refractory patients, selinexor plus dexamethasone achieved a partial or better response of 26%, with two stringent complete responses. The median PFS and OS were 3.7 months and 8.6 months, respectively, demonstrating a favorable efficacy for these heavily pretreated and refractory patients. ¹⁴¹ The combination of once‐per‐week selinexor with BTZ and dexamethasone was assessed. The median PFS was 13.9 months in this triplet regimen and 9.5 months in the BTZ and dexamethasone regimen. Despite that, adverse events occurred more frequently in the selinexor group including thrombocytopenia, anemia, fatigue, and pneumonia. ¹⁴² Thereafter, patients treated with selinexor need supportive management properly. In addition, the combination of selinexor with carfilzomib is under exploration. ¹⁴³

3.1.6. Other novel therapies

Immunotherapy has been a powerful strategy in tumor treatment. This approach may be the key to regaining immune balance and generating durable control of myeloma. ¹⁴⁴ In addition to mAbs and CAR T‐cell therapies, bispecific T‐cell engagers have been introduced into preclinical studies and clinical trials. AMG‐420 is a bispecific T‐cell engager that binds to BCMA on target cells, leading to T cell‐mediated lysis. The first‐in‐human study showed an ORR of 70% while requiring continuous infusions. ¹⁴⁵ Teclistamab is a humanized bispecific antibody that binds to BCMA and CD3, and demonstrated promising efficacy and durable responses in a phase 1 study. ¹⁴⁶ An antibody‐drug conjugate is the combination of a recombinant mAb with a cytotoxic chemodrug. ¹⁴⁷ It first binds to the target and then delivers the cytotoxic agent into myeloma cells. Belantamab mafodotin targeting BCMA showed 31 and 34% overall response in different dose cohorts in a two‐arm phase 2 study. ¹⁴⁸ The most common adverse events included anemia, keratopathy, and thrombocytopenia. As more agents are approved, more studies are needed to properly incorporate these strategies with present therapies, and reduce treatment‐related toxicities.

3.2. Autologous stem cell transplantation

Although numerous therapeutic agents have been introduced for the treatment of myeloma, ASCT is still a cornerstone in MM after initial treatment. Hematopoietic stem cells are mobilized into peripheral blood by granulocyte colony‐stimulating factors with or without chemotherapy. The CD34⁺ stem cells are collected at least 2 × 10⁶ cells/kg. After that, patients receive conditioning therapy, with high‐dose melphalan at the 200 mg/m² level as the standard regimen. Other reduced dose levels, such as 140 mg/m², are always considered for patients who are older than 65 and have worse renal function. ¹⁴⁹ A study reported that the at least very good partial response rate in the melphalan (200 mg/m²) group was higher than that in the lower dose group, and melphalan (200 mg/m²) was associated with a lower disease progression rate. ¹⁵⁰ Other clinical trials are now investigating combination regimens for conditioning therapy, for instance, busulfan in combination with melphalan. ¹⁵¹ Debates on the role of ASCT still exist, and several clinical trials have demonstrated enhanced responses and survival benefits. Attal et al. reported that ASCT after the RVd combination therapy was associated with a higher complete response and a longer PFS than RVd therapy alone. ¹⁵² Recently, a study pooled four randomized clinical trials for conventional meta‐analysis and five randomized clinical trials for network meta‐analysis. The results indicated that high‐dose melphalan, followed by ASCT was associated with superior PFS compared to standard‐dose therapy using novel agents, while there was no OS benefit. ¹⁵³ In addition, the optimal timing for ASCT and whether single or tandem ASCT still remains to be determined. Ongoing studies and long‐term follow‐up will continue to figure out a favorable profile to apply ASCT properly for patients with different risk profiles and performance status.

4. NANOMEDICINE‐BASED STRATEGIES FOR MULTIPLE MYELOMA

Despite the advances of effective managements, many MM patients eventually relapse and develop resistance to drugs. ¹⁵⁴ In addition to that, systemic toxicity and adverse events are obstacles of numerous regimens. Accordingly, nanomedicine‐based strategies are underway to address these potential issues and improve the treatment efficacy of MM.

