Gelişmiş Arama

Basit öğe kaydını göster

dc.contributor.authorAkun E.
dc.contributor.authorOkutur K.
dc.contributor.authorSeber S.
dc.contributor.authorKorkmaz T.
dc.contributor.authorAydin K.
dc.contributor.authorBozkurt M.
dc.contributor.authorDemir G.
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:53:21Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:53:21Z
dc.date.issued2012
dc.identifier.issn1107-0625
dc.identifier.urihttp://hdl.handle.net/11446/1905
dc.descriptionPubMed ID: 23335523en_US
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.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBevacizumaben_US
dc.subjectBleedingen_US
dc.subjectColorectal canceren_US
dc.subjectGastrointestinal perforationen_US
dc.subjectHypertensionen_US
dc.subjectThromboembolismen_US
dc.titleSafety and tolerability of first-line bevacizumab in metastatic colorectal canceren_US
dc.typearticleen_US
dc.relation.journalJournal of B.U.ON.en_US
dc.departmentDBÜen_US
dc.identifier.issue4en_US
dc.identifier.volume17en_US
dc.identifier.startpage669en_US
dc.identifier.endpage676en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempDBÜen_US


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster