Division of Hematology, Mayo Clinic, Rochester, MN
Matthew J. Rees , Aytaj Mammadzadeh , Abiola Bolarinwa , Mohammed E Elhaj , Arwa Bohra , Sikander Ailawadhi , Ricardo Parrondo , Saurabh Chhabra , Yi Lin , Moritz Binder , Suzanne R. Hayman , Angela Dispenzieri , Francis Buadi , David Dingli , Rahma M. Warsame , Radhika Bansal , Prashant Kapoor , Morie A. Gertz , Eli Muchtar , Shaji Kumar
Background: BCMA directed CAR T cells, antibody drug conjugates (ADCs), and T cell engagers (TCEs) each have distinct strengths and weaknesses. While these agents have shown unprecedented response rates and survival outcomes, no head-head comparisons exist. We assessed the relative efficacy of different BCMA-therapies in relapsed myeloma, with a focus on high-risk subgroups. Methods: Retrospective study of MM patients treated at Mayo Clinic with commercial or investigational BCMA targeted therapies between April 2018-June 2023. Results: 385 patients (ADC=59, TCE=134, CAR T=192) with a median follow up of 20-months. The median time from diagnosis was 6.1 years. The table shows disease, and treatment characteristics. Amongst ADCs and TCEs recipients, the median treatment duration was 1.9 and 3.5 months respectively, disease progression (64% and 79%) and intolerance (22% and 10%) were the most common reasons for discontinuation. The overall response rates were 27, 50, and 86% for ADCs, TCEs and CAR T, respectively. Compared to ADCs, CAR T was associated with improved PFS (adjusted HRPFS=0.29, 95%CI=0.20-0.43) and OS (aHROS=0.28, 95%CI=0.18-0.44) when adjusting for age, R-ISS, double hit high risk cytogenetic abnormalities (HRCAs), extramedullary disease (EMD, excluding paraskeletal plasmacytomas), triple class refractoriness, and the number of lines of therapy (LOTs) received in the preceding 1 year. Likewise compared to ADCs, TCEs were associated with superior PFS (aHRPFS=0.59, 95%CI=0.40-0.86) and OS (aHROS=0.60, 95%CI=0.39-0.93). Amongst patients with plasma cell leukemia (PCL) or EMD at the time of BCMA therapy (n=123), median PFS was poor irrespective of the therapeutic class at 1.3, 1.7 and 6.1 months for ADCs, TCEs and CAR T, respectively. Equally, for patients previously treated with BCMA therapy (n=58), median PFS was poor regardless of class at 1.9, 2.4 and 3 months for ADCs, TCEs and CAR T, respectively. Of 229 relapses the mode of relapse was known in 192 cases (84%), with 101 (52%) having EMD at relapse. Conclusions: While contingent on myriad other factors, patients able to receive BCMA-directed CAR T therapy experience superior survival compared to ADC and TCEs. EMD, PCL and BCMA-exposed populations are recalcitrant to BCMA-directed immunotherapy, and EMD is a common means of relapse.
ADC, N = 591 | CAR T, N = 1921 | TCE, N = 1341 | p-value2 | |
---|---|---|---|---|
Age (years) | 61 (56, 68) | 58 (48, 64) | 59 (53, 66) | 0.008 |
R-ISS 3 at diagnosis | 5 (8.5%) | 20 (10%) | 17 (13%) | 0.7 |
Double hit HRCA prior to BCMA | 4 (6.8%) | 43 (22%) | 25 (19%) | 0.027 |
Triple class refractory | 50 (85%) | 149 (78%) | 119 (89%) | 0.029 |
Penta class refractory | 37 (63%) | 61 (32%) | 65 (49%) | <0.001 |
≥4 LOTs in preceding 1-year | 10 (17%) | 14 (7.3%) | 13 (9.7%) | 0.089 |
No. of LOTs prior to BCMA | 7.00 (5.00, 8.50) | 5.00 (4.00, 7.00) | 6.00 (4.00, 7.00) | <0.001 |
EMD/PCL prior to BCMA | 19 (40%) | 56 (30%) | 48 (39%) | 0.2 |
BCMA exposed | 13 (22%) | 15 (7.8%) | 30 (22%) | <0.001 |
1 Median(IQR); n(%), 2 Kruskal-Wallis rank sum test; Pearson's Chi-squared test.
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