Nanomedicine is the intentional design and application of nanoscale biomaterials in the field of medicine. ¹⁵⁵ Nanobiomaterials mainly include two broad categories, organic nanomaterials and inorganic nanomaterials. ¹⁵⁶ Liposomes, micelles, and polymeric nanoparticles have been widely applied as drug carriers; metal particles, graphene, and silicon dioxide nanoparticles can serve as both nanocarriers and diagnostic tools. ¹⁵⁷ , ¹⁵⁸ , ¹⁵⁹ , ¹⁶⁰ The physicochemical properties, such as composition, size, and surface charge, can influence the process of blood circulation, biodistribution, and cellular internalization in vivo. Tailoring the properties and responsive conditions of nanomedicine provides opportunities to achieve different goals. Encapsulating drugs into nanoparticle platforms can enhance the solubility and stability, control drug release, increase drug concentration at the tumor site, and reduce side‐effects at the same time. ¹⁶¹ , ¹⁶²

The enhanced permeability and retention (EPR) effect contributes to the upgraded efficacy of nanomedicine in solid tumors, owing to the abundant generation of blood vessels and defective vascular structure inside and around neoplasms. ¹⁶³ However, the EPR effect varied among different types of tumors because of significant heterogeneity. Tumor type, size, location, surrounding environment, and mononuclear phagocytic system are critical factors correlated with the EPR effect. ¹⁶⁴ Meanwhile, pressure inside solid tumors and other biological barriers impedes the deep penetration of nanomedicine to some extent. In comparison, hematological malignancies benefit little from the EPR property. ¹⁶⁵ The long circulation property contributes to the retention of nanomedicine in the blood and BM, thus, facilitating the interaction of nanomedicine with hematological tumor cells. ¹⁶⁶ The increased angiogenesis and abundant blood flow in the BM contribute to the augmented passive accumulation. Furthermore, active targeting nanomedicine performs better among solid tumors and hematological tumors. Targeting strategies are established according to the different properties and molecular expression levels of tumors. Some specific molecules, such as peptides, antibodies, aptamers, and proteins, can be used as high‐affinity targeting agents or ligands to achieve precise treatment. ¹⁶⁷ , ¹⁶⁸ For MM, multidrug combination therapies have been broadly adopted, and codelivery of two or more drugs in one nanoparticle platform guarantees the synergistic drug ratios. In addition, nanotechnology also assists in immunotherapy and refines these strategies. ¹⁶⁹ In this section, we summarize the development and recent advances in nanomedicine‐based strategies for MM, elaborating the nanoparticle design and antitumor potency.

4.1. Liposomes

The liposome is one of the ideal and widely applied nanomaterials for drug delivery. Liposomes are composed of phospholipids and cholesterol. The aqueous core is capable of loading hydrophilic drugs, and the lipid bilayer can encapsulate hydrophobic drugs. Pegylated liposomal doxorubicin (PLD) was introduced into the market in 1995 for the treatment of MM and other tumors. ¹⁷⁰ To verify the efficacy of PLD, several clinical trials have been carried out. PLD reduced systemic toxicity, including cardiotoxicity, by long blood circulation and passive accumulation in the tumor sites. ¹⁷¹ Dexamethasone occupies an essential position in standard regimens for MM. In an advanced human‐mouse hybrid MM model, the liposomal dexamethasone showed prolonged circulation and strong tumor inhibition, while free dexamethasone was ineffective at the same dosage. ¹⁷² Other chemodrugs, such as gemcitabine, have also been loaded by pegylated unilamellar liposomes and showed increased apoptosis induction and cell proliferation inhibition compared to the free drug. ¹⁷³

To synthesize the BTZ prodrug, Ashley et al. mixed the pegylated lipids and BTZ‐conjugated lipids to obtain liposomal BTZ with a reversible boronic ester linkage. This liposomal BTZ exhibited upgraded pharmacokinetics and better efficacy in tumor growth inhibition. ¹⁷⁴ Several factors and preparation steps are essential for the design of liposomes. Entrapping agents, temperature, incubation duration, total lipid ratio, and drug concentration may change the properties. The diameter of liposomal carfilzomib was approximately 70 nm. Compared to free carfilzomib, the liposomal carfilzomib displayed improved effectiveness and decreased systemic toxicity. Notably, the combination of liposomal carfilzomib with doxorubicin (DOX) demonstrated a superior synergistic outcome than the free drug combination. ¹⁷⁵ Besides, combination therapy tends to perform synergistically at a specific drug ratio. ¹⁷⁶ The blood circulation, biodistribution, and metabolism can disturb the drug ratio when arriving at the tumor site. The application of nanomedicine‐based delivery systems ensures the maintenance of optimal synergistic ratios. Carfilzomib and DOX were loaded into liposomes at a 1:1 ratio. Although DOX and carfilzomib were released at different rates, a synergistic drug ratio was maintained between 1:1 and 2:1 in a controlled release manner and demonstrated significant tumor inhibition, achieving synergistic therapeutic efficacy. ¹⁷⁷

