Bevacizumab induced intestinal perforation in patients with colorectal cancer
- Author:
Sun Young BAEK
1
;
Seung Hun LEE
;
Seung Hyun LEE
Author Information
- Publication Type:Original Article
- Keywords: Colorectal neoplasms; Tumor; Intestinal perforation; Bevacizumab
- MeSH: Bevacizumab; Colon, Sigmoid; Colorectal Neoplasms; Drug Therapy; Hemorrhage; Humans; Intestinal Perforation; Liver; Medical Records; Rectum; Retrospective Studies; Sepsis
- From: Korean Journal of Clinical Oncology 2019;15(1):15-18
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: Bevacizumab has been used as a promising drug for metastatic colorectal cancer in combination with chemotherapeutic agents. However, it has a few serious adverse effects, such as intestinal bleeding or perforation. The purpose of this study is to identify the clinical characteristics of intestinal perforation induced by bevacizumab in colorectal cancer patients.METHODS: From January 2007 to June 2018, a total of 488 patients underwent chemotherapy with bevacizumab for metastatic colorectal cancer. Medical records were reviewed retrospectively.RESULTS: Nine patients (1.8%) were identified with intestinal perforation induced with bevacizumab. The median age was 59 years (range, 36–68 years). The primary tumor site was the sigmoid colon in six patients, the rectum in three patients. The liver was the most common metastatic organ (7 patients). Perforation sites were primary tumor site of the colorectum in four patients and the small bowel in five patients. Intestinal perforation was developed after a median of 3 chemotherapy cycles (range, 1–15 cycles), and a median of 7 days (range, 3–32 days) after chemotherapy. One patient expired due to sepsis.CONCLUSION: Bevacizumab induced intestinal perforation is a lethal adverse effect in patients with colorectal cancers. The characteristics of intestinal perforation varied according to perforation site, previous chemotherapy cycles, and clinical course. Careful monitoring is necessary with the use of bevacizumab in conjunction with chemotherapeutic agents.
