Departments of Medicine Thoracic Oncology Service, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.
Cancer Discov. 2013 Jun;3(6):630-5. doi: 10.1158/2159-8290.CD-13-0035. Epub 2013 Mar 26.
The discovery of RET fusions in lung cancers has uncovered a new therapeutic target for patients whose tumors harbor these changes. In an unselected population of non-small cell lung carcinomas (NSCLCs), RET fusions are present in 1% to 2% of cases. This incidence increases substantially, however, in never-smokers with lung adenocarcinomas that lack other known driver oncogenes. Although preclinical data provide experimental support for the use of RET inhibitors in the treatment of RET fusion-positive tumors, clinical data on response are lacking. We report preliminary data for the first three patients treated with the RET inhibitor cabozantinib on a prospective phase II trial for patients with RET fusion-positive NSCLCs (NCT01639508). Confirmed partial responses were observed in 2 patients, including one harboring a novel TRIM33-RET fusion. A third patient with a KIF5B-RET fusion has had prolonged stable disease approaching 8 months (31 weeks). All three patients remain progression-free on treatment.
肺癌中 RET 融合的发现为其肿瘤携带这些变化的患者揭示了一个新的治疗靶点。在非小细胞肺癌(NSCLC)的未选择人群中,1%至 2%的病例存在 RET 融合。然而,在不吸烟的肺腺癌患者中,这一发病率显著增加,这些患者缺乏其他已知的驱动致癌基因。尽管临床前数据为 RET 融合阳性肿瘤使用 RET 抑制剂提供了实验支持,但缺乏关于反应的临床数据。我们报告了在一项前瞻性 II 期试验中,前 3 名接受 RET 抑制剂卡博替尼治疗的 RET 融合阳性 NSCLC 患者的初步数据(NCT01639508)。在 2 名患者中观察到了确认的部分缓解,其中包括 1 名携带新型 TRIM33-RET 融合的患者。另一名 KIF5B-RET 融合患者的疾病稳定时间延长至接近 8 个月(31 周)。所有 3 名患者在治疗过程中均无疾病进展。