奥西替尼治疗后EGFR t790m获得性肺腺癌共存并向不同器官小细胞癌转化。病例报告

IF 0.2 Q4 ONCOLOGY
Masahide Takeda, Mariko Asano, Sho Sakamoto, Yuka Izumiya, Yuji Okuda, Kazuhiro Sato, Katsutoshi Nakayama
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引用次数: 0

摘要

我们报告一例罕见的59岁男性egfr突变肺腺癌患者出现奥西替尼耐药,同时存在不同器官的t790m阳性腺癌和t790m阴性小细胞癌。经吉非替尼、化疗、奥西替尼及后续化疗治疗后,患者病情进展,包括心包积液和纵隔淋巴结病。心包液细胞学证实为腺癌,而淋巴结活检显示为小细胞癌。再次使用奥西替尼成功地控制了心包积液,但疾病最终进展。该病例强调了重新活检对了解耐药机制的重要性,并强调了处理肺癌双重组织学转化的挑战,特别是当转化为小细胞癌发生在不同解剖部位时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-existence of EGFR T790M-acquired lung adenocarcinoma and transformation into small-cell carcinoma in different organs after osimertinib treatment. A case report
We report a rare case of a 59-year-old man with EGFR-mutated lung adenocarcinoma who developed osimertinib resistance, with coexisting T790M-positive adenocarcinoma and T790M-negative small-cell carcinoma in different organs. After treatment with gefitinib, chemotherapy, osimertinib, and subsequent chemotherapy, the patient presented with progressive disease, including pericardial effusion and mediastinal lymphadenopathy. Cytology of the pericardial fluid confirmed adenocarcinoma, while lymph node biopsy revealed transformation to small-cell carcinoma. Rechallenge with osimertinib successfully controlled the pericardial effusion, but the disease ultimately progressed. This case emphasizes the importance of re-biopsy for understanding resistance mechanisms and highlights the challenges of managing dual histologic transformation in lung cancer, particularly when transformation to small-cell carcinoma occurs in different anatomical sites.
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CiteScore
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