Dietrich Martin Frederik, Yan Shirley Xiao, Schiller Joan Hoff
Department of Internal Medicine, Division of Hematology/Oncology, UT Southwestern Medical Center, Dallas, Texas.
Department of Pathology, UT Southwestern Medical Center, Dallas, Texas.
J Thorac Oncol. 2015 May;10(5):e23-e25. doi: 10.1097/JTO.0000000000000448.
Targeted therapy has become a valuable approach in adenocarcinoma of the lung. The number of actionable mutations has been continuously increasing with significant acceleration from discovery to clinical application. Herein, we present a case of innovative treatment using targeted therapy of a 75-year-old female with two primary adenocarcinomas of the lung. The first tumor was found to carry an activating mutation in the exon 19 of the epidermal growth factor receptor and responded favorably to treatment with erlotinib. The second primary tumor was found to carry an isolated amplification of the c-met gene but no epidermal growth factor receptor mutation. Off-label use of crizotinib, a potent inhibitor of c-met, was prescribed. Within 4 weeks of treatment initiation, the tumor and the dependent lymphadenopathy responded with rapid shrinkage. This observation stresses the need for rebiopsy of tumors upon progression or change of biological behavior for selection of appropriate targeted therapy.
靶向治疗已成为肺癌腺癌治疗中的一种重要方法。可操作的突变数量一直在不断增加,从发现到临床应用的加速显著。在此,我们报告一例75岁女性患有双原发性肺癌腺癌的创新靶向治疗病例。第一个肿瘤在表皮生长因子受体外显子19中发现有激活突变,对厄洛替尼治疗反应良好。第二个原发性肿瘤发现有c-met基因的孤立扩增,但无表皮生长因子受体突变。因此使用了c-met的强效抑制剂克唑替尼进行非标签用药。在开始治疗的4周内,肿瘤和相关淋巴结病迅速缩小。这一观察结果强调了在疾病进展或生物学行为改变时对肿瘤进行再次活检以选择合适靶向治疗的必要性。