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. 2025 May 21:S2152-2650(25)00181-8.
doi: 10.1016/j.clml.2025.05.015. Online ahead of print.

Retreatment With Anti-CD38-Based Combinations in Multiple Myeloma in Real-Life: Results From the Emmy Cohort Study

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Retreatment With Anti-CD38-Based Combinations in Multiple Myeloma in Real-Life: Results From the Emmy Cohort Study

Alexis Talbot et al. Clin Lymphoma Myeloma Leuk. .
Free article

Abstract

Introduction: Anti-CD38 monoclonal antibodies (aCD38) are increasingly used in early lines of therapies in multiple myeloma (MM). Retreatment with aCD38-based regimen is a widely used practice in later lines. However, data coming from clinical trials are currently limited. EMMY is a noninterventional, prospective dynamic cohort study conducted in 73 centers in France to assess the real-life management of MM in France and which can explore the efficacy of aCD38-based retreatment.

Methods: Patients who initiated a second line of treatment with aCD38-based combinations after a first exposure to aCD38 were identified and described and the outcomes of progression-free survival (PFS) and overall survival (OS) were estimated.

Results: In the EMMY cohort, 286 patients received 2 lines of treatment including aCD38. For all aCD38-retreated patients, median PFS was estimated at 5.1 months. Median PFS was 23.6 m in patients sensitive to aCD38 and 4.6 in nonsensitive patients, P = .0003. Median OS was estimated at 17.3 months for all patients,14.8 months in patients nonsensitive to aCD38, and not reached (NR) in sensitive patients, P = .0004. No significant differences in PFS or OS were observed between the refractory and nonrefractory to aCD38 groups.

Conclusion: These results of aCD38 retreatment in a large sample of real-life patients (n = 286) in extensively pretreated patients show that retreatment may be a meaningful strategy for aCD38 sensitive patients. These findings need to be investigated further while the use of aCD38 is emerging as a first-line treatment for newly diagnosed patients.

Keywords: Immunotherapy; Monoclonal antibody; Real-life data; Rechallenge; Relapsed or refractory multiple myeloma.

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Conflict of interest statement

Disclosure Alexis Talbot: Board Pfizer, Sanofi. Cyrille Hulin: Amgen, BMS, GSK, Janssen, Sanofi, Takeda. Aurore Perrot: received honoraria from Abbvie, Amgen, BMS, GSK, Janssen, Pfizer, Sanofi and Takeda. Margaret Macro: Honoraria: Amgen, BMS, GSK, Janssen, Sanofi, Takeda. Karim Belhadj Merzoug: Honoraria: Amgen, BMS, Janssen, Pfizer, Sanofi. Mohamed Mohty: received honoraria from Janssen, Sanofi, BMS, Amgen, Takeda, GSK, Pfizer, Novartis, Jazz pharmaceuticals, Stemline and Astellas. Arthur Bobin: Johnson & Johnson, Sanofi, Amgen, Pfizer, Stemline Menarini. Lionel Karlin: Amgen, Abbvie, Celgene-BMS, Pfizer, Takeda, Sanofi, Janssen: honoraires, advisory boards, travel support (congress). Salomon Manier: AbbVie, Adaptative Biotechnology, Amgen, BMS, GSK, Janssen, Regeneron, Roche, Sanofi, Takeda. Laure Vincent: being a board member for Bristol Myers Squib and Takeda. And receiving honoraria from Janssen and Pfizer. Abderazzak El Yamani: None. Wajed Abarah: None. Régis Kaphan: None. Thomas Chalopin: Consulting / advisory boards: Amgen, Stemline, Janssen, Sanofi, Pfizer, BMS. Daniel Re: None. Adrienne de Labarthe: None. Olivier Fitoussi: None. Chanaz Lounis: None. Ronan Garlantezec: None. Olivier Decaux: Honoraria: BMS, GSK, Janssen, Sanofi, Takeda, Roche, Gilead.

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