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. 2024 Aug 12;14(1):137.
doi: 10.1038/s41408-024-01114-7.

Sustained remission following finite duration bispecific antibody therapy in patients with relapsed/refractory myeloma

Affiliations

Sustained remission following finite duration bispecific antibody therapy in patients with relapsed/refractory myeloma

Rajshekhar Chakraborty et al. Blood Cancer J. .
No abstract available

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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.

Figures

Fig. 1
Fig. 1
Kaplan–Meier curve for progression-free survival from discontinuation of bispecific antibody in patients with relapsed/refractory myeloma.
Fig. 2
Fig. 2
Swimmer plot for outcomes in all 23 patients who discontinued bispecific antibodies for a reason other than progression or death and had at least 3 months of follow-up after drug discontinuation, commencing at the time of discontinuation.

References

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