Triplet Therapy, Transplantation, and Maintenance until Progression in Myeloma

Paul G. Richardson(Harvard University), Susanna Jacobus(Harvard University), Edie Weller(Boston Children's Hospital), Hani Hassoun(Memorial Sloan Kettering Cancer Center), Sagar Lonial(Emory University), Noopur Raje(Harvard University), Eva Medvedova(Oregon Health & Science University), Philip L. McCarthy(Roswell Park Comprehensive Cancer Center), Edward N. Libby(University of Washington), Peter M. Voorhees(Levine Cancer Institute), Robert Z. Orlowski(The University of Texas MD Anderson Cancer Center), Larry D. Anderson(Dana-Farber Cancer Institute), Jeffrey A. Zonder(Wayne State University), Carter P. Milner(University of Mississippi Medical Center), Cristina Gasparetto(Dana-Farber Cancer Institute), Mounzer Agha(Dana-Farber Cancer Institute), Abdullah Khan(Dana-Farber Cancer Institute), David D. Hurd(Atrium Health Wake Forest Baptist), Krisstina Gowin(University of Arizona), Rammurti T. Kamble(Baylor College of Medicine), Sundar Jagannath(Dana-Farber Cancer Institute), Nitya Nathwani(City of Hope), Melissa Alsina(Moffitt Cancer Center), Robert F. Cornell(Dana-Farber Cancer Institute), Hamza Hashmi(Medical University of South Carolina), Erica Campagnaro(University of Michigan), Astrid C. Andreescu(Eastern Maine Medical Center), Teresa Gentile(SUNY Upstate Medical University), Michaela Liedtke(Dana-Farber Cancer Institute), Kelly Godby(University of Alabama at Birmingham), Adam D. Cohen(Dana-Farber Cancer Institute), Thomas H. Openshaw(Cape Cod Hospital), Marcelo C. Pasquini(Medical College of Wisconsin), Sergio Giralt(Memorial Sloan Kettering Cancer Center), Jonathan L. Kaufman(Emory University), Andrew J. Yee(Massachusetts General Hospital), Emma C. Scott(Oregon Health & Science University), Pallawi Torka(Roswell Park Comprehensive Cancer Center), Amy Foley(National Marrow Donor Program), Mariateresa Fulciniti(Dana-Farber Cancer Institute), Kyle Hebert(Harvard University), Mehmet Samur(Harvard University), Kelly Masone(Harvard University), Michelle E. Maglio(Harvard University), Andrea A. Zeytoonjian(Harvard University), Omar Nadeem(Harvard University), Robert Schlossman(Harvard University), Jacob P. Laubach(Harvard University), Claudia E. Paba‐Prada(Harvard University), Irene M. Ghobrial(Harvard University), Aurore Perrot(Dana-Farber Cancer Institute), Philippe Moreau(Hotel Dieu Hospital), Hervé Avet‐Loiseau(Dana-Farber Cancer Institute), Michel Attal(Dana-Farber Cancer Institute), Kenneth C. Anderson(Harvard University), Nikhil C. Munshi(Harvard University)
New England Journal of Medicine
June 5, 2022
Cited by 454Open Access
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Abstract

BACKGROUND: In patients with newly diagnosed multiple myeloma, the effect of adding autologous stem-cell transplantation (ASCT) to triplet therapy (lenalidomide, bortezomib, and dexamethasone [RVD]), followed by lenalidomide maintenance therapy until disease progression, is unknown. METHODS: In this phase 3 trial, adults (18 to 65 years of age) with symptomatic myeloma received one cycle of RVD. We randomly assigned these patients, in a 1:1 ratio, to receive two additional RVD cycles plus stem-cell mobilization, followed by either five additional RVD cycles (the RVD-alone group) or high-dose melphalan plus ASCT followed by two additional RVD cycles (the transplantation group). Both groups received lenalidomide until disease progression, unacceptable side effects, or both. The primary end point was progression-free survival. RESULTS: Among 357 patients in the RVD-alone group and 365 in the transplantation group, at a median follow-up of 76.0 months, 328 events of disease progression or death occurred; the risk was 53% higher in the RVD-alone group than in the transplantation group (hazard ratio, 1.53; 95% confidence interval [CI], 1.23 to 1.91; P<0.001); median progression-free survival was 46.2 months and 67.5 months. The percentage of patients with a partial response or better was 95.0% in the RVD-alone group and 97.5% in the transplantation group (P = 0.55); 42.0% and 46.8%, respectively, had a complete response or better (P = 0.99). Treatment-related adverse events of grade 3 or higher occurred in 78.2% and 94.2%, respectively; 5-year survival was 79.2% and 80.7% (hazard ratio for death, 1.10; 95% CI, 0.73 to 1.65). CONCLUSIONS: Among adults with multiple myeloma, RVD plus ASCT was associated with longer progression-free survival than RVD alone. No overall survival benefit was observed. (Funded by the National Heart, Lung, and Blood Institute and others; DETERMINATION ClinicalTrials.gov number, NCT01208662.).


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