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Autologous transplantation and maintenance therapy in multiple myeloma.
Palumbo, Antonio; Cavallo, Federica; Gay, Francesca; Di Raimondo, Francesco; Ben Yehuda, Dina; Petrucci, Maria Teresa; Pezzatti, Sara; Caravita, Tommaso; Cerrato, Chiara; Ribakovsky, Elena; Genuardi, Mariella; Cafro, Anna; Marcatti, Magda; Catalano, Lucio; Offidani, Massimo; Carella, Angelo Michele; Zamagni, Elena; Patriarca, Francesca; Musto, Pellegrino; Evangelista, Andrea; Ciccone, Giovannino; Omedé, Paola; Crippa, Claudia; Corradini, Paolo; Nagler, Arnon; Boccadoro, Mario; Cavo, Michele.
Afiliación
  • Palumbo A; From the Myeloma Unit, Division of Hematology, University of Turin (A.P., F.C., F.G., C. Cerrato, M.G., P.O., M.B.), and Unit of Clinical Epidemiology and Centro di Referimento per l'Epidemiologia-Piemonte, Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino (A.E., G.C.), Turin, Division of Hematology, Ospedale Ferrarotto, Azienda Policlinico-Ospedale Vittorio Emanuele, University of Catania, Catania (F.D.R.), Hematology, Sapienza University of Rome (M.T.P.), and Catte
N Engl J Med ; 371(10): 895-905, 2014 Sep 04.
Article en En | MEDLINE | ID: mdl-25184862
ABSTRACT

BACKGROUND:

This open-label, randomized, phase 3 study compared melphalan at a dose of 200 mg per square meter of body-surface area plus autologous stem-cell transplantation with melphalan-prednisone-lenalidomide (MPR) and compared lenalidomide maintenance therapy with no maintenance therapy in patients with newly diagnosed multiple myeloma.

METHODS:

We randomly assigned 273 patients 65 years of age or younger to high-dose melphalan plus stem-cell transplantation or MPR consolidation therapy after induction, and 251 patients to lenalidomide maintenance therapy or no maintenance therapy. The primary end point was progression-free survival.

RESULTS:

The median follow-up period was 51.2 months. Both progression-free and overall survival were significantly longer with high-dose melphalan plus stem-cell transplantation than with MPR (median progression-free survival, 43.0 months vs. 22.4 months; hazard ratio for progression or death, 0.44; 95% confidence interval [CI], 0.32 to 0.61; P<0.001; and 4-year overall survival, 81.6% vs. 65.3%; hazard ratio for death, 0.55; 95% CI, 0.32 to 0.93; P=0.02). Median progression-free survival was significantly longer with lenalidomide maintenance than with no maintenance (41.9 months vs. 21.6 months; hazard ratio for progression or death, 0.47; 95% CI, 0.33 to 0.65; P<0.001), but 3-year overall survival was not significantly prolonged (88.0% vs. 79.2%; hazard ratio for death, 0.64; 95% CI, 0.36 to 1.15; P=0.14). Grade 3 or 4 neutropenia was significantly more frequent with high-dose melphalan than with MPR (94.3% vs. 51.5%), as were gastrointestinal adverse events (18.4% vs. 0%) and infections (16.3% vs. 0.8%); neutropenia and dermatologic toxic effects were more frequent with lenalidomide maintenance than with no maintenance (23.3% vs. 0% and 4.3% vs. 0%, respectively).

CONCLUSIONS:

Consolidation therapy with high-dose melphalan plus stem-cell transplantation, as compared with MPR, significantly prolonged progression-free and overall survival among patients with multiple myeloma who were 65 years of age or younger. Lenalidomide maintenance, as compared with no maintenance, significantly prolonged progression-free survival. (Funded by Celgene; ClinicalTrials.gov number, NCT00551928.).
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Talidomida / Protocolos de Quimioterapia Combinada Antineoplásica / Trasplante de Células Madre / Melfalán / Mieloma Múltiple Tipo de estudio: Clinical_trials Límite: Adult / Aged / Humans / Middle aged Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Talidomida / Protocolos de Quimioterapia Combinada Antineoplásica / Trasplante de Células Madre / Melfalán / Mieloma Múltiple Tipo de estudio: Clinical_trials Límite: Adult / Aged / Humans / Middle aged Idioma: En Año: 2014 Tipo del documento: Article