Choosing a suitable target is crucial and challenging for active targeting systems. Two target peptides, CD38 and CD138, were compared. CD138 is a heparin sulfate proteoglycan and is expressed on plasma cells. CD138 regulates the adherence and differentiation of MM cells, which enables it to be a therapeutic target. Although the binding ability of CD138‐targeted liposomes was better than that of CD38‐targeted liposomes in vitro, CD138‐targeted liposomes were prone to accumulate in the nontumor site and bind to normal cells, leading to worse performance in vivo. In addition, a long‐lasting period of in vivo study verified the superior efficacy of CD38‐targeted liposomes. ¹⁷⁸ A high targeting rate in vitro may not represent success in vivo, and utilization of the multivalent low‐affinity property may contribute to better binding. Chang et al. established dioleoyl phosphatidic acid (DOPA)‐based liposomes with two surface modifications, alendronate and transferrin (Tf). Both DOPA and alendronate have a bone affinity, and the Tf modification enhanced cellular uptake. This liposome demonstrated higher targeting capability and cellular uptake with pH sensitivity, around 1.6‐fold higher than the control group. Meanwhile, this system showed a higher Tf‐mediated internalization rate, enhanced apoptosis induction, and increased survival time. ¹⁷⁹ While there were some inconsistent results between in vitro and in vivo studies, the more complicated microenvironment in vivo may be the explanation.

Scholars added VLA‐4 antagonist and LPAM‐1 antagonist to the liposome surface to augment the selectivity of liposome. The two kinds of peptides on the surface of liposomes bound to myeloma cells cooperatively, and the optimal peptide density consisted of 0.75% VLA‐4 peptide and 1% LPAM‐1 peptide, demonstrating 28‐fold cellular uptake compared to the nontargeted liposome and approximately ten times over either one targeted liposome. ¹⁸⁰ Such excellent performance in vitro may promote further exploration and application of this system. BTZ was combined with Rho‐kinase inhibitor Y27632, a BM microenvironment‐disrupting agent, and both were loaded in liposomes targeting P‐selectin. ¹⁸¹ Rho‐kinase is a downstream target of the MM‐BM microenvironment interaction signaling pathway, and this system attempted to target the tumor‐associated endothelium rather than tumor cells. ¹⁸² With the precise targetability and combinational delivery in vivo, the efficacy was more dramatic than that of other formulations. This approach achieved the goal of increasing treatment sensitivity and overcoming the BM microenvironment‐induced drug resistance.

The liposomal bispecific T‐cell engager (nanoBiTE) was decorated with anti‐CD3 mAb and anti‐CD20 mAb to target T cells and tumor cells. ¹⁸³ In an aggressive Waldenstrom macroglobulinemia mouse model, the CD20/CD3 nanoBiTE group achieved eradication of the disease by day 35. Furthermore, scholars developed liposome‐based multispecific T‐cell engagers (nanoMuTEs), decorating with anti‐CD3 mAbs and multiple mAbs, including anti‐BCMA, anti‐CS1, and anti‐CD38 mAbs, against myeloma cells simultaneously. The nanoMuTEs had a long half‐life of 50–60 h, and this multispecific formulation was able to prevent the antigen‐less tumor escape. Meanwhile, nanoMuTEs exhibited a prolonged survival time in MM mouse models of approximately 10–20 days. This platform created a specific and efficacious immunotherapy strategy.

4.2. Micelles

Micelles are self‐assembled nanocarriers formed by amphiphilic polymers. A polymeric micelle using polyethylene glycol (PEG)‐polycaprolactone (PCL) blocks increased the stability of carfilzomib in MM cells and lung cancer cells. ¹⁸⁴ Zhang et al. developed core‐disulfide‐crosslinked micelles with A6 peptide‐tagged (A6‐PMs). ¹⁸⁵ The system increased the stability of the drug and controlled drug release according to the glutathione level. More importantly, improved tumor inhibition and better tolerance compared to the free formulation provide favorable indications for these studies. Another VLA‐4‐targeted micelle incorporated with a novel camptothecin prodrug aimed to solve cell adhesion‐mediated drug resistance. Once the nanoparticle arrived at the target, it fused with the cell membrane and transferred the payload into the cell. This system decreased tumor burden in vivo without causing severe toxicity, and provided a strategy to treat chemoresistant myeloma in combination with free chemotherapy. ¹⁸⁶

5‐Aza‐2ʹ‐deoxycytidine (DAC) belongs to deoxycytidine analogs, which can activate methylated and silenced genes by promoter demethylation. ¹⁸⁷ DAC and BTZ were encapsulated into NH₂‐PEG‐PCL nanoparticles simultaneously. The dual‐drug micelle showed good stability and slow‐release properties, inducing reactive oxygen species (ROS) release and apoptosis at the cellular level. ¹⁸⁸ LP‐1 human MM cells overexpress CD44, and hyaluronic acid has a high affinity for CD44 on the cell surface. The lipophilized BTZ was encapsulated in the hyaluronic acid‐shelled and core‐disulfide‐crosslinked micelle. Because of the enhanced hydrophobic interaction, the loading efficacy was markedly increased and exhibited quick intracellular release. This complex inhibited tumor growth better than free BTZ at the same dose level, and more importantly, showed high toleration. Moreover, this platform prolonged the survival time compared with liposomal BTZ as well. ¹⁸⁹

