Zhu You-Cai, Xu Chun-Wei, Ye Xiao-Qian, Yin Man-Xiang, Zhang Jin-Xian, Du Kai-Qi, Zhang Zhi-Hao, Hu Jian
Department of Thoracic Surgery, The First Affiliated Hospital of Medical School of Zhejiang University, Hangzhou; Department of Thoracic Surgery, Chinese People's Armed Police Force, Zhejiang Corps Hospital, Jiaxing, Zhejiang.
Department of Pathology, Affiliated Hospital of Academy of Military Medical Sciences, Beijing.
Onco Targets Ther. 2016 Jul 15;9:4301-5. doi: 10.2147/OTT.S109415. eCollection 2016.
ROS1 rearrangement has recently emerged as a new molecular subtype in non-small cell lung cancer, and is predominantly found in lung adenocarcinomas compared with other oncogenes such as EGFR, KRAS, or ALK. Patients who have both mutations are extremely rare. Here we report a 50-year-old female diagnosed with adenocarcinoma with sarcomatoid differentiation, who was shown to have EGFR and ROS1 mutations. The patient was treated surgically and received three cycles of adjuvant postoperative chemotherapy. In addition, we reviewed the previously reported cases and related literature. This presentation will provide further understanding of the underlying molecular biology and optimal treatment for non-small cell lung cancer patients with more than one driver mutation.
ROS1重排最近已成为非小细胞肺癌中的一种新分子亚型,与其他致癌基因如表皮生长因子受体(EGFR)、 Kirsten大鼠肉瘤病毒癌基因(KRAS)或间变性淋巴瘤激酶(ALK)相比,主要在肺腺癌中发现。同时具有这两种突变的患者极为罕见。在此,我们报告一名50岁女性,诊断为伴有肉瘤样分化的腺癌,该患者被证实存在EGFR和ROS1突变。患者接受了手术治疗,并接受了三个周期的术后辅助化疗。此外,我们回顾了先前报道的病例及相关文献。本报告将进一步加深对具有不止一种驱动突变的非小细胞肺癌患者潜在分子生物学及最佳治疗方法的理解。