Real‐world outcomes of brexucabtagene autoleucel (brexu‐cel) for relapsed or refractory mantle cell lymphoma (r/r MCL): A CIBMTR subgroup analysis by prior treatment
Year: 2023
Type: article
Abstract: Introduction: Brexu-cel is a CAR T-cell therapy approved for adult patients (pts) with r/r MCL. In a 3-year follow-up of ZUMA-2 (Wang et al. 2022), ORR was 91% (CR, 68%). Median DOR, PFS, and OS were 28.2, 25.8, and 46.6 mo, respectively. Here, we describe real-world outcomes with brexu-cel analyzed by prior receipt of BTK inhibitor (BTKi), bendamustine, or autoHCT, and 1–2 versus ≥3 prior lines (L) of therapy. Methods: From July 2020 to August 2022, 397 pts who received brexu-cel for r/r MCL in 79 US centers were registered in the CIBMTR observational database. This analysis included 272 pts (median follow-up, 6.6 mo; range, 0.3–16.5), excluding pts with prior non-HCT cellular therapy (n = 7), missing data on prior treatment, or no follow-up. Descriptive analyses were used for all outcomes. Results: Median age was 65.8 y (range, 34.1–84.9); most pts were male (78%). Prior to infusion, 7% had ECOG PS ≥2; 76% had clinically significant comorbidities; 4% had extranodal CNS involvement. At diagnosis, Ki-67 ≥30%, Ki-67 ≥50%, and TP53/17p deletion were reported in 69% (n = 111/160), 44% (n = 70/160), and 19% (n = 29/153) of pts, respectively. Pts had a median of 4L of prior therapy (range, 1–12L; 6% as 2L). Prior to leukapheresis, 87% and 54% of pts had received BTKi or bendamustine, respectively, and 31% were autoHCT recipients. Median time from leukapheresis to infusion was 28 d (IQR, 26–34 d); 18% of pts received bridging therapy. Overall ORR was 89% (CR, 78%). At 6 mo, cumulative incidence of relapse/PD was 21%; DOR, PFS, and OS were 76%, 73%, and 83%, respectively. Grade ≥3 (ASTCT consensus) CRS and ICANS occurred in 9% and 27% of pts, respectively (88% and 62% for any grade). Most CRS (94%) and ICANS (79%) resolved within 3 weeks. Prolonged cytopenia by 30 d occurred in 23% of pts. NRM at 100 d and 180 d were 3% and 6%, respectively, mainly due to infections. ORR in BTKi-naive (n = 36) versus -exposed (n = 233) pts was 85% (CR, 79%; 6-mo DOR, 84%) versus 89% (CR, 77%; 6-mo DOR, 74%); in pts with (n = 145) versus without (n = 124) prior bendamustine was 88% (CR, 75%; 6-mo DOR, 75%) versus 89% (CR, 80%; 6-mo DOR, 77%); in pts with (n = 83) versus without (n = 188) prior autoHCT was 90% (CR, 82%; 6-mo DOR, 83%) versus 88% (CR, 76%; 6-mo DOR, 72%). CR rates were higher in pts with brexu-cel as 2/3L (n = 56) versus 4L+ (n = 213) (91% vs. 74%; ORR, 92% vs. 88%; 6-mo DOR, 77% vs. 75%). Safety profiles were similar regardless of prior BTKi or autoHCT. Pts with prior bendamustine had lower rates of Grade ≥3 ICANS (19% vs. 36%) but higher prolonged cytopenia (29% vs. 16%) versus those without. Conclusions: These early findings suggest that real-world outcomes with brexu-cel are consistent regardless of prior BTKi, bendamustine, or autoHCT. Use of brexu-cel in earlier lines may help achieve a higher CR rate. Further studies with longer follow-up are warranted to contextualize response rates in relation to long-term clinical benefits of brexu-cel. Updated data with longer follow-up will be presented. NA and SK contributed equally. Encore Abstract - previously submitted to ASCO 2023 and EHA 2023 The research was funded by: Kite, a Gilead Company; and NCI grant: National Cancer Institute (CIDR [U24 CA233032]) Keywords: aggressive B-cell non-Hodgkin lymphoma, cellular therapies, immunotherapy Conflicts of interests pertinent to the abstract. M. Hamadani Consultant or advisory role: Incyte Corporation, MorphoSys, Kite, Genmab, SeaGen, Gamida Cell, Novartis, Legend Biotech, Kadmon. ADC Therapeutics; Omeros, Abbvie Research funding: Takeda Pharmaceutical Company: ADC Therapeutics; Spectrum Pharmaceuticals; Astellas Pharma N. Grover Consultant or advisory role: Seattle Genetics; Genentech; ADC Therapeutics Stock ownership: Sangamo Honoraria: Novartis Research funding: Tessa