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Use of bevacizumab before or after radiotherapy increases the risk of fistula formation in patients with cervical cancer

DC Field Value Language
dc.contributor.author김건민-
dc.contributor.author김나리-
dc.contributor.author김상운-
dc.contributor.author김영태-
dc.contributor.author김용배-
dc.contributor.author장지석-
dc.contributor.author최서희-
dc.date.accessioned2021-04-29T16:53:50Z-
dc.date.available2021-04-29T16:53:50Z-
dc.date.issued2021-01-
dc.identifier.issn1048-891X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/182076-
dc.description.abstractObjective: Several reports have documented the risk of fistula formation after bevacizumab in patients previously treated with radiation therapy. The aim of this study was to investigate the risk of fistula formation with bevacizumab and radiotherapy compared with radiotherapy alone. Methods: We retrospectively analyzed patients with stage I-IV cervical cancer between January 2013 and December 2018. Patients who had a history of pelvic radiotherapy, who were treated with intracavitary brachytherapy alone, received radiotherapy at another hospital, received concurrent bevacizumab and radiotherapy, or had missing follow-up data or a short follow-up period (<6 months) were excluded. The fistula rates were compared between the groups using the Cox proportional hazards model and propensity score analyses. Results: A total of 302 patients were included in the study: 249 patients were treated with definitive or adjuvant radiotherapy, and 53 patients were treated with radiotherapy before or after bevacizumab. With a median follow-up of 35.9 (IQR 22.8-53.5) months, the 3 year cumulative fistula incidence rate was significantly higher in the radiotherapy + bevacizumab group than in the radiotherapy group (27.0% vs 3.0%, p<0.001). Bevacizumab administration was significantly associated with fistula formation in the multivariable adjusted model (HR 4.76, 95% CI 1.71 to 13.23) and three propensity score adjusted model (all p<0.05). Biologically equivalent dose in 2 Gy fractions for 2 cc of the rectum more than 76 Gy was also associated with fistula formation (HR 4.30, 95% CI 1.52 to 12.18). Additionally, a 10 month interval between radiotherapy and bevacizumab reduced the incidence of fistula formation in the radiotherapy + bevacizumab group (p=0.032). Conclusions: In patients with cervical cancer treated with pelvic radiotherapy, the addition of bevacizumab substantially increased the risk of fistula formation. Physicians should perform pelvic radiotherapy in combination with bevacizumab with caution; moreover, close monitoring for fistula formation is warranted in these patients.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherLippincott Williams & Wilkins-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleUse of bevacizumab before or after radiotherapy increases the risk of fistula formation in patients with cervical cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorNalee Kim-
dc.contributor.googleauthorSeo Hee Choi-
dc.contributor.googleauthorJee Suk Chang-
dc.contributor.googleauthorYoung-Tae Kim-
dc.contributor.googleauthorSang Wun Kim-
dc.contributor.googleauthorGun Min Kim-
dc.contributor.googleauthorYong Bae Kim-
dc.identifier.doi10.1136/ijgc-2020-002031-
dc.contributor.localIdA00287-
dc.contributor.localIdA05709-
dc.contributor.localIdA00526-
dc.contributor.localIdA00729-
dc.contributor.localIdA00744-
dc.contributor.localIdA04658-
dc.contributor.localIdA04867-
dc.relation.journalcodeJ01115-
dc.identifier.eissn1525-1438-
dc.identifier.pmid33273018-
dc.identifier.urlhttps://ijgc.bmj.com/content/31/1/59.long-
dc.subject.keywordcervical cancer-
dc.subject.keywordradiotherapy-
dc.subject.keywordrectovaginal fistula-
dc.subject.keywordvaginal fistula-
dc.contributor.alternativeNameKim, Gun Min-
dc.contributor.affiliatedAuthor김건민-
dc.contributor.affiliatedAuthor김나리-
dc.contributor.affiliatedAuthor김상운-
dc.contributor.affiliatedAuthor김영태-
dc.contributor.affiliatedAuthor김용배-
dc.contributor.affiliatedAuthor장지석-
dc.contributor.affiliatedAuthor최서희-
dc.citation.volume31-
dc.citation.number1-
dc.citation.startPage59-
dc.citation.endPage65-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, Vol.31(1) : 59-65, 2021-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers

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