Lenalidomide after Stem-Cell Transplantation for Multiple Myeloma

Philip L. McCarthy(Roswell Park Comprehensive Cancer Center), Kouros Owzar, Craig C. Hofmeister(The Ohio State University), David D. Hurd(Wake Forest University), Hani Hassoun(Memorial Sloan Kettering Cancer Center), Paul G. Richardson(Dana-Farber Cancer Institute), Sergio Giralt(Memorial Sloan Kettering Cancer Center), Edward A. Stadtmauer(University of Pennsylvania), Daniel J. Weisdorf(University of Minnesota Medical Center), Ravi Vij(Washington University in St. Louis), Jan S. Moreb(University of Florida), Natalie S. Callander(University of Wisconsin–Madison), Koen van Besien(University of Chicago), Teresa Gentile(State University of New York), Luis Isola(Mount Sinai Medical Center), Richard T. Maziarz(Oregon Health & Science University), Don A. Gabriel(University of North Carolina at Chapel Hill), Asad Bashey, Heather Landau(Memorial Sloan Kettering Cancer Center), Thomas Martin(University of California, San Francisco), Muzaffar H. Qazilbash(The University of Texas MD Anderson Cancer Center), Denise Levitan(Duke University), Brian McClune(University of Minnesota Medical Center), Robert Schlossman(Dana-Farber Cancer Institute), Vera Hárs, John Postiglione, Chen Jiang, Elizabeth Bennett, Susan Barry, Linda R. Bressler(University of Chicago), Michael E. Kelly(University of Chicago), Michele Seiler(University of Chicago), Cara A. Rosenbaum(University of Chicago), Parameswaran Hari(Medical College of Wisconsin), Marcelo C. Pasquini(Medical College of Wisconsin), Mary M. Horowitz(Medical College of Wisconsin), Thomas C. Shea(University of North Carolina at Chapel Hill), Steven M. Devine(The Ohio State University), Kenneth C. Anderson(Dana-Farber Cancer Institute), Charles Linker(University of California, San Francisco)
New England Journal of Medicine
May 9, 2012
Cited by 1,140Open Access
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Abstract

BACKGROUND: Data are lacking on whether lenalidomide maintenance therapy prolongs the time to disease progression after autologous hematopoietic stem-cell transplantation in patients with multiple myeloma. METHODS: Between April 2005 and July 2009, we randomly assigned 460 patients who were younger than 71 years of age and had stable disease or a marginal, partial, or complete response 100 days after undergoing stem-cell transplantation to lenalidomide or placebo, which was administered until disease progression. The starting dose of lenalidomide was 10 mg per day (range, 5 to 15). RESULTS: The study-drug assignments were unblinded in 2009, when a planned interim analysis showed a significantly longer time to disease progression in the lenalidomide group. At unblinding, 20% of patients who received lenalidomide and 44% of patients who received placebo had progressive disease or had died (P<0.001); of the remaining 128 patients who received placebo and who did not have progressive disease, 86 crossed over to lenalidomide. At a median follow-up of 34 months, 86 of 231 patients who received lenalidomide (37%) and 132 of 229 patients who received placebo (58%) had disease progression or had died. The median time to progression was 46 months in the lenalidomide group and 27 months in the placebo group (P<0.001). A total of 35 patients who received lenalidomide (15%) and 53 patients who received placebo (23%) died (P=0.03). More grade 3 or 4 hematologic adverse events and grade 3 nonhematologic adverse events occurred in patients who received lenalidomide (P<0.001 for both comparisons). Second primary cancers occurred in 18 patients who received lenalidomide (8%) and 6 patients who received placebo (3%). CONCLUSIONS: Lenalidomide maintenance therapy, initiated at day 100 after hematopoietic stem-cell transplantation, was associated with more toxicity and second cancers but a significantly longer time to disease progression and significantly improved overall survival among patients with myeloma. (Funded by the National Cancer Institute; ClinicalTrials.gov number, NCT00114101.).


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