- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
查看更多
读书报告 汇报人:罗娜 Background Patients with metastatic colorectal cancer (mCRC) previously-treated with oxaliplatin benefit significantly from the addition of aflibercept to FOLFIRI in relation to overall survival, progression-free survival and response rate. typically regimen Treatment of metastatic colorectal cancer (mCRC) typically involves a fluoropyrimidine-based hemotherapy regimen, combining infusional fluorouracil (5-FU) and leucovorin with oxaliplatin (FOLFOX regimen) or rinotecan (FOLFIRI regimen). FOLFOX+bevacizumab In the E3200 study, it was shown that the addition of bevacizumab to FOLFOX improves survival duration for patients with previously treated mCRC who had not received first-line treatment with oxaliplatin or bev-acizumab. FOLFIRI+aflibercept VEGF Trap (aflibercept) with irinotecan in colorectal cancer after failure of oxaliplatin regimen (VELOUR) was the first randomised, placebo-controlled, phase III trial to show a statistically significant improvement in OS, progression-free survival (PFS) and response rate (RR) for an anti-angiogenic in combination with FOLFIRI compared with FOLFIRI alone in a prior oxaliplatin-treated population. FOLFIRI+aflibercept Patients receiving FOLFIRI plus aflibercept had a median OS of 13.5 months versus 12.0 months for patients receiving FOLFIRI plus placebo, representing a relative reduction in the risk of death of 18.3% for the aflibercept arm compared with the placebo arm. Patients?and Methods The results for efficacy and safety over the time course of the VEGF Trap (aflibercept) with irinotecan in colorectal cancer after failure of oxaliplatin regimen trial were analysed based on data from 1226 patients randomised to receive FOLFIRI plus either aflibercept (n = 612) or placebo (n = 614). Hazard ratios (HR) by 6-month time period were estimated using a piecewise Cox proportional hazard model. Severity of adverse events (AEs) was graded using National Cancer Institute Common Terminology Criteria, version 3.0. Fig
您可能关注的文档
最近下载
- 2024年浙江省镇海中学自主招生数学试卷及答案 .pdf VIP
- 自治区取暖费补贴文件2010.pdf VIP
- 500kV变电站运维精益化管理探究(电力系统及自动化论文资料).doc VIP
- 第一单元--观察物体(单元测试)-2025-2026学年三年级上册数学人教版.docx VIP
- (入党志愿书空白表格.doc VIP
- 第一单元-观察物体(单元测试)-2025-2026学年三年级上册数学人教版.docx VIP
- 企业级数据湖建设项目解决方案.pptx VIP
- 2025年新能源微电网稳定性分析与智能电网技术发展动态报告.docx
- DLT616-2006 火力发电厂汽水管道与支吊架维护调整导则.pdf VIP
- 春秋酒店改造装修项目投标文件技术部分.doc VIP
文档评论(0)