A phase 1, open-label study of LCAR-B38M, a chimeric antigen receptor T cell therapy directed against B cell maturation antigen, in patients with relapsed or refractory multiple myeloma

1Multiple myeloma is a neoplasm of plasma cells that represents 13% of hematologic cancers and 1% of all cancers. Despite the development of novel agents such as proteasome inhibitors, immunomodulatory drugs, and monoclonal antibodies that have significantly improved patient outcomes, multiple myeloma is still considered to be an incurable disease. The majority of patients will eventually relapse or become refractory to treatment; therefore, the development of new therapies for multiple myeloma remains a major unmet medical need.

2B cell maturation antigen (BCMA) is a member of the tumor necrosis factor superfamily and represents an ideal target for multiple myeloma immunotherapy. BCMA is widely expressed on the surface of multiple myeloma cells, but has low expression on normal cells and no expression on CD34+ hematopoietic cells.

3Chimeric antigen receptor (CAR) T cell therapy has emerged as an efficacious treatment in some relapsed/refractory hematologic cancers. CAR T cell therapies have been approved in the US for the treatment of relapsed or refractory acute lymphoblastic leukemia and large B cell lymphoma based on the high level of durable remissions that were achieved. In multiple myeloma, 2 phase 1 studies using CAR T cells targeting BCMA in heavily pretreated patients showed encouraging preliminary responses. In the CAR-BCMA study, of the 16/24 patients treated at the highest CAR T cell dose, 13 patients achieved a partial response (PR) or better, demonstrating an overall response rate (ORR) of 81%. In updated results of the bb-2121 study (N = 43), an ORR of 95.5% was observed in the 22 evaluable patients treated with the highest CAR T cell dose range. The promising efficacy shown in these preliminary studies suggests that BCMA-targeted CAR T cell therapy may be a viable approach in the treatment of relapsed or refractory multiple myeloma.

4LCAR-B38M is a dual epitope-binding CAR T cell therapy directed against 2 distinct BCMA epitopes. The bi-epitope BCMA-binding moieties confer high avidity binding and distinguish LCAR-B38M from other BCMA CAR constructs. Here, we report results from the full data set of 57 patients from our study site’s clinical experience with an ongoing phase 1 study of LCAR-B38M CAR T cell therapy in patients with relapsed or refractory multiple myeloma. Preliminary results of the first 35 patients treated at our site were presented at scientific meetings in 2017.

5A phase 1 trial of LCAR-B38M CAR T cells (LEGEND-2) has been explored at multiple centers in China, each with their own protocol for lymphodepletion and timing of CAR T cell administration. Study enrollment has ended at all 4 of these sites.

6The analysis reported here represents the clinical experience (N = 57) from The Second Affiliated Hospital of Xi’an Jiaotong University, which used cyclophosphamide alone as the lymphodepleting therapy and infused CAR T cells in 3 split doses. The study was initiated on March 30, 2016, and the analysis reported here is from a data cutoff date of February 6, 2018. A study schema is presented in Additional file 1.

7Eligible patients were between 18 and 80 years of age with confirmed diagnosis of relapsed or refractory multiple myeloma. Multiple myeloma was defined by the International Myeloma Working Group (IMWG) criteria, and relapse was defined by the National Comprehensive Cancer Network criteria.

8All patients underwent leukapheresis to obtain peripheral blood mononuclear cells from which T cells were purified. CD3+ T cells were transduced with LCAR-B38M lentiviral vector to express anti-BCMA CAR (Additional file 2). The engineered T cells were further expanded ex vivo under interleukin-2 stimulation. Lymphodepletion using 3 doses of cyclophosphamide 300 mg/m2 on days − 5, − 4, and − 3 was followed by infusion of the engineered LCAR-B38M CAR T cells 5 days after the initiation of lymphodepletion chemotherapy. The total weight-adjusted CAR+ T cell dose (median, 0.5 × 106 cells/kg [range, 0.07 to 2.1 × 106]) was split into 3 infusions (20, 30, and 50% of total dose) administered over 7 days.

