Lenalidomide maintenance after stem-cell transplantation for multiple myeloma.


Autoria(s): Attal M.; Lauwers-Cances V.; Marit G.; Caillot D.; Moreau P.; Facon T.; Stoppa A.M.; Hulin C.; Benboubker L.; Garderet L.; Decaux O.; Leyvraz S.; Vekemans M.C.; Voillat L.; Michallet M.; Pegourie B.; Dumontet C.; Roussel M.; Leleu X.; Mathiot C.; Payen C.; Avet-Loiseau H.; Harousseau J.L.; IFM Investigators
Data(s)

2012

Resumo

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 β(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. (Funded by the Programme Hospitalier de Recherche Clinique and others; ClinicalTrials.gov number, NCT00430365.).

Identificador

http://serval.unil.ch/?id=serval:BIB_A51FB5B0019E

isbn:1533-4406 (Electronic)

pmid:22571202

doi:10.1056/NEJMoa1114138

isiid:000303817000007

Idioma(s)

en

Fonte

New England Journal of Medicine, vol. 366, no. 19, pp. 1782-1791

Palavras-Chave #Adult; Aged; Antineoplastic Agents/adverse effects; Antineoplastic Agents/therapeutic use; Disease-Free Survival; Double-Blind Method; Female; Follow-Up Studies; Humans; Kaplan-Meier Estimate; Maintenance Chemotherapy; Male; Middle Aged; Multiple Myeloma/drug therapy; Multiple Myeloma/mortality; Neoplasms, Second Primary/epidemiology; Stem Cell Transplantation; Thalidomide/adverse effects; Thalidomide/analogs & derivatives; Young Adult
Tipo

info:eu-repo/semantics/article

article