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三阴性乳腺癌临床试验的人群和目标考虑因素。

Population and target considerations for triple-negative breast cancer clinical trials.

机构信息

Department of Pharmacology & Experimental Therapeutics, Division of Biostatistics, Thomas Jefferson University, Kimmel Cancer Center, Philadelphia, PA, USA.

出版信息

Biomark Med. 2013 Feb;7(1):11-21. doi: 10.2217/bmm.12.114.

Abstract

Triple-negative breast cancer (TNBC) is an aggressive disease subtype that has a poor prognosis. Extensive epidemiological evidence demonstrates clear socioeconomic and demographic associations with increased likelihood of TNBC in both poorer and minority populations. Thus, biological aggressiveness with few known therapeutic directions generates disparities in breast cancer outcomes for vulnerable populations. Emerging molecular evidence of potential targets in triple-negative subpopulations offers great potential for future clinical trial directions. However, trials must appropriately consider populations at risk for aggressive subtypes of disease in order to address this disparity most completely. New US FDA draft guidance documents provide both flexible outcomes for accelerated approvals as well as flexibility in design with adaptive trials. Careful planning with design, potential patient population and choices of molecular targets informed by biomarkers will be critical to address TNBC clinical care.

摘要

三阴性乳腺癌(TNBC)是一种侵袭性疾病亚型,预后不良。广泛的流行病学证据表明,在贫困和少数族裔人群中,TNBC 的发生与社会经济地位和人口统计学因素密切相关。因此,生物学侵袭性强而治疗方向有限,导致弱势群体的乳腺癌结局存在差异。在三阴性亚群中发现的潜在靶点的分子证据为未来临床试验提供了很大的方向。然而,试验必须充分考虑患有侵袭性疾病亚型风险的人群,以最全面地解决这一差异。美国食品和药物管理局(FDA)新的草案指导文件为加速批准提供了灵活的结果,并为适应性试验提供了设计上的灵活性。通过设计、潜在患者人群和生物标志物指导下的分子靶点选择进行精心规划,对于解决 TNBC 的临床护理问题至关重要。

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