To the editor
The prognosis of patients with relapsed or refractory (R/R) multiple myeloma (MM) is generally poor, and new therapeutic methods are urgently demanded. G protein-coupled receptor family C group 5 member D (GPRC5D) is primarily expressed on myeloma cells, and normal tissue expression is limited to the hair follicle, making it a promising therapeutic target for patients with MM [1‐4]. We summarized some impressive developments in GPRC5D-targeted immunotherapies for R/R MM from the 2022 ASH Annual Meeting (ASH 2022).
GPRC5D CAR-T cell therapy in R/R MM
In patients with R/R MM, anti-GPRC5D chimeric antigen receptor (CAR)-T cell treatment exhibited encouraging clinical efficacy and a manageable safety profile [2‐4]. Dr. Bal reported the results of BMS-986393 (CC-95266) trial[5], a phase 1 first-in-human GPRC5D-targeted CAR-T cell therapy in patients with R/R MM (Table 1). In this heavily pretreated population (median four prior therapies, 90% previous transplant, 41% previous B cell maturation antigen [BCMA] -targeted therapies), the initial (1-month) overall response rate (ORR) was 86% (12/14), including 4/6 patients treated with previous BCMA-targeted therapies. No grade ≥ 3 cytokine release syndrome (CRS), on-target/off-tumor activity, or immune effector cell-associated neurotoxicity syndrome (ICANS) events were presented (Table 2).
Table 1
Properties of GPRC5D-targeted agents in MM
Author | Agent | Clinical Trial Identifier | Phase | Target | Mechanism | Cell source | References |
|---|---|---|---|---|---|---|---|
Sham Mailankody et al. | MCARH109 | NCT04555551 | 1 | GPRC5D | CAR-T | Autologous | [2] |
Jieyun Xia et al. | GPRC5D CAR-T | ChiCTR2100048888 | 2 | GPRC5D | CAR-T | Autologous | [3] |
Mingming Zhang et al. | OriCAR-017 | NCT05016778 | 1 | GPRC5D | CAR-T | Autologous | [4] |
Susan Bal et al. | BMS-986393 | NCT04674813 | 1 | GPRC5D | CAR-T | Autologous | [5] |
Ajai Chari et al. | Tal (JNJ-64407564) | NCT03399799/NCT04634552 | 1/2 | GPRC5D,CD3 | BiTE | Off-the-shelf | [6] |
Yaël C. Cohen et al. | Tal (JNJ-64407564) -DP or Tal-D versus DPd | NCT05455320 | 3 | GPRC5D,CD3 | BiTE | Off-the-shelf | [7] |
Carmelo Carlo-Stella et al. | RG6234 | NCT04557150 | 1 | GPRC5D,CD3 | BiTE | Off-the-shelf | [9] |
John Reiser | FT555 | – | Preclinical | GPRC5D,CD38 | CAR-NK | iPSCs master cell line | [11] |
Table 2
Outcomes of GPRC5D-targeted clinical trials in MM
Author | Agent | Clinical Trial Identifier | Patients (n) | Medium number of prior LOT | Prior BCMA directed therapy | ORR | ≥ CR | ORR in patients with Prior BCMA directed therapy | Grade ≥ 3 CRS | Grade ≥ 3 ICANS | On-target/off-tumor | Nail disorders | References |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Sham Mailankody et al. | MCARH109 | NCT04555551 | 17 | 6 | 59% | 71% | 35% | 70% | 6% | 6% | – | 65% | [2] |
Jieyun Xia et al. | GPRC5D CAR-T | ChiCTR2100048888 | 33 | 4 | 27% | 91% | 64% | 100% | 0% | 3% | – | 27% | [3] |
Mingming Zhang et al. | OriCAR-017 | NCT05016778 | 10 | 5.5 | 50% | 100% | 60% | 100% | 0% | 0% | – | 30% | [4] |
Susan Bal et al. | BMS-986393 | NCT04674813 | 17 | 4 | 41% | 86% | – | 67% | 0% | 0% | 29% | 12% | [5] |
Ajai Chari et al. | Tal (JNJ-64407564) | NCT03399799/NCT04634552 | 0.4 mg/kg weekly:143; 0.8 mg/kg biweekly:145 | 5 | – | 0.4 mg/kg weekly:73%; 0.8 mg/kg biweekly:74% | 0.4 mg/kg weekly:29% | – | 0.4 mg/kg weekly:2%; 0.8 mg/kg biweekly:1% | – | – | 0.4 mg/kg weekly:52%; 0.8 mg/kg biweekly:43% | [6] |
Carmelo Carlo-Stella et al. | RG6234 | NCT04557150 | IV: 51; SC: 54 | IV: 5; SC: 4 | IV: 19.6%; SC: 20.4% | IV: 71.4%; SC: 60.4% | IV: 28.5%; SC: 18.8% | 55.6% | IV: 2.0%; SC: 1.9% | 1.90% | IV: 72.5%; SC: 81.5% (cutaneous AEs) | IV: 17.6%; SC: 22.2%, (hair and nail changes) | [9] |
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Besides GPRC5D CAR-T cell monotherapy, BCMA and GPRC5D dual-target CAR-T cell therapies (NCT05509530, NCT05325801), concurrent administration of GPRC5D-targeted CAR-T cells and BCMA-targeted CAR-T cells (NCT05431608) in patients with R/R MM are being investigated in clinical settings.
