4.7 Article

Safety and Efficacy of Combination Maintenance Therapy with Ixazomib and Lenalidomide in Patients with Posttransplant Myeloma

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CLINICAL CANCER RESEARCH
卷 28, 期 7, 页码 1277-1284

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-21-3420

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  1. Millenium Pharmaceuticals
  2. Takeda Pharmaceuticals
  3. Comprehensive Cancer Center Support Grant (NCI)
  4. Leukemia & Lymphoma Society [SCOR-12206-17]
  5. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
  6. Paula and Rodger Riney Foundation
  7. MD Anderson Cancer Center High Risk Multiple Myeloma Moon Shot

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This study evaluated the addition of ixazomib to lenalidomide maintenance therapy after autologous stem cell transplantation (ASCT) in patients with multiple myeloma. The study found that the addition of ixazomib resulted in better progression-free survival compared to lenalidomide alone, and was well tolerated by patients.
Purpose: In this study, the addition of ixazomib to lenalidomide maintenance post-autologous stem cell transplant (ASCT) in 64 patients with newly diagnosed multiple myeloma was evaluated on the basis of the observed benefit of lenalidomide-only maintenance in prior studies. Patients and Methods: Patients were started on maintenance therapy with lenalidomide and ixazomib within 60-180 days of stem cell infusion. Results: Response rates deepened over time from baseline post-ASCT for 39 patients. The complete response (CR)/stringent CR rate was 43% and median overall survival was not reached with a median follow-up of 62 months (range, 25-82 months). Median PFS (mPFS) for all patients was 73 months and has not been reached for those with International Staging System (ISS) stage 1 disease. mPFS in 9 patients who had ISS stage 3 disease and 14 patients who had high-risk cytogenetics was 34 and 25 months, respectively. Twenty-two patients had progressive disease, while 19 patients continue to receive dual maintenance. The most common grade 3/4 adverse events included neutropenia, leukopenia, thrombocytopenia, lung infections, diarrhea, and maculopapular rash. Second primary malignancies occurred in 9 patients. Toxicity led to dose reductions in ixazomib and lenalidomide in 20 and 31 patients, respectively. Discontinuation of ixazomib due to toxicity occurred in 4 patients. Grade 1/2 neuropathy occurred in 22 patients and led to reduction or discontinuation of ixazomib in 2 patients. Conclusions: The addition of ixazomib to lenalidomide maintenance demonstrated a better than expected PFS compared with historical data using lenalidomide alone and was safe and tolerable.

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