Bevacizumab in combination with biweekly capecitabine and irinotecan, as first-line treatment for patients with metastatic colorectal cancer

被引:16
作者
Garcia-Alfonso, P. [1 ]
Munoz-Martin, A. J. [1 ]
Alvarez-Suarez, S. [1 ]
Jerez-Gilarranz, Y. [1 ]
Riesco-Martinez, M. [1 ]
Khosravi, P. [1 ]
Martin, M. [1 ]
机构
[1] Hosp Gen Univ Gregorio Maranon, Med Oncol Serv, Madrid 28007, Spain
关键词
bevacizumab; capecitabine; irinotecan; metastatic colorectal cancer; combined modality treatment; 2 DIFFERENT SCHEDULES; PHASE-II TRIAL; ORAL FLUOROPYRIMIDINES; PLUS OXALIPLATIN; LINE TREATMENT; LEUCOVORIN; FLUOROURACIL; CHEMOTHERAPY; BOLUS;
D O I
10.1038/sj.bjc.6605907
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: Combination of capecitabine and irinotecan (XELIRI regimen) is an active and well tolerated treatment for metastatic colorectal cancer (mCRC). The aim of this study was to evaluate the efficacy and safety of this regimen in combination with bevacizumab (BV), as first-line treatment for mCRC. PATIENTS AND METHODS: A total of 46 consecutive patients received a combination of BV (5 mg kg(-1), day 1), irinotecan (175 mg m(-2), day 1) and capecitabine (1000 mg m(-2) twice daily on day 2-8), every 2 weeks. Patients were treated until disease progression or unacceptable toxicity. The primary objective was to determine the progression-free survival (PFS) and safety profile. RESULTS: The overall response rate (ORR) was 67.4%, with a disease control rate (ORR+stable disease) of 93.5%. Median PFS and overall survival (OS) were 12.3 months (95% confidence interval (CI): 6.5-18.1 months) and 23.7 months (95% CI: 16.7-30.6 months), respectively. The most frequent grade 3/4 treatment-related adverse events were asthenia (7%), diarrhoea (7%), nausea (9%) and vomiting (7%). CONCLUSION: Bevacizumab combined with biweekly XELIRI is a highly active first-line regimen for mCRC treatment, showing encouraging PFS, ORR and OS with a good tolerability. British Journal of Cancer (2010) 103, 1524-1528. doi:10.1038/sj.bjc.6605907 www.bjcancer.com Published online 26 October 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1524 / 1528
页数:5
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