9The primary objective is to evaluate the safety of LCAR-B38M, and the secondary objective is to assess the antimyeloma activity of CAR T cell therapy. Adverse events (AEs) were identified and toxicity was graded using the National Cancer Institute Common Terminology Criteria for Adverse Events, v.4.03. Cytokine release syndrome (CRS) was assessed using the modified criteria proposed by Lee et al.. No prophylactic treatment was given for CRS.

10Response assessments were based on the general guidelines from the IMWG. Disease evaluations were conducted using serum quantitative immunoglobulin or free light chain levels followed by immunofixation (serum and urine) and bone marrow biopsy/flow cytometry after normalization of serum quantitative immunoglobulin and free light chain levels. Two eight-color flow cytometry panels were used for minimal residual disease (MRD) assessment. The first panel included CD38, CD45, CD19, CD56, CD27, CD81, CD200, and CD20 antibodies. The second panel included CD38, CD138, CD19, CD45, CD117, and CD28 antibodies; cytoplasmic kappa and cytoplasmic lambda antibodies were used to assess clonality. Samples were analyzed on a Canto II flow cytometer (Becton Dickenson). The sensitivity of MRD assessment was up to 1 × 10−4.

11BCMA expression was measured in malignant plasma cells from either bone marrow or plasmacytoma by flow cytometry. Whole blood was collected at serial time points to measure the number of LCAR-B38M CAR T cells using an exploratory quantitative polymerase chain reaction (PCR) assay. Preliminary assay results were generated with a research grade real-time PCR assay, which represents a semi-quantitative assessment of CAR gene copy numbers over time.

12The all-treated population included all patients who received at least 1 dose of LCAR-B38M CAR T cells and was used for all safety and efficacy analyses. Categorical variables were summarized using frequency counts and percentages. Continuous variables included the mean, standard deviation, median, and range (minimum and maximum) and were summarized using descriptive statistics.

13The ORR was defined as the proportion of patients who achieved a complete response (CR), very good partial response (VGPR), or PR, after receiving study treatment. Two-sided 95% exact confidence intervals (CIs) based on exact method of binomial distribution were calculated for each response category. The median duration of response, progression-free survival, and overall survival and corresponding 95% CI were calculated using Kaplan-Meier method.

14At data cutoff (February 6, 2018), 57 patients were enrolled in the study site and had received LCAR-B38M CAR T cell therapy. The median age was 54 years (range, 27 to 72), and more men (60%) were enrolled in the study (Table 1). The median number of prior lines of therapy was 3 (range, 1 to 9), including prior proteasome inhibitor therapy (68%), immunomodulatory agents (86%), and both proteasome inhibitors and immunomodulatory agents (60%; Table 1). At the time of enrollment, 37% of patients had stage III disease as assessed by the International Staging System. The median duration of follow-up for all patients was 8 months (range, 0.7 to 20.7). Due to clinical practice differences, refractoriness could not be systematically assessed by the study physician.

15AEs were reported in all patients. The most common (≥ 40%) AEs of any grade were pyrexia (91%), CRS (90%), thrombocytopenia (49%), and leukopenia (47%; Table 2). Grade ≥ 3 AEs were reported in 37 patients (65%); the most common (≥ 20%) grade ≥ 3 events were leukopenia (30%), thrombocytopenia (23%), and aspartate aminotransferase increased (21%).

16CRS, assessed according to Lee et al. criteria, was mostly grades 1 (47%) and 2 (35%); 4 patients (7%) had grade 3 cases (Table 2). Liver function abnormalities, particularly aspartate aminotransferase increased, were the most common signs of end organ injury among patients with CRS (Table 3). Coagulopathies were also observed in patients who had CRS. Among patients who had CRS and available laboratory assessments, prolongation of activated partial thromboplastin time and decreased fibrinogen occurred in 67 and 37% of patients, respectively. Kidney, pulmonary, and vascular system abnormalities were less frequent (2 to 35%) than those observed for the liver (Table 3).

17The median time to onset of any grade CRS was 9 days (range, 1 to 19). Tocilizumab (46%), vasopressor (11%), and supplemental oxygen (35%) were used to manage the CRS. One patient, who had received a dose of 1.8 × 106 CAR+ T cells/kg, developed grade 2 CRS. While the CRS was resolving, the patient developed sudden onset of respiratory distress 22 days after receiving the first dose of CAR T cells. The patient required intubation for ventilator support and died 1 h later with cause of death reported as grade 5 pulmonary embolism and acute coronary syndrome. The intubation was performed as part of final resuscitation efforts and not specifically to treat the CRS. Except for the patient who had grade 5 AEs, all CRS events resolved, with a median duration of 9 days (range, 3 to 57).

