The Paterson Institute for Cancer Research, Manchester, United Kingdom.
Cancer Res. 2013 Feb 1;73(3):1046-9. doi: 10.1158/0008-5472.CAN-12-3236. Epub 2012 Dec 7.
The mechanisms of genetically determined mechanisms of resistance to several target drugs were discussed in breast cancer, melanoma, colorectal and prostate cancers, chronic myelogenous leukemia, small cell lung cancer, and medulloblastoma. In each case, heterogeneity of mechanisms was emphasized. In melanoma, therapeutic interference with the effects of BRAF mutations was repeatedly discussed. It was also reported that anti-CTLA4 antibodies provided the first treatment improving survival of patients with stage IV melanoma. Epithelial-mesenchymal transition (EMT) was introduced as a mechanism of resistance, particularly in lung and pancreatic cancer, where the role of microenvironment factors was also indicated. In colorectal and prostate cancers, the use of liquid biopsies, namely, measurements of tumor nucleic acid in blood, were indicated as a way to obtain whole-tumor assessment instead of the partial assessment obtainable with traditional biopsies. Knowledge of the mechanisms of drug action and resistance was stressed to be essential for the design of new agents and combination of agents aimed at increasing antitumor effectiveness and overcoming resistance.
探讨了乳腺癌、黑色素瘤、结直肠癌和前列腺癌、慢性髓性白血病、小细胞肺癌和髓母细胞瘤中几种靶向药物的遗传决定耐药机制。在每种情况下,都强调了机制的异质性。在黑色素瘤中,反复讨论了治疗性干扰 BRAF 突变的影响。据报道,抗 CTLA4 抗体提供了首个改善 IV 期黑色素瘤患者生存的治疗方法。上皮-间充质转化 (EMT) 被引入作为一种耐药机制,特别是在肺癌和胰腺癌中,还指出了微环境因素的作用。在结直肠癌和前列腺癌中,液体活检(即血液中肿瘤核酸的测量)的使用被认为是获得全肿瘤评估的一种方法,而不是传统活检可获得的部分评估。强调了解药物作用和耐药机制对于设计旨在提高抗肿瘤效果和克服耐药性的新药物和联合药物至关重要。