Publication: Safety and tolerability of first-line bevacizumab in metastatic colorectal cancer
| dc.contributor.authors | Akun, E.; Okutur, K.; Seber, S.; Korkmaz, T.; Aydin, K.; Bozkurt, M.; Namal, E.; Hasbal, B.; Tecimer, C.; Demir, G. | |
| dc.date.accessioned | 2022-03-12T18:06:30Z | |
| dc.date.accessioned | 2026-01-11T17:12:59Z | |
| dc.date.available | 2022-03-12T18:06:30Z | |
| dc.date.issued | 2012 | |
| dc.description.abstract | Purpose: 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.doi | doiWOS:000313394000008 | |
| dc.identifier.eissn | 2241-6293 | |
| dc.identifier.issn | 1107-0625 | |
| dc.identifier.pubmed | 23335523 | |
| dc.identifier.uri | https://hdl.handle.net/11424/230915 | |
| dc.identifier.wos | WOS:000313394000008 | |
| dc.language.iso | eng | |
| dc.publisher | IMPRIMATUR PUBLICATIONS | |
| dc.relation.ispartof | JOURNAL OF BUON | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | bevacizumab | |
| dc.subject | bleeding | |
| dc.subject | colorectal cancer | |
| dc.subject | gastrointestinal perforation | |
| dc.subject | hypertension | |
| dc.subject | thromboembolism | |
| dc.subject | RANDOMIZED PHASE-III | |
| dc.subject | FLUOROURACIL | |
| dc.subject | LEUCOVORIN | |
| dc.subject | THERAPY | |
| dc.subject | CHEMOTHERAPY | |
| dc.subject | OXALIPLATIN | |
| dc.subject | COMBINATION | |
| dc.subject | IRINOTECAN | |
| dc.subject | MANAGEMENT | |
| dc.subject | TRIAL | |
| dc.title | Safety and tolerability of first-line bevacizumab in metastatic colorectal cancer | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 676 | |
| oaire.citation.issue | 4 | |
| oaire.citation.startPage | 669 | |
| oaire.citation.title | JOURNAL OF BUON | |
| oaire.citation.volume | 17 |
