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International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

机译:国际胰腺癌筛查(CAPS)联合会峰会探讨家族性胰腺癌高风险患者的治疗

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摘要

Screening individuals at increased risk for pancreatic cancer (PC) detects early, potentially curable, pancreatic neoplasia. To develop consortium statements on screening, surveillance and management of high-risk individuals with an inherited predisposition to PC. A 49-expert multidisciplinary international consortium met to discuss pancreatic screening and vote on statements. Consensus was considered reached if ≥ 75% agreed or disagreed. There was excellent agreement that, to be successful, a screening programme should detect and treat T1N0M0 margin-negative PC and high-grade dysplastic precursor lesions (pancreatic intraepithelial neoplasia and intraductal papillary mucinous neoplasm). It was agreed that the following were candidates for screening: first-degree relatives (FDRs) of patients with PC from a familial PC kindred with at least two affected FDRs; patients with Peutz-Jeghers syndrome; and p16, BRCA2 and hereditary non-polyposis colorectal cancer (HNPCC) mutation carriers with ≥ 1 affected FDR. Consensus was not reached for the age to initiate screening or stop surveillance. It was agreed that initial screening should include endoscopic ultrasonography (EUS) and/or MRI/magnetic resonance cholangiopancreatography not CT or endoscopic retrograde cholangiopancreatography. There was no consensus on the need for EUS fine-needle aspiration to evaluate cysts. There was disagreement on optimal screening modalities and intervals for follow-up imaging. When surgery is recommended it should be performed at a high-volume centre. There was great disagreement as to which screening abnormalities were of sufficient concern to for surgery to be recommended. Screening is recommended for high-risk individuals, but more evidence is needed, particularly for how to manage patients with detected lesions. Screening and subsequent management should take place at high-volume centres with multidisciplinary teams, preferably within research protocols
机译:筛查罹患胰腺癌(PC)风险增高的个体,可以发现早期,可能可治愈的胰腺肿瘤。制定财团对筛查,监视和管理具有PC遗传倾向的高危人群的声明。一个由49名专家组成的国际跨学科财团开会讨论了胰腺筛查并就声明进行投票。如果≥75%同意或不同意,则认为已达成共识。达成了一项极好的协议,即成功的筛查程序应检测并治疗T1N0M0边缘阴性PC和高度不典型增生的前体病变(胰腺上皮内瘤变和导管内乳头状黏液性肿瘤)。同意以下筛选对象:家族性PC的PC患者的一级亲属(FDR),其家族中至少有两个受影响的FDR。 Peutz-Jeghers综合征患者; p16,BRCA2和遗传性非息肉性大肠直肠癌(HNPCC)突变携带者,其中FDR≥1。未达到开始筛查或停止监测的年龄共识。同意最初的筛查应包括内镜超声检查(EUS)和/或MRI /磁共振胰胆管造影,而不是CT或内窥镜逆行胰胆管造影。对于需要进行EUS细针抽吸术评估囊肿尚无共识。对于最佳的筛查方式和随访影像学的间隔存在分歧。建议进行手术时,应在大容量中心进行。对于哪些筛查异常值得推荐的手术存在很大的分歧。建议对高危人群进行筛查,但还需要更多证据,尤其是对于如何处理发现病变的患者。筛选和后续管理应在具有多学科团队的高容量中心进行,最好在研究方案内

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