Calles Antonio, Rubio-Viqueira Belén, Hidalgo Manuel
Clinical Research Programme, Spanish National Cancer Research Centre-CNIO, Madrid, Spain.
Curr Protoc Pharmacol. 2013 Jun;Chapter 14:Unit 14.26. doi: 10.1002/0471141755.ph1426s61.
The number of therapeutic options for lung and pancreatic cancer is increasing because of the identification of new druggable molecular targets and development of new drug combinations. Reproducible, biologically relevant in vivo pre-clinical models are critical for this effort. The generation of patient-derived tumor xenografts has proven useful for integrating drug screening with biomarker discovery, discovering fundamental information in tumor biology, prioritizing drugs for clinical investigation, and personalizing treatments for these tumors. The protocol described in this unit details how to establish a direct in vivo subcutaneous primary tumorgraft and maintenance passages. The predictive value of a tumorgraft platform to guide personalized medicine is illustrated with the case of a patient with refractory advanced non-small cell lung cancer (NSCLC). The outcome of a patient for whom their own pancreatic tumorgraft revealed a remarkable sensitivity to mitomycin C based on a PALB2 mutation is also detailed.
由于新的可成药分子靶点的发现以及新药物组合的开发,肺癌和胰腺癌的治疗选择数量正在增加。可重复的、具有生物学相关性的体内临床前模型对于这项工作至关重要。患者来源的肿瘤异种移植的产生已被证明有助于将药物筛选与生物标志物发现相结合,发现肿瘤生物学的基础信息,确定临床研究的优先药物,以及为这些肿瘤进行个性化治疗。本单元中描述的方案详细介绍了如何建立直接体内皮下原发性肿瘤移植瘤并进行维持传代。通过一名难治性晚期非小细胞肺癌(NSCLC)患者的病例,说明了肿瘤移植平台对指导个性化医疗的预测价值。还详细介绍了一名患者的情况,其自身的胰腺肿瘤移植瘤基于PALB2突变显示对丝裂霉素C具有显著敏感性。