Division of Respirology, Neurology, and Rheumatology, Kurume University Hospital, Kurume, Japan.
Department of Diagnostic Pathology, Kurume University Hospital, Kurume, Japan.
Thorac Cancer. 2018 Jun;9(6):754-757. doi: 10.1111/1759-7714.12646. Epub 2018 Apr 19.
Pulmonary pleomorphic carcinoma (PPC) is a very rare type of primary lung cancer with an aggressive clinical course. Few reports have documented therapeutic options for PPC with EGFR mutations. Herein, we report a case of PPC with EGFR mutation treated with EGFR-tyrosine kinase inhibitors (TKIs). A 65-year-old Japanese woman was diagnosed with stage IV lung adenocarcinoma with L858R point mutation in exon 21. Despite treatment with erlotinib, the patient died after two weeks as a result of rapid disease progression. Postmortem examination indicated that the thoracic tumors consisted primarily of spindle/sarcomatous components, while expression of the mutated EGFR protein was only observed in adenocarcinoma components. We speculate that the tumor was not driven by EGFR mutation. Clinicians should bear in mind the possibility of pleomorphic carcinoma if EGFR-TKI treatment fails to achieve a clinical response for adenocarcinoma harboring an activating EGFR mutation diagnosed on the basis of small biopsy specimens.
肺多形性癌(PPC)是一种非常罕见的原发性肺癌,具有侵袭性的临床病程。很少有报道记录了具有 EGFR 突变的 PPC 的治疗选择。在此,我们报告一例 EGFR 突变型 PPC 患者接受 EGFR 酪氨酸激酶抑制剂(TKI)治疗的病例。一名 65 岁的日本女性被诊断为 IV 期肺腺癌,伴有外显子 21 的 L858R 点突变。尽管接受了厄洛替尼治疗,但由于疾病快速进展,两周后患者死亡。尸检表明,胸内肿瘤主要由梭形/肉瘤样成分组成,而突变型 EGFR 蛋白的表达仅在腺癌成分中观察到。我们推测肿瘤不是由 EGFR 突变驱动的。如果基于小活检标本诊断的携带激活 EGFR 突变的腺癌患者接受 EGFR-TKI 治疗未能获得临床反应,临床医生应牢记多形性癌的可能性。