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Impact of extramedullary multiple myeloma on outcomes with idecabtagene vicleucel.

Authors :
Zanwar S
Sidana S
Shune L
Puglianini OC
Pasvolsky O
Gonzalez R
Dima D
Afrough A
Kaur G
Davis JA
Herr M
Hashmi H
Forsberg P
Sborov D
Anderson LD Jr
McGuirk JP
Wagner C
Lieberman-Cribbin A
Rossi A
Freeman CL
Locke FL
Richard S
Khouri J
Lin Y
Patel KK
Kumar SK
Hansen DK
Source :
Journal of hematology & oncology [J Hematol Oncol] 2024 Jun 06; Vol. 17 (1), pp. 42. Date of Electronic Publication: 2024 Jun 06.
Publication Year :
2024

Abstract

Idecabtagene vicleucel (Ide-cel) has demonstrated excellent efficacy and durable responses in patients with relapsed/refractory multiple myeloma (RRMM). However, the outcomes with ide-cel in patients with extramedullary disease (EMD) remain incompletely characterized. We included patients with RRMM treated with ide-cel between May 2021 and April 2023 across 11 US academic institutions. Visceral or soft tissue lesions non-contiguous from bone was classified as EMD. Time-to-event analyses were performed from date of ide-cel infusion. Among 351 patients, 84 (24%) had EMD prior to infusion. The median follow-up from ide-cel infusion was 18.2 months (95% CI: 17-19.3). The day 90 overall response rates (ORR) were 52% vs. 82% for the EMD and non-EMD cohorts, respectively (p < 0.001). The median progression-free survival (PFS) was 5.3 months (95% CI: 4.1-6.9) for the EMD cohort vs. 11.1 months (95% CI: 9.2-12.6; p < 0.0001) for the non-EMD cohort. In a multivariable analysis, EMD was an independent predictor of inferior PFS [hazard ratio 1.5 (1.1-2.2), p = 0.02]. The median overall survival was 14.8 months [95% CI: 9-Not reached (NR)] vs. 26.9 months (26.3 vs. NR, p = 0.006) for the EMD and non-EMD cohorts, respectively. Extramedullary disease represents an independent predictor of inferior day 90 ORR and PFS among patients treated with ide-cel.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1756-8722
Volume :
17
Issue :
1
Database :
MEDLINE
Journal :
Journal of hematology & oncology
Publication Type :
Report
Accession number :
38845015
Full Text :
https://doi.org/10.1186/s13045-024-01555-4