Nensi Shrestha, Ashton John
Department of Pharmacology & Toxicology, Otago School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
Curr Cancer Drug Targets. 2021;21(9):737-748. doi: 10.2174/1568009621666210729100647.
Advances in chromosomally rearranged ALK positive non-small cell lung cancer have been dramatic in only the last few years. Survival times have improved dramatically due to the introduction of ever more efficacious ALK inhibitors. These improvements have been due largely to improvements in blood-brain barrier penetration and the breadth of ligand binding pocket mutations against which the drugs are effective. However, the advances maybe slow due to the frequency of cancers with compound resistance mutations are appearing, suggesting the need to develop multiple ALK inhibitors to target different compound mutations.Another research area that promises to provide further gains is the use of drug combinations, with an ALK inhibitor combined with a drug targeting a "second driver" to overcome resistance. In this review, the range of secondary targets for ALK+ lung cancer and the potential for their clinical success are reviewed.
仅在过去几年中,染色体重排的ALK阳性非小细胞肺癌就取得了显著进展。由于越来越有效的ALK抑制剂的引入,生存时间得到了显著改善。这些改善很大程度上归功于血脑屏障穿透性的提高以及药物有效的配体结合口袋突变的广度。然而,由于出现复合耐药突变的癌症频率,进展可能会缓慢,这表明需要开发多种ALK抑制剂来靶向不同的复合突变。另一个有望带来进一步进展的研究领域是药物联合使用,将ALK抑制剂与靶向“第二驱动因素”的药物联合使用以克服耐药性。在这篇综述中,对ALK+肺癌的一系列次要靶点及其临床成功的潜力进行了综述。