Combinational immunotherapy based on immune checkpoints inhibitors in small cell lung cancer: is this the beginning to reverse the refractory situation?

Abstract

Small cell lung cancer (SCLC), a particular neuroendocrine tumor, occupies 13% of lung cancers, with the highest mortality among cancers. Immune checkpoints inhibitors (ICIs) based on programmed cell death protein-1 (PD-1)/programmed cell death one ligand (PD-L1) inhibitors and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors have been one of the most favorable therapies in SCLC. Simultaneously, not all the patients respond to ICIs due to the lack of biomarkers to predict the immunotherapeutic effect. Multiple combinational approaches are under exploration, including the integrated or successive assessment of additional immunotherapeutic agents, chemotherapy, radiotherapy, and targeted therapy with ICIs. The current review offers a general view of the rationale for clinical studies exploring the experimental result of combinational immunotherapy based on ICIs, with both available results and ongoing trials. Moreover, the development of more predictive biomarkers, specific clinical trial designs, enhancement of the efficacy, and decreasing the financial toxicity will become the trend of future research and clinical applications of ICIs. Understanding the evolving immuno-oncology is increasingly relevant and crucial to solve those problems and define therapeutic strategies and potential target populations of combinational immunotherapy. Ultimately, emerging combinational immunotherapy will transform SCLC into a chronic disease to help patients survive from tumors.

Introduction

Small cell lung cancer (SCLC), a particular neuroendocrine tumor, occupies 13% of lung cancers, with the highest mortality among cancers (1). SCLC consists of a limited stage (LS) and an extensive stage (ES). Although surgical resections are the most common therapy in cancers, SCLC, regardless of ES-SCLC or LS-SCLC, is usually treated with a combination of radiotherapy and chemotherapy, where the response is initially good but quickly developing resistance and relapse (1). Furthermore, the 5-year overall survival (OS) of ES-SCLC is merely 2% (2). Nowadays, immune checkpoint inhibitors (ICIs) are revolutionary representatives of immunotherapy to reverse refractory cancers, including SCLC, which is targeting the immune checkpoint pathway that tumor cells evade immune surveillance and progress.

However, immunotherapy based on ICIs faces a range of challenges in SCLC, including long response time and severe side effects. For example, the average response time of pembrolizumab in SCLC is 8.6 weeks (7.7–16.1 weeks), which is detrimental to some patients with high-grade malignant and rapidly progressing SCLC (3). Meanwhile, SCLC patients receiving immunotherapy are experiencing various degrees of side effects during the trial, even death (3). As a result, other immunotherapeutic agents, chemotherapy, radiotherapy, and targeted therapy are being developed to improve these defects. It has been validated that ICIs can be safely combined with a variety of immunotherapeutic agents, albeit at about half a dose.

Moreover, response rates were significantly higher with combinations of ICIs or other immunotherapy than monotherapy (4). Previous studies have found chemotherapy and radiation therapy can accelerate the development of tumor antigen-presenting cells (APCs), enhance the level of PD-L1 on tumor cells, and down-regulate pro-tumor immune cells at the tumor microenvironment (TME), such as regulatory T cells (Tregs) and myeloid-derivative suppressive cells (MDSC), and recruit CD8⁺ T cells and macrophages into the TME (5). The above evidence reveals the potential of chemotherapy and radiotherapy in enhancing the function of ICIs. Further, immunotherapy, combined with targeted therapy in cancer, can complement each other. Immunotherapy enhances the immune system's activity, reduces tumor tolerance to targeted therapy, and expands the beneficiary group of targeted therapy. On the other hand, the utilization of targeted therapy shortens the host response time to immunotherapy and activates the immune system through specific signal pathways.

The current review offers a general view of the rationale for clinical studies exploring the experimental result of combinational immunotherapy based on ICIs, with both available results and ongoing trials.

The focus of immunotherapy: immune checkpoints and checkpoint inhibitors

Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and its inhibitors

CTLA-4 pathway in tumor immunity

CTLA-4 (CD152) is a surface or intracellular molecule on activated T cells that curbs the initial period of T cells activation as a competitive ligand for the T-cell costimulatory receptor CD28 (6). CTLA-4 is mostly found in intracellular compartments and is transported to the surface upon activated by T cell receptor (TCR) (7). Additionally, CTLA-4 can both regulate CD4⁺ T cells and selective depletion of Tregs by removing CD80 and CD86 from the cell surfaces of antigen-presenting cells (APCs) via trans-endocytosis (8-10) (Figure 1). Further, a recent study developed a dual variable domain immunoglobulin of anti-CTLA4 antibody, which could deplete intratumor Tregs, but spares tissue-resident Tregs, minimizing potential toxicities of CTLA-4 blockades (11).

Figure 1.

The immune suppression of Tregs via trans-endocytosis of CD80/86 from APCs. Upon activation by the combination of CTLA-4: CD80/86, Tregs will endocytose CD80/86 on the surface of antigen presentation cells (APC), the binding receptor of the costimulatory receptor CD28 on naïve T cells. Therefore, the activated pathway of naïve T cells is blocked.

The efficacy of monotherapy with inhibitors of CTLA-4 in SCLC

There are two critical inhibitors of CTLA-4 currently studied in the treatment of lung cancers, which are tremelimumab (ticilimumab, CP-675,206) and ipilimumab (MDX-010, Yervoy, BMS-734016), hampering the joint of CTLA-4 on T cells with ligands (CD80/CD86) on APCs to enhance antitumor immune responses. Few completed clinical trials of ipilimumab or tremelimumab adopted monotherapy in SCLC patients. Therefore, combining inhibitors of CTLA-4 with additional therapies may lead to breakthroughs in SCLC treatment activity.

The programmed cell death protein -1 (PD-1)/programmed cell death one ligand (PD-L1) pathway and their inhibitors

PD-1/PD-L1 pathway in tumor immunity

PD-1 (CD279) is mostly detected on the exterior of lymphocytes, primarily CD8⁺ T cells, and overexpressed on exhausted CD8⁺ T cells (Tex) (12). Currently, the ligands of PD-1 were confirmed to be PD-L1 (B7-H1) and PD-L2 (B7-DC), while PD-L1 is highly associated with tumor immunity. Besides tumor cells, PD-L1 and PD-L2 can also be found on other cells such as macrophages (13), myeloid DCs (14), MDSC (15), stromal fibroblasts (16), and endothelial cells (17). The expression of PD-1 not only inhibits T cells (CD8⁺) mediated cell killing and promotes the differentiation of exhausted CD8⁺ T cells (Tex) (18) but also facilitates the differentiation of the Treg (CD4⁺ Foxp3⁺) cells from naive CD4⁺ T cells (19,20). Moreover, the inhibitory effect of PD-1 on B cells improves immune responses to antigen-specific antibody, showing that PD-1 can also impede B cell-mediated T-cell activation (20). Importantly, the cytokines secreted by inflammatory cells, especially interferon-γ (IFN-γ), can induce or maintain the PD-L1 protein expressions (21), showing an IFN-γ/PD-L1 axis between tumor cells and the TME (Figure 2).

Figure 2.

