| Literature DB >> 30858549 |
Ujjawal H Gandhi1, Robert F Cornell1, Arjun Lakshman2, Zhubin J Gahvari3, Elizabeth McGehee4, Megan H Jagosky5, Ridhi Gupta6, William Varnado7, Mark A Fiala8, Saurabh Chhabra9, Ehsan Malek10, Joshua Mansour11, Barry Paul12, Alyssa Barnstead13, Saranya Kodali14, Amarendra Neppalli11, Michaela Liedtke6, Swapna Narayana9, Kelly N Godby7, Yubin Kang12, Ankit Kansagra4, Elvira Umyarova14, Emma C Scott13, Parameswaran Hari9, Ravi Vij8, Saad Z Usmani5, Natalie S Callander3, Shaji K Kumar2, Luciano J Costa15.
Abstract
The introduction of CD38-targeting monoclonal antibodies (CD38 MoABs), daratumumab and isatuximab, has significantly impacted the management of patients with multiple myeloma (MM). Outcomes of patients with MM refractory to CD38 MoABs have not been described. We analyzed outcomes of 275 MM patients at 14 academic centers with disease refractory to CD38 MoABs. Median interval between MM diagnosis and refractoriness to CD38 MoAB (T0) was 50.1 months. The median overall survival (OS) from T0 for the entire cohort was 8.6 [95% C.I. 7.5-9.9] months, ranging from 11.2 months for patients not simultaneously refractory to an immunomodulatory (IMiD) agent and a proteasome inhibitor (PI) to 5.6 months for "penta-refractory" patients (refractory to CD38 MoAB, 2 PIs and 2 IMiDs). At least one subsequent treatment regimen was employed after T0 in 249 (90%) patients. Overall response rate to first regimen after T0 was 31% with median progression-free survival (PFS) and OS of 3.4 and 9.3 months, respectively. PFS was best achieved with combinations of carfilzomib and alkylator (median 5.7 months), and daratumumab and IMiD (median 4.5 months). Patients with MM refractory to CD38 MoAB have poor prognosis and this study provides benchmark for new therapies to be tested in this population.Entities:
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Year: 2019 PMID: 30858549 PMCID: PMC6820050 DOI: 10.1038/s41375-019-0435-7
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528