4.3. Polymeric nanoparticles

Polymeric nanoparticles are formed by natural or synthetic polymers. The preparation process of nanoparticles can be manipulated with pH level, temperature, solvent conditions, and targetability, aiming to tailor the properties to meet variable goals. In addition, therapeutic agents can be encapsulated, conjugated, or attached to the core or surface of nanoparticles. Zhong et al. encapsulated DOX in lipoic acid‐crosslinked hyaluronic acid nanoparticles, and the disulfide crosslink structure helped stabilize the nanoparticles. The release of the DOX nanoparticle was mainly concentrated at the tumor site rather than in normal organs or tissues. ¹⁹⁰ Several immunotherapy modalities targeting BCMA have emerged for durable and deep responses. ¹⁹¹ Nevertheless, patient‐specific procedures require complicated protocols, which limit wide applications. An off‐the‐shelf vaccine can reduce the workload and promote the activation of effective T cells. Bae et al. found an immunogenic BCMA_72‐80 [YLMFLLRKI] peptide and developed nanoparticle‐based BCMA delivery systems. The poly(lactic‐co‐glycolic acid) (PLGA)‐based nanoparticles showed gradual increased uptake by antigen‐presenting cells, and exhibited the highest polyfunctional antitumor activity, with CD107a degranulation‐based cytotoxicity and production of cytokines. It evoked higher proliferation of CD8⁺cytotoxic T cells and antimyeloma effect than the free BCMA peptide. ¹⁹² This nanoparticle‐based cancer vaccine can be utilized to maintain a long‐lasting immune response. Guo et al. formulated the PLGA/polyethyleneimine nanoparticles containing programmed cell death ligand 1 (PD‐L1) and DKK‐1 antigens. ¹⁹³ This formulation activated the responses of dendritic cells and T cells, which were essential for antitumor activity.

Active targeting strategies have excellent potential to realize precise accumulation of delivered drugs in the ideal site. Multiple avenues for active targeting strategies have been established with nanoparticles. The CD44‐specific A6 short peptide (KPSSPPEE) showed a solid affinity for CD44. Gu et al. encapsulated epirubicin into the functionalized A6‐polymersome (A6‐PS‐EPI). A6‐PS showed high drug loading ability with a simplified fabrication process. An in vivo study showed that the median survival was 240 days in the group treated with A6‐PS‐EPI and 72 days in the nontargeted PS‐EPI group, demonstrating striking efficacy. ¹⁹⁴ Granzyme B, the key player in NK cells, was loaded in the hyaluronic acid‐directed reduction‐responsive chimeric polymersome (HA‐RCP‐GrB). With the property of reduction‐triggered protein release and CD44 targetability, HA‐RCP‐GrB achieved a noticeable survival benefit and less weight loss than nontargeted polymersomes and blank control groups in both subcutaneous and orthotopic mouse models. Besides, decreased osteolysis in the BM was identified. ¹⁹⁵ In summary, these platforms improved the antitumor effect and tolerability of free drugs, providing a new avenue.

Daratumumab immunopolymersomes loaded with vincristine sulfate (Dar‐IPs‐VCR) showed superb stability, efficacious vincristine (VCR) loading rate, high targetability, and glutathione‐responsive release property. It exhibited a particular binding ability to CD38‐positive MM cells in the BM with sequential release of VCR through the glutathione‐triggered mechanism to inhibit microtubule formation and cause cell apoptosis. Dar‐IPs‐VCR completely depleted LP‐1‐Luc cells in the orthotopic MM model in vivo, with no bodyweight loss and less bone damage. ¹⁹⁶ Puente et al. labeled anti‐CD38 mAbs with biotin to obtain the CD38‐targeted nanoparticles loaded with BTZ. The chitosan nanoparticle had an increasable swelling property in the MM‐conditioned microenvironment, presenting with a faster release, and the 50 nm size allowed deep penetration. The CD38‐targeted nanoparticles were taken up fourfold by CD38‐positive myeloma cells than by normal cells and entered target cells through endocytosis, resulting in a much higher drug concentration. ¹⁹⁷ The STAT3 inhibitor is limited by its poor hydrophilic property and severe adverse events in clinical application. To overcome these defects, Huang et al. loaded S3I‐1757, a STAT3 inhibitor, into anti‐CD38 decorated nanoparticles. The researchers used a covalent thioester bond to conjugate the antibody and exhibited higher stability than biotinylation conjugations. The IC₅₀ of CD38‐targeted S3I‐1757 nanoparticle was significantly lower. The nanoparticle minimized the tumor volume more efficiently than the free inhibitor, and showed increased bioavailability of the drug. ¹⁹⁸

