Risk of Venous Thromboembolism in Patients With Cancer Treated With Cisplatin: A Systematic Review and Meta-Analysis

被引:174
|
作者
Seng, Sonia
Liu, Ziyue [3 ]
Chiu, Sophia K.
Proverbs-Singh, Tracy
Sonpavde, Guru [4 ]
Choueiri, Toni K. [2 ]
Tsao, Che-Kai
Yu, Menggang [5 ]
Hahn, Noah M. [3 ]
Oh, William K.
Galsky, Matthew D. [1 ]
机构
[1] Mt Sinai Med Ctr, Mt Sinai Sch Med, Tisch Canc Inst, New York, NY 10029 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Indiana Univ Sch Med, Indianapolis, IN USA
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Univ Wisconsin, Sch Med, Madison, WI USA
关键词
CELL LUNG-CANCER; RANDOMIZED PHASE-II; COOPERATIVE-ONCOLOGY-GROUP; ADVANCED GASTRIC-CANCER; DOCETAXEL PLUS CISPLATIN; CLINICAL-TRIALS GROUP; OF-THE-LITERATURE; COMBINATION CHEMOTHERAPY; 1ST-LINE TREATMENT; BREAST-CANCER;
D O I
10.1200/JCO.2012.42.4358
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Several reports suggest that cisplatin is associated with an increased risk of thromboembolism. However, because the excess risk of venous thromboembolic events (VTEs) with cisplatin-based chemotherapy has not been well described, we conducted a systemic review and meta-analysis of randomized controlled trials evaluating the incidence and risk of VTEs associated with cisplatin-based chemotherapy. Methods PubMed was searched for articles published from January 1, 1990, to December 31, 2010. Eligible studies included prospective randomized phase II and III trials evaluating cisplatin-based versus non-cisplatin-based chemotherapy in patients with solid tumors. Data on all-grade VTEs were extracted. Study quality was calculated using Jadad scores. Incidence rates, relative risks (RRs), and 95% CIs were calculated using a random effects model. Results A total of 8,216 patients with various advanced solid tumors from 38 randomized controlled trials were included. The incidence of VTEs was 1.92% (95% CI, 1.07 to 2.76) in patients treated with cisplatin-based chemotherapy and 0.79% (95% CI, 0.45 to 1.13) in patients treated with non-cisplatin-based regimens. Patients receiving cisplatin-based chemotherapy had a significantly increased risk of VTEs (RR, 1.67; 95% CI, 1.25 to 2.23; P = .01). Exploratory subgroup analysis revealed the highest RR of VTEs in patients receiving a weekly equivalent cisplatin dose > 30 mg/m(2) (2.71; 95% CI, 1.17 to 6.30; P = .02) and in trials reported during 2000 to 2010 (1.72; 95% CI, 1.27 to 2.34; P = .01). Conclusion Cisplatin is associated with a significant increase in the risk of VTEs in patients with advanced solid tumors when compared with non-cisplatin-based chemotherapy. J Clin Oncol 30:4416-4426. (c) 2012 by American Society of Clinical Oncology
引用
收藏
页码:4416 / 4426
页数:11
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