Sustained remission following finite duration bispecific antibody therapy in patients with relapsed/refractory myeloma
- PMID: 39134535
- PMCID: PMC11319778
- DOI: 10.1038/s41408-024-01114-7
Sustained remission following finite duration bispecific antibody therapy in patients with relapsed/refractory myeloma
Conflict of interest statement
RC: Consulting/Advisory Board-Janssen, Sanofi, Adaptive Biotech. SL: Consultant and/or Advisor for Adaptive Biotechnologies, Alexion Therapeutics, Bristol-Meyers-Squibb, Caelum Biosciences, Janssen Pharmaceuticals, Karyopharm Therapeutics, Oncopeptides AB, GSK, Abbvie, Janssen, Pfizer, and Takeda Pharmaceutical Company; receives research funding from Celgene, Inc., Sanofi, Zentalis; received honoraria from Clinical Care Options and Regeneron Pharmaceuticals; and has Royalties/Patents with Caelum Biosciences. In addition, SL has a patent CAEL-101 with royalties paid to Columbia University. AD: Institutional research funding from AbbVie, Caelum, Janssen, Novartis, Prothena, Sanofi, Takeda, and TeneoBio; advisory board fees from BMS, Pfizer, and Janssen; and consulting fees from Prothena and Janssen. BD: Consultant-BMS, Genentech, Janssen, Karyopharm, Natera, Pfozer. SH: Consultant-Celgene, Genentech, Janssen, Novartis. MK: Honoraria: Janssen, Takeda, AbbVie, and Sanofi; consulting or advisory role: AbbVie, GSK, Janssen, Pfizer, Seattle Genetics, Takeda, Adaptive and Poolbeg Pharma. Research funding: BMS/Celgene (to institution) and Janssen (to institution). MM: Institutional Research Funding: Sanofi S.A, GlaxoSmithKline plc, Takeda Pharmaceutical Company, Ionis Pharmaceuticals, Bristol-Myers Squibb Company, Celgene Corporation, Sanofi S.A, and Amgen Inc; Consultancy: Sanofi S.A, Bristol-Myers Squibb Company, and Pfizer; Honorarium: Blood Cancer Today, MJH life sciences. The remaining authors declare no relevant financial conflicts of interest.
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References
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- D’Souza A, Shah N, Rodriguez C, Voorhees PM, Weisel K, Bueno OF, et al. A phase I first-in-human study of ABBV-383, a B-cell maturation antigen × CD3 bispecific T-cell redirecting antibody, in patients with relapsed/refractory multiple myeloma. J Clin Oncol. 2022;40:3576–86. 10.1200/JCO.22.01504 - DOI - PMC - PubMed
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- Jagannath S, Richter J, Dhodapkar MV, Hoffman JE, Lee HC, Suvannasankha A, et al. Patterns of response to 200 Mg linvoseltamab in patients with relapsed/refractory multiple myeloma: longer follow-up of the linker-MM1 study. Blood. 2023;1424746. 10.1182/blood-2023-177968 - DOI
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- Bar N, Mateos MV, Ribas P, Hansson M, Paris L, Hofmeister CC, et al. Alnuctamab (ALNUC; BMS-986349; CC-93269), a 2+1 B-cell maturation antigen (BCMA) × CD3 T-cell engager (TCE), administered subcutaneously (SC) in patients (Pts) with relapsed/refractory multiple myeloma (RRMM): updated results from a phase 1 first-in-human clinical study. Blood. 2023;142:2011. 10.1182/blood-2023-180013 - DOI
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