Morris Michael J, Basch Ethan M, Wilding George, Hussain Maha, Carducci Michael A, Higano Celestia, Kantoff Philip, Oh William K, Small Eric J, George Daniel, Mathew Paul, Beer Tomasz M, Slovin Susan F, Ryan Charles, Logothetis Christopher, Scher Howard I
Genitourinary Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Clin Genitourin Cancer. 2009 Jan;7(1):51-7. doi: 10.3816/CGC.2009.n.009.
In 2005, the US Department of Defense, through the US Army Medical Research and Materiel Command, Office of the Congressionally Directed Medical Research Programs, created a funding mechanism to form a clinical trials consortium to conduct phase I and II studies in prostate cancer. This is the first report of the Prostate Cancer Clinical Trials Consortium (PCCTC).
The Department of Defense award supports a consortium of 10 prostate cancer research centers. Memorial Sloan-Kettering Cancer Center was awarded the Coordinating Center grant for the consortium and charged with creating an infrastructure to conduct early-phase multicenter clinical trials. Each participating center was required to introduce >or=1 clinical trial per year and maintain accrual of a minimum of 35 patients per year.
The PCCTC was launched in 2006 and now encompasses 10 leading prostate cancer research centers. Fifty-one trials have been opened, and 1386 patients have been accrued at member sites. Members share an online clinical trial management system for protocol tracking, electronic data capture, and data storage. A legal framework has been instituted, and standard operating procedures, an administrative structure, editorial support, centralized budgeting, and mechanisms for scientific review are established.
The PCCTC fulfills a congressional directive to create a clinical trials instrument dedicated to early-phase prostate cancer studies. The member institutions have built an administrative, informatics, legal, financial, statistical, and scientific infrastructure to support this endeavor. Clinical trials are open and accruing in excess of federally mandated goals.
2005年,美国国防部通过美国陆军医学研究与物资司令部、国会指令医学研究项目办公室,设立了一种资助机制,以组建一个临床试验联盟,开展前列腺癌的I期和II期研究。这是前列腺癌临床试验联盟(PCCTC)的首份报告。
国防部的资助支持了一个由10个前列腺癌研究中心组成的联盟。纪念斯隆凯特琳癌症中心获得了该联盟的协调中心资助,并负责创建开展早期多中心临床试验的基础设施。每个参与中心每年需引入≥1项临床试验,并每年至少招募35名患者。
PCCTC于2006年启动,目前涵盖10个领先的前列腺癌研究中心。已开展了51项试验,成员机构已招募了1386名患者。成员共享一个在线临床试验管理系统,用于方案跟踪、电子数据采集和数据存储。已建立了法律框架,并制定了标准操作程序、行政结构、编辑支持、集中预算以及科学审查机制。
PCCTC履行了国会的指令,创建了一个专门用于早期前列腺癌研究的临床试验工具。成员机构构建了行政、信息学、法律、财务、统计和科学基础设施来支持这一工作。临床试验正在开放进行,且招募人数超过了联邦规定的目标。