Annals of Surgical Oncology Sign the Guestbook
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

10.1245/s10434-006-9337-9
Annals of Surgical Oncology 14:1860-1869 (2007)
© 2007 Society of Surgical Oncology
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Saif, M. W.
Right arrow Articles by Salem, R. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Saif, M. W.
Right arrow Articles by Salem, R. R.

Original Article

Gastrointestinal Perforation Due to Bevacizumab in Colorectal Cancer

Muhammad Wasif Saif, MD, MBBS, Aymen Elfiky, MD and Ronald R. Salem, MB, ChB

Yale Cancer Center, Yale University School of Medicine, Divisions of Medical and Surgical Oncology, 333 Cedar Street, FMP 116, New Haven, Connecticut 06520, USA

Correspondence: Address correspondence and reprint requests to: Muhammad Wasif Saif, MD, MBBS; E-mail: wasif.saif{at}yale.edu

Bevacizumab is the first U.S. Food and Drug Association-approved vascular endothelial growth factor-targeted agent that greatly increases progression-free and overall survival in combination with standard chemotherapy regimens in patients with metastatic colorectal cancer. Although bevacizumab is generally well tolerated, some serious adverse events have occurred in some patients in clinical trials, including arterial thromboembolism and gastrointestinal (GI) perforation. GI perforation was first observed in the pivotal phase 3 trial, in which six events occurred in bevacizumab group (1.5%), compared with no events in the control group. Since then, similar rates of GI perforation have been observed in other large trials. Typical presentation was abdominal pain associated with constipation and vomiting. Such events occurred throughout treatment and were not correlated with duration of exposure. No difference in rate of GI perforations was found in patients who did and did not have a baseline history of peptic ulcer disease, diverticulosis, and history of chronic use of non-steroidal anti-inflammatory drugs. However, the incidence of GI perforation seemed to be higher in patients with primary tumor intact, recent history of sigmoidoscopy or colonoscopy, or previous adjuvant radiotherapy, but it is necessary to confirm these preliminary findings by multivariate analyses. The mechanism responsible for causing GI perforation is not known and may be multifactorial. Bevacizumab should be permanently discontinued in patients who develop GI perforation. This article reviews the incidence, presentation, pathogenesis, risk factors, and management of GI perforation in patients with colorectal cancer who are treated with bevacizumab.

Key Words: Bevacizumab • Colorectal cancer • Gastrointestinal perforation




This article has been cited by other articles:


Home page
Clin. Cancer Res.Home page
K. Sakamoto, S. Maeda, Y. Hikiba, H. Nakagawa, Y. Hayakawa, W. Shibata, A. Yanai, K. Ogura, and M. Omata
Constitutive NF-{kappa}B Activation in Colorectal Carcinoma Plays a Key Role in Angiogenesis, Promoting Tumor Growth
Clin. Cancer Res., April 1, 2009; 15(7): 2248 - 2258.
[Abstract] [Full Text] [PDF]


Home page
Neuro OncolHome page
A. D. Norden, J. Drappatz, A. S. Ciampa, L. Doherty, D. C. LaFrankie, S. Kesari, and P. Y. Wen
Colon perforation during antiangiogenic therapy for malignant glioma
Neuro-oncol, January 1, 2009; 11(1): 92 - 95.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
C. L. Estilo, M. Fornier, A. Farooki, D. Carlson, G. Bohle III, and J. M. Huryn
Osteonecrosis of the Jaw Related to Bevacizumab
J. Clin. Oncol., August 20, 2008; 26(24): 4037 - 4038.
[Full Text] [PDF]


Home page
Ann OncolHome page
S. Cowman, J. Stebbing, and M. Tuthill
Large bowel perforation associated with capecitabine treatment for breast cancer
Ann. Onc., August 1, 2008; 19(8): 1510 - 1511.
[Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
G. K. Dudar, L. D. D'Andrea, R. Di Stasi, C. Pedone, and J. L. Wallace
A vascular endothelial growth factor mimetic accelerates gastric ulcer healing in an iNOS-dependent manner
Am J Physiol Gastrointest Liver Physiol, August 1, 2008; 295(2): G374 - G381.
[Abstract] [Full Text] [PDF]


Home page
Ann OncolHome page
J. Tol, M. Koopman, C. J. Rodenburg, A. Cats, G. J. Creemers, J. G. Schrama, F. L. G. Erdkamp, A. H. Vos, L. Mol, N. F. Antonini, et al.
A randomised phase III study on capecitabine, oxaliplatin and bevacizumab with or without cetuximab in first-line advanced colorectal cancer, the CAIRO2 study of the Dutch Colorectal Cancer Group (DCCG). An interim analysis of toxicity
Ann. Onc., April 1, 2008; 19(4): 734 - 738.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Society of Surgical Oncology.