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美国胃肠病学会关于高危个体胰腺癌筛查的临床实践更新:专家综述

AGA Clinical Practice Update on Pancreas Cancer Screening in High-Risk Individuals: Expert Review.

作者信息

Aslanian Harry R, Lee Jeffrey H, Canto Marcia Irene

机构信息

Yale University, New Haven, Connecticut.

University of Texas, MD Anderson Cancer Center, Houston, Texas.

出版信息

Gastroenterology. 2020 Jul;159(1):358-362. doi: 10.1053/j.gastro.2020.03.088. Epub 2020 May 19.

Abstract

DESCRIPTION

The purpose of this American Gastroenterological Association Institute Clinical Practice Update is to describe the indications for screening for pancreas cancer in high-risk individuals.

METHODS

The evidence reviewed in this work is based on reports of pancreas cancer screening studies in high-risk individuals and expert opinion. BEST PRACTICE ADVICE 1: Pancreas cancer screening should be considered in patients determined to be at high risk, including first-degree relatives of patients with pancreas cancer with at least 2 affected genetically related relatives. BEST PRACTICE ADVICE 2: Pancreas cancer screening should be considered in patients with genetic syndromes associated with an increased risk of pancreas cancer, including all patients with Peutz-Jeghers syndrome, hereditary pancreatitis, patients with CDKN2A gene mutation, and patients with 1 or more first-degree relatives with pancreas cancer with Lynch syndrome, and mutations in BRCA1, BRCA2, PALB2, and ATM genes. BEST PRACTICE ADVICE 3: Genetic testing and counseling should be considered for familial pancreas cancer relatives who are eligible for surveillance. A positive germline mutation is associated with an increased risk of neoplastic progression and may also lead to screening for other relevant associated cancers. BEST PRACTICE ADVICE 4: Participation in a registry or referral to a pancreas Center of Excellence should be pursued when possible for high-risk patients undergoing pancreas cancer screening. BEST PRACTICE ADVICE 5: Clinicians should not screen average-risk individuals for pancreas cancer. BEST PRACTICE ADVICE 6: Pancreas cancer screening in high-risk individuals should begin at age 50 years, or 10 years younger than the initial age of familial onset. Screening should be initiated at age 40 years in CKDN2A and PRSS1 mutation carriers with hereditary pancreatitis and at age 35 years in the setting of Peutz-Jeghers syndrome. BEST PRACTICE ADVICE 7: Magnetic resonance imaging and endoscopic ultrasonography (EUS) should be used in combination as the preferred screening modalities in individuals undergoing pancreas cancer screening. BEST PRACTICE ADVICE 8: The target detectable pancreatic neoplasms are resectable stage I pancreatic ductal adenocarcinoma and high-risk precursor neoplasms, such as intraductal papillary mucinous neoplasms with high-grade dysplasia and some enlarged pancreatic intraepithelial neoplasias. BEST PRACTICE ADVICE 9: Screening intervals of 12 months should be considered when there are no concerning pancreas lesions, with shortened intervals and/or the performance of EUS in 6-12 months directed towards lesions determined to be low risk (by a multidisciplinary team). EUS evaluation should be performed within 3-6 months for indeterminate lesions and within 3 months for high-risk lesions, if surgical resection is not planned. New-onset diabetes in a high-risk individual should lead to additional diagnostic studies or change in surveillance interval. BEST PRACTICE ADVICE 10: Decisions regarding therapy directed towards abnormal findings detected during screening should be made by a dedicated multidisciplinary team together with the high-risk individual and their family. BEST PRACTICE ADVICE 11: Surgical resection should be performed at high-volume centers. BEST PRACTICE ADVICE 12: Clinicians should consider discontinuing pancreas cancer screening in high-risk individuals when they are more likely to die of non-pancreas cancer-related causes due to comorbidity and/or are not candidates for pancreas resection. BEST PRACTICE ADVICE 13: The limitations and potential risks of pancreas cancer screening should be discussed with patients before initiating a screening program.

摘要

描述

本美国胃肠病学会临床实践更新的目的是描述高危个体胰腺癌筛查的指征。

方法

本研究中所回顾的证据基于高危个体胰腺癌筛查研究报告及专家意见。最佳实践建议1:对于确定为高危的患者应考虑进行胰腺癌筛查,包括有至少2名受影响的遗传相关亲属的胰腺癌患者的一级亲属。最佳实践建议2:对于与胰腺癌风险增加相关的遗传综合征患者应考虑进行胰腺癌筛查,包括所有黑斑息肉综合征、遗传性胰腺炎、携带CDKN2A基因突变的患者,以及有1名或更多患胰腺癌的一级亲属且患有林奇综合征、携带BRCA1、BRCA2、PALB2和ATM基因突变的患者。最佳实践建议3:对于符合监测条件的家族性胰腺癌亲属应考虑进行基因检测和咨询。种系突变阳性与肿瘤进展风险增加相关,还可能导致对其他相关联癌症的筛查。最佳实践建议4:对于接受胰腺癌筛查的高危患者,应尽可能让其参与登记或转诊至胰腺癌卓越中心。最佳实践建议5:临床医生不应为平均风险个体筛查胰腺癌。最佳实践建议6:高危个体的胰腺癌筛查应在50岁开始,或比家族发病初始年龄早10年。对于遗传性胰腺炎的CKDN2A和PRSS1突变携带者,筛查应在40岁开始,对于黑斑息肉综合征患者,筛查应在35岁开始。最佳实践建议7:磁共振成像和内镜超声检查(EUS)应联合使用,作为胰腺癌筛查个体的首选筛查方式。最佳实践建议8:目标可检测胰腺肿瘤为可切除的I期胰腺导管腺癌和高危前体肿瘤,如伴有高级别异型增生的导管内乳头状黏液性肿瘤和一些增大的胰腺上皮内瘤变。最佳实践建议9:当没有可疑胰腺病变时,应考虑12个月的筛查间隔,对于确定为低风险的病变(由多学科团队判定),筛查间隔应缩短和/或在6 - 12个月内进行EUS检查。对于不确定病变,应在3 - 6个月内进行EUS评估,对于高危病变,如果不计划手术切除,应在3个月内进行EUS评估。高危个体新发糖尿病应导致额外的诊断检查或监测间隔的改变。最佳实践建议10:针对筛查期间发现的异常结果的治疗决策应由专门的多学科团队与高危个体及其家属共同做出。最佳实践建议11:手术切除应在大型中心进行。最佳实践建议12:当高危个体因合并症更可能死于非胰腺癌相关原因和/或不是胰腺切除候选者时,临床医生应考虑停止对其进行胰腺癌筛查。最佳实践建议13:在启动筛查项目前,应与患者讨论胰腺癌筛查的局限性和潜在风险。

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