Therapeutics M. Shadman Employment or leadership position: Spouse employment for BMS Consultant or advisory role: Abbvie, Genentech, AstraZeneca, Sound Biologics, Pharmacyclics, Beigene, Bristol Myers Squibb, Morphosys/Incyte, TG Therapeutics, Innate Pharma, Kite Pharma, Adaptive Biotechnologies, Epizyme, Eli Lilly, Adaptimmune, Mustang Bio, Regeneron, Merck, Fate therapeutics, MEI pharma and Atara Biotherapeutic Research funding: Mustang Bio, Celgene, Bristol Myers Squibb, Pharmacyclics, Gilead, Genentech, AbbVie, TG Therapeutics, Beigene, AstraZeneca, Sunesis, Atara Biotherapeutics, Genmab, Morphosys/Incyte F. L. Locke Consultant or advisory role: A2, Allogene, Amgen, Bluebird Bio, BMS/Celgene, Calibr, Caribou, Cellular Biomedicine Group, Cowen, Daiichi Sankyo, EcoR1, Emerging Therapy Solutions, GammaDelta Therapeutics, Gerson Lehrman Group (GLG), Iovance, Kite Pharma, Janssen, Legend Biotech, Novartis, Sana, Takeda, Wugen, Umoja Research funding: Aptitude Health, ASH, BioPharma Communications CARE Education, Clinical Care Options Oncology, Imedex, Society for Immunotherapy of Cancer Educational grants: A2 Bio J. Gerson Consultant or advisory role: Abbvie, Genentech, Kite Research funding: Loxo M. J. Frank Employment or leadership position: Roche/Genentech Stock ownership: Roche/Genentech L. E. Budde Consultant or advisory role: AstraZeneca, Roche, ADC Therapeutics Research funding: Amgen, Merck, AstraZeneca, Mustang Bio M. Wang Consultant or advisory role: AbbVie, Acerta Pharma, AstraZeneca, BeiGene, BioInvent, Deciphera, InnoCare, Janssen, Kite Pharma, Leukemia & Lymphoma Society, Lilly, Merck, Milken Institute, Oncternal, Parexel, Pepromene Bio, Pharmacyclics, VelosBio Honoraria: AbbVie, Acerta Pharma, AstraZeneca, BeiGene, BioInvent, Dava Oncology, Eastern Virginia Medical School, IDEOlogy Health, Janssen, Kite Pharma, Leukemia & Lymphoma Society, LLC TS Oncology, Medscape, Meeting Minds Experts, MJH Life Sciences, Merck, Moffit Cancer Center, Oncology Specialty Group, OncLive, Pharmacyclics, Physicians Education Research funding: Acerta Pharma, AstraZeneca, BeiGene, BioInvent, Celgene, Genmab, Genentech, Innocare, Janssen, Juno Therapeutics, Kite Pharma, Lilly, Loxo Oncology, Molecular Templates, Oncternal, Pharmacyclics, VelosBio, Vincerx Z. Hu Employment or leadership position: Kite, a Gilead Company Stock ownership: Gilead Sciences, Inc. A. Nunes Employment or leadership position: Gilead Sciences Europe, Ltd. Stock ownership: Gilead, Amgen Honoraria: Gilead D. Dalton Employment or leadership position: Kite, a Gilead Company Stock ownership: Gilead, Bristol-Myers Squibb I. Kloos Employment or leadership position: Kite, a Gilead Company Stock ownership: Gilead Sciences, Inc. D. Lee Employment or leadership position: Kite, a Gilead Company Stock ownership: Gilead Sciences, Inc H. Xu Employment or leadership position: Kite, a Gilead Company Stock ownership: Gilead Sciences, Inc M. Pasquini Consultant or advisory role: BMS Research funding: Kite, Novartis, BMS, Janssen, GSK A. Herrera Consultant or advisory role: Karyopharm, Takeda, Tubulis, Regeneron, Genmab, Pfizer, Caribou, Adicet bio, Abbie, BMS, Genentech, Astrazeneca, ADC, Seattle Genetics, Merck Research funding: BMS, Genentech, AstraZeneca, ADC, Merck, Seattle Genetics, Kite, Gilead
Source: Hematological Oncology
DOI: 10.1002/hon.3164_358
Authors: N. Ahmed, S. Kambhampati, M. Hamadani, N. Grover, M. Shadman, F. L. Locke, J. Gerson, M. J. Frank, L. E. Budde, M. Wang, Z. Hu, A. Nunes, D. Dalton, I. Kloos, D. Lee, H. Xu, M. Pasquini, A. Herrera
Institutions: University of Kansas Medical Center, City Of Hope National Medical Center, Medical College of Wisconsin, University of North Carolina at Chapel Hill, Fred Hutch Cancer Center, Moffitt Cancer Center, University of Vermont Medical Center, Stanford University, The University of Texas MD Anderson Cancer Center, Kite (United States)
Language: English
Topic: CAR-T cell therapy research
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W4380084511
