TY - JOUR
T1 - Efficacy of Daratumumab-Containing Regimens Among Patients With Multiple Myeloma Progressing on Lenalidomide Maintenance
T2 - Retrospective Analysis
AU - Mian, Hira
AU - Eisfeld, Christine
AU - Venner, Christopher P.
AU - Masih-Khan, Esther
AU - Kardjadj, Moustafa
AU - Jimenez-Zepeda, Victor H.
AU - Khandanpour, Cyrus
AU - Lenz, Georg
AU - McCurdy, Arleigh
AU - Sebag, Michael
AU - Song, Kevin
AU - LeBlanc, Richard
AU - White, Darrell
AU - Stakiw, Julie
AU - Reiman, Anthony
AU - Louzada, Martha
AU - Aslam, Muhammad
AU - Kotb, Rami
AU - Gul, Engin
AU - Reece, Donna
N1 - Publisher Copyright:
Copyright © 2022 Mian, Eisfeld, Venner, Masih-Khan, Kardjadj, Jimenez-Zepeda, Khandanpour, Lenz, McCurdy, Sebag, Song, LeBlanc, White, Stakiw, Reiman, Louzada, Aslam, Kotb, Gul and Reece.
PY - 2022/2/18
Y1 - 2022/2/18
N2 - Background: Daratumumab, a monoclonal antibody directed against CD38 is a recent class of drugs introduced into the multiple myeloma therapeutic landscape. While clinical trial data have shown a remarkable impact on outcomes, the efficacy of daratumumab combination therapies in specific clinically relevant subgroups including among patients refractory to lenalidomide maintenance remains unknown. Methods: In this study, retrospective data were reviewed from the Canadian Myeloma Research Group and the German Munster Myeloma databases to identify patients that received daratumumab in combination with pomalidomide (DPd), lenalidomide (DRd), and bortezomib (DVd) in a population that had relapsed on lenalidomide maintenance postautologous stem cell transplant. The primary aim of the study was to look at outcomes of these patients in different daratumumab combinations. Results: A total of 73 patients were identified. The median age of the patients at the time of daratumumab initiation was 60 (38-72) and 64.4% (n = 47) were men. In the selected cohort, 43.8% (n = 32) were treated with DRd, 31.5% (n = 23) with DVd, and 24.7% (n = 18) with DPd regimen. The median progression-free survival (PFS) of the entire cohort was 15.8 months (95% CI, 12.9–37.1 months). The median PFS of the individual regimens was as follows: DPd 18.9 months (95% CI, 13.7-not reached), DRd 21.7 months (95% CI, 11.6-not reached), and DVd 12.9 months (95% CI, 3.1-not reached). Conclusions: Daratumumab-containing therapies are effective regimens in patients progressing on lenalidomide maintenance. Additional studies are required to decide the optimal regimen post-lenalidomide maintenance.
AB - Background: Daratumumab, a monoclonal antibody directed against CD38 is a recent class of drugs introduced into the multiple myeloma therapeutic landscape. While clinical trial data have shown a remarkable impact on outcomes, the efficacy of daratumumab combination therapies in specific clinically relevant subgroups including among patients refractory to lenalidomide maintenance remains unknown. Methods: In this study, retrospective data were reviewed from the Canadian Myeloma Research Group and the German Munster Myeloma databases to identify patients that received daratumumab in combination with pomalidomide (DPd), lenalidomide (DRd), and bortezomib (DVd) in a population that had relapsed on lenalidomide maintenance postautologous stem cell transplant. The primary aim of the study was to look at outcomes of these patients in different daratumumab combinations. Results: A total of 73 patients were identified. The median age of the patients at the time of daratumumab initiation was 60 (38-72) and 64.4% (n = 47) were men. In the selected cohort, 43.8% (n = 32) were treated with DRd, 31.5% (n = 23) with DVd, and 24.7% (n = 18) with DPd regimen. The median progression-free survival (PFS) of the entire cohort was 15.8 months (95% CI, 12.9–37.1 months). The median PFS of the individual regimens was as follows: DPd 18.9 months (95% CI, 13.7-not reached), DRd 21.7 months (95% CI, 11.6-not reached), and DVd 12.9 months (95% CI, 3.1-not reached). Conclusions: Daratumumab-containing therapies are effective regimens in patients progressing on lenalidomide maintenance. Additional studies are required to decide the optimal regimen post-lenalidomide maintenance.
UR - http://www.scopus.com/inward/record.url?scp=85125878535&partnerID=8YFLogxK
U2 - 10.3389/fonc.2022.826342
DO - 10.3389/fonc.2022.826342
M3 - Journal articles
AN - SCOPUS:85125878535
SN - 2234-943X
VL - 12
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 826342
ER -