Department of Cancer Studies, University of Leicester, Leicester, United Kingdom.
Centre for Analytical Science, Department of Chemistry, Loughborough University, Loughborough, Leicestershire, United Kingdom.
Cancer Res. 2017 Apr 15;77(8):2029-2039. doi: 10.1158/0008-5472.CAN-16-1121. Epub 2017 Feb 15.
To improve treatment outcomes in non-small cell lung cancer (NSCLC), preclinical models that can better predict individual patient response to novel therapies are urgently needed. Using freshly resected tumor tissue, we describe an optimized explant culture model that enables concurrent evaluation of NSCLC response to therapy while maintaining the tumor microenvironment. We found that approximately 70% of primary NSCLC specimens were amenable to explant culture with tissue integrity intact for up to 72 hours. Variations in cisplatin sensitivity were noted with approximately 50% of cases responding Notably, explant responses to cisplatin correlated significantly with patient survival ( = 0.006) irrespective of tumor stage. In explant tissue, cisplatin-resistant tumors excluded platinum ions from tumor areas in contrast to cisplatin-sensitive tumors. Intact TP53 did not predict cisplatin sensitivity, but a positive correlation was observed between cisplatin sensitivity and mutation status ( = 0.003). Treatment of NSCLC explants with the targeted agent TRAIL revealed differential sensitivity with the majority of tumors resistant to single-agent or cisplatin combination therapy. Overall, our results validated a rapid, reproducible, and low-cost platform for assessing drug responses in patient tumors , thereby enabling preclinical testing of novel drugs and helping stratify patients using biomarker evaluation. .
为了改善非小细胞肺癌(NSCLC)的治疗效果,迫切需要能够更好地预测新型治疗方法对个体患者反应的临床前模型。本研究使用新鲜切除的肿瘤组织,描述了一种优化的离体培养模型,该模型能够在保持肿瘤微环境的同时,同时评估 NSCLC 对治疗的反应。我们发现,约 70%的原发性 NSCLC 标本可进行离体培养,组织完整性完整,最长可达 72 小时。约 50%的标本对顺铂的敏感性存在差异,其中约有 50%的标本对顺铂敏感。值得注意的是,离体组织中顺铂耐药肿瘤将铂离子从肿瘤区域排除,而顺铂敏感肿瘤则没有。完整的 TP53 并不能预测顺铂的敏感性,但顺铂敏感性与 突变状态之间存在正相关( = 0.003)。用靶向药物 TRAIL 处理 NSCLC 离体组织显示出不同的敏感性,大多数肿瘤对单药或顺铂联合治疗均耐药。总的来说,我们的研究结果验证了一种快速、可重复、低成本的平台,用于评估患者肿瘤中的药物反应,从而能够对新型药物进行临床前测试,并通过生物标志物评估帮助分层患者。