Outcomes in frail patients receiving BCMA-directed bispecific antibodies for relapsed/refractory multiple myeloma

Patients with relapsed/refractory (R/R) multiple myeloma (MM) are often frail with preexisting comorbidities and poor performance status (PS). To evaluate clinical characteristics and outcomes based on frailty, we conducted a single-center retrospective study of patients with R/R MM who received B-cell maturation antigen (BCMA)-directed bispecific antibodies (BsAbs). Frailty was defined using the simplified frailty index based on age, Eastern Cooperative Oncology Group (ECOG) PS, and Charlson comorbidity index (CCI; nonfrail score 0-1 and frail score ≥2). Of 102 patients analyzed (age range, 40-88 years), 40 (39%) were considered frail. The frail group had more patients aged ≥70 years (73% vs 29%; P < .001), with ECOG PS ≥2 (36% vs 0%; P < .001), and worse median CCI (2 vs 1; P < .001). Patients in the frail group experienced similar rates of all-grade cytokine release syndrome (58% vs 60%; P = .99), immune effector cell-associated neurotoxicity syndrome (15% vs 8%; P = .44), and treatment-related mortality (13% vs 21%; P = .27) compared to the nonfrail group. The best overall response rate was 80% (stringent complete response [sCR]/CR, 15%; very good partial response [VGPR], 48%) in the frail group vs 73% (sCR/CR, 23%; VGPR, 31%) in the nonfrail group (P = .40). With a median follow-up of 8.6 months (range, 3-14), there was no significant difference in median progression-free survival (not reached vs 11 months; P = .051) or overall survival (37 vs 25 months; P = .37) between the frail and nonfrail groups. Hence, BsAbs were deemed safe and effective for older and frail patients with R/R MM.

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Publication Details

Journal
Blood Advances
Published
2025-05-02
DOI
https://doi.org/10.1182/bloodadvances.2025015973
Citations
6
Primary Topic
Multiple Myeloma Research and Treatments
Type
article
Field-Weighted Citation Impact
10.62

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article

Outcomes in frail patients receiving BCMA-directed bispecific antibodies for relapsed/refractory multiple myeloma

Heather Jolie Landau, Benjamin Adegbite, Kylee H. Maclachlan, Hamza Hashmi et al.
6 citations
Blood Advances
Multiple Myeloma Research and Treatments
10.62
article

Outcomes in frail patients receiving BCMA-directed bispecific antibodies for relapsed/refractory multiple myeloma

Heather Jolie Landau, Benjamin Adegbite, Kylee H. Maclachlan, Hamza Hashmi, Issam S. Hamadeh, Saad Z. Usmani, Tala Shekarkhand, Malin L. Hultcrantz, Gunjan L. Shah, Kevin C. Miller, Urvi Ashok Shah, Alexander M. Lesokhin, Michael Scordo, Eric Matthew Jurgens, Hani Hassoun, Sham Mailankody, Neha Korde, Sridevi Rajeeve, Sergio A. Giralt, David Nemirovsky, Andriy Derkach, Carlyn Rose C. Tan, Ross Firestone
article en
6 citations

Abstract

Patients with relapsed/refractory (R/R) multiple myeloma (MM) are often frail with preexisting comorbidities and poor performance status (PS). To evaluate clinical characteristics and outcomes based on frailty, we conducted a single-center retrospective study of patients with R/R MM who received B-cell maturation antigen (BCMA)-directed bispecific antibodies (BsAbs). Frailty was defined using the simplified frailty index based on age, Eastern Cooperative Oncology Group (ECOG) PS, and Charlson comorbidity index (CCI; nonfrail score 0-1 and frail score ≥2). Of 102 patients analyzed (age range, 40-88 years), 40 (39%) were considered frail. The frail group had more patients aged ≥70 years (73% vs 29%; P < .001), with ECOG PS ≥2 (36% vs 0%; P < .001), and worse median CCI (2 vs 1; P < .001). Patients in the frail group experienced similar rates of all-grade cytokine release syndrome (58% vs 60%; P = .99), immune effector cell-associated neurotoxicity syndrome (15% vs 8%; P = .44), and treatment-related mortality (13% vs 21%; P = .27) compared to the nonfrail group. The best overall response rate was 80% (stringent complete response [sCR]/CR, 15%; very good partial response [VGPR], 48%) in the frail group vs 73% (sCR/CR, 23%; VGPR, 31%) in the nonfrail group (P = .40). With a median follow-up of 8.6 months (range, 3-14), there was no significant difference in median progression-free survival (not reached vs 11 months; P = .051) or overall survival (37 vs 25 months; P = .37) between the frail and nonfrail groups. Hence, BsAbs were deemed safe and effective for older and frail patients with R/R MM.

Blood AdvancesVol. 9(15)
Mount Sinai Hospital (US), Memorial Sloan Kettering Cancer Center (US)
Amgen, Bristol-Myers Squibb, Pfizer, GlaxoSmithKline, Sanofi, Gilead Sciences, Celgene, Memorial Sloan-Kettering Cancer Center, Array BioPharma, SkylineDx, Omeros Corporation, Seagen, Springworks Therapeutics, Genentech, Pharmacyclics
No poverty
Openalex Percentile: Top 2%
Multiple Myeloma Research and Treatments
10.62
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