The suppression of antitumor immunity activated by the PD-1/PD-L1 pathway in the tumor microenvironment (TME) of lung cancers. The core of this network is tumor-specific T cells. The PD-1 protein is expressed both on activated T cells by the combination of major histocompatibility (MHC) complex with T cell receptor (TCR), and also exhausted CD8⁺ T cells (Tex). PD-L1 is expressed on various immune cells and stromal cells in TME. The engagement of the PD-1/PD-L1 pathway facilitates the transformation of Texs and the differentiation of regulatory T cells (Treg). Meanwhile, the secretion of IFN-γ by infiltrating immune cells mentioned in the figure upgrades the expression of the PD-L1 protein.

The efficacy of monotherapy with inhibitors of PD-1/PD-L1 in SCLC

The inhibitors of the PD-1/PD-L1 that have been utilized in lung cancers are classified as anti-PD-1 agents and anti-PD-L1 agents. Nivolumab (opdivo, BMS 936558), durvalumab (imfinzi, MEDI4736), and pembrolizumab (Keytruda, MK-3475) are human-derived PD-1 monoclonal IgG4 antibodies in SCLC, which pair the PD-1 proteins expressed on T cells. Nivolumab monotherapy is approved in metastatic SCLC based on CheckMate 032, a significant study of nivolumab with or without ipilimumab (NCT01928394, phase I/II) (22,23). Durvalumab monotherapy was proved with enduring efficacy in some patients with the extensive pretreated disease (ED)-SCLC without additional security warnings (24). However, pembrolizumab monotherapy did not extend median progression-free survival (PFS) in ES-SCLC patients after receiving platinum and etoposide (25).

PD-L1 inhibitors also reported activity in the treatment of SCLC. Atezolizumab (tecentriq, MPDL3280A) is the earliest PD-L1 inhibitor in SCLC (26). Another clinical study investigating the outcomes and safety of atezolizumab in NSCLC or SCLC patients treated in routine clinical practice is ongoing (NCT03782207).

Other immune checkpoints and their inhibitors

In addition to the above two earliest and widely studied immune checkpoints, a few novel immune checkpoints and inhibitors such as T cell Ig and mucin-domain-3-containing molecule 3 (TIM-3), lymphocyte activation gene 3 (LAG-3) and et, al. have emerged in SCLC (Table 1).

Table 1. Selected immune checkpoint inhibitors in SCLC.

Target	Expressing cells	Roles in cancer immunity	Agents	Class	Ongoing monotherapy studies
CTLA-4	Tumor cells and T cells(activated/exhausted/Tregs)	Negatively regulates the early stage of naïve T cells activation by blocking costimulatory pathway	Ipilimumab	Fully human IgG1 antibody	–
			Tremelimumab	Fully human IgG2 antibody	–
PD-1	Tumor-infiltrating lymphocytes including T cells and B cells	Promote the exhaustion of CD8+ T cells and the differentiation of Tregs	Nivolumab	Fully human IgG4 antibody	NCT02481830
			Durvalumab	Humanized IgG1 antibody	NCT03043872
			Pembrolizumab	Humanized IgG4 antibody	NCT03526887
					NCT01840579
					NCT02721732
					NCT02628067
					NCT02963090
			PDR001		–
PD-L1	Tumor cells, macrophages, myeloid DCs, MDSC, stromal fibroblasts, and endothelial cells		Atezolizumab	Fully human IgG1 antibody	NCT03782207
					NCT03059667
			Sintilimab		–
			Avelumab		–
TIM-3	T cells (including Tregs), macrophages, DCs, NK cells, and mast cells	Mediate T-cell exhaustion and suppress innate antitumor immunity	RO7121661(PD-1/TIM-3 bispecific antibody)	Bispesific antibody	NCT03708328
			INCAGN02390	Fully human Fc-engineered IgG1κ antibody	NCT03652077
LAG-3	Tumor cells, T cells (including Tregs), B cells, NK cells, DCs, and TILs	Inhibit the activation of T cells and the differentiation of macrophages or fully competent antigen-presenting DCs	INCAGN02385	Fc-engineered IgG1κ	NCT03538028
			XmAb®22841	Bispesific antibody	NCT03849469
			LAG525	Monoclonal antibody	NCT03365791
OX40	Endothelial cells, mast cells, activated NK cells, DCs, B cells, microglial cells, activated T cells and Foxp3+ Tregs	Enhance the differentiation of CD4 memory T cell, CD4+ T cells and Th2 cells and activate NK cells	INCAGN01949	IgG1 monoclonal antibody	–
GITR	Expressed high levels on Tregs and at low levels on naïve and memory T cells	Promote NFκB activation, IL-9 production and cytotoxic T lymphocyte responses, enhance the function of DCs and Tregs expansion, and inhibits Tregs suppressive function	INCAGN01876	–	–
IDO1	Mature DCs, pulmonary and placental endothelial cells and tumor cells	Favor the growth of tumors, promote the differentiation of Tregs and induce inflammation-associated tumorigenesis	Epacadostat	–	–
TIGT	CD8+ TILs, Foxp3+ Tregs, monocytes, and NK cells	Inhibit activation of T cells and NK cells	Tiragolumab	Fully human IgG1 antibody	–
CD137	Tumor cells, CD4+ and CD8+ T cells, Foxp3+ Tregs, NK cells, and DCs	Activate and proliferate monocytes and NK cells, promote T cell activation, proliferation, and differentiation, and also induce T cell apoptosis	Utomilumab	IgG2 monoclonal antibody	–

CTLA-4, cytotoxic T-lymphocyte-associated protein 4; PD-1, programmed cell death protein-1; PD-L1, programmed cell death 1 ligand; TIM-3, T cell Ig and mucin-domain-3-containing molecule 3; LAG-3, lymphocyte-activation gene 3; GITR, glucocorticoid-induced TNFR-related protein; IDO1, indoleamine 2, 3-dioxygenase 1; TIGT, tyrosine-based inhibitory motif domain; Tregs, regulatory T cells; NK cells, nature killer cells; TILs, tumor infiltrating lymphocytes; MDSC, myeloid suppressor cells.

Tim-3 is an immune checkpoint on T cells, FoxP3⁺ Tregs, macrophages, DCs, nature killer (NK) cells, and mast cells to regulate immunity, upon interaction with ligands which are galectin-9 (Gal-9), carcinoembryonic antigen cell adhesion molecule 1 (CEACAM-1), high-mobility group protein B1 (HMGB1), and phosphatidylserine (PS) (27,28). As a result, TIM-3 can hinder immune responses by inducing T cells exhaustion (29) and suppressing innate antitumor immunity, such as decreasing the production of IL-12 by monocytes (30). The expressions of TIM-3 on Tregs and NK cells were associated with lung cancer progression (31,32). Additionally, blocking TIM3 promotes the cytotoxicity of NK cells might be a promising target for immunotherapy in lung cancer (33).

LAG-3 (CD223) is an immune checkpoint that inhibits T cells stimulation and restrains cytokine production, therefore making the status of immune homeostasis (34). What is more, LAG-3 inhibits macrophages' differentiation or fully competent antigen-presenting DCs from monocytes (35). Even though the exact process of LAG-3 signaling and interplay with additional immune checkpoints are generally unknown, LAG-3 blockades combined with PD-1 blockades are promising to suppress immune escape (34).

More immune checkpoints, along with their inhibitors involved in this review, were detailed in Table 1.

Combinations with other immunotherapies

Combinations of immune checkpoints inhibitors

The combination of ICIs is significant in SCLC treatment, most of which are the mixture of PD-1/PD-L1 and CTLA-4 pathway blockades, based on previous studies showing two pathways are nonredundant without additive or synergistic effects (36). Currently, there are two classic combos in the combination of PD-1/PD-L1 and CTLA-4 inhibitors, such as nivolumab plus ipilimumab and durvalumab plus tremelimumab.