18Neurotoxicity was observed in 1 patient, dosed at 1.0 × 106 CAR+ T cells/kg, who developed grade 1 aphasia, agitation, and seizure-like activity. The patient was treated with 10 mg diazepam, and the events resolved within 1 day.

19In total, 50 of 57 patients responded; the ORR was 88% (95% CI, 76 to 95). CR was achieved by 39 patients (68%; 95% CI, 55 to 80), VGPR was achieved by 3 patients (5%; 95% CI, 1 to 15), and PR was achieved by 8 patients (14%; 95% CI, 6 to 26; Fig. 1a). MRD was negative for 36/57 patients (63%; 95% CI, 49 to 76), as assessed by bone marrow eight-color flow cytometry assay, and all MRD negative patients achieved CR. The median time to initial response was 1 month (range, 0.4 to 3.5).

20LCAR-B38M CAR T cells also demonstrated activity in patients with extramedullary disease, with observed decreases in tumor mass (Fig. 1b, c).

21At data cutoff, 10 patients (20%) who achieved a PR or better subsequently progressed. The Kaplan-Meier estimate of median duration of response was 14 months (95% CI, 12 to not estimable). The median progression-free survival was 15 months (95% CI, 11 to not estimable; Fig. 2a). Six patients died during the study due to disease progression (n = 4), suicide after disease progression (n = 1), and pulmonary embolism and acute coronary syndrome (n = 1). The median overall survival was not reached (Fig. 2b).

22Among the patients with BCMA expression data, 26/53 (49%) had < 40% BCMA expression and 27/53 (51%) had ≥ 40% BCMA expression (Additional file 3). BCMA expression did not appear to correlate with clinical response. An ORR of 92% was observed in patients with < 40% BCMA expression compared with an ORR of 82% in patients with ≥ 40% BCMA expression. Correlation between BCMA expression and median PFS or OS was not observed. Median PFS was 15 months for patients who had < 40% BCMA expression and 11 months for patients who had ≥ 40% BCMA expression. Median OS was not reached for both the < 40 and ≥ 40% BCMA expression groups (Additional file 3).

23The median number of total CAR+ T cells infused was 32.3 × 106 (range, 3.3 to 126.2 × 106). The body weight-adjusted median number of CAR+ T cells administered was 0.5 × 106 cells/kg (range, 0.07 to 2.1 × 106). The overall incidence and severity of CRS was higher with increasing median LCAR-B38M CAR T cell dose; however, the small number of patients with higher grade events limits the interpretation of the data. There was no clear relationship between LCAR-B38M CAR T cell dose and disease response (Additional file 4).

24Among the patients who had blood samples for analysis (n = 31), the majority had peak levels of LCAR-B38M signal greater than 1 × 104 copies/μg genomic DNA following infusion. LCAR-B38M CAR T cells in most patients (71%) were not detectable (signal below the lower limit of detection) in peripheral blood at 4 months, and only 5 patients showed CAR T cell persistence up to 10 months (Additional file 5).

25Serum interleukin-6 increased transiently within the first month following LCAR-B38M CAR T cell infusion. The peak levels of interleukin-6 increased with severity of CRS (Additional file 6). Similar results were observed with interleukin-2, interleukin-8, interleukin-10, and tumor necrosis factor alpha.

26Infusion of LCAR-B38M CAR T cells resulted in a rapid reduction of serum immunoglobulin levels in all patients. IgA and IgG levels eventually increased for some patients who also had disease progression (Additional file 7).

27In this analysis of an ongoing phase 1, first-in-human clinical study, LCAR-B38M, a CAR T cell therapy directed against 2 distinct BCMA epitopes, displayed a manageable safety profile and demonstrated durable responses in patients with relapsed or refractory multiple myeloma.

28CRS occurred in 90% of patients and were mostly grades 1 and 2 (83%), with 4 (7%) grade 3 cases. The overall response rate was 88%, and 39 patients (68%) achieved CR at a median follow-up of 8 months (range, 0.7 to 20.7).

