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特泊替尼用于治疗MET扩增的胆管癌:一例报告

Tepotinib in Cholangiocarcinoma with MET Amplification: A Case Report.

作者信息

Chen Yen-Hao, Huang Yu-Ting, Kuo Fang-Ying

机构信息

Division of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, 833, Taiwan.

School of Medicine, College of Medicine, Chang Gung University, Taoyuan, 333, Taiwan.

出版信息

Onco Targets Ther. 2024 Oct 29;17:857-861. doi: 10.2147/OTT.S483155. eCollection 2024.

DOI:10.2147/OTT.S483155
PMID:39493678
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11531238/
Abstract

Cholangiocarcinoma is a malignant tumor that affects the bile ducts and is usually aggressive with poor prognosis. The treatment of cholangiocarcinoma depends on the stage and location of the tumor as well as the patient's overall health status. Systemic therapy, such as chemotherapy using gemcitabine and cisplatin, is the first choice for patients with cholangiocarcinoma who were inoperable. After no response to first-line chemotherapy, second-line chemotherapy or targeted therapy focusing on signaling pathway inhibition are subsequent treatment. The present report described a case of cholangiocarcinoma involving bilateral lobes of liver. He received one cycle of chemotherapy with gemcitabine plus cisplatin and exhibited rapid progression. Next-generation sequencing was performed, and the results showed that MET amplification had a gene copy number of 68. After that, he underwent tepotinib and tumor shrinkage occurred. After a follow‑up period of 12 months, the treatment response was partial response, and the benefit of tepotinib is ongoing. The development of precision medicine has expanded the paradigm of targeted therapies to increasingly favorable options in the second line and beyond, and prolong overall survival. Detecting druggable mutations (mutations potentially amenable to treatment with) for identifying a landscape of therapeutic options is imperative for managing cholangiocarcinoma.

摘要

胆管癌是一种影响胆管的恶性肿瘤,通常具有侵袭性,预后较差。胆管癌的治疗取决于肿瘤的分期和位置以及患者的整体健康状况。全身治疗,如使用吉西他滨和顺铂的化疗,是无法手术的胆管癌患者的首选治疗方法。在一线化疗无反应后,二线化疗或针对信号通路抑制的靶向治疗是后续治疗方法。本报告描述了一例累及肝脏双侧叶的胆管癌病例。他接受了一个周期的吉西他滨加顺铂化疗,但病情迅速进展。进行了二代测序,结果显示MET扩增的基因拷贝数为68。之后,他接受了替泊替尼治疗,肿瘤出现缩小。经过12个月的随访,治疗反应为部分缓解,替泊替尼的疗效仍在持续。精准医学的发展将靶向治疗的模式扩展到了二线及以后越来越有利的选择,并延长了总生存期。检测可靶向治疗的突变(可能适合治疗的突变)以确定治疗方案对于胆管癌的管理至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2706/11531238/4bfab46780c0/OTT-17-857-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2706/11531238/7e93ca086e21/OTT-17-857-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2706/11531238/4bfab46780c0/OTT-17-857-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2706/11531238/7e93ca086e21/OTT-17-857-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2706/11531238/4bfab46780c0/OTT-17-857-g0002.jpg

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本文引用的文献

1
Durvalumab plus Gemcitabine and Cisplatin in Advanced Biliary Tract Cancer.度伐利尤单抗联合吉西他滨和顺铂治疗晚期胆道癌。
NEJM Evid. 2022 Aug;1(8):EVIDoa2200015. doi: 10.1056/EVIDoa2200015. Epub 2022 Jun 1.
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Precision Oncology Targets in Biliary Tract Cancer.胆管癌中的精准肿瘤学靶点
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Final Overall Survival Efficacy Results of Ivosidenib for Patients With Advanced Cholangiocarcinoma With IDH1 Mutation: The Phase 3 Randomized Clinical ClarIDHy Trial.
晚期 IDH1 突变型胆管癌患者ivosidenib 的最终总生存疗效结果:III 期随机临床 ClarIDHy 试验。
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Capmatinib in Exon 14-Mutated or -Amplified Non-Small-Cell Lung Cancer.卡马替尼治疗外显子 14 突变或扩增的非小细胞肺癌。
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Tepotinib in Non-Small-Cell Lung Cancer with Exon 14 Skipping Mutations.特泊替尼治疗伴有外显子 14 跳跃突变的非小细胞肺癌。
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Pemigatinib for previously treated, locally advanced or metastatic cholangiocarcinoma: a multicentre, open-label, phase 2 study.培米替尼治疗既往治疗过的局部晚期或转移性胆管癌:一项多中心、开放标签、2 期研究。
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First-in-Man Phase I Trial of the Selective MET Inhibitor Tepotinib in Patients with Advanced Solid Tumors.首个人体 I 期试验评估选择性 MET 抑制剂特泊替尼治疗晚期实体瘤患者的疗效。
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Nat Rev Cancer. 2019 Sep;19(9):495-509. doi: 10.1038/s41568-019-0179-8. Epub 2019 Aug 12.
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Known and novel roles of the MET oncogene in cancer: a coherent approach to targeted therapy.MET 癌基因在癌症中的已知和新作用:一种针对靶向治疗的连贯方法。
Nat Rev Cancer. 2018 Jun;18(6):341-358. doi: 10.1038/s41568-018-0002-y.
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Does c-Met remain a rational target for therapy in patients with EGFR TKI-resistant non-small cell lung cancer?在 EGFR TKI 耐药的非小细胞肺癌患者中,c-Met 是否仍然是一个合理的治疗靶点?
Cancer Treat Rev. 2017 Dec;61:70-81. doi: 10.1016/j.ctrv.2017.10.003. Epub 2017 Oct 25.