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

被引:0
|
作者
Akun, E. [1 ]
Okutur, K. [2 ]
Seber, S. [3 ]
Korkmaz, T. [3 ]
Aydin, K. [2 ]
Bozkurt, M. [2 ]
Namal, E. [2 ]
Hasbal, B. [2 ]
Tecimer, C. [4 ]
Demir, G. [2 ]
机构
[1] Gayrettepe Florence Nightingale Hosp, Dept Internal Med, Istanbul, Turkey
[2] Istanbul Sci Univ, Sch Med, Dept Med Oncol, Istanbul, Turkey
[3] Marmara Univ, Sch Med, Dept Med Oncol, Istanbul, Turkey
[4] Gayrettepe Florence Nightingale Hosp, Dept Med Oncol, Istanbul, Turkey
来源
JOURNAL OF BUON | 2012年 / 17卷 / 04期
关键词
bevacizumab; bleeding; colorectal cancer; gastrointestinal perforation; hypertension; thromboembolism; RANDOMIZED PHASE-III; FLUOROURACIL; LEUCOVORIN; THERAPY; CHEMOTHERAPY; OXALIPLATIN; COMBINATION; IRINOTECAN; MANAGEMENT; TRIAL;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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收藏
页码:669 / 676
页数:8
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