Cetuximab/Irinotecan-Chemotherapy in KRAS Wild-type Pretreated Metastatic Colorectal Cancer: A Pooled Analysis and Review of Literature.

伊立替康 西妥昔单抗 医学 克拉斯 内科学 肿瘤科 奥沙利铂 结直肠癌 荟萃分析 化疗 置信区间 癌症
作者
Sandro Barni,Mara Ghilardi,Karen Borgonovo,Mary Cabiddu,Alberto Zaniboni,Fausto Petrelli
出处
期刊:Reviews on Recent Clinical Trials [Bentham Science Publishers]
卷期号:8 (2): 101-109 被引量:8
标识
DOI:10.2174/15748871113089990042
摘要

Cetuximab and irinotecan are effective agents in advanced colorectal cancer (CRC) after either irinotecanor oxaliplatin-based first-line chemotherapy. Here, the efficacy of this combination in patients with the KRAS wild-type gene as second- or further-line therapy is reviewed and data are collected in a pooled analysis.Studies that enrolled pretreated CRC patients for second-line therapy or beyond were identified using electronic databases (PubMed and EMBASE). A systematic analysis was conducted using Comprehensive Meta Analysis (version 2.2.064) to calculate the event rate of response and the 95% confidence interval. The weighted median overall survival (OS) and progression-free survival (PFS) were also calculated with NCSS 2007 software. We tested for significant heterogeneity using Cochran's chi-square test and the I(2) index.Twenty-five studies published between 2007 and 2012 were eligible for this analysis, with a total of 1,712 KRAS wild-type patients enrolled. The overall response rate was 31.9% with similar response rates of 28. 7% for second-line treatment and 31.1% for third or further lines. The overall weighted median OS and PFS were 12.5 and 6 months with a weighted OS of 11.56 and 12.2 months for second- and further-line CRC settings, respectively.In metastatic KRAS wild-type CRC patients pretreated with one or more lines of therapy, cetuximab plus irinotecan-based chemotherapy is an active treatment. Response rates and survival outcomes appear similar in second-line therapy or beyond.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
李爱国应助小胖卷毛采纳,获得30
刚刚
聪慧毛衣完成签到,获得积分10
1秒前
JamesPei应助白华苍松采纳,获得10
2秒前
李澳发布了新的文献求助10
2秒前
3秒前
5秒前
8秒前
yuge发布了新的文献求助10
9秒前
9秒前
取个名儿吧完成签到,获得积分10
9秒前
zhoujunjie完成签到,获得积分10
9秒前
哇哈哈哈哈哈完成签到,获得积分10
12秒前
yyy完成签到,获得积分10
13秒前
科研通AI6.2应助nini采纳,获得10
13秒前
苹果追命发布了新的文献求助10
15秒前
16秒前
DrW完成签到,获得积分0
20秒前
眼睛大的尔蝶完成签到,获得积分10
20秒前
星河发布了新的文献求助30
20秒前
21秒前
sea完成签到 ,获得积分10
22秒前
科研通AI6.2应助nxdsz采纳,获得10
25秒前
花花完成签到,获得积分10
26秒前
26秒前
littleE发布了新的文献求助10
27秒前
安静的寒风完成签到,获得积分10
27秒前
等待黎云完成签到,获得积分20
28秒前
30秒前
狂奔的蜗牛完成签到,获得积分10
31秒前
123456789完成签到,获得积分10
32秒前
wang完成签到,获得积分10
35秒前
路过发布了新的文献求助10
35秒前
田小冉发布了新的文献求助10
36秒前
37秒前
liuxinyu完成签到,获得积分10
37秒前
orixero应助勤恳的凝云采纳,获得10
37秒前
37秒前
djfndnn完成签到,获得积分10
40秒前
健壮的书蕾完成签到,获得积分10
40秒前
隐形曼青应助科研通管家采纳,获得10
41秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Cronologia da história de Macau 5000
Petrology and Plate Tectonics 800
Electrode Potentials 550
Matrix Methods in Data Mining and Pattern Recognition 510
Association of Reentry Well-Being with Psychological Distress, Employment, and Housing Instability 15-Months After Incarceration 500
Trees of tropical Asia : an illustrated guide to diversity 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7034117
求助须知:如何正确求助?哪些是违规求助? 8702958
关于积分的说明 18437718
捐赠科研通 6538438
什么是DOI,文献DOI怎么找? 3113986
关于科研通互助平台的介绍 2193961
邀请新用户注册赠送积分活动 2089411