Nivolumab ± ipilimumab has been evaluated in advanced or metastatic SCLC patients after platinum therapy in phase I/II trial (CheckMate 032) (37). According to CheckMate032, both overall response rate and the incidence of grade 3–4 adverse effects (AEs) in nivolumab combined with ipilimumab (overall response rate: 23%, AEs incidence: 33%) are higher than those in nivolumab monotherapy (overall response rate: 10%, AEs incidence: 14%), demonstrating a considerable tumor response and acceptable side effects in recurrent SCLC, regardless of PDL-1 expression and platinum-sensitivity/resistance. The same intervention was performed in another randomized expansion cohort, with an overall response rate of 12% and 21% in nivolumab monotherapy and nivolumab plus ipilimumab, sharing a similar 3-month OS of 64% and 65% in monotherapy and combined therapy (23). Based on these promising results, more clinical trials on nivolumab combined with ipilimumab are ongoing (Table 2). A phase III trial (CheckMate 451; NCT02538666) is ongoing to evaluate nivolumab plus ipilimumab compared with nivolumab monotherapy and placebo for ES-SCLC after first-line platinum-based doublet chemotherapy (PT-DC) (38). Moreover, NCT03670056 observes the changes in tumor antigen-specific effector T (Teff)/Treg cells as a primary outcome measure, which strongly influences antitumor immunity (23). Further, triple ICIs combinations based on nivolumab plus ipilimumab are also started to come out. A phase I/II trial explores the security, tolerability, and efficacy of INCAGN01876, an anti-GITR agonistic monoclonal antibody, plus nivolumab and (or) ipilimumab in advanced or metastatic malignancies including SCLC. Similarly, another attempt to combine an anti-OX40 agonistic antibody INCAGN01949 with nivolumab and ipilimumab in advanced or metastatic malignancies has been recently completed, but the result has not been reported (NCT03241173; phase I/II).

Table 2. Ongoing studies on combination of ICIs and other immunotherapeutic agents in SCLC.

PD-1/PD-L1 inhibitors	Other ICIs/other immunotherapeutic agents	Target	Clinical trial	Phase	Stage	Status	Estimated study completion	Primary outcome measures
Combination of PD-1/PD-L1 inhibitors with other ICIs
Nivolumab	Ipilimumab	CTLA-4	NCT03670056	Phase II	ES	Not yet recruiting	30-Sep-22	Change in the ratio of Teff/Treg cells
			NCT03043599	Phase I/II	ES	Active, not recruiting	Apr-22	PFS
			NCT02046733	Phase II	LS	Active, not recruiting	Jan-22	OS, PFS
			NCT03083691	Phase II	All	Enrolling by invitation	Aug-21	ORR
			NCT02538666	Phase III	ES	Active, not recruiting	Jun-20	OS
			NCT02538666 (CheckMate 451)	Phase III	ES	Active, not recruiting	11-Jun-20	OS
Nivolumab or Ipilimumab or Nivolumab + Ipilimumab	INCAGN01876	GITR	NCT03126110	Phase I/II	Unknown	Recruiting	28-Oct-21	AEs, ORR
	INCAGN01949	OX40	NCT03241173	Phase I/II	Unknown	Completed	23-Nov-19	TEAEs, ORR
Durvalumab	Tremelimumab	CTLA-4	NCT03703297	Phase III	LS	Recruiting	19-Feb-24	PFS and OS
			NCT02937818	Phase II	ES	Active, not recruiting	22-Jan-21	Overall Response Rate
			NCT03923270	Phase I	ES	Recruiting	1-May-25	SAEs, PFS
			NCT02701400	Phase II	Unknown	Active, not recruiting	Oct-21	PFS, ORR
			NCT03043872	Phase III	ES	Active, not recruiting	30-Sep-20	OS
			NCT03509012	Phase I	ES	Recruiting	4-Apr-22	DLTs, AEs
Pembrolizumab	Ipilimumab	CTLA-4	NCT01840579	Phase I	ES	Active, not recruiting	30-Jun-20	DLTs, AEs
	XmAb®22841	CTLA-4 x LAG-3	NCT03849469	Phase I	Unknown	Recruiting	Mar-27	AEs
	INCAGN01876+ Epacadostat	GITR+IDO1	NCT03277352	Phase I/II	Unknown	Active, not recruiting	May-20	TEAEs, ORR, CRR
	Epacadostat	IDO1	NCT03361228	Phase I/II	Unknown	Completed	30-Mar-19	TEAEs, ORR
Atezolizumab	Tiragolumab	TIGIT	NCT04256421	Phase III	ES	Recruiting	31-Aug-23	PFS, OS
PDR001	LAG525	LAG-3	NCT03365791	Phase II	Unknown	Active, not recruiting	19-Oct-20	CBR, PFS
Avelumab	Utomilumab	CD137	NCT02554812	Phase II	Unknown	Recruiting	16-Dec-22	Cmax, ADA, TTR, DR, PFS, OS, Tumor tissue biomarkers
Combination of ICIs with other immunotherapy agents
Nivolumab or Pembrolizumab or Atezolizumab or Avelumab	ALT-803	IL-15	NCT03228667	Phase II	Unknown	Recruiting	Aug-20	ORR
Pembrolizumab	SO-C101	IL-15	NCT04234113	Phase I	Unknown	Recruiting	Mar-22	DLTs, AEs, SAEs, laboratory test abnormalities, Clinically Significant Change and ECOG
Atezolizumab	BNT411	TLR7	NCT04101357	Phase I/II	ES	Not yet recruiting	Dec-23	DLTs, TEAEs, IMP dose reductions, IMP treatment discontinuations due to toxicity
Nivolumab	BMS-986012	fucosyl-GM1	NCT02247349	Phase I/II	Unknown	Active, not recruiting	28-Sep-20	AEs, worst grade SAEs
Pembrolizumab	Galinpepimut-S	Wilms tumor 1 (WT1) protein	NCT03761914	Phase I/II	Unknown	Recruiting	30-Jul-21	TRAEs, Overall response rate
Nivolumab + Pembrolizumab + Atezolizumab	FT500	NK cells	NCT03841110	Phase I	Unknown	Recruiting	Jun-22	DLTs
Nivolumab + Ipilimumab	INGN-225 (Ad. p53-DC)	Dendritic cell p53	NCT03406715	Phase II	LS + ES	Recruiting	Apr-21	DCR

ICIs, immune checkpoint inhibitors; OS, overall survival; PFS, progression-free survival; LS, limited stage; ES, extensive stage; AEs, adverse events; DCR, disease control rate; IMP, investigational medicinal products; DLTs, dose-limiting toxicities; SAEs, serious adverse events; MTD, maximum tolerated dose; ORR, objective response rate; RR, response rate; CRR, complete response rate; TEAEs, treatment-emergent adverse events; CBR, clinical benefit rate; Cmax, maximum plasma concentration; ADA, anti-drug antibody; TTR, time to tumor response; DR, duration of response; ECOG, Eastern Cooperative Oncology Group.

