通过国家癌症研究所治疗转介中心尽早获得研究药物。

Tali M Johnson, Matthew J Boron
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引用次数: 0

摘要

背景:美国国家癌症研究所(NCI)的癌症治疗与诊断部(DCTD)作为研究用新药的赞助商,可以尽早提供用于治疗的研究用药物。直到最近,NCI 通过治疗转介中心(TRC)(NCI 的 DCTD 癌症治疗评估计划内的药品管理处(PMB)提供的一项服务)有 3 种协议机制来分发研究用制剂。第一种机制是 C 组方案,第二种机制是 TRC 方案,第三种也是最常见的一种机制是特殊例外方案:本文旨在描述和报告技术资源中心自 2000 年至 2011 年底在 PMB 开展的活动:资本技术信息服务部对 PMB 2000 年 1 月 1 日至 2011 年 12 月 31 日期间的所有治疗方案进行了数据挖掘。向 PMB 提出的申请以电子表格格式按处理方式分类,或转介、或批准、或拒绝,并按类型计数,或列为 C 组、TRC、或特殊例外:结果:2000 年至 2011 年间,60% 以上的申请被转介或批准。2000 年至 2011 年间,申请数量的峰值出现在 2003 年,为 1664 份。高峰期主要是由特殊例外申请造成的;不过,当年也批准了 400 多份传统习俗审查申请和 20 份 C 组申请。2003 年后,申请总数急剧下降,自 2008 年以来,每年的申请总数不到 50 项。2006 年 3 月,所有 C 组和 TRC 协议均已完成。治疗用途申请数量最少的年份是 2011 年:结论:通过 "特殊例外 "机制提供药物是有前途的新药研究药物能够被危及生命的患者使用的一种方式。总体而言,对于开展肿瘤学临床研究的研究机构来说,PMB 的治疗用药申请中心是一个有用的药物信息资源,为肿瘤学界提供了宝贵的服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Access to Investigational Agents through the National Cancer Institute's Treatment Referral Center.

Background: The National Cancer Institute's (NCI) Division of Cancer Treatment and Diagnosis (DCTD), as an investigational new drug sponsor, may provide early access to investigational agents for treatment use. Until recently, the NCI had 3 protocol mechanisms for distributing investigational agents through the Treatment Referral Center (TRC), a service provided by the Pharmaceutical Management Branch (PMB) within the Cancer Therapy Evaluation Program of the NCI's DCTD. The first mechanism is the Group C protocol, the second mechanism is the TRC protocol, and the third, and most common, mechanism is the Special Exception protocol.

Objectives: The purpose of this article is to describe and report on the activities of the TRC at the PMB since 2000 through the end of 2011.

Methods: Capital Technology Information Services performed PMB data mining for all treatment protocols from January 1, 2000, to December 31, 2011. Requests to PMB were sorted in spreadsheet format by disposition, either as referred, approved, or denied, and were counted by type, either as Group C, TRC, or Special Exception.

Results: More than 60% of requests were either referred or approved between 2000 and 2011. The peak number of requests was 1664 between 2000 and 2011 and occurred in 2003. The peak was mostly a result of Special Exception requests; however, more than 400 TRC requests and 20 Group C requests were approved that year. The total number of requests dropped precipitously after 2003, and since 2008 have totaled fewer than 50 annually. All Group C and TRC protocols were completed by March 2006. The lowest number of treatment use requests occurred in 2011.

Conclusion: Providing agents through the Special Exception mechanism is one way that promising investigational new drug agents can get to patients with life-threatening illnesses. In general, the PMB's TRC is a useful drug information resource for sites conducting clinical research in oncology, and it provides a valuable service to the oncology community.

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