Bisphosphonates are pyrophosphate analogs, and they can selectively bind to the surface of bone owing to their affinity for hydroxyapatite crystals. Bisphosphonates are also able to inhibit the progression of osteoclastic activity and are capable of inhibiting tumor cell adhesion and migration, acting as supportive agents. ¹⁹⁹ Due to the affinity for the bone surface of alendronate, Swami and coworkers reported a nanoparticle system with bone tissue orienting and microenvironment manipulation properties. In biodistribution studies, this bone‐targeted nanoparticle showed a 9.6‐fold accumulation compared to the nontargeted one. The targeted nanoparticle loaded with BTZ (Ald‐BTZ‐NP) contributed to bone formation and decreased tumor burden in the xenograft osteolytic bone disease model, demonstrating a promising benefit in MM treatment. ²⁰⁰

4.4. Inorganic nanoparticles

Inorganic nanoparticles have attracted great attention in the nanomedicine area, exhibiting unique features. Metal nanoparticles have high stability, high purity, optical and electromagnetic properties, and the surface can be easily modified. Zhang et al. developed iron oxide magnetic nanoparticles (MNPs) with modified dimercaptosuccinic acid. BTZ and gambogic acid (GA) were encapsulated in MNPs. The combination platform of BTZ‐GA/MNPs showed increased inhibition of cell proliferation, as well as induction of cell apoptosis. ²⁰¹ In comparison, free BTZ and GA had a mild antitumor effect at the equivalent dose level. Since the poor water solubility limits the clinical utilization of paclitaxel, researchers synthesized paclitaxel‐loaded Fe₃O₄ nanoparticles (PTX‐NPs). ²⁰² The PTX‐NP group showed the strongest tumor volume inhibition among other groups. ²⁰³ Moreover, superparamagnetic iron oxide nanoparticles (SPIONs) were utilized as a magnetic hyperthermia treatment, which induced endoplasmic reticulum stress and caused MM cell death. ²⁰⁴ In addition, SPIONs combined tumor imaging with targeted treatment. Coating with folic acid, SPIONs selectively accumulated in the tumor site, localized the tumor by MRI, and generated heat to selectively kill tumor cells in mouse plasmacytoma models. ²⁰⁵ Much work has been done to refine the properties of VCR because of its high lipophilicity and severe side‐effects. ²⁰⁶ A gold nanoparticle loaded with low‐dose VCR reduced the risk of side‐effects, in which the nanomaterial acted as both a carrier and a combinational drug component, arresting cells at the S phase. ²⁰⁷ The radionuclide ⁸⁹Zr naturally homes to the bone and could be used to sensitize the therapeutic effects of drugs. ²⁰⁸ Titanium dioxide (TiO₂) nanoparticles coated with Tf and radiolabeled with ⁸⁹Zr were able to target the BM and image the distribution of nanoparticles in mouse models. Besides, in the presence of ⁸⁹Zr, the TiO₂ nanoparticles were able to generate ROS and induce cell death through the apoptosis pathway. ²⁰⁹

Silica is a safe and biocompatible inorganic material, and mesoporous silica nanoparticles (MSNs) are easily degraded and expelled from urine. ²¹⁰ Nigro et al. grafted folic acid on the surface of MSN and then encapsulated BTZ in the nanoparticle (FOL‐MSN‐BTZ). ²¹¹ FOL‐MSN‐BTZ affected the metabolic pathway of MM cells by damaging mitochondrial function, decreasing ATP levels, and concurrently increasing ROS production. Meanwhile, FOL‐MSN did not impact the metabolism of normal cells, guaranteeing the safety profile of the material. This drug delivery system increased the therapeutic index and provided a safe treatment choice.

4.5. Other platforms

Dendrimers are a specific type of polymers with a strictly defined structure. They are globular‐shaped nanosized macromolecules with high branching, presenting with a central core and dendritic branches starting radially from the core. Besides, the outer surface of dendrimers can be modified with functional groups. ²¹² BTZ is currently available only by intravenous and subcutaneous injection, with no oral formulation due to its poor oral absorption. Chaudhary et al. increased the solubility and stability of BTZ using dendrimers. They synthesized two kinds of dendrimers, G4‐PAMAM‐NH₂ and G5‐PPI‐NH₂, both of which can excessively improve the solubility of BTZ by more than 1000 times. And the solubility was concentration‐ and pH‐dependent through hydrophobic interactions and electrostatic interactions. ²¹³ Although NK cell‐based therapy has been a powerful tool to fight with malignancy, iterating infusions with a large number of NK cells after engraftment are needed. The technique of selective NK cell proliferation remains a problem. ²¹⁴ The synthetic reagents, poly(phosphorhydrazone) dendrimers, showed immunomodulatory properties in vitro, and were evidenced to activate the proliferation of NK cells. Dendrimer‐expanded NK cells were examined in subcutaneous tumor models and exhibited antitumor ability. ²¹⁵ The high reproducibility of ex vivo amplification with precise control makes it possible to be widely applied.