The combination of durvalumab plus tremelimumab has been confirmed to show antitumor activity in NSCLC, regardless of PD-L1 status, with an objective response rate of 23% (36). As a result, similar clinical trials are being conducted in SCLC to investigate whether durvalumab plus tremelimumab has a more potent antitumor activity than either drug alone (Table 2). The ADRIATIC (NCT03703297) is a phase III study in durvalumab with or without tremelimumab for patients with LS-SCLC following chemoradiation therapy to compare PFS and OS (approximately 5 years). An ongoing phase II study in ES-SCLC compares the combination of durvalumab plus tremelimumab with another two chemotherapies, based on overall response rate and other indexes (NCT02937818). The rest ongoing studies attempt to build a joint therapy of durvalumab plus tremelimumab, with chemotherapy or radiotherapy (NCT03923270, NCT02701400, NCT03043872, NCT03509012).

Except for these two classic combos, there are more new combinational ICIs combos. The first star agent is pembrolizumab, which is explored to be combined with ipilimumab (NCT01840579), XmAb®22841 (a CTLA-4 x LAG-3 bispecific antibody; NCT03849469), INCAGN01876 (a GITR agonist antibody; NCT03277352) and epacadostat (an inhibitor of indoleamine 2,3-dioxygenase-1 (IDO1); NCT03277352, NCT03361228), which are still at initial stages. A phase III study named SKYSCRAPER-02 exerts an efficacy comparison between tiragolumab plus atezolizumab, cisplatin (or carboplatin), and etoposide (EC) with placebo plus atezolizumab and EC (NCT04256421). Finally, the JAVELIN Medley (NCT02554812) explores the safety and effect of avelumab plus utomilumab in advanced malignancies, including SCLC. Another ongoing phase II trial (NCT02554812) determines whether a PD-1 blockade PDR001 plus a LAG-3 inhibitor LAG525 demonstrates sufficient efficacy in advanced malignancies, including SCLC.

Combinations with other immunotherapeutic agents

Agonists of cytokines and proteins

Interleukin (IL-15) is a promising target in immunotherapy, which can upgrade the production, function, and survival of CD8⁺ T and NK cells (39). A current report has shown that the combination of IL-15 superagonist named ALT803 and nivolumab in metastatic NSCLC was well-tolerated, with an objective response rate of 29% (40). Meanwhile, the addition of AL-803 may increase the objective responses in patients with PD-1-resistance (40). Based on this research, more trials are ongoing for applying IL-15 superagonists to assist PD-1/PD-L1 blockades in SCLC. NCT03228667 (phase II) sets up four interventions, including ALT-803 plus pembrolizumab or nivolumab or atezolizumab or avelumab in SCLC patients. Further, NCT04234113 looks into whether there is an improvement or decreased safety in SO-C101 combined with pembrolizumab, another IL-15 superagonist, compared with SO-C101 alone.

Toll-like receptor-7 (TLR-7) has been detected on the endosomes of immune cells such as macrophages, NK cells, DCs, and B cells. Activation of TLR7 ligands is beneficial to the differentiation and stimulation of immune cells and the secretion of pro-inflammatory cytokines (41). A TLR-7 agonist called BNT411 can amplify the potential immune-stimulating and antitumor activities of TLR-7, combined with atezolizumab and EC in an ongoing phase I/II trial (NCT04101357) in ES-SCLC.

Agents targeting tumor surface proteins

The ganglioside fucosyl-GM1 (FucGM1) is a specific tumor antigen on SCLC cells, but missing in normal tissues, which is a favorable therapeutic option for specific antitumor immunity. Previous researches had shown that a fully human anti-fucosyl-GM1 antibody (BMS-986012) may induce antitumor activity by complement-dependent cytotoxicity (CDC) and antibody-dependent cellular phagocytosis (ADCP) assays, while the tumor response enhanced when BMS-986012 was in combination with PD-1 or CD137 blockades (42). Therefore, a phase I/II study (NCT02247349) is ongoing to detect the effect and safety of the combination of BMS-986012 and nivolumab in relapsed or refractory SCLC.

The Wilms’ tumor suppressor gene (WT1) was initially recognized as a tumor suppressor gene in Wilm’s tumor and was then found overexpression in various solid tumors, including lung cancer (43). Caihua Xu et al. found that WT1 promoted proliferation of NSCLC cells by upgrading Cyclin D1 and p-pRb (44). Galinpepimut-S (GPS) is a novel cancer vaccine that targets the WT1 protein and has been adopted by FDA for mesothelioma. Hence, a phase I/II study is recruiting to combine pembrolizumab with GPS in selected advanced cancers, including SCLC.

Agents targeting innate immune cells

FT500 is a first NK cell immunotherapeutic agent produced from a self-renewing clonal master pluripotent cell line (MPCL). Current studies have found that FT500 can facilitate the recruitment and activation of tumor-infiltrating lymphocytes (TILs), suggesting an ability to reduce tumor burden and resistance of ICIs (45). A phase I study on FT500 monotherapy and in combination of nivolumab, pembrolizumab, and atezolizumab along with chemotherapy in selected advanced solid tumors, including SCLC, is recruiting.

p53 gene mutations often occur in cancers, leading to tumor proteins’ expression and making p53-specific cytotoxic T cells recognize tumor cells. Thence, INGN-225 (Ad. p53-DC), a p53-modified adenovirus-transduced dendritic cell vaccine, was developed, which has been proved well tolerated in SCLC, with all side effects ≤ grade 2 in a phase I/II trial (NCT03406715) (46). Also, specific anti-p53 immune responses and overall post-INGN-225 responses were observed in 41.8% and 51.5% of SCLC patients, respectively (46). Considering these post-INGN-225 immune responses, a phase II trial is ongoing to combine Ad. p53-DC with ipilimumab and nivolumab in LS-SCLC to explore whether there is an enhanced antitumor activity of ICIs (NCT03406715).

Combinations with chemotherapy or(and) radiotherapy

Chemotherapy and radiotherapy are beneficial to mature antigen-presenting cells, increase PD-L1 expression on tumor cells, decrease tumor-infiltrating Tregs or MDSCs, and recruit CD8⁺ TILs and macrophages (5). These shaping of TME from chemotherapy and radiotherapy make them become the first choice in combination with immunotherapy.

Combinations with chemotherapy

NCT01331525 proved the combination of ipilimumab with EC improved a subgroup of patients’ outcomes but also caused severe neurological toxicity in advanced SCLC (47). 72.4% and 84.8% of patients presented an objective response by RECIST and the immune-related response criteria. However, grade 3 or higher toxicity occurred in 89.7% of patients. Moreover, another phase III study (NCT01450761) revealed that the addition of ipilimumab to etoposide and platinum did not improve OS compared with chemotherapy alone in ES-SCLC patients, also without new adverse events (48). Thus, current researches shift the redemptions to the combination of other ICIs with chemotherapy.

