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Multicenter Study
. 2023 Dec 8;13(1):181.
doi: 10.1038/s41408-023-00946-z.

Real world data on outcomes of anti-CD38 antibody treated, including triple class refractory, patients with multiple myeloma: a multi-institutional report from the Canadian Myeloma Research Group (CMRG) Database

Affiliations
Multicenter Study

Real world data on outcomes of anti-CD38 antibody treated, including triple class refractory, patients with multiple myeloma: a multi-institutional report from the Canadian Myeloma Research Group (CMRG) Database

A Visram et al. Blood Cancer J. .

Abstract

Multiple myeloma (MM) remains incurable despite the availability of novel agents. This multi-center retrospective cohort study used the Canadian Myeloma Research Group Database to describe real-world outcomes of patients withanti-CD38 monoclonal antibody (mAb) refractory MM subsequently treated with standard of care (SoC) regimens. Patients with triple class refractory (TCR) disease (refractory to a proteasome inhibitor, immunomodulatory drug, and anti-CD38 mAb) were examined as a distinct cohort. Overall, 663 patients had disease progression on anti-CD38 mAb therapy, 466 received further treatment (346 with SoC regimens were included, 120 with investigational agents on clinical trial and were excluded). The median age at initiation of subsequent SoC therapy of 67.9 (range 39.6-89.6) years with a median of 3 prior lines (range 1-9). The median PFS and OS from the start of subsequent therapy was 4.6 (95% CI 4.1-5.6) months and 13.3 (95% CI 10.6-16.6) months, respectively. The median PFS and OS of patients with TCR disease (n = 199) was 4.4 (95% CI 3.6-5.3) months and 10.5 (95% CI 8.5-13.8) months. Our results reinforce that real-world patients with relapsed MM, particularly those with TCR disease, have dismal outcomes. There remains an urgent unmet need for the development of and access to effective therapeutics for these patients.

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Conflict of interest statement

AV: Consultancy/Honoraria fees from Janssen, Sanofi, Pfizer. HM: Consultancy/Honoraria fees from Celgene/BMS, Takeda, Janssen, Amgen, Sanofi, Pfizer, GSK; Research funding Janssen. RL: Consultancy/Honoraria fees from Janssen, BMS, Amgen, Sanofi, Forus Therapeutics. CPV: Honoraria from Janssen, BMS, Sanofi, Pfizer, Amgen, BMS/Celgene, Takeda, Forus. VJZ Honoraria Janssen, BMS, Sanofi, Pfizer, Amgen, BMS/Celgene, Takeda and Forus Therapeutics. TR: consultancy/honoraria from Janssen, Pfizer, Sanofi, Celgene/BMS, Takeda, Amgen.

Figures

Fig. 1
Fig. 1. Consort diagram of included patients.
Abbreviations: monoclonal antibody (mAb) triple class refractory (TCR).
Fig. 2
Fig. 2. Frequency of standard of care (SoC) drug regimens used after relapse on the index anti-CD38 monoclonal antibody containing regimen.
All regimens were given in conjunction with steroids. Of the patients with MM relapsing on 1st SoC therapy after index progression, 130 were treated with a 2nd Soc therapy and 81 were treated on clinical trial.
Fig. 3
Fig. 3. Outcomes of patients with TCR versus non-TCR RRMM.
A Progression-free survival (PFS) and B Overall survival (OS) from initiation of subsequent standard of care therapy post anti-CD38 mAb progression.

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