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Lenalidomide Maintenance after Stem-Cell Transplantation for Multiple Myeloma

  作者 Attal, M; Lauwers-Cances, V; Marit, G; Caillot, D; Moreau, P; Facon, T; Stoppa, AM; Hulin, C; Benboubker, L; Garderet, L; Decaux, O; Leyvraz, S; Vekemans, MC; Voillat, L; Michallet, M; Pegourie, B; Dumontet, C; Roussel, M; Leleu, X; Mathiot, C; Payen, C; Avet-Loiseau, H; Harousseau, JL  
  选自 期刊  New England Journal of Medicine;  卷期  2012年366-19;  页码  1782-1791  
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[摘要]Background High-dose chemotherapy with autologous stem-cell transplantation is a standard treatment for young patients with multiple myeloma. Residual disease is almost always present after transplantation and is responsible for relapse. This phase 3, placebo-controlled trial investigated the efficacy of lenalidomide maintenance therapy after transplantation. Methods We randomly assigned 614 patients younger than 65 years of age who had nonprogressive disease after first-line transplantation to maintenance treatment with either lenalidomide (10 mg per day for the first 3 months, increased to 15 mg if tolerated) or placebo until relapse. The primary end point was progression-free survival. Results Lenalidomide maintenance therapy improved median progression-free survival (41 months, vs. 23 months with placebo; hazard ratio, 0.50; P<0.001). This benefit was observed across all patient subgroups, including those based on the beta(2)-microglobulin level, cytogenetic profile, and response after transplantation. With a median follow-up period of 45 months, more than 70% of patients in both groups were alive at 4 years. The rates of grade 3 or 4 peripheral neuropathy were similar in the two groups. The incidence of second primary cancers was 3.1 per 100 patient-years in the lenalidomide group versus 1.2 per 100 patient-years in the placebo group (P=0.002). Median event-free survival (with events that included second primary cancers) was significantly improved with lenalidomide (40 months, vs. 23 months with placebo; P<0.001). Conclusions Lenalidomide maintenance after transplantation significantly prolonged progression-free and event-free survival among patients with multiple myeloma. Four years after randomization, overall survival was similar in the two study groups.

 
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