A phase II trial (NCT02551432) has shown a moderate activity with acceptable toxicity of pembrolizumab combined with paclitaxel in refractory ES-SCLC, where the objective response rate was 23.1%, among which complete response rate is 3.8% and confirmed partial response is 19.2% (49). Various kinds of grade 3 or 4 AEs appeared among 4–8% patients. However, a significantly decreased NK cell activity was found in responders from flow cytometric analysis. Moreover, the PembroPlus (NCT02331251) explored the possible combos of pembrolizumab combined with common chemotherapies, including gemcitabine (G), docetaxel (D), nab-paclitaxel (NP), vinorelbine (V), irinotecan (I) and liposomal doxorubicin (LD) in advanced cancers including SCLC. The result showed the safety of standard-dose pembrolizumab combination with G, G+NP, G+V, I, and LD, indicating possible future research directions (50). Recently, MK-3475-604/KEYNOTE-604 (NCT03066778; phase III) has shown mixed results in ES-SCLC that pembrolizumab plus etoposide/platinum could potentially prolong PFS (P=0.0023; median 4.5 vs. 4.3 months) but OS (P=0.0164; median 10.8 vs. 9.7 months) (51). Further, pembrolizumab is being combined with more chemotherapies, such as topotecan (NCT02963090), amrubicin (NCT03253068), EC (NCT03043872, NCT02580994, NCT01840579), paclitaxel or pemetrexed (NCT01840579) (Table 3).

Table 3. Ongoing studies on combination of ICIs and chemotherapy and (or) radiotherapy in SCLC.

ICIs	Chemotherapy/radiotherapy/chemo-radiotherapy	Clinical trial	Phase	Stage	Status	Estimated study completion	Primary outcome measures
Combination with chemotherapy
Nivolumab	Irinotecan	NCT04173325	Phase I	Unknown	Recruiting	Nov-21	AEs
Nivolumab	EC	NCT03382561	Phase II	ES	Active, not recruiting	2-Jun-20	PFS
Nivolumab	Temozolomide	NCT03728361	Phase II	Stage IV	Recruiting	31-Dec-21	ORR
Nivolumab	Gemcitabine	NCT03662074	Phase II	Stage IV	Recruiting	10-Sep-21	Radiographic RR
Durvalumab	Placebo	NCT03703297	Phase III	LS	Recruiting	19-Feb-24	PFS, OS
Durvalumab	Olaparib	NCT02734004	Phase I/II	Unknown	Recruiting	5-Aug-22	DCR, ORR
Durvalumab	EC	NCT03043872	Phase III	ES	Active, not recruiting	30-Sep-20	OS
Durvalumab + Tremelimumab	EC	NCT03043872	Phase III	ES	Active, not recruiting	30-Sep-20	OS
Pembrolizumab	Topotecan	NCT02963090	Phase II	Unknown	Active, not recruiting	20-Aug-19	PFS
Pembrolizumab	Amrubicin	NCT03253068	Phase II	ES	Recruiting	31-Aug-20	OS
Pembrolizumab	EC	NCT03066778	Phase III	ES	Active, not recruiting	5-Oct-21	PFS, OS
Pembrolizumab	EC	NCT02580994	Phase II	ES	Active, not recruiting	Aug-20	PFS
Pembrolizumab	Cisplatin + Pemetrexed/Carboplatin + Paclitaxel/EC/EC + G-CSF	NCT01840579	Phase I	ES	Active, not recruiting	30-Jun-20	DLTs, AEs
Atezolizumab + Tiragolumab	EC + Placebo	NCT04256421	Phase III	ES	Recruiting	31-Aug-23	PFS, OS
Atezolizumab	EC + Placebo	NCT03041311	Phase II	ES	Active, not recruiting	May-20	Chemotherapy-induced myelosuppression
Atezolizumab	EC	NCT04028050	Phase III	ES	Recruiting	30-Dec-22	SAEs, Serious and Non-Serious Immune Related Adverse Events
Atezolizumab	EC	NCT02763579	Phase III	ES	Active, not recruiting	30-Dec-20	PFS, OS
Atezolizumab	EC	NCT04221529	Phase II	ES	Recruiting	Jun-24	OS
Avelumab	EC	NCT03568097	Phase II	Unknown	Recruiting	Aug-21	1-year PFS
Combination with radiotherapy
Nivolumab	Lutathera	NCT03325816	Phase I/II	ES	Active, not recruiting	Dec-20	PFS
Nivolumab	Stereotactic radiosurgery	NCT02978404	Phase II	Stage IV	Recruiting	Jun-21	PFS
Nivolumab + Ipilimumab	Stereotactic body radiation therapy	NCT03223155	Phase I	Stage IV	Recruiting	Dec-20	SAEs
Durvalumab + Tremelimumab	Stereotactic body radiation therapy	NCT02701400	Phase II	Unknown	Active, not recruiting	Oct-21	PFS, ORR
Atezolizumab	Hypofractionated radiation therapy	NCT03262454	Phase II	Unknown	Recruiting	31-Jul-24	ORR
Combination with chemo-radiotherapy
Nivolumab + Ipilimumab	Thoracic radiation therapy + platinum-based chemotherapy	NCT03043599	Phase I/II	ES	Active, not recruiting	Apr-22	PFS
Durvalumab	EC + thoracic radiotherapy	NCT03585998	Phase II	LS	Recruiting	19-Dec-21	PFS
Durvalumab	Olaparib pill + thoracic radiotherapy or Tremelimumab + thoracic radiotherapy	NCT03923270	Phase I	ES	Recruiting	1-May-25	SAEs, PFS
Durvalumab or Durvalumab + Tremelimumab	EC + external beam radiation	NCT03509012	Phase I	ES	Recruiting	4-Apr-22	DLTs, AEs
Pembrolizumab	EC + radiation	NCT02934503	Phase II	ES	Recruiting	Oct-20	PD-L1 expression status, PFS, OS, RR
Pembrolizumab	EC + radiation	NCT02402920	Phase I	LS	Recruiting	31-Jul-23	MTD
Pembrolizumab	EC + radiation	NCT02402920	Phase I	LS	Recruiting	31-Jul-23	MTD
Atezolizumab	Chemo-radiotherapy	NCT03540420	Phase II	LS	Recruiting	Dec-26	2-year OS
Atezolizumab	EC + intensity-modulated radiation therapy	NCT03811002	Phase II/III	LS	Recruiting	28-Dec-26	PFS, OS

ICIs, immune checkpoint inhibitors; OS, overall survival; PFS, progression-free survival; EC, cisplatin or carboplatin plus etoposide; LS, limited stage; ES, extensive stage; AEs, adverse events; DCR, disease control rate; DLTs, dose-limiting toxicities; SAEs, serious adverse events; MTD, maximum tolerated dose; ORR, objective response rate; RR, response rate.

IMpower133 (NCT02763579) demonstrated a synergistic potential of ICIs combined with first-line chemotherapy, that the addition of atezolizumab to EC in ED-SCLC brought remarkably extended OS and PFS than chemotherapy alone, with a manageable safety profile (52). Based on this promising result, emerging clinical trials on the addition of atezolizumab to EC (NCT04028050, NCT02763579, NCT04221529) with placebo (NCT03041311) in ES-SCLC are ongoing. Moreover, the SKYSCRAPER-02 (NCT04256421) is probing whether atezolizumab plus EC combined with tiragolumab have a different efficacy from atezolizumab plus EC alone in ES-SCLC.

Nivolumab, in combination with PT-DC has shown that nivolumab plus pemetrexed-cisplatin or paclitaxel-carboplatin or gemcitabine-cisplatin, achieved an objective response rate, a 24-week PFS and a 2-year OS up to 47%, 71% and 62%, respectively (NCT01454102) (53). Herein, clinical scientists are exploring the potential combos of nivolumab plus more chemotherapies, including irinotecan (NCT04173325), temozolomide (NCT03728361), gemcitabine (NCT03662074), and EC (NCT03382561) (Table 3).

