her -2阳性壶腹腺癌1例报告。

Case reports in pancreatic cancer Pub Date : 2015-11-01 eCollection Date: 2015-01-01 DOI:10.1089/crpc.2015.29004.koh
Kevin O'Hayer, John Farber, Charles J Yeo, Ashwin R Sama
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引用次数: 5

摘要

背景:壶腹腺癌是壶腹周围肿瘤中一种罕见的亚型,总体预后较差。治疗决定通常是从胰腺化疗方案推断出来的,主要由传统的化疗药物组成。目前还没有已知的壶腹腺癌治疗干预的靶点。下一代测序和其他新的肿瘤分子图谱,包括循环肿瘤DNA (ctDNA),最近使得更好地理解肿瘤生物学和阐明可用于靶向治疗的驱动突变成为可能。本病例描述了使用新的DNA测序技术,为HER-2过表达壶腹腺癌患者提供靶向治疗选择,HER-2抑制。这是第一次在文献中描述这种情况。病例介绍:患者是一名63岁的白人男性,最初以梗阻性黄疸的症状出现,后来发现壶腹周围有肿瘤。他接受了肿瘤切除术,病理证实为IIB期壶腹腺癌。不幸的是,两年后他的肝脏和肺部又复发了。切除时肿瘤的下一代测序以及ctDNA分析显示HER-2过表达肿瘤。在FOLFOX一线治疗后,患者病情出现进展,并在多灶性肺炎最终死亡前接受曲妥珠单抗和帕妥珠单抗治疗,病情趋于稳定。结论:下一代测序和ctDNA技术的使用为我们的患者带来了一种新的治疗干预。随着这些技术的普及,更有针对性的治疗方法可能会用于这些难以治疗的疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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HER-2-Positive Ampullary Adenocarcinoma: A Case Report.

Background: Ampullary adenocarcinomas are a rare subset of periampullary tumors with an overall poor prognosis. Treatment decisions are generally extrapolated from pancreatic chemotherapy protocols and consist mainly of traditional chemotherapy drugs. There are no known targets for therapeutic intervention in ampullary adenocarcinoma at this time. Next generation sequencing and other novel molecular profiling of tumors, including circulating tumor DNA (ctDNA), have recently made it possible to better understand tumor biology and elucidate driver mutations which are amenable to targeted therapy. This case describes the use of novel DNA sequencing technology to provide a targeted treatment option, HER-2 inhibition, in a patient with HER-2 overexpressing ampullary adenocarcinoma. This is the first time this has been described in the literature. Case presentation: The patient is a 63-year-old Caucasian man who initially presented with symptoms of obstructive jaundice and was found to have a periampullary tumor. He underwent resection of his tumor and pathology confirmed a stage IIB ampullary adenocarcinoma. He unfortunately developed a recurrence in the liver and lung two years later. Next generation sequencing of his tumor at the time of resection as well as ctDNA analysis demonstrated a HER-2 overexpressing tumor. Following first line therapy with FOLFOX he had progression and was treated with trastuzumab and pertuzumab with stabilization of his disease prior to his ultimate demise from multifocal pneumonia. Conclusion: The use of next generation sequencing as well as ctDNA technology generated a novel therapeutic intervention in our patient. As these techniques become more widespread, it is likely more targeted therapies will be used in these difficult to treat diseases.

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