Journal
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
Volume 93, Issue 3, Pages 257-276Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.critrevonc.2014.11.006
Keywords
Vascular endothelial growth factor receptor; Tyrosine kinase inhibitors; Approved; Hepatotoxicity; Meta-analysis
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Funding
- DF/HCC Kidney Cancer SPORE [P50 CA101942-01]
- Trust Family
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A meta-analysis of randomized controlled trials (RCT) was conducted to determine the relative risk (RR) of hepatotwdcity with vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKI). Citations from PubMed/Medline, abstracts from major conferences, clinicaltrials.gov and package inserts were reviewed to include RCTs comparing arms with or without a VEGFR TKI. The RRs of all-grade ALT, AST, ALP and bilirubin elevation in 18,282 patients from 52 trials were 1.57 (95% CI 1.38-1.79, p < 0.001), 1.57 (95% CI 1.36-1.81, p < 0.001), 1.20 (95% CI 1.09-1.83, p < 0.001) and 1.55 (95% CI 1.21-1.97, p < 0.001) respectively, and high-grade elevations were 1.66(95% CI 1.25-2.20,p = 0.001), 1.61 (95% CI 1.21-2.14, p = 0.001), 1.02(95% CI 0.70-1.47,p = 0.932) and 1.34 (95% CI 1.0-1.81, p = 0.054) respectively compared to those in the non-TKI group. The incidence of hepatic failure with VEGFR TKIs was 0.8%. Published by Elsevier Ireland
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