An ongoing phase III trial (CASPIAN; NCT03043872) proved that durvalumab combined with platinum-etoposide was related to a considerably increased survival (median OS: 13 months, 18-month OS: 34%) from the platinum-etoposide group (median OS: 10.3 months, 18-month OS: 25%). Meanwhile, the incidence of grade 3 or 4 AEs is the same between the two groups, at 62% (54). Another ongoing phase II trial (MEDIOLA) has revealed the combination of olaparib and durvalumab was relatively well tolerated, but the efficacy did not reach the target disease control rates (DCRs) and was below the futility boundary (<40%) (55). ADRIATIC (NCT03703297) is an ongoing phase III trial to study the combo of durvalumab and placebo, compared with durvalumab plus tremelimumab, and placebo alone in LS-SCLC.

Finally, PAVE (NCT03568097, phase II) is in the process to explore the mixture of avelumab with first-line chemotherapy of EC in SCLC patients with carcinoma.

Combinations with radiotherapy

177Lu-DOTATATE (lutathera) is a promising target in patients with metastatic thoracic neuroendocrine tumors that express somatostatin receptors (56). An ongoing phase I/II trial (NCT03325816) has shown early evidence that lutathera combined with nivolumab is safe and well-tolerated with initial signs of antitumor activity (57). NCT02978404 (phase II) is looking into combining nivolumab and stereotactic radiosurgery (SRS), which is increasingly applied as the sole treatment of brain metastases in selected cancers, including SCLC. Stereotactic body radiation (SBRT) therapy (NCT03223155) is also being tested to combine with the classic combo of nivolumab plus ipilimumab in stage-IV SCLC.

An ongoing randomized phase II study of tremelimumab plus durvalumab±SBRT, showing no significant difference of efficacy for ICIs with or without SBRT in relapsed SCLC (58). Further, NCT03262454 (phase II) is attempting to add atezolizumab to the hypofractionated radiation therapy in SCLC.

Combinations with chemoradiotherapy

Most chemoradiotherapy combined with ICIs in current trials of SCLC are based on first-line EC, including durvalumab (NCT03585998, NCT03509012), pembrolizumab (NCT02934503, NCT02402920, NCT02402920) and atezolizumab (NCT03540420, NCT03811002) (Table 3). Of note, the CLOVER (NCT03509012, phase I) is setting four arms to evaluate the addition of tremelimumab to the combination of durvalumab and EC with external beam radiation, determining the different efficacy between hypofractionated and standard external beam radiation.

Except for the combination with EC, NCT03923270 (phase II) is setting three arms to assess the activity and safety of durvalumab plus thoracic radiotherapy, durvalumab combined tremelimumab plus thoracic radiotherapy and durvalumab combined olaparib pills plus thoracic radiotherapy.

Finally, a prospective single-arm phase I/II study (NCT03043599) utilized ipilimumab and nivolumab with consolidative thoracic radiotherapy after platinum doublet chemotherapy for patients with ES-SCLC. The result did not significantly improve the 6-month PFS compared to historical estimates, while the OS estimate at one year compares favorably with historical estimates (59).

Combinations with targeted therapy

Antiangiogenic agents

A series of mice models demonstrated that the antiangiogenic therapy targeting vascular endothelial growth factor (VEGF) and Angiopoietin-2 (ANG2) (60), and vascular endothelial growth factor receptor 2 (VEGFR2) (61) raised the level of PD-L1 on endothelial cells (ECs) and tumor cells, leading to the suppression of antitumor immunity. Thus, a piece of equitable evidence supports the combination of antiangiogenic agents and ICIs, to solve the resistance during the antiangiogenic therapy.

Tyrosine kinase inhibitors (TKIs)

Receptor tyrosine kinases (RTKs) are transmembrane glycoproteins, which serve as the connection of cellular growth factors and extracellular ligands (62). Currently, targeted RTK inhibitors have been a new representative of targeted therapy in cancers, including SCLC (63).

Anlotinib (AL3818) is an orally multiple TKI, targeting c-kit, fibroblast growth factor receptor (FGFR), VEGFR, and platelet-derived growth factor receptor (PDGFR), which has been permitted for the treatment in NSCLC in China (62). Based on these outcomes in NSCLC, two clinical trials are recruiting to explore more potential of anlotinib combined with nivolumab (NCT04165330) and sintilimab (NCT04055792) in SCLC.

Vorolanib (X-82) is an orally dual inhibitor targeting VEGFRs and PDGFRs with antiangiogenic and antineoplastic activities, which has demonstrated reduced tissue toxicity by 95% with first-generation kinase inhibitors. NCT03583086 (phase I/II) estimates the tolerability and effect of nivolumab plus vorolanib in patients with refractory thoracic tumors, including SCLC.

Cabozantinib (XL184), an orally bioavailable TKI with activity against MET, VEGFR 2, AXL, ROS1, and RET, has been tested in some advanced solid tumors (64). NCT04079712 is a recruiting phase II trial to test the combination of XL184, nivolumab, and ipilimumab for differentiated neuroendocrine cancers.

VEGF inhibitors

VEGF is immensely expressed in SCLC cells, and it is related to cancer cell proliferation, metastasis, and invasion, while clinical evaluation of angiogenesis inhibitors has not improved OS in SCLC (2). Bevacizumab is a humanized anti-VEGF-A monoclonal IgG₁ antibody (65), which is also the VEGF inhibitor most studied in SCLC (2). NCT02734004 (phase I/II) is a study to assess the antitumor activity and safety of the mixture of bevacizumab, durvalumab, and olaparib, compared with the other arms of durvalumab plus olaparib, and bevacizumab plus olaparib.

Cyclin-dependent protein kinase (Cdks) inhibitors

Once combing with cyclin D, cyclin-dependent kinases (CDK4/6) firstly phosphorylate retinoblastoma protein (Rb), leading to the cell transition from G1 to S phase (66). CDK4/6 inhibitors can obstruct cell cycle and induce cell senescence and disruption by a cytotoxic T-cell-mediated effect in cancer (67). Trilaciclib is a CDK4/6 inhibitor that has been used for breast cancer in postmenopausal women. In SCLC, NCT03041311 (phase II) is in the process of evaluating the addition of trilaciclib to the combination of carboplatin, etoposide, and atezolizumab in ES-SCLC.

Additionally, a selective CDK7 inhibitor, YKL-5-124, was another potent treatment in SCLC mice models in Hua Zhang et al.’s study (68). Anti-PD-1 + YKL-5-124 presented with a better response than a single treatment. Strikingly, the mice treated with four-drug combination (YKL-5-124 + anti-PD-1+EC) appeared to live significantly longer than those treated with anti-PD-1+EC or EC alone. Moreover, this study also indicated that YKL-5-124 induced antitumor immune reactions engaging DCs (MHCII⁺CD11c⁺CD103⁺), effector CD4⁺T cells (CD44^highCD62L^low/Ki67⁺/ICOS⁺) and cytotoxic CD8+T cells (Granzyme B⁺), which could be heightened by the combination with PD-1 blockades.

Arginase and its inhibitor

Arginase in the TME can inhibit antitumor NO secreted by pro-inflammation macrophages, synthesis of polyamines supporting tumor cells multiplication, and topical arginine reduction, which result in T-cell dysfunction and immunosuppression (69). Current studies have demonstrated that arginase was expressed on various cancers (69) while its inhibitors could cause suppression of breast cancer cell proliferation (70). INCB001158 is an orally available inhibitor of arginase, which inhibits the breakdown of arginine by arginase and restores arginine levels. Thus, NCT03361228 (phase I/II) is a study to explore the security, tolerability, and preclinical effect of INCB001158 plus epacadostat, with or without pembrolizumab in advanced solid tumors, including SCLC.

