Outcomes of Penta-Refractory Multiple Myeloma Patients Treated with or without BCMA-Directed Therapy

Author:

Atrash Shebli12ORCID,Mammadzadeh Aytaj3,Peng Fulei4,Alkharabsheh Omar25ORCID,Afrough Aimaz26,Cui Wei27,Mahmoudjafari Zahra28,Abdallah Al-Ola29,Hashmi Hamza210

Affiliation:

1. Levine Cancer Institute, Carolinas Healthcare System, Charlotte, NC 28204, USA

2. US Myeloma Research Innovations Research Collaborative (USMIRC), Westwood, KS 66205, USA

3. Division of Hematology/Oncology, Mayo Clinic, Rochester, MN 55905, USA

4. Department of Internal Medicine, Mercy St. Louis Hospital, St. Louis, MO 63141, USA

5. Division of Hematology/Oncology, The University of South Alabama Mitchell Cancer Institute, Mobile, AL 36604, USA

6. Division of Hematology/Oncology, UT Southwestern Medical Center, Dallas, TX 75390, USA

7. Department of Pathology & Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160, USA

8. Division of Pharmacy, University of Kansas Medical Center, Westwood, KS 66160, USA

9. Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Medical Center, Westwood, KS 66160, USA

10. Division of Hematology/Oncology, Medical University of South Carolina, Charleston, SC 29425, USA

Abstract

Despite advances in treatment, outcomes remain poor for patients with penta-relapsed refractory multiple myeloma (RRMM). In this retrospective analysis, we evaluated the survival outcomes of penta-RRMM patients treated with (BCMA)- directed therapy (BDT). We identified 78 patients with penta-RRMM. Median age was 65 years, 29 (37%) had R-ISS stage III disease, 63 (81%) had high-risk cytogenetics, and 45 (58%) had extra-medullary disease. Median LOT prior to penta-refractory state was 5 (3–12). Amongst penta-RRMM, 43 (55%) were treated with BDT, 35 (45%) were not treated with BDT. Type of BDT received included belantamab mafadotin 15 (35%), Chimeric Antigen Receptor T-cell therapy 9 (21%), BCMA monoclonal antibody 6 (14%), and Bispecific T-cell engager 2 (5%). Eleven (25%) patients received more than one BDT. No significant differences were identified between baseline characteristics for the two groups. Patients treated with a BDT had better median overall survival, 17 vs. 6 months, HR 0.3 p-value < 0.001. Poor performance status, white race, and high-risk cytogenetics were associated with worse outcomes, whereas using a BDT was associated with better outcomes. Patients with penta-refractory MM have poor outcomes. Our retrospective analysis showed a significant survival benefit using BDT when compared to non-BDT for patients with penta-RRMM.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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