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Leveraging Learning From a Phase III Colorectal Cancer Clinical Trial: Outcomes Methodology Meta-Analysis and Pharmacogenetics

机译:利用来自第三阶段结直肠癌临床试验的学习成果方法论Meta分析和药物遗传学

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摘要

This paper summarizes the results of a National Cancer Institute (NCI) sponsored Phase III clinical trial led by the North Central Cancer Treatment Group (NCCTG) that enrolled patients with metastatic colorectal cancer (MCRC) on combination chemotherapy regimens in the late 1990s through 2003. The study changed clinical practice in the US and led to a new Food and Drug Agency (FDA) indication for the drug oxaliplatin. The time was opportune in the management of MCRC, when, after 50 years of using the single active agent 5-Fluorouracil (5-FU), two new cytotoxic agents, irinotecan and oxaliplatin, were found to be active in MCRC. Patients were randomized to receive two of those three agents in each arm of the trial. Over 500 of the > 1700 enrolled patients permitted their germline DNA and plasma samples to be banked. Consequently this is one of the largest cancer populations available for pharmacogenetic studies and for the study of other biomarkers. Data derived from N9741 led to publications related to treatment of MCRC and trial methodology, used pooled meta-analyses and helped to pioneer the field of pharmacogenetics. This review highlights some of those observations. Initiated in 1997, the trial has spawned 26 published or in press papers and 39 abstracts.
机译:本文总结了由美国国家癌症研究所(NCI)赞助的,由北部中部癌症治疗小组(NCCTG)领导的III期临床试验的结果,该试验招募了1990年代后期至2003年末接受转移化疗的转移性结直肠癌(MCRC)患者。该研究改变了美国的临床实践,并导致食品和药物管理局(FDA)对奥沙利铂进行了新的适应症。在MCRC的管理上是时候了,当时使用单一活性剂5-氟尿嘧啶(5-FU)50年后,发现两种新的细胞毒剂,伊立替康和奥沙利铂在MCRC中具有活性。在试验的每组中,患者被随机分配接受这三种药物中的两种。登记的1700多个患者中,有500多个允许将其种系DNA和血浆样品保存起来。因此,这是可用于药物遗传学研究和其他生物标志物研究的最大癌症人群之一。来自N9741的数据导致发表了有关MCRC治疗和试验方法的出版物,使用了汇总的荟萃分析,并帮助开拓了药物遗传学领域。这篇评论重点介绍了其中一些观察。该试验始于1997年,已经产生了26篇已发表或在报纸上发表的论文和39篇摘要。

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