Arginine is a kind of semi-essential amino acid, while several cancers fail to endogenously synthesize enough arginine for survival and proliferation, mainly because of decreased level of argininosuccinate synthase (ASS1) (71). Pegzilarginase is a highly potent human arginine-degrading enzyme, while SCLC has been validated with the highest incidence of decreased ASS1 expression and the highest rate of responding to pegzilarginase in patient-derived xenografts (PDX) models (71). Moreover, pegzilarginase prevented tumor growth and promoted the infiltration of CD8⁺ T cells in the TME in mouse models (71). Thus, an ongoing phase I/II study (NCT03371979) explores the security and effect of pegzilarginase plus pembrolizumab in ED-SCLC with relapsed or progressive disease on or in 6 months of platinum-based chemotherapy.

DNA damage response (DDR) drugs

PARP (poly (ADP-ribose) polymerase) inhibitors can induce cell death by inhibiting the activity of PARP, which is a protein involved in DNA repair (72). A phase II trial (NCT03958045) is recruiting to combine rucaparib with nivolumab in stage-IV SCLC, evaluating their potential to prolong PFS and OS.

WEE1 is a protein kinase that regulates the cell cycle by serving as a checkpoint preventing DNA replication in the presence of DNA damage (73). The inhibition of WEE1 aims to generate sufficient DNA damage in cancer cells to cause apoptosis and prevent tumor growth. ZN-c3 is an orally administered WEE1 inhibitor, which is investigated in phase I/II study (NCT04158336) as monotherapy and in combination with pembrolizumab or talazoparib in solid cancers including SCLC.

Topoisomerase II (Top 2) is an enzyme incredible in DNA replication, chromosome condensation, and chromosome segregation (74). As a result, inhibitors of Top 2 are increasingly utilized in the therapy of various cancers, including lung cancer. Amrubicin, a third-generation anthracycline and potent, which has been permitted for relapsed small cell lung carcinoma in Japan (75). NCT03253068 (phase II) is continuing to explore the overall response rate per RECIST 1.1 as assessed by investigators in subjects with refractory SCLC treated with pembrolizumab combined amrubicin.

PM01183 is a novel antitumor agent binding to selected DNA sequences and promoting apoptosis via double-strand breaks at nanomolar concentrations (76). NCT04253145 is a phase I trial to assess the safety, tolerability, and efficacy of PM01183 combined with atezolizumab in SCLC patients.

Notch pathway inhibitors

The Notch is a surface receptor in regulating cell proliferation, survival, differentiation, and cell death by interacting with transmembrane ligands on neighboring cells (77), which is one of the most prevalently activated signaling pathways in cancers (78). A study of colorectal carcinoma revealed the blockade of Notch pathway could stimulate tumor-infiltrating CD8⁺ cytotoxic T lymphocytes (CTL), and the production of IFN-γ, TNF-α, IL-1β, IL-6, and IL-8 (79). What is more, the PD1 expression on CD8⁺ CTL was also declined with the inhabitation of Notch pathway, demonstrating the great potential to assist PD-1 blockers.

Delta-like ligand 3 (DLL3) is an inhibitory Notch ligand that is overexpressed in SCLC cells but hardly expressed in normal tissues (80). AMG 757 is a bispecific antibody targeting DLL3 and CD3, which has been demonstrated to turn T cells to eliminate DLL3⁺ SCLC cells in vitro (80). A phase I trial (NCT03319940) is attempting to compare AMG 757 monotherapy and AMG 757 combined with pembrolizumab in small cell lung carcinoma. Rovalpituzumab tesirine (Rova-T) is an anti-DLL3 conjugate, with early signs of efficacy as a third- or fourth-line setting in SCLC (80). Therefore, NCT03026166 is a phase I/II study of Rova-T with nivolumab ± ipilimumab for ES-SCLC, where Rova-T with nivolumab and ipilimumab is not appropriate, attributable to dose-limiting toxicities (DLTs). However, Rova-T plus nivolumab demonstrated some durable responses and required optimizing dose and schedule (81).

Kirsten rat sarcoma viral oncogene homolog (KRAS) pathway inhibitors

KRAS activation is one of the most often oncogenic events in some cancers and is correlated with poor survival (82). Although there has not been a clear conclusion in SCLC, several surprising ICIs in KRAS mutant NSCLC have been reported. According to a meta-analysis, ICIs prolonged the OS of KRAS mutant NSCLC, compared with chemotherapy (P=0.03) (83). Therefore, whether KRAS mutation could also be a potential biomarker for the efficacy of ICIs in SCLC is worth discussion. Plinabulin is a novel agent that inhibits tubulin polymerization and growth of KRAS-driven cancer cells with a manageable safety profile in previous studies (82). Currently, a phase1/2 study (NCT03575793) determines the different outcomes between nivolumab plus plinabulin, and nivolumab combined with ipilimumab plus plinabulin in recurrent SCLC patients.

Lysine-specific demethylase 1 (LSD1) inhibitors

Lysine-specific demethylase 1 (LSD1, KDM1A) promotes cancer cell proliferation, metastasis, and invasion (84). Inhibitors of LSD1 has been validated with significant antitumor activity in vitro and vivo in a series of solid tumors, including SCLC (85). Mounting results in breast mice models showed that the combination of LSD1 inhibitors with PD-1 antibody significantly inhibited tumor growth, decreased Ki-67 level, and enhanced CD8⁺ TILs (86). Overall, these results proved that LSD1 inhibition could be an approach to assist with immunotherapy.

INCB059872 is a demethylase that suppresses LSD1 pathway and being combined with azacytidine and nivolumab in advanced malignancies, including SCLC (NCT02712905, phase I/II). CC-90011 is another demethylase binding to and inhibiting LSD1, which is being tested in combination with nivolumab and EC in ES-SCLC (NCT03850067, phase I/II).

Liver-X nuclear hormone receptor (LXR) agonist

LXR-α and β are vital regulators in lipid and carbohydrate metabolism, cellular differentiation, apoptosis, and many immune responses (87). LXR-α is highly expressed in fat tissue, liver, kidney, intestine, and macrophages, while LXR-β expression is universal (88), both of which have demonstrated anticancer activities in a variety of cancer cell lines (89). RGX-104, an oral administered LXR agonist, was proved to upgrade LXR-mediated expression of apolipoprotein E (ApoE), which induced apoptosis of peripheral or tumor-infiltrating MDSCs, and then supported T cell-engaging antitumor immunity (90). Consequently, this therapy was considered to promote the curative effect of ICIs. Hence, NCT02922764 (phase I) sets up five arms to assess the activity and tolerability of RGX-104 monotherapy, RGX-104 plus nivolumab, or ipilimumab or docetaxel and the combination of RGX-104 with pembrolizumab, carboplatin, and pemetrexed.

More details of these above ongoing clinical trials were demonstrated in Table S1.

Table S1. Ongoing studies on combination of ICIs and target therapy in SCLC.

