Yamagata Akira, Yokoyama Toshihide, Fukuda Yasushi, Ishida Tadashi
Department of Respiratory Medicine, Ohara Healthcare Foundation, Kurashiki Central Hospital, 1-1-1 Miwa, Kurashiki, Okayama, 710-8602, Japan.
Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.
Respir Med Case Rep. 2021 Jun 1;33:101440. doi: 10.1016/j.rmcr.2021.101440. eCollection 2021.
Small cell lung cancer (SCLC) transformation is a rare resistance mechanism to anaplastic lymphoma kinase-tyrosine kinase inhibitors (ALK-TKIs), for which cytotoxic chemotherapy is often initiated. However, no case has been reported so far in which the SCLC component disappeared after chemotherapy and the tumor responded to ALK-TKI treatment again. A 41-year-old, never-smoker man was diagnosed with multiple metastatic lung adenocarcinoma harboring ALK gene rearrangements. After tumor re-growth was treated with alectinib, histological analysis of re-biopsy of the primary lesion showed combined small cell carcinoma, and cytotoxic chemotherapy was administered. After resistance to chemotherapy developed, the third biopsy of the primary lesion showed the original ALK gene rearrangements without the SCLC component. Alectinib was re-administered, and partial response was obtained. Biopsy for ALK-positive lung cancer that progressed after chemotherapy for SCLC transformation might be useful for decision-making regarding the therapeutic strategy.
小细胞肺癌(SCLC)转化是间变性淋巴瘤激酶-酪氨酸激酶抑制剂(ALK-TKIs)罕见的耐药机制,对此常启动细胞毒性化疗。然而,迄今为止,尚无化疗后SCLC成分消失且肿瘤再次对ALK-TKI治疗产生反应的病例报道。一名41岁从不吸烟的男性被诊断为患有ALK基因重排的多发转移性肺腺癌。在用阿来替尼治疗肿瘤复发后,对原发灶再次活检的组织学分析显示为小细胞癌合并,随后给予细胞毒性化疗。在出现化疗耐药后,对原发灶的第三次活检显示存在原始的ALK基因重排,而无SCLC成分。再次给予阿来替尼后,获得了部分缓解。对于SCLC转化化疗后进展的ALK阳性肺癌进行活检,可能有助于制定治疗策略。