Meta-Analysis of the Efficacy and Safety of Bortezomib Re-Treatment in Patients With Multiple Myeloma

被引:32
|
作者
Knopf, Kevin B. [1 ]
Duh, Mei Sheng [2 ]
Lafeuille, Marie-Helene [3 ]
Gravel, Jonathan [3 ]
Lefebvre, Patrick [3 ]
Niculescu, Liviu [4 ]
Ba-Mancini, Abbie [4 ]
Ma, Esprit [4 ]
Shi, Hongliang [4 ]
Comenzo, Raymond L. [5 ]
机构
[1] Sutter Hlth, Calif Pacific Med Ctr, San Francisco, CA 94118 USA
[2] Anal Grp Inc, Boston, MA USA
[3] Grp Anal Ltee, Montreal, PQ, Canada
[4] Millennium Takeda Oncol Co, Cambridge, MA USA
[5] Tufts Med Ctr, Dept Hematol Oncol, Boston, MA USA
来源
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | 2014年 / 14卷 / 05期
关键词
Meta-regression analysis; Overall response rate; Random-effect model; Refractory; Relapsed; RANDOMIZED PHASE-III; PEGYLATED LIPOSOMAL DOXORUBICIN; PLUS BORTEZOMIB; PERIPHERAL NEUROPATHY; MELPHALAN-PREDNISONE; APEX TRIAL; COMBINATION; THERAPY; RISK; DEXAMETHASONE;
D O I
10.1016/j.clml.2014.03.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This meta-analysis of 23 studies of bortezomib-based retreatment in relapsed/refractory myeloma demonstrated a pooled, weighted average response rate of 39.1% and median time to progression (TTP) and overall survival (OS) of 7.5 and 16.6 months, respectively. Grade 3/4 adverse events (AEs) included thrombocytopenia (35%), neutropenia (15%), and anemia (14%). These data demonstrate the efficacy and tolerability of bortezomib retreatment in previously treated patients. Introduction: Bortezomib is administered for a finite course; thus, patients might remain sensitive to bortezomib-based therapy at relapse. We report a meta-analysis of bortezomib-based retreatment in relapsed/refractory myeloma. Patients and Methods: A systematic literature review identified studies of bortezomib-based retreatment in relapsed/refractory myeloma. Proportions of bortezomib-refractory patients and additional prognostic factors were extracted and used in weighted stratified analyses of TTP and OS. Random-effect pooled estimates were calculated for overall response rate (ORR) and rates of common AEs. Results: Twenty-three studies (n = 1051 patients) were identified. Bortezomib was administered intravenously in all studies. Across studies in which data were available, pooled, weighted average ORR was 39.1% (95% confidence interval, 30.8%-47.4%), and pooled, weighted average median TTP and OS were 7.5 and 16.6 months, respectively. Patients with fewer previous therapies (<= 4) and relapsed (not refractory) patients achieved higher ORRs, of 43.4% and 57.2%, respectively. Random-effects meta-regression analysis confirmed that relapsed patients were associated with a higher ORR by 28 to 41 percentage points versus refractory patients. In relapsed patients, median TTP and OS were 8.5 and 19.7 months, respectively. Common Grade 3/4 AEs included thrombocytopenia (35%), neutropenia (15%), anemia (14%), pneumonia (10%), and peripheral neuropathy (3%). Conclusion: Based on these findings, bortezomib retreatment is well tolerated and appears efficacious in relapsed patients. In an era of new and emerging treatment options for relapsed and/or refractory myeloma, these data indicate that bortezomib retreatnnent might be a highly effective option in previously treated patients.
引用
收藏
页码:380 / 388
页数:9
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