Literature DB >> 20382413

Which factors predict bowel complications in patients with recurrent epithelial ovarian cancer being treated with bevacizumab?

D L Richardson1, F J Backes, J D Hurt, L G Seamon, L J Copeland, J M Fowler, D E Cohn, D M O'Malley.   

Abstract

BACKGROUND: Increased rates of bowel perforation in patients with recurrent epithelial ovarian cancer (EOC) treated with bevacizumab have been reported, but the risk factors for this association are uncertain. We sought to identify factors associated with bowel perforation and fistula formation in recurrent EOC patients treated with bevacizumab.
METHODS: A chart review of all patients treated with bevacizumab for recurrent EOC at a single institution was performed. Pertinent patient characteristics and treatment information were collected. Univariate logistic regression was performed to analyze multiple variables.
RESULTS: One hundred twelve patients who were treated with 160 different bevacizumab regimens were identified. The median age was 60 years (range, 29-78 years). Patients had received a median of 4 prior chemotherapy regimens (range, 1-10). The median number of cycles was 4 (range, 0.5-31). Ten patients (9%) were diagnosed with bowel perforations, and another 2 patients (1.8%) were diagnosed with fistulas. The 30-day mortality following perforation was 50%, with 30% of patients dying within 1 week. Patients with rectovaginal nodularity were more likely to develop a bowel perforation or fistula than those who did not have this finding, OR=3.64 (95% CI=1.1 to 12.1, p=0.04). None of the other variables were significantly associated with bowel perforations or fistula formation.
CONCLUSIONS: Rectovaginal nodularity is associated with an increased risk of bowel perforation or fistula formation for patients with recurrent EOC treated with bevacizumab. Careful consideration should be given prior to initiating bevacizumab treatment in EOC patients with rectovaginal nodularity since the mortality rate with bevacizumab associated bowel perforations is 50%. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20382413     DOI: 10.1016/j.ygyno.2010.01.011

Source DB:  PubMed          Journal:  Gynecol Oncol        ISSN: 0090-8258            Impact factor:   5.482


  11 in total

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Authors:  Gillian M Keating
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Review 2.  Bevacizumab use in the frontline, maintenance and recurrent settings for ovarian cancer.

Authors:  Carolyn E Haunschild; Krishnansu S Tewari
Journal:  Future Oncol       Date:  2019-11-20       Impact factor: 3.404

3.  Clinical predictors of bevacizumab-associated intestinal perforation in non-small cell lung cancer.

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Journal:  Invest New Drugs       Date:  2018-03-14       Impact factor: 3.850

4.  Imaging features of bowel toxicities in the setting of molecular targeted therapies in cancer patients.

Authors:  E Thornton; S A Howard; J Jagannathan; K M Krajewski; A B Shinagare; K O'Regan; J M Cleary; N H Ramaiya
Journal:  Br J Radiol       Date:  2012-06-06       Impact factor: 3.039

5.  Intestinal perforation in gynecologic oncology: do all patients benefit from surgical management?

Authors:  Gunjal Garg; L Stewart Massad; Shabnam Pourabolghasem; Gongfu Zhou; Matthew A Powell; Premal H Thaker; Andrea R Hagemann; Ivy Wilkinson-Ryan; David G Mutch
Journal:  Gynecol Oncol       Date:  2013-03-13       Impact factor: 5.482

6.  A recurrent ovarian cancer patient with a history of nine prior chemotherapy regimens who was safely treated with weekly paclitaxel plus bevacizumab and achieved a complete response: a case report.

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7.  Bevacizumab toxicity in heavily pretreated recurrent epithelial ovarian, fallopian tube, and primary peritoneal cancers.

Authors:  Jovana Y Martin; Renata R Urban; John B Liao; Barbara A Goff
Journal:  J Gynecol Oncol       Date:  2016-05-10       Impact factor: 4.401

8.  An open-label, randomized, phase II trial evaluating the efficacy and safety of standard of care with or without bevacizumab in platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer patients previously treated with bevacizumab for front-line or platinum-sensitive ovarian cancer: rationale, design, and methods of the Japanese Gynecologic Oncology Group study JGOG3023.

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Journal:  BMC Cancer       Date:  2018-07-31       Impact factor: 4.430

Review 9.  Targeted anti-vascular therapies for ovarian cancer: current evidence.

Authors:  M Hall; C Gourley; I McNeish; J Ledermann; M Gore; G Jayson; T Perren; G Rustin; S Kaye
Journal:  Br J Cancer       Date:  2013-02-05       Impact factor: 7.640

10.  Increased genitourinary fistula rate after bevacizumab in recurrent cervical cancer patients initially treated with definitive radiochemotherapy and image-guided adaptive brachytherapy.

Authors:  Alina Sturdza; Sandra Hofmann; Marlene Kranawetter; Stephan Polterauer; Christoph Grimm; Michael Krainer; Christian Kirisits; Richard Pötter; Alexander Reinthaller; Richard Schwameis
Journal:  Strahlenther Onkol       Date:  2017-07-18       Impact factor: 3.621

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