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Published on: October 27, 2014
Incidence and management of gastrointestinal perforation from bevacizumab in advanced cancers
Taher Abu-Hejleh1, James J Mezhir, Michael J Goodheart
1Department of Internal Medicine, Division of Hematology, Oncology, and Bone Marrow Transplantation, The University of Iowa Hospitals and Clinics, 200 Hawkins Dr., C32 GH, Iowa City, IA 52242-1081, USA. taher-hejleh@uiowa.edu
Abstract:
Bevacizumab (Avastin™, Genentech) is a monoclonal antibody that deactivates the vascular endothelial growth factor leading to disruption of vital cancer signaling pathways and inhibition of angiogenesis which results in its anti-tumor activity. The use of bevacizumab in treating cancers has steadily increased since it was initially approved by the Food and Drug Administration for metastatic colorectal cancer. Clinical trials have revealed that bevacizumab has serious side effects, including spontaneous bowel perforation, which can occur in patients who have no involvement of the gastrointestinal tract by cancer. Although risk factors for bevacizumab-associated bowel perforation have been identified, it is still unclear which patients are specifically at risk for this complication. The management of bevacizumab-induced bowel perforation depends on the clinical presentation and the goals of care set by the treating physicians and the patient.
Insights
Bevacizumab, a cancer drug, can cause serious bowel perforation even without gastrointestinal tumors. Identifying at-risk patients remains a challenge for effective cancer treatment management.
Area of Science:
- Oncology
- Pharmacology
- Gastroenterology
Background:
- Bevacizumab (Avastin) is a monoclonal antibody targeting vascular endothelial growth factor (VEGF).
- It inhibits angiogenesis, a key process in tumor growth and metastasis.
- Its use has expanded for various cancers since FDA approval for metastatic colorectal cancer.
Purpose of the Study:
- To review the anti-tumor activity of bevacizumab.
- To highlight the serious side effect of bowel perforation associated with bevacizumab therapy.
- To discuss the current understanding of risk factors and management strategies for bevacizumab-induced bowel perforation.
Main Methods:
- Review of clinical trial data and scientific literature.
- Analysis of bevacizumab's mechanism of action and its impact on angiogenesis.
- Examination of reported cases of bevacizumab-associated bowel perforation.
Main Results:
- Bevacizumab effectively disrupts cancer signaling and inhibits angiogenesis.
- Serious side effects include spontaneous bowel perforation, even in patients without GI cancer involvement.
- While some risk factors are known, precise identification of susceptible patients remains unclear.
Conclusions:
- Bevacizumab is an effective anti-cancer agent but carries significant risks.
- Bowel perforation is a critical complication requiring careful consideration.
- Management strategies are guided by clinical presentation and patient-specific goals of care.
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