Abstract
Background
The aim of this meta-analysis was to gather current data and evaluate not only the risk of gastrointestinal (GI) perforation with bevacizumab, but also the potential risk factors for this adverse event.
Materials and methods
We carried out a literature search in PubMed for randomized controlled trials (RCTs) reported from January 2000 to December 2013. Summary incidence, relative risks (RRs) and 95 % confidence intervals (CIs) were calculated using random-effects or fixed-effects models based on the heterogeneity of the included studies.
Results
A total of 26,833 patients from 33 RCTs were included in the meta-analysis. Bevacizumab-containing therapy significantly increased the risk of developing all-grade (RR 3.35, 95 % CI 2.35–4.79, P < 0.001) and fatal GI perforation (RR 3.08, 95%CI: 1.04–9.08, P = 0.042). On subgroup analysis, no significant risk differences were found based on bevacizumab dosage, treatment duration, treatment line, type of clinical trial and median age. When stratified by tumor types, a significantly increased risk of GI perforation with bevacizumab was observed in colorectal cancer (RR 2.84, 95% CI 1.43–5.61, P = 0.003), gynecologic cancer (RR 3.37, 95% CI 1.71–6.62, P < 0.001) and prostate cancer (RR 6.01, 95% CI 1.78–20.28, P = 0.004). Additionally, the use of bevacizumab significantly increased the risk of GI perforation when used in conjunction with taxanes (RR 3.09, 95% CI 1.92–4.96, P < 0.001) or oxaliplatin (RR 2.85, 95% CI 1.07–7.57, P = 0.036).
Conclusions
Bevacizumab treatment is associated with a significantly increased risk of developing GI perforation, and clinicians should be aware of the risks of GI perforation with the administration of this drug in cancer patients.
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Supplemental Figure 1
Meta-regression analysis of trends between treatment duration and relative risk of GI perforation, Symbols Each study is represented by a circle, the diameter of which is proportional to its statistical weight (JPEG 358 kb)
Supplemental Figure 2
Funnel plot of standard error by log-relative risk for GI perforation. (JPEG 209 kb)
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Qi, WX., Shen, Z., Tang, LN. et al. Bevacizumab increases the risk of gastrointestinal perforation in cancer patients: a meta-analysis with a focus on different subgroups. Eur J Clin Pharmacol 70, 893–906 (2014). https://doi.org/10.1007/s00228-014-1687-9
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DOI: https://doi.org/10.1007/s00228-014-1687-9