Title | Lenalidomide after stem-cell transplantation for multiple myeloma. |
Publication Type | Journal Article |
Year of Publication | 2012 |
Authors | McCarthy, PL, Owzar, K, Hofmeister, CC, Hurd, DD, Hassoun, H, Richardson, PG, Giralt, S, Stadtmauer, EA, Weisdorf, DJ, Vij, R, Moreb, JS, Callander, NScott, van Besien, K, Gentile, T, Isola, L, Maziarz, RT, Gabriel, DA, Bashey, A, Landau, H, Martin, T, Qazilbash, MH, Levitan, D, McClune, B, Schlossman, R, Hars, V, Postiglione, J, Jiang, C, Bennett, E, Barry, S, Bressler, L, Kelly, M, Seiler, M, Rosenbaum, C, Hari, P, Pasquini, MC, Horowitz, MM, Shea, TC, Devine, SM, Anderson, KC, Linker, C |
Journal | N Engl J Med |
Volume | 366 |
Issue | 19 |
Pagination | 1770-81 |
Date Published | 2012 May 10 |
ISSN | 1533-4406 |
Keywords | Adult, Aged, Antineoplastic Agents, Disease-Free Survival, Double-Blind Method, Female, Follow-Up Studies, Humans, Lenalidomide, Maintenance Chemotherapy, Male, Middle Aged, Multiple Myeloma, Neoplasms, Second Primary, Stem Cell Transplantation, Thalidomide |
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 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.). |
DOI | 10.1056/NEJMoa1114083 |
Alternate Journal | N Engl J Med |
PubMed ID | 22571201 |
PubMed Central ID | PMC3744390 |
Grant List | U10 HL069294 / HL / NHLBI NIH HHS / United States U10 HL109526 / HL / NHLBI NIH HHS / United States UG1 HL069286 / HL / NHLBI NIH HHS / United States U10 HL069290 / HL / NHLBI NIH HHS / United States U10 HL069330 / HL / NHLBI NIH HHS / United States U10 HL069334 / HL / NHLBI NIH HHS / United States U01 HL069294 / HL / NHLBI NIH HHS / United States P50 CA100707 / CA / NCI NIH HHS / United States U10 HL069315 / HL / NHLBI NIH HHS / United States U10 HL069348 / HL / NHLBI NIH HHS / United States U24 CA076518 / CA / NCI NIH HHS / United States U10 CA021115 / CA / NCI NIH HHS / United States U10 HL069286 / HL / NHLBI NIH HHS / United States U10 CA031946 / CA / NCI NIH HHS / United States U10 CA033601 / CA / NCI NIH HHS / United States U10 HL069301 / HL / NHLBI NIH HHS / United States |