TY - JOUR
T1 - Clinical efficacy of retreatment of daratumumab-based therapy (D2) in daratumumab-refractory multiple myeloma
AU - Abdallah, Al Ola
AU - Mahmoudjafari, Zahra
AU - Ahmed, Nausheen
AU - Cui, Wei
AU - Shune, Leyla
AU - McGuirk, Joseph
AU - Mohan, Meera
AU - Mohyuddin, Ghulam Rehman
AU - Afrough, Aimaz
AU - Alkharabsheh, Omar
AU - Atrash, Shebli
N1 - Funding Information:
Al‐Ola Abdallah, Nausheen Ahmed, Wei Cui, Leyla Shune, Ghulam Rehman Mohyuddin, Aimaz Afrough, and Omar Alkharabsheh report no conflict of interest. Joseph McGuirk reports the following conflicts: Novartis: Research Funding; Fresenius Biotech: Research Funding; Astellas: Research Funding; Bellicum Pharmaceuticals: Research Funding; Kite Pharmaceuticals: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Gamida Cell: Research Funding; Pluristem Ltd: Research Funding; Articulate Science LLC: Other: Assistance with manuscript preparation; Juno Therapeutics: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding. Meera Mohan reports research funding from Norvatis, Celgene, and Takeda. Zahra Mahmoudjafari reports the following conflicts: Omeros: Advisory Board; Bristol Myers Squibb, Omeros, Incyte: Advisory Board. Shebli Atrash reports honorarium from Celgene, Jansen, Karyopharm, GSK, Sanofi. Speakers Bureau: Celgene, Jansen, Sanofi.
Publisher Copyright:
© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2023
Y1 - 2023
N2 - Daratumumab demonstrates activity as a single agent and in combination with either immunomodulatory agents (IMiDs) or proteasome inhibitors (PIs) in relapsed refractory multiple myeloma (RRMM). However, little is known about the benefit of daratumumab retreatment in daratumumab-refractory MM. This study aimed to analyze the clinical efficacy of daratumumab-based retreatment (D2) in patients who are daratumumab refractory MM. Retrospectively, we identified 43 RRMM patients from a single-center database review. The median age was 65 years, 42% patients had high-risk cytogenetics, and 23% had an extramedullary disease, while the median time between D2 and prior daratumumab was 1 (0.25–39) month. All D2 patients received combination therapy with either pomalidomide, carfilzomib, bortezomib, or lenalidomide. The response rate, median progression-free, and overall survival were 49%, 7.97 and 32.6 months, respectively. Our study raises the possibility of re-utilizing daratumumab in combination with different classes of anti-myeloma drugs to generate responses in RRMM patients who are daratumumab-refractory.
AB - Daratumumab demonstrates activity as a single agent and in combination with either immunomodulatory agents (IMiDs) or proteasome inhibitors (PIs) in relapsed refractory multiple myeloma (RRMM). However, little is known about the benefit of daratumumab retreatment in daratumumab-refractory MM. This study aimed to analyze the clinical efficacy of daratumumab-based retreatment (D2) in patients who are daratumumab refractory MM. Retrospectively, we identified 43 RRMM patients from a single-center database review. The median age was 65 years, 42% patients had high-risk cytogenetics, and 23% had an extramedullary disease, while the median time between D2 and prior daratumumab was 1 (0.25–39) month. All D2 patients received combination therapy with either pomalidomide, carfilzomib, bortezomib, or lenalidomide. The response rate, median progression-free, and overall survival were 49%, 7.97 and 32.6 months, respectively. Our study raises the possibility of re-utilizing daratumumab in combination with different classes of anti-myeloma drugs to generate responses in RRMM patients who are daratumumab-refractory.
KW - daratumumab
KW - relapsed myeloma
KW - triple-class refractory myeloma
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U2 - 10.1111/ejh.13942
DO - 10.1111/ejh.13942
M3 - Article
C2 - 36752328
AN - SCOPUS:85148636848
SN - 0902-4441
JO - European Journal of Haematology
JF - European Journal of Haematology
ER -