ICIs	Other therapies	Target	Clinical trial	Phase	Stage	Status	Estimated Study Completion	Primary outcome measures
Anti-angiogenic agents
Nivolumab	Anlotinib (AL3818)	VEGFR, FGFR, PDGFR, c-kit	NCT04165330	Phase I/II	Unknown	Recruiting	31-Dec-22	ORR
Sintilimab	Anlotinib (AL3818)	VEGFR, FGFR, PDGFR, c-kit	NCT04055792	Phase II	Unknown	Recruiting	1-Mar-22	PFS
Nivolumab	Vorolanib (X-82)	VEGFR/PDGFR	NCT03583086	Phase I/II	Stage IV	Recruiting	Jul-24	RP2D, Phase II best response
Nivolumab + Ipilimumab	XL184 (cabozantinib)	MET, VEGFR 2, AXL, ROS1, RET	NCT04079712	Phase II	Unknown	Not yet recruiting	17-Jul-22	Overall response rate
Durvalumab	Bevacizumab	VEGF-A	NCT02734004	Phase I/II	Unknown	Recruiting	5-Aug-22	DCR, ORR
Cyclin-dependent protein kinase inhibitors
Atezolizumab	Trilaciclib	CDK4/6	NCT03041311	Phase II	ES	Active, not recruiting	May-20	Chemotherapy-induced myelosuppression
Arginase and its inhibitor
Pembrolizumab	Pegzilarginase	Arginase 1	NCT03371979	Phase I/II	Unknown	Active, not recruiting	Dec-20	TEAEs, ORR
Pembrolizumab + Epacadostat	INCB001158	Arginase	NCT03361228	Phase I/II	Unknown	Completed	30-Mar-19	TEAEs, ORR
DNA damage response drugs
Nivolumab	Rucaparib	PARP	NCT03958045	Phase II	Stage IV	Recruiting	Jul-24	PFS
Pembrolizumab	Amrubicin	Top 2	NCT03253068	Phase II	ES	Recruiting	31-Aug-20	Overall response rate
Pembrolizumab	ZN-c3	WEE1	NCT04158336	Phase I/II	Unknown	Recruiting	Aug-23	MTD, RP2D, ORR
Atezolizumab	PM01183	Trans-activated transcription	NCT04253145	Phase I	Unknown	Recruiting	Feb-22	MTD, RD
Notch pathway inhibitors
Pembrolizumab	AMG-757	DLL3	NCT03319940	Phase I	Unknown	Recruiting	4-Aug-23	DLTs, TEAEs, significant changes
Nivolumab + Ipilimumab	Rovalpituzumab tesirine	DLL3	NCT03026166	Phase I/II	Unknown	Completed	3-Jul-19	CBR, DOR, ORR, PFS, OS
KRAS pathway inhibitors
Nivolumab + Ipilimumab	Plinabulin	Tubulin polymerization	NCT03575793	Phase I/II	ES	Recruiting	Sep-22	MTD, PFS
LSD1 inhibitors
Nivolumab	CC-90011	LSD1	NCT03850067	Phase I/II	ES	Recruiting	30-Sep-22	DLT, MTD, AEs
Nivolumab	INCB059872	LSD1	NCT02712905	Phase I/II	Unknown	Recruiting	14-Dec-21	AEs, RD
LXR inhibitors
Docetaxel	RGX-104	LXR	NCT02922764	Phase I	Unknown	Recruiting	Mar-21	MTD, Overall response rate, PFS, TEAEs

ICIs, immune checkpoint inhibitors; OS, overall survival; PFS, progression-free survival; LS, limited stage; ES, extensive stage; VEGFR, endothelial growth factor receptor, FGFR, fibroblast growth factor receptor, PDGFR, platelet-derived growth factor receptors; LDS-1,lysine-specific demethylase 1; LXR, liver-X nuclear hormone receptor; KARS, Kirsten rat sarcoma viral oncogene homolog; PARP, poly (ADP-ribose) polymerase; Top 2, topoisomerase II; RP2D, recommended Phase II dose; DOR, duration of response; RD, recommended dose; AEs, adverse events; DCR, disease control rate; DLTs, dose-limiting toxicities; SAEs, serious adverse events; MTD, maximum tolerated dose; ORR, objective response rate; RR, response rate; TEAEs, treatment-emergent adverse events; CBR, clinical benefit rate.

Future perspectives

In the next years, ICIs alone or in combination with additional immunotherapeutic agents, targeted therapy, chemotherapy, and (or) radiotherapy promise to reverse the refractory situation of SCLC. Multiple trials are investigating the benefit of ICIs in various neoadjuvant settings. Thus, oncologists have to deal with more difficulty and complicated selectivity.

Development of more predictive biomarkers

First, lacking potential biomarkers to predict the therapeutic effect of ICIs alone or in combination with other therapies is concerned in SCLC (91). High level of PD-L1 in multiple tumor cells or TME had been assumed as a predictor for a better response and survival after ICIs treatment, which has been approved by the FDA as an indicator for variable solid tumors, including lung cancers. However, recent evidence suggested that the clinical benefit of ICIs might not be restricted in PD-L1 high patients, leading to the full doubt of the predictive capability of PD-L1 (92). Thereby, multimodal detection of PD-L1, such as PD-L1 protein, PD-L1 mRNA, circulating PD-L1, and dynamic PD-L1 monitoring, might provide a comprehensive method for screening candidates for ICIs. Moreover, combined biomarkers, such as PD-L1 combined with tumor mutation burden (TMB) and microsatellite instability-high/mismatch repair deficient, nomograms, and deep learning, could better provide advice for therapeutic decisions (93).

Specific clinical trial designs

Ten to twenty-five percent of patients beneficial from ICIs are not counted by the traditional response criteria, due to the similar imaging performance of inflammation and tumor growth, the antitumor activity of immunotherapy might be more substantial than measured by standard response criteria (94). Secondly, due to the immunotherapy is based on slow stimulation of the immune system rather than rapidly assaulting tumor cells, the efficacy and antitumor responses are always delayed (95). Thereby, the endpoints of traditional anticancer treatment may be insufficient for immunotherapy, and long-term disease-free survival is more appropriate for immunotherapy (96). Moreover, the assessment of multiple immune cells in the TME or peripheral blood should be counted as additional endpoints for immunotherapy (96).

Enhancement of the efficacy

Tumor heterogeneity and treatment resistance are the most two mechanisms to hinder the efficacy of cancer immunotherapy (92). Liquid biopsies, containing the genomic analysis of circulating free DNA or cancer cells, could noninvasively obtain the level of tumor heterogeneity and also dynamically monitor resistance (97). Moreover, liquid biopsies are promising for personalized medicine to screen optimal combinational therapy (97).

Decreasing the financial toxicity

Cancer immunotherapies are known as one of the most promising treatments for malignant tumors, while they are also the most expensive ones in cancer, considering the enormous research costs (98). The cost for each lung cancer patient to treat with nivolumab was estimated at $44,100 per year (99). Thence, screening potential patients for immunotherapy is critical to reducing the unnecessary financial burden on patients. Meanwhile, cost-effectiveness, cost-benefit, and quality of life (QoL) is another approach to weigh the clinical benefit and financial cost (92).

Understanding the evolving immuno-oncology is increasingly relevant and crucial to solve those problems and define therapeutic strategies and potential target populations of combinational immunotherapy. Ultimately, emerging combinational immunotherapy will transform SCLC into a chronic disease to help patients survive from tumors.

Supplementary

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