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病例报告:经抗血管内皮生长因子受体酪氨酸激酶抑制剂阿帕替尼治疗的伴有重排的胃肠道PEComa

Case Report: Gastrointestinal PEComa With Rearrangement Treated With Anti-VEGFR TKI Apatinib.

作者信息

Xu Jiaming, Gong Xiao-Lei, Wu Huanwen, Zhao Lin

机构信息

Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Front Oncol. 2020 Nov 23;10:582087. doi: 10.3389/fonc.2020.582087. eCollection 2020.

Abstract

Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors. Unresectable malignant PEComas with rearrangement have no recommended therapy to date. Here, we report the first case of malignant gastrointestinal PEComa with rearrangement which has a response to the targeted therapy of an anti-VEGFR tyrosine kinase inhibitor (TKI), apatinib. A 31-year-old female was diagnosed with malignant gastrointestinal PEComa with rearrangement and hepatic metastases. A resection of the giant retroperitoneal mass was performed. The patient received the anti-VEGFR TKI apatinib to treat the hepatic metastasis. The tumor remained stable during apatinib treatment and the progression-free survival (PFS) lasted about 7 months. This case suggests that targeting the VEGF/VEGFR signaling pathway may be an essential new therapeutic choice for -associated malignant PEComas.

摘要

血管周上皮样细胞肿瘤(PEComas)是罕见的间叶组织肿瘤。迄今,对于伴有重排的不可切除恶性PEComas尚无推荐治疗方案。在此,我们报告首例伴有重排的恶性胃肠道PEComa,其对抗血管内皮生长因子受体(VEGFR)酪氨酸激酶抑制剂(TKI)阿帕替尼的靶向治疗有反应。一名31岁女性被诊断为伴有重排及肝转移的恶性胃肠道PEComa。对巨大的腹膜后肿块进行了切除。患者接受抗VEGFR TKI阿帕替尼治疗肝转移。在阿帕替尼治疗期间肿瘤保持稳定,无进展生存期(PFS)持续约7个月。该病例提示,针对VEGF/VEGFR信号通路可能是与相关恶性PEComas相关的一种重要新治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7063/7719820/bf3b38fd7244/fonc-10-582087-g001.jpg

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