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

Author:

Seng Sonia1,Liu Ziyue1,Chiu Sophia K.1,Proverbs-Singh Tracy1,Sonpavde Guru1,Choueiri Toni K.1,Tsao Che-Kai1,Yu Menggang1,Hahn Noah M.1,Oh William K.1,Galsky Matthew D.1

Affiliation:

1. Sonia Seng, Southcoast Centers for Cancer Care, Fairhaven; Toni K. Choueiri, Dana-Farber Cancer Institute, Boston, MA; Ziyue Liu and Noah M. Hahn, Indiana University School of Medicine, Indianapolis, IN; Sophia K. Chiu, Tracy Proverbs-Singh, Che-Kai Tsao, William K. Oh, and Matthew D. Galsky, Mount Sinai School of Medicine, New York, NY; Guru Sonpavde, Baylor College of Medicine, Houston, TX; and Menggang Yu, University of Wisconsin School of Medicine, Madison, WI.

Abstract

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/m2 (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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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