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晚期小肠腺癌:分子特征与治疗前景

Advanced small bowel adenocarcinoma: Molecular characteristics and therapeutic perspectives.

作者信息

Zaaimi Yosra, Aparicio Thomas, Laurent-Puig Pierre, Taieb Julien, Zaanan Aziz

机构信息

Department of Gastroenterology and Digestive Oncology, European Georges Pompidou Hospital, AP-HP, 20, rue Leblanc, 75015 Paris, France.

Department of Gastroenterology and Digestive Oncology, Avicenne Hospital, AP-HP, Bobigny, France.

出版信息

Clin Res Hepatol Gastroenterol. 2016 Apr;40(2):154-60. doi: 10.1016/j.clinre.2015.09.008. Epub 2015 Nov 4.

DOI:10.1016/j.clinre.2015.09.008
PMID:26547136
Abstract

Small bowel cancer represents less than 5% of all gastrointestinal cancers, while small bowel adenocarcinoma (SBA) accounts for about one third of all cancers of the small bowel. Although SBA frequently appears sporadically, some diseases are risk factors, such as Crohn's disease and some genetic predispositions to cancer. Progress in the identification of molecular alterations suggests some similarities in carcinogenesis between SBA and colorectal cancer. Evidence levels for the treatment and prognosis of these tumors are insufficient because of the scarcity of this disease and the absence of randomized trials. Chemotherapy based on fluoropyrimidine plus a platinum salt appears to be the most effective treatment regimen in non-randomized prospective trials for advanced SBA. Targeted therapy, against the angiogenic pathway or the epidermal growth factor receptor (EGFR) pathway, for example, is not yet established, but seems promising given the over-expression of vascular epithelial growth factor (VEGF)-A or EGFR observed in SBA. Phase I and II studies are currently evaluating the safety and efficacy of these targeted therapies in SBA treatment. The low incidence of SBA should promote the development of international collaborations to improve our knowledge of the biological mechanisms underlying these tumors and to set up therapeutic trials.

摘要

小肠癌占所有胃肠道癌症的比例不到5%,而小肠腺癌(SBA)约占所有小肠癌症的三分之一。尽管SBA常常散发出现,但一些疾病是风险因素,如克罗恩病以及某些癌症的遗传易感性。分子改变识别方面的进展表明SBA和结直肠癌在致癌过程中存在一些相似之处。由于这种疾病罕见且缺乏随机试验,这些肿瘤治疗和预后的证据水平不足。在晚期SBA的非随机前瞻性试验中,基于氟嘧啶加铂盐的化疗似乎是最有效的治疗方案。例如,针对血管生成途径或表皮生长因子受体(EGFR)途径的靶向治疗尚未确立,但鉴于在SBA中观察到血管上皮生长因子(VEGF)-A或EGFR的过度表达,似乎很有前景。I期和II期研究目前正在评估这些靶向治疗在SBA治疗中的安全性和有效性。SBA的低发病率应推动国际合作的开展,以增进我们对这些肿瘤潜在生物学机制的了解并开展治疗试验。

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