Long-term follow-up on overall survival from the MM-009 and MM-010 phase III trials of lenalidomide plus dexamethasone in patients with relapsed or refractory multiple myeloma

被引:0
作者
M A Dimopoulos
C Chen
A Spencer
R Niesvizky
M Attal
E A Stadtmauer
M T Petrucci
Z Yu
M Olesnyckyj
J B Zeldis
R D Knight
D M Weber
机构
[1] University of Athens School of Medicine,Department of Clinical Therapeutics
[2] Princess Margaret Hospital,Department of Medical Oncology and Hematology
[3] The Alfred Hospital,Department of Clinical Haematology and Bone Marrow Transplantation
[4] Weill Cornell Medical College,Department of Medicine
[5] C.H.U. Purpan,Department of Hematology
[6] Abramson Cancer Center,Department of Cellular Biotechnologies and Hematology
[7] University of Pennsylvania,Department of Lymphoma and Myeloma
[8] University ‘Sapienza’,undefined
[9] Celgene Corporation,undefined
[10] The M.D. Anderson Cancer Center,undefined
来源
Leukemia | 2009年 / 23卷
关键词
multiple myeloma; lenalidomide; dexamethasone; myelosuppression;
D O I
暂无
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学科分类号
摘要
We present a pooled update of two large, multicenter MM-009 and MM-010 placebo-controlled randomized phase III trials that included 704 patients and assessed lenalidomide plus dexamethasone versus dexamethasone plus placebo in patients with relapsed/refractory multiple myeloma (MM). Patients in both studies were randomized to receive 25 mg daily oral lenalidomide or identical placebo, plus 40 mg oral dexamethasone. In this pooled analysis, using data up to unblinding (June 2005 for MM-009 and August 2005 for MM-010), treatment with lenalidomide plus dexamethasone significantly improved overall response (60.6 vs 21.9%, P<0.001), complete response rate (15.0 vs 2.0%, P<0.001), time to progression (median of 13.4 vs 4.6 months, P<0.001) and duration of response (median of 15.8 months vs 7 months, P<0.001) compared with dexamethasone-placebo. At a median follow-up of 48 months for surviving patients, using data up to July 2008, a significant benefit in overall survival (median of 38.0 vs 31.6 months, P=0.045) was retained despite 47.6% of patients who were randomized to dexamethasone-placebo receiving lenalidomide-based treatment after disease progression or study unblinding. Low β2-microglobulin and low bone marrow plasmacytosis were associated with longer survival. In conclusion, these data confirm the significant response and survival benefit with lenalidomide and dexamethasone.
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页码:2147 / 2152
页数:5
相关论文
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