Jänne Pasi A, Gray Nathanael, Settleman Jeff
Dana Farber Cancer Institute and Harvard Medical School, Boston, Massachusetts, USA.
Nat Rev Drug Discov. 2009 Sep;8(9):709-23. doi: 10.1038/nrd2871. Epub 2009 Jul 24.
Selective small-molecule kinase inhibitors have emerged over the past decade as an important class of anti-cancer agents, and have demonstrated impressive clinical efficacy in several different diseases, including relatively common malignancies such as breast and lung cancer. However, clinical benefit is typically limited to a fraction of treated patients. Genomic features of individual tumours contribute significantly to such clinical responses, and these seem to vary tremendously across patients. Additional factors, including pharmacogenomics, the tumour microenvironment and rapidly acquired drug resistance, also contribute to the clinical sensitivity of various cancers, and should be considered and applied in the development and use of new kinase inhibitors.
在过去十年中,选择性小分子激酶抑制剂已成为一类重要的抗癌药物,并在几种不同疾病中展现出令人瞩目的临床疗效,其中包括乳腺癌和肺癌等相对常见的恶性肿瘤。然而,临床获益通常仅限于一部分接受治疗的患者。个体肿瘤的基因组特征对这种临床反应有显著影响,而且这些特征在患者之间似乎差异极大。其他因素,包括药物基因组学、肿瘤微环境和迅速产生的耐药性,也对各种癌症的临床敏感性有影响,在新型激酶抑制剂的研发和使用中应予以考虑并应用。