GPRC5D x CD3 bispecific T cell engagers (BiTEs) in R/R MM
Talquetamab (JNJ-64407564) is a first-in-class, off-the-shelf, bispecific T cell engager antibody that targets both GPRC5D and CD3 (Table 1). In the phase 1/2 MonumenTAL-1 study (NCT03399799/NCT04634552) [6], measurable improvement of cancer was observed in 73% of patients receiving 0.4 mg/kg of talquetamab weekly and 74% of patients receiving 0.8 mg/kg every other week, with 29% achieving a complete response. The most common adverse events (AEs) at 0.4 mg/kg weekly /0.8 mg/kg biweekly dose were CRS (79%/72%; grade 3: 2%/1%); skin-related AEs occurred in 56%/68% and nail disorders in 52%/43% of patients (Table 2). In addition, the MonumenTAL-3 trial (NCT05455320) will compare the efficacy and safety of talquetamab plus daratumumab (with or without pomalidomide) with those of daratumumab plus pomalidomide and dexamethasone in patients with RRMM who received ≥ 1 prior line of therapy [7] (Table 1).
RG6234 is another exciting novel GPRC5DxCD3 BiTE[8‐10]. Carlo-Stella et al. presented the initial results of an ongoing phase I study (NCT04557150; Table 1, Table 2) [9]. The median number of previous lines of therapy was five in the intravenous (IV) cohorts and four in the subcutaneous (SC) cohorts. Some patients had received BCMA-targeted therapies previously (IV: 19.6%; SC: 20.4%). Clinical activity was observed in both routes of dose escalation (ORR: IV 71.4%, SC 60.4%), including 55.6% of patients who had received previous BCMA-targeted therapies. The drug was well tolerated; CRS and ICANS > grade 2 were both ≤ 2%, and only two patients (3.9%) in the IV group and two patients (3.7%) in the SC group discontinued treatment due to RG6234-related AEs. Biomarker analysis demonstrated rapid T cell activation and T cell-mediated anti-myeloma activity independent of the route of administration [10].
Several GPRC5D CAR-T cell studies reported higher ORR (86%-100%) compared with GPRC5DxCD3 BiTEs (60.4%-74%); CR rates of GPRC5D CAR-T were also higher [2‐6, 9] (Table 2). However, the frequency and severity of CRS and ICANS were similar in both the treatments.
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GPRC5D CAR-NK Cell therapy in MM
FT555 is a multiplexed-engineered GRPC5D CAR-NK cell derived from an induced pluripotent stem cells (iPSC) master cell line[11] (Table 1). Compared to isogenic GPRC5D knockout targets, FT555 exhibited persistent specific anti-tumor activity against GPRC5D-positive myeloma cells in the preclinical study. In the disseminated in vivo xenograft model of MM, a single dose of FT555 showed robust killing kinetics and tumor clearance, controlled disease progression for up to 42 days and improved survival to 80 days compared to the untreated control arm of 37 days. The durability of FT555 was further strengthened by the addition of daratumumab, an anti-CD38 monoclonal antibody. Also, tumor growth inhibition was enhanced and survival was significantly prolonged.
In conclusion, the ASH 2022 Annual Meeting exhibited notable advances in the field of GPRC5D-targeted therapies in MM, as summarized in Tables 1 and 2. Although data from GPRC5D-related clinical trials need to be accumulated further, GPRC5D CAR-T cells have shown high ORR and CR rates, low incidence of ≥ grade 3 CRS and ICANS, and encouraging efficacy in patients who do not respond to or relapse after BCMA-targeted therapy. These results demonstrate that GPRC5D is a very potential immunotherapeutic target for R/R MM after BCMA.
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