Lenalidomide in combination with dexamethasone at first relapse in comparison with its use as later salvage therapy in relapsed or refractory multiple myeloma

被引:89
|
作者
Stadtmauer, Edward A. [1 ]
Weber, Donna M. [2 ]
Niesvizky, Ruben [3 ]
Belch, Andrew [4 ]
Prince, Miles H. [5 ,10 ]
San Miguel, Jesus F. [6 ]
Facon, Thierry [7 ]
Olesnyckyj, Marta [8 ]
Yu, Zhinuan [8 ]
Zeldis, Jerome B. [8 ]
Knight, Robert D. [8 ]
Dimopoulos, Meletios A. [9 ]
机构
[1] Univ Penn, Abramson Canc Ctr, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Weill Cornell Med Coll, New York, NY USA
[4] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[5] Peter MacCallum Canc Inst, Div Haematol Med Oncol, Melbourne, Vic 3000, Australia
[6] IBMCC USAL CSIC, Serv Hematol, CIC, Hosp Univ Salamanca, Salamanca, Spain
[7] Hop Claude Huriez, Lille, France
[8] Celgene Corp, Summit, NJ USA
[9] Univ Athens, Sch Med, GR-11527 Athens, Greece
[10] Univ Melbourne, Melbourne, Vic, Australia
关键词
lenalidomide; multiple myeloma; relapse; time to progression; survival; NEWLY-DIAGNOSED MYELOMA; PLUS DEXAMETHASONE; THALIDOMIDE; BORTEZOMIB; TIME;
D O I
10.1111/j.1600-0609.2009.01257.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This subset analysis of data from two phase III studies in patients with relapsed or refractory multiple myeloma (MM) evaluated the benefit of initiating lenalidomide plus dexamethasone at first relapse. Multivariate analysis showed that fewer prior therapies, along with beta(2)-microglobulin (<= 2.5 mg/L), predicted a better time to progression (TTP; study end-point) with lenalidomide plus dexamethasone treatment. Patients with one prior therapy showed a significant improvement in benefit after first relapse compared with those who received two or more therapies. Patients with one prior therapy had significantly prolonged median TTP (17.1 vs. 10.6 months; P = 0.026) and progression-free survival (14.1 vs. 9.5 months, P = 0.047) compared with patients treated in later lines. Overall response rates were higher (66.9% vs. 56.8%, P = 0.06), and the complete response plus very good partial response rate was significantly higher in first relapse (39.8% vs. 27.7%, P = 0.025). Importantly, overall survival was significantly prolonged for patients treated with lenalidomide plus dexamethasone with one prior therapy, compared with patients treated later in salvage (median of 42.0 vs. 35.8 months, P = 0.041), with no differences in toxicity, dose reductions, or discontinuations despite longer treatment. Therefore, lenalidomide plus dexamethasone is both effective and tolerable for second-line MM therapy and the data suggest that the greatest benefit occurs with earlier use.
引用
收藏
页码:426 / 432
页数:7
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