Efficacy and safety of long-term treatment with lenalidomide and dexamethasone in patients with relapsed/refractory multiple myeloma

被引:40
作者
Dimopoulos, M. A. [1 ]
Swern, A. S. [2 ]
Li, J. S. [2 ]
Hussein, M. [3 ]
Weiss, L. [4 ]
Nagarwala, Y. [3 ]
Baz, R. [5 ]
机构
[1] Univ Athens, Sch Med, Dept Clin Therapeut, Athens 11528, Greece
[2] Celgene Corp, Dept Biostat, Summit, NJ USA
[3] Celgene Corp, Dept Med Affairs, Summit, NJ USA
[4] Celgene Corp, Dept Drug Safety, Summit, NJ USA
[5] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Hematol Malignancies, Tampa, FL 33612 USA
关键词
PLUS DEXAMETHASONE; SURVIVAL; THERAPY; NEUTROPENIA; IMPACT;
D O I
10.1038/bcj.2014.77
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Data from two randomized pivotal, phase 3 trials evaluating the combination of lenalidomide and dexamethasone in relapsed/refractory multiple myeloma (RRMM) were pooled to characterize the subset of patients who achieved long-term benefit of therapy (progression-free survival >= 3 years). Patients with long-term benefit of therapy (n = 45) had a median duration of treatment of 48.1 months and a response rate of 100%. Humoral improvement (uninvolved immunoglobulin A) was more common in patients with long-term benefit of therapy (79% vs 55%; P = 0.002). Significant predictors of long-term benefit of therapy in multivariate analysis were age <65 years (P = 0.03), beta 2-microglobulin <2.5 mg/l (P = 0.002) and fewer prior therapies (P = 0.002). The exposure-adjusted incidence rate (EAIR) of grade 3-4 neutropenia was lower in patients with long-term benefit of therapy (13.9 vs 38.2 per 100 patient-years). The EAIR for invasive second primary malignancy was the same in patients with long-term benefit of therapy and other patients (1.7 per 100 patient-years). These findings indicate that patients with RRMM can experience long-term benefit with lenalidomide and dexamethasone treatment with manageable side effects.
引用
收藏
页码:e257 / e257
页数:8
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