Division of Thoracic Oncology, Kobe Minimally Invasive Cancer Center, Kobe, Japan.
Department of Clinical Pathology, Kobe City Medical Center General Hospital, Kobe, Japan.
Thorac Cancer. 2022 Aug;13(16):2394-2397. doi: 10.1111/1759-7714.14563. Epub 2022 Jul 6.
Histological transformation from adenocarcinoma to small cell lung cancer (SCLC) occurs ~10% after acquired resistance to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors. Transformed SCLC generally responds well to chemotherapy regimens for SCLC such as platinum plus etoposide. After the response, histological nature and clinical course could be complicated by possible heterogeneity or transformation. Therefore, monitoring rebiospy is desirable to seize its histological nature at that moment. We report a case of EGFR-mutated adenocarcinoma, where histological transformations from adenocarcinoma and SCLC alternated. In this case, first rebiopsy after gefitinib revealed adenocarcinoma, but second rebiopsy after osimertinib identified SCLC transformation. After failure of platinum plus etoposide, adenocarcinoma-induced leptomeningeal metastases were controlled by osimertinib reintroduction. Optimal therapies could be provided according to the result of monitoring rebiopsy.
腺癌对表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂获得性耐药后,约有 10%会发生向小细胞肺癌(SCLC)的组织学转化。转化后的 SCLC 通常对 SCLC 的化疗方案(如铂类加依托泊苷)反应良好。在缓解后,组织学性质和临床过程可能因异质性或转化而变得复杂。因此,监测再活检以抓住其当时的组织学性质是可取的。我们报告了一例 EGFR 突变型腺癌,其中腺癌和 SCLC 交替发生组织学转化。在这种情况下,吉非替尼治疗后的首次再活检显示为腺癌,但奥希替尼治疗后的第二次再活检确定为 SCLC 转化。铂类加依托泊苷治疗失败后,奥希替尼再次引入控制了腺癌引起的软脑膜转移。根据监测再活检的结果,可以提供最佳治疗方案。