Hydrogels are crosslinked hydrophilic polymer chains formed networks, demonstrating a sol‐gel phase transition property. ²¹⁶ They can respond to external stimuli, including temperature, pH level, and light, according to different designs. Injectable biodegradable hydrogels have become a matter of importance for drug delivery. In addition, the incorporation of nanoparticles into hydrogels has integrated the multifunction and advantages with high tunability. ²¹⁷ To achieve sustained release of BTZ, Lee et al. encapsulated BTZ into PEG‐P(Cat)₁₃ micelles with pH‐sensitive boronic ester bonds and incorporated these micelles into a hydrogel network. The BTZ‐loaded micelle/hydrogel composite served as a subcutaneously injectable and biodegradable dosage form with readily tunable mechanical properties. BTZ was released sustainedly in the acidic environment within 9 days. This composite acted as a drug reservoir and showed a meaningful delay in tumor progression after one treatment. ²¹⁸

Biomimetic nanoparticles are novel strategies for drug delivery. Cells and their derivatives possess specific features, and nanoparticles coated with cell membranes exhibit cell‐like behaviors. ²¹⁹ Besides, these nanoparticles also retain the physicochemical properties of synthetic vehicles. Biomimetic nanoparticles are capable of immune escape, long circulation, and active targeting. ²²⁰ Several source cells, including red blood cells, macrophages, platelets, and tumor cells, have been studied for superior targeting capacity and therapeutic efficacy. The pH‐responsive nanoparticles were coated with platelet membrane (PM‐NP), and the affinity between P‐selectin and CD44 enabled the nanoparticles to target NCI‐H929 cells. Once the nanoparticles were internalized by myeloma cells, the drugs inside were released owing to the acid‐responsive behavior. In addition, alendronate was attached to the surface of nanoparticles, aiming to accumulate in the bone site. The codelivery of BTZ and tissue plasminogen activator (tPA) enabled the PM‐NP to inhibit tumor growth and dissolve thrombus, reducing the risk of thrombus complications. The targeted‐NP‐BTZ showed higher cytotoxicity against NCI‐H929 cells with significantly lower IC₅₀ value than the NP‐BTZ. Moreover, the sequential targeting strategy aimed at bone and MM cells resulted in superior treatment efficacy. ²²¹ MM cells mainly survive in the BM and exhibit the BM homing property. Cell membrane‐coated nanomedicine can inherit the properties of the source cell. Researchers took advantage of this phenomenon and designed an MM cell membrane‐coated BTZ nanoparticle (MPCEC@BTZ). This MM‐mimicking nanocarrier efficiently transported BTZ into BM and targeted MM cells. In addition, the system exhibited the property of immune escape. In the orthotopic MM model, the MPCEC@BTZ group demonstrated the lowest bioluminescence imaging intensity and Kappa light chain concentration. In addition, the MPCEC@BTZ formulation prolonged the median survival time of the disease model and avoided serious adverse effects (Figure 5). ²²²

FIGURE 5.

(A) Schematic illustration of MM cell membrane‐coated bortezomib (BTZ) nanoparticles for treatment of multiple myeloma. These biomimetic nanoparticles could enter the bone marrow cavity after intravenous injection, and then target tumor cells through homologous targeting. (B) Bioluminescence images of mice treated with saline (control), blank MPCEC nanoparticles, free BTZ, PCEC@BTZ nanoparticles, and MPCEC@BTZ nanoparticles (Copyright 2022, John Wiley and Sons ²²² )

With the property of high spatiotemporal accuracy, photodynamic therapy can control tumor‐killing precisely. ²²³ , ²²⁴ Nevertheless, the poor penetration of external light and indeterminate tumor location limits its application in disseminated tumors. Transforming hydrophobic light‐sensitive drugs into phototherapeutic agents with tumor‐targeted lipid micelles or serum albumin nanoparticles and radiopharmaceuticals extends the application range. This strategy facilitated the treatment efficacy in the disseminated MM model with the effects of Cerenkov radiation‐induced therapy. ²²⁵ The epirubicin‐loaded and anti‐ABCG2 mAb conjugated microbubbles, along with ultrasound exposure, attempted to eradicate the MM stem cells in the engrafted tumor mouse models. The targeted drug delivery system could anchor at the tumor site and retain for a long time; nevertheless, apart from the targeting ability, it did not enhance the therapeutic effect. When combined with ultrasound, epirubicin invaded myeloma cells facilely through membrane perforations. ²²⁶ The preclinical results demonstrated a new strategy to target MM cells and enhance efficacy.