29All cases of CRS started with pyrexia with a median time to onset of 9 days (range, 1 to 19) after the first infusion of LCAR-B38M CAR T cells, suggesting that careful monitoring for fever during the first several days following CAR T cell infusion could be used in future studies to identify patients likely to require additional support for the CRS.

30Cytopenias (thrombocytopenia and neutropenia) were common (54%); prolonged grade 4 cytopenias with duration exceeding 35 days occurred in 16% of patients. Infection AEs were reported, although the rate (9%) did not exceed that expected for patients with multiple myeloma.

31Time to response was rapid, with a median time of 1 month (range, 0.4 to 3.5). Consistent efficacy was observed across all subgroups examined, including prior autologous stem cell transplant, age, number of prior therapies, and prior proteasome and immunomodulatory agent treatment. Ten responders (20%) progressed or died at data cutoff.

32BCMA expression did not appear to correlate with clinical response and was highly variable, as has been described by others. In the dose expansion phase of the bb-2121 study, BCMA expression is not an eligibility requirement, suggesting that clinical response might be independent of BCMA expression levels.

33This was an exploratory study conducted to evaluate the effects of different preconditioning chemotherapy and treatment regimens for LCAR-B38M. Because this was the first clinical experience with LCAR-B38M, cyclophosphamide alone, rather than cyclophosphamide plus fludarabine, was used as the preconditioning treatment for safety considerations. Typically, CAR T cell therapy has a broad range of efficacious doses, and it is not uncommon for CAR T cell studies to start without a dose escalation phase. The dose used in our study was determined by both the sponsor and the investigator. Several factors were considered to determine the dose for each patient: the patient’s disease status, overall condition prior to infusion, and available total CAR T cells manufactured.

34In this study, the median age of patients was 54 years, which is consistent with reported differences in the median age at diagnosis between Chinese and Western patients with multiple myeloma (59 vs. 70 years, respectively). Taking the median age of patients into consideration, a median of 3 prior lines of therapy and ISS stage III disease in 37% of patients suggest that the patients in this study had advanced myeloma.

35The 88% ORR observed in this study was higher than that observed with CAR-BCMA. Among the 10 patients treated at the lowest dose of 0.3 × 106 CAR-BCMA CAR+ T cells/kg, only 2 patients (20.0%) achieved PR or better. For the 16 patients treated at the highest dose of 9 × 106 CAR-BCMA CAR+ T cells/kg, 13 (81%) achieved PR or better. The observed difference in response may be related to the design of the CAR and the dose of CAR+ T cells infused. The CAR-BCMA design incorporates a 11D-5-3 single anti-BCMA single chain variable region, a CD28 costimulatory domain, and a CD3ζ T cell activation domain and is different from the design of LCAR-B38M, which binds to 2 distinct BCMA epitopes. Although it is not possible to compare across studies, the efficacious doses used in the CAR-BCMA study were also considerably higher than those of LCAR-B38M used in this study (median dose of 0.5 × 106 CAR+ T cells/kg [range, 0.07 to 2.10 × 106]).

36The bb-2121 study (N = 43) tested a range of study doses from 50 × 106 to 800 × 106 CAR+ T cells. Among the 22 evaluable patients in the cohort receiving > 150 × 106 CAR+ T cells, the ORR was 95.5%. The final doses under evaluation for the phase 2 study of bb-2121 are 150 to 450 × 106 CAR+ T cells, which are higher than the doses used in this study with LCAR-B38M (median total CAR+ T cells = 32.3 × 106). The dual epitope-binding of LCAR-B38M, which confers high avidity binding, may result in clinical responses at lower cell doses, with less toxicity.

37This ongoing first-in-human study has provided initial proof-of-concept that dual epitope-binding LCAR-B38M CAR T cells may be a highly effective therapy for patients with relapsed or refractory multiple myeloma. LCAR-B38M displayed a manageable safety profile consistent with its known mechanism of action. Further clinical evaluation of this promising and potentially transformational treatment approach is underway, with an ongoing phase 1b/2 study in the US (ClinicalTrials.gov, NCT03548207).