序贯alk -酪氨酸激酶抑制剂治疗间变性淋巴瘤激酶重排鳞状细胞肺癌一例报告

Q4 Medicine
R. Ozawa, H. Kuraishi, Yuki Takeuchi, Shunnosuke Tanaka, M. Yamamoto, I. Hase, T. Masubuchi, Hidetoshi Satomi, I. Ito, Shigeru Koyama
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引用次数: 0

摘要

━━背景。间变性淋巴瘤激酶(ALK)重排是鳞状细胞肺癌(SCC)的罕见亚群。alk -酪氨酸激酶抑制剂(TKIs)在alk重排SCC患者中的疗效尚不清楚。的情况。一名49岁日本女性以咳嗽和锁骨上窝淋巴结肿大的症状来我院就诊。她被诊断为SCC (cT4N3M1c, c期IVB),通过经皮锁骨上窝淋巴结穿刺活检。由于患者是一名不吸烟的女性,且病情进展迅速,我们怀疑存在致癌驱动因素。免疫染色和荧光原位杂交显示ALK融合基因的存在。由于患者患有特发性血小板减少性紫癜,细胞毒性化疗不可行。因此,她接受序贯ALK-TKI治疗,包括阿勒替尼、布加替尼和洛拉替尼。经过这些治疗,肿瘤变小了,但效果持续的时间比预期的要短,她最终在确诊后12个月去世了。结论。ALK-TKIs是alk重排SCC患者的治疗选择;然而,它们的功效是有限的。即使在SCC中,如果患者的背景表明存在致癌驱动因素,也建议进行ALK融合基因的分子检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Anaplastic Lymphoma Kinase-rearranged Squamous Cell Lung Cancer Treated with Sequential ALK-tyrosine Kinase Inhibitor Therapy: a Case Report
━━ Background. Anaplastic lymphoma kinase (ALK) rearrangement is a rare subset of squamous cell lung cancer (SCC). The efficacy of ALK-tyrosine kinase inhibitors (TKIs) in ALK-rearranged SCC patients re-mains unclear. Case. A 49-year-old Japanese woman presented to our hospital with symptoms of cough and supraclavicular fossa lymph node swelling. She was diagnosed with SCC (cT4N3M1c, cStage IVB) by a percutane-ous core needle biopsy from the supraclavicular fossa lymph node. As the patient was a non-smoking woman, and the progression of the disease was rapid, we suspected the presence of an oncogenic driver. Immunostaining and fluorescence in situ hybridization revealed the presence of an ALK fusion gene. Cytotoxic chemotherapy was not feasible because the patient was suffering from idiopathic thrombocytopenic purpura. She was therefore treated with sequential ALK-TKI therapy involving alectinib, brigatinib, and lorlatinib. The tumors decreased in size with these treatments, but the duration of the effect was shorter than expected, and she ultiamtly died 12 months after the diagnosis. Conclusion. ALK-TKIs are treatment options for ALK-rearranged SCC patients; however, their efficacy is limited. Molecular testing for the ALK fusion gene is recommended even in SCC if the patient has a background that suggests the presence of an oncogenic driver.
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