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鉴定出对克唑替尼有反应的肝内胆管癌中的新型 EHBP1-MET 融合。

Identification of a Novel EHBP1-MET Fusion in an Intrahepatic Cholangiocarcinoma Responding to Crizotinib.

机构信息

Department of Medical Oncology, Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.

OrigiMed, Shanghai, People's Republic of China.

出版信息

Oncologist. 2020 Dec;25(12):1005-1008. doi: 10.1634/theoncologist.2020-0535. Epub 2020 Oct 12.

Abstract

As an aggressive tumor, intrahepatic cholangiocarcinoma (ICC) originates in the epithelium of the bile duct and has a poor prognosis. The therapeutic options for ICC are challenging and limited because of poor response to chemotherapy and the lack of targeted therapy. Here we report on a 41-year-old female patient with ICC with EHBP1-MET fusion and multiple intrahepatic metastases responding to crizotinib. Next-generation sequencing-based tumor mutation profiling was performed on the tumor biopsy and circulating tumor DNA from plasma. A novel EHBP1-MET fusion was identified and confirmed by Sanger sequencing. Immunohistochemistry of biopsy sample also revealed c-MET positivity. Subsequently, the patient started treatment with MET inhibitor crizotinib. Magnetic resonance imaging scan demonstrated a partial response for 8 months. To the best of our knowledge, this is the first clinical case report of a patient with MET-rearranged ICC successfully treated with crizotinib. This case suggests that crizotinib may be a promising treatment option for patients with ICC with MET fusion, warranting further clinical investigation. KEY POINTS: To the authors' knowledge, this is the first reported case of EHBP1-MET fusion. This is also the first clinical case report of clinical benefit from crizotinib treatment in an intrahepatic cholangiocarcinoma (ICC) with MET fusion. MET fusion is rare in ICC, and inhibition of MET could be a viable option for ICC that warrants further clinical investigation.

摘要

作为一种侵袭性肿瘤,肝内胆管癌 (ICC) 起源于胆管上皮,预后较差。由于对化疗反应不佳和缺乏靶向治疗,ICC 的治疗选择具有挑战性且有限。在这里,我们报告了一例 EHBP1-MET 融合和多发肝内转移的 41 岁女性 ICC 患者对克唑替尼有反应。对肿瘤活检和来自血浆的循环肿瘤 DNA 进行了基于下一代测序的肿瘤突变分析。通过 Sanger 测序鉴定并确认了一种新的 EHBP1-MET 融合。活检样本的免疫组化也显示 c-MET 阳性。随后,患者开始接受 MET 抑制剂克唑替尼治疗。磁共振成像扫描显示 8 个月部分缓解。据我们所知,这是首例 MET 重排 ICC 患者成功接受克唑替尼治疗的临床病例报告。该病例表明,克唑替尼可能是 MET 融合型 ICC 患者有前途的治疗选择,值得进一步临床研究。关键点:据作者所知,这是首例报道的 EHBP1-MET 融合病例。这也是首例 MET 融合型肝内胆管癌 (ICC) 患者接受克唑替尼治疗有临床获益的临床病例报告。MET 融合在 ICC 中很少见,抑制 MET 可能是 ICC 的一种可行选择,值得进一步临床研究。

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