4.6. Clinical applications of nanomedicine

Nanomedicine aims to improve the therapeutic index of chemotherapeutic drugs by modifying their physicochemical properties, pharmacokinetics, and distribution in vivo. Optimized delivery of drugs to the ideal site has also been emphasized in the clinic. Several liposomes and polymeric nanoparticles have been approved to treat malignant neoplasms. The FDA has granted liposomal DOX and liposomal VCR for MM and acute lymphoblastic leukemia. Liposomal DOX achieved long circulation and preferential accumulation at the tumor site, attenuating cardiac toxicity in both animal models and humans. ²²⁷ The PLD has been evaluated in different combination regimens including PIs or IMiDs. The BTZ, PLD, and dexamethasone regimen seems highly effective for initial therapy. In a pivotal trial, patients who received PLD and BTZ showed superior effects than the BTZ monotherapy group in the interim analysis. ²²⁸ However, the final results indicated that this combination did not improve OS compared to monotherapy in long‐term follow‐up. ²²⁹ CPX‐351 gains satisfying outcomes as a dual‐drug liposomal formulation that encapsulates daunorubicin and cytarabine at a fixed ratio of 5:1. ²³⁰ The results of clinical trials demonstrated clinical benefits and confirmed CPX‐351 as a standard intensive therapy for high‐risk or secondary acute myeloid leukemia in older patients. ²³¹ Although nanomedicine has shown inspiring efficacy in preclinical studies, many limitations and difficulties remain in the path of clinical translation. The limited gain in OS has not satisfied clinicians and patients. Rare active targeting nanoparticles have been applied in the clinic so far. The complicated preparation process restricts large‐scale output. In addition, clinical trials and long‐term outcomes are required to verify the efficacy and safety of nanomedicine.

4.7. Challenges of nanomedicine in multiple myeloma

Nanomedicine has demonstrated promising efficacy in tumor treatment. Several factors are essential for designing nanomedicine including preparation methods, different targeting peptides or antibodies, length, and hydrophilicity of conjugated linkers. ²³² In addition, excellent performance in vitro cannot guarantee a satisfying outcome in vivo. The complicated situation in vivo, including blood circulation, biodistribution, tumor cell penetration, and the interaction between nanoparticles and healthy tissues, hindered the voyage to the target site, leading to disappointing behavior. ²³³ In vivo estimation remains crucial for clinical application. The hydrophilicity of the targeting peptides, the valency of the peptides on the surface, and nanoparticle size matter greatly. Therefore, upgrading these parameters and finding the balance among these factors is essential to uplift the in vivo therapeutic results.

MM is highly heterogeneous, and stemming from the heterogeneous expression levels of surface molecules on MM cells, there still exist limitations to achieving precise targeting. Therefore, digging the highly unique surface marker of MM, creating dual‐targeted nanoparticles, and optimizing the preparation are essential steps to improve the efficacy. Other significant issues of MM are drug resistance and disease relapse. Many patients suffer from relapse, showing double or even triple refractory. Mapping out a strategy to achieve MRD‐negativity may be the key point to solve the problem. Several organic nanoparticles formulated by polymeric materials have been widely studied and have shown high biocompatibility, biodegradability, and low toxicity based on tests in cells and animal models. Because of the different characteristics of ingredients and surface modifications, the metabolic pathways of nanomedicine in vivo vary from each other. Therefore, safety issues should be considered. The long‐term effects of nanomaterials are essential for biosafety assessment and clinical application but are currently less explored.

The two main myeloma animal models are xenogeneic model and syngeneic tumor model. Culturing myeloma cells in human fetal bone or rabbit bone and then implanting them into severe combined immune deficiency mice can sustain myeloma cell growth and recreate the look‐alike microenvironment. ²³⁴ Syngeneic tumor models, such as the transplantable murine model 5T33 and genetically engineered mouse models, can present aggressive late‐stage disease. ²³⁵ Gu et al. established an orthotopic MM mouse model by intravenous injection of LP‐1‐Luc MM cells, which were disseminated to the whole body. ¹⁹⁴ Another A6 peptide targeted nanoparticle was studied in a subcutaneous model with an implanted human BM‐like scaffold, providing an advanced manner to verify the effectiveness of micelle‐drug formulations. ¹⁸⁵ However, subcutaneous xenograft mouse models are mostly used for their viability and convenience, although they cannot genuinely imitate the complicated microenvironment. Even though nanoparticles showed validation in these models, they may not demonstrate matching efficacy in the clinical situation. Establishing orthotopic animal models and patient‐derived xenograft models can be more reliable to verify the power of nanomedicine.

