Impact of bortezomib‐based versus lenalidomide maintenance therapy on outcomes of patients with high‐risk multiple myeloma

Author:

Bumma Naresh1,Dhakal Binod2ORCID,Fraser Raphael34,Estrada‐Merly Noel4,Anderson Kenneth5,Freytes César O.6,Hildebrandt Gerhard C.7,Holmberg Leona8,Krem Maxwell M.9,Lee Cindy10,Lekakis Lazaros11,Lazarus Hillard M.12,Mian Hira13ORCID,Murthy Hemant S.14,Nathan Sunita15,Nishihori Taiga16ORCID,Parrondo Ricardo14ORCID,Patel Sagar S.17,Solh Melhem18,Strouse Christopher19,Vesole David H.20,Kumar Shaji21ORCID,Qazilbash Muzaffar H.22ORCID,Shah Nina23ORCID,D’Souza Anita4ORCID,Sidana Surbhi24

Affiliation:

1. James Cancer Center Ohio State Medical Center Columbus Ohio USA

2. Bone Marrow Transplant and Cellular Therapy Program Division of Hematology/Oncology Medical College of Wisconsin Milwaukee Wisconsin USA

3. Division of Biostatistics Institute for Health and Equity Medical College of Wisconsin Milwaukee Wisconsin USA

4. Center for International Blood and Marrow Transplant Research (CIBMTR) Department of Medicine Medical College of Wisconsin Milwaukee Wisconsin USA

5. Dana‐Farber Cancer Institute Boston Massachusetts USA

6. Bone Marrow Transplant Program University of Texas Health Science Center at San Antonio San Antonio Texas USA

7. Markey Cancer Center University of Kentucky Lexington Kentucky USA

8. Fred Hutchinson Cancer Research Center Seattle Washington USA

9. Division of Hematology/BMT Kansas City Veterans Affairs Medical Center Kansas City Missouri USA

10. Department of Hematology, Royal Adelaide Hospital Adelaide South Australia Australia

11. Division of Transplantation and Cellular Therapy University of Miami Hospital and Clinics Sylvester Comprehensive Cancer Center Miami Florida USA

12. University Hospital Seidman Cancer Center Case Western Reserve University Cleveland Ohio USA

13. Department of Oncology McMaster University Hamilton Ontario Canada

14. Blood and Marrow Transplantation Program Division of Hematology‐Oncology Mayo Clinic Jacksonville Florida USA

15. Section of Bone Marrow Transplant and Cell Therapy Division of Hematology, Oncology, and Cell Therapy Rush University Medical Center Chicago Illinois USA

16. Department of Blood and Marrow Transplant and Cellular Immunotherapy H. Lee Moffitt Cancer Center and Research Institute Tampa Florida USA

17. Transplant and Cellular Therapy Program Huntsman Cancer Center Institute University of Utah Salt Lake City Utah USA

18. The Blood and Marrow Transplant Group of Georgia Northside Hospital Atlanta Georgia USA

19. Division of Hematology, Oncology, and Bone Marrow Transplantation University of Iowa Iowa City Iowa USA

20. Jonn Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey USA

21. Hematology/Oncology, Mayo Clinic Rochester Minnesota USA

22. Department of Blood and Marrow Transplantation, The University of Texas MD Anderson Cancer Center Houston Texas USA

23. Division of Hematology‐Oncology University of California San Francisco San Francisco California USA

24. Division of Blood and Marrow Transplantation Department of Medicine Stanford Health Care Stanford California USA

Abstract

AbstractBackgroundLenalidomide maintenance after autologous stem cell transplant (ASCT) in multiple myeloma (MM) results in superior progression‐free survival and overall survival. However, patients with high‐risk multiple myeloma (HRMM) do not derive the same survival benefit from lenalidomide maintenance compared with standard‐risk patients. The authors sought to determine the outcomes of bortezomib‐based maintenance compared with lenalidomide maintenance in patients with HRMM undergoing ASCT.MethodsIn total, the authors identified 503 patients with HRMM who were undergoing ASCT within 12 months of diagnosis from January 2013 to December 2018 after receiving triplet novel‐agent induction in the Center for International Blood and Marrow Transplant Research database. HRMM was defined as deletion 17p, t(14;16), t(4;14), t(14;20), or chromosome 1q gain.ResultsThree hundred fifty‐seven patients (67%) received lenalidomide alone, and 146 (33%) received bortezomib‐based maintenance (with bortezomib alone in 58%). Patients in the bortezomib‐based maintenance group were more likely to harbor two or more high‐risk abnormalities and International Staging System stage III disease (30% vs. 22%; p = .01) compared with the lenalidomide group (24% vs. 15%; p < .01). Patients who were receiving lenalidomide maintenance had superior progression‐free survival at 2 years compared with those who were receiving either bortezomib monotherapy or combination therapy (75% vs. 63%; p = .009). Overall survival at 2 years was also superior in the lenalidomide group (93% vs. 84%; p = .001).ConclusionsNo superior outcomes were observed in patients with HRMM who received bortezomib monotherapy or (to a lesser extent) in those who received bortezomib in combination as maintenance compared with lenalidomide alone. Until prospective data from randomized clinical trials are available, post‐transplant therapy should be tailored to each patient with consideration for treating patients in clinical trials that target novel therapeutic strategies for HRMM, and lenalidomide should remain a cornerstone of treatment.

Funder

Office of Naval Research

National Heart, Lung, and Blood Institute

Health Resources and Services Administration

Publisher

Wiley

Subject

Cancer Research,Oncology

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