Outcomes of patients with multiple myeloma refractory to CD38-targeted monoclonal antibody therapy

被引:0
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作者
Ujjawal H. Gandhi
Robert F. Cornell
Arjun Lakshman
Zhubin J. Gahvari
Elizabeth McGehee
Megan H. Jagosky
Ridhi Gupta
William Varnado
Mark A. Fiala
Saurabh Chhabra
Ehsan Malek
Joshua Mansour
Barry Paul
Alyssa Barnstead
Saranya Kodali
Amarendra Neppalli
Michaela Liedtke
Swapna Narayana
Kelly N. Godby
Yubin Kang
Ankit Kansagra
Elvira Umyarova
Emma C. Scott
Parameswaran Hari
Ravi Vij
Saad Z. Usmani
Natalie S. Callander
Shaji K. Kumar
Luciano J. Costa
机构
[1] Vanderbilt University Medical Center,Department of Medicine, Division of Hematology & Oncology
[2] Mayo Clinic,Division of Hematology
[3] University of Wisconsin,Division of Hematology/Oncology
[4] University of Texas Southwestern Medical Center,Department of Medicine, Division of Oncology
[5] Department of Hematologic Oncology & Blood Disorders Levine Cancer Institute/Carolinas Health Care,Division of Hematology/Oncology, Department of Medicine
[6] Stanford Cancer Institute,Adult Hematologic Malignancies & Stem Cell Transplant Section, Seidman Cancer Center
[7] University of Alabama at Birmingham,Hollings Cancer Center
[8] Washington University School of Medicine,Department of Medicine, Division of Hematologic Malignancies and Cellular Therapy
[9] Medical College of Wisconsin,undefined
[10] University Hospitals Cleveland Medical Center,undefined
[11] Medical University of South Carolina,undefined
[12] Duke University School of Medicine,undefined
[13] Oregon Health & Science University,undefined
[14] University of Vermont,undefined
[15] College of Medicine,undefined
来源
Leukemia | 2019年 / 33卷
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摘要
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.
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页码:2266 / 2275
页数:9
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