使用精准医学工具定义、识别和理解肿瘤学中的“特殊应答者”

A. Tsimberidou, R. Said, L. Staudt, B. Conley, N. Takebe
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引用次数: 2

摘要

包括下一代测序在内的广泛应用的分子分析技术已经改变了癌症药物开发的格局。越来越多的早期药物开发临床试验需要根据分子改变来选择患者。与此同时,在用标准药物或研究性药物进行全身治疗后表现出异常反应的肿瘤中,鉴定分子改变的努力已经发表或正在进行中。这些发现可能最终成为未来治疗的预测性标记或“可操作的突变”。为了测试从建议的特殊应答者患者中收集档案组织并成功进行后续分子分析的可行性,美国国家癌症研究所于2014年启动了一项全国性的特殊应答者倡议协议。此外,已从学术机构确定并公布了越来越多的例外应对案例。网络的神秘的特殊反应研究使用众包来识别特殊的反应者,并将分子分析肿瘤,以识别与异常反应的分子相关性。在这篇综述中,我们讨论了异常反应分子分析在新的生物标志物发现工作中的潜在作用,以进一步推进肿瘤治疗中的精准医学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Defining, Identifying, and Understanding “Exceptional Responders” in Oncology Using the Tools of Precision Medicine
Abstract Widely available molecular profiling technology, including next-generation sequencing has changed the landscape of drug development in cancer. An increasing number of clinical trials in early drug development require patient selection based on molecular alterations. Concurrently, efforts to identify molecular alterations in tumors that exhibited exceptional response after systemic treatment with standard or investigational agents have been published or are in progress. These discoveries may ultimately serve as predictive markers or “actionable mutations” for future therapies. To test the feasibility of collecting the archival tissues from proposed exceptional responder patients and successful subsequent molecular profiling, the National Cancer Institute opened a nationwide exceptional responder initiative protocol in 2014. In addition, an increasing number of exceptional responder cases have been identified and published from academia institutions. The Network of Enigmatic Exceptional Responders study uses crowdsourcing to identify exceptional responders and will molecularly profile tumors to discern molecular correlates with exceptional response. In this review, we discuss the potential role of exceptional responder molecular analysis in new biomarker discovery efforts to further advance precision medicine in oncology therapeutics.
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