5. CONCLUSIONS AND PERSPECTIVES

Improved understanding of biological development, molecular abnormalities, and the BM microenvironment of MM enables effective treatment and management for patients. To date, the survival of MM patients has improved as large amount of therapeutic agents have emerged. Next‐generation PIs, IMiDs, mAbs, CAR T‐cell therapies, and novel agents are favorable advancements, and ASCT is still a cornerstone during management. In addition to currently adopted approaches, drug delivery strategies should be considered. Nanomedicine can meliorate the pharmacokinetic and pharmacodynamic properties of conventional agents. Nanoplatforms loaded with cytotoxic drugs and PIs have achieved controlled drug release, prolonged circulation, and reduced systemic toxicity. Active targeting nanoparticles with particular affinity for MM cells, bone, or BM have been designed for precise treatment (Table 3). Besides, nanomedicine acts as an aide in immunotherapy to strengthen immune effects. However, challenges still exist, and a portion of patients have poor outcomes.

TABLE 3.

Studies of active targeting nanoparticles for multiple myeloma

Targets	Types	Agents	Injection method	In vivo model	Refs.
CD38	Liposome	Doxorubicin	iv	NCI‐H929 subcutaneous model	178
Bone/transferrin receptor	Liposome	Paclitaxel	ip	MM.1S orthotopic model	179
P‐selectin	Liposome	Bortezomib/Y27632	iv	MM.1S orthotopic model	181
CD3/BCMA, CS1, CD38	Liposomal multispecific T‐cell engager	–	iv	MM.1S orthotopic model	183
CD44	Core‐disulfide‐crosslinked micelle	Carfilzomib	iv	LP‐1 subcutaneous model	185
VLA‐4	Micelle	Camptothecin prodrug	iv	5TGM1 orthotopic model	186
CD44	Hyaluronic acid‐shelled and core‐disulfide‐crosslinked micelle	Bortezomib	iv	LP‐1 subcutaneous model	192
CD44	Lipoic acid‐crosslinked hyaluronic acid nanoparticle	Doxorubicin	iv	LP‐1 subcutaneous model	190
CD44	Polymersome	Epirubicin	iv	LP‐1 orthotopic model	194
CD44	Chimeric polymersome	Granzyme B	iv	LP‐1 subcutaneous/orthotopic model	195
CD38	Immunopolymersome	Vincristine sulfate	iv	LP‐1 orthotopic model	196
CD38	Chitosan nanoparticle	Bortezomib	iv	MM.1S orthotopic model	197
CD38	Polymeric nanoparticle	S3I‐1757	iv	U266 orthotopic model	198
Bone	Polymeric nanoparticle	Bortezomib	ip	MM.1S orthotopic model	200
Bone marrow/transferrin receptor	Titanium dioxide nanoparticle	89Zr	iv	MM.1S orthotopic model	209
Bone/CD44	Platelet membrane‐coated nanoparticle	Bortezomib/tPA	iv	NCI‐H929 orthotopic model	221
Bone marrow	MM cell membrane‐coated nanoparticle	Bortezomib	iv	MRD orthotopic model	222

Abbreviations. ip, intraperitoneal injection; iv, intravenous injection.

When designing treatment strategies, personalized situations, tolerability, and molecular information should be taken into account. Patients with high‐risk features need to be identified early, and the application of biomarkers can help to select subgroups for appropriate treatment. Besides, real‐world evidence is needed to assess the benefits, toxicity, and long‐term effects. Studies are underway to figure out potential combination strategies, mechanisms of drug resistance, new targets, and new drug classes. Regarding the further development of nanomedicine, several aspects deserve the attention of researchers. The precision, efficacy, and safety of nanomedicine systems are crucial issues, thus, requiring rational and ingenious design. Combination therapies, multiple targeting strategies, and immunotherapies are promising paths for nanotechnology application. In addition, orthotopic animal models are needed as standards to judge the effect of nanomedicine platforms. Moreover, the convenience of large‐scale manufacture and long‐term storage for clinical translation should be considered as well.

CONFLICT OF INTEREST

Zhiyong Qian is an editorial board member of MedComm. Author Zhiyong Qian was not involved in the journal's review of, or decisions related to, this manuscript. The other authors declared no conflict of interest.

AUTHOR CONTRIBUTIONS

Ting Niu and Zhiyong Qian conceived the ideas of the manuscript and supervised the writing. Peipei Yang and Ying Qu drafted and revised the manuscript. Mengyao Wang, Bingyang Chu, Yuhuan Zheng, and Wen Chen edited the manuscript and summarized related research. All authors read and approved the final manuscript.

ETHICS APPROVAL

Not applicable.

Yang P, Qu Y, Wang M, et al. Pathogenesis and treatment of multiple myeloma. MedComm. 2022;3:e146. 10.1002/mco2.146

DATA AVAILABILITY STATEMENT

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