Brower Stacey L, Fensterer Jeffrey E, Bush Jason E
Precision Therapeutics, Pittsburgh, PA, USA.
Methods Mol Biol. 2008;414:57-78. doi: 10.1007/978-1-59745-339-4_6.
The ChemoFx Assay is an ex vivo assay designed to predict the sensitivity and resistance of a given patient's solid tumor to a variety of chemotherapy agents. A portion of a patient's solid tumor, as small as a core biopsy, is mechanically disaggregated and established in primary culture where malignant epithelial cells migrate out of tumor explants to form a monolayer. Cultures are verified as epithelial and exposed to increasing doses of selected chemotherapeutic agents. The number of live cells remaining post-treatment is enumerated microscopically using automated cell-counting software. The resultant cell counts in treated wells are compared with those in untreated control wells to generate a dose-response curve for each chemotherapeutic agent tested on a given patient specimen. Features of each dose-response curve are used to score a tumor's response to each ex vivo treatment as "responsive," "intermediate response," or "non-responsive." Collectively, these scores are used to assist an oncologist in making treatment decisions.
化疗敏感性检测(ChemoFx检测)是一种体外检测方法,旨在预测特定患者实体瘤对多种化疗药物的敏感性和耐药性。患者实体瘤的一部分,小至芯针活检样本,经机械解离后进行原代培养,恶性上皮细胞从肿瘤外植体迁移出来形成单层。培养物经鉴定为上皮细胞后,用递增剂量的选定化疗药物处理。使用自动细胞计数软件通过显微镜对处理后剩余的活细胞数量进行计数。将处理孔中的细胞计数结果与未处理的对照孔中的细胞计数结果进行比较,以生成在给定患者样本上测试的每种化疗药物的剂量反应曲线。每条剂量反应曲线的特征用于将肿瘤对每种体外治疗的反应评为“敏感”、“中度反应”或“无反应”。这些评分共同用于协助肿瘤学家做出治疗决策。