Publication:
Safety and tolerability of first-line bevacizumab in metastatic colorectal cancer

dc.contributor.authorsAkun, E.; Okutur, K.; Seber, S.; Korkmaz, T.; Aydin, K.; Bozkurt, M.; Namal, E.; Hasbal, B.; Tecimer, C.; Demir, G.
dc.date.accessioned2022-03-12T18:06:30Z
dc.date.accessioned2026-01-11T17:12:59Z
dc.date.available2022-03-12T18:06:30Z
dc.date.issued2012
dc.description.abstractPurpose: To determine the clinical features of bevacizumab-associated toxicities in metastatic colorectal cancer (MCRC) patients. Methods: The medical records of 60 patients with MCRC who were treated with chemotherapy including bevacizumab in the first-line setting were retrospectively evaluated. Results: Bevacizumab was administered along with irinotecan plus 5-fluorouracil/leucovorin (5-FU/LV) to 44 patients, 5-FU/LV+oxaliplatin to 8 patients, capecitabine+oxaliplatin to 6 patients and 5-FU/LV to 2 patients. The total number of the cycles received was 381 (median 6, range 1-13). The most common bevacizumab-related toxicity was grade 1-2 bleeding (28%) followed by hypertension (17%). Grade 1-2 proteinuria was seen in 8% of the patients (no grade 3-4 proteinuria). Arterial thromboembolic events (ATE) were not observed, however 3 patients (5%) had experienced grade 3-4 venous thromboembolic events. In 3 patients (5%) grade 1-2 wound complications were seen (delayed wound healing in the place of the venous access device in 2, and wound infection in 1). In addition, gastrointestinal perforation (GIP) was seen in 3 (5%) patients. Two of the patients were treated by surgical intervention and one patient died of sepsis. Conclusion: Bevacizumab is well tolerated when combined with various chemotherapy regimens. As bevacizumab is becoming widely used in the routine oncology practice, further studies which investigate the mechanism of bevacizumab-associated toxicities are warranted to develop effective management strategies for these adverse events.
dc.identifier.doidoiWOS:000313394000008
dc.identifier.eissn2241-6293
dc.identifier.issn1107-0625
dc.identifier.pubmed23335523
dc.identifier.urihttps://hdl.handle.net/11424/230915
dc.identifier.wosWOS:000313394000008
dc.language.isoeng
dc.publisherIMPRIMATUR PUBLICATIONS
dc.relation.ispartofJOURNAL OF BUON
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectbevacizumab
dc.subjectbleeding
dc.subjectcolorectal cancer
dc.subjectgastrointestinal perforation
dc.subjecthypertension
dc.subjectthromboembolism
dc.subjectRANDOMIZED PHASE-III
dc.subjectFLUOROURACIL
dc.subjectLEUCOVORIN
dc.subjectTHERAPY
dc.subjectCHEMOTHERAPY
dc.subjectOXALIPLATIN
dc.subjectCOMBINATION
dc.subjectIRINOTECAN
dc.subjectMANAGEMENT
dc.subjectTRIAL
dc.titleSafety and tolerability of first-line bevacizumab in metastatic colorectal cancer
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage676
oaire.citation.issue4
oaire.citation.startPage669
oaire.citation.titleJOURNAL OF BUON
oaire.citation.volume17

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