Boughey Annabelle, Hopley Phil, Sarantitis Ioannis, Thomas Paul, Gubacsi Beata, Jevons Kayleigh, Crowe Emma, Hughes Eleri, Quinn Isobel, Royle Liam, Jackson Richard J, Greenhalf William, Halloran Chris
Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, England, UK.
Royal Liverpool University Hospital, Liverpool, UK.
BMJ Open. 2025 Apr 3;15(4):e100027. doi: 10.1136/bmjopen-2025-100027.
Pancreatic cancer is a devastating disease and one of the top causes of cancer death worldwide. Over 30% of cases are potentially avoidable, and while screening for this disease should be possible, the current methods, without risk stratification to detect high-risk groups, are unlikely to detect these individuals. A tailored screening pathway could be applied to individuals with a germline genetic cause of pancreatic cancer, which may account for around 10% of cases.
EUROPAC, although having international reach, is described here in relation to the UK only. This national prospective observational study has run for several decades but was modified into the current trial in 2019, which aims to recruit and screen 10 000 individuals with either familial pancreatic cancer or hereditary pancreatitis (HP). Applicants are assessed for eligibility by generating an individual pedigree and by attributing a family risk score (FR). Individual risk is assessed according to age. Individuals over 40 with an FR >30 are offered baseline imaging and then three yearly triplets of annual endoscopic ultrasound (EUS) and an MRI (in the third year). Those with an FR >60 are offered both EUS and MRI yearly. HP patients are screened by CT and/or MRI dependent on risk stratification using the presence of diabetes, smoking or alcohol consumption. Low-risk (absence of these factors) patients have a CT every 2 years, and high-risk (one or more of the above factors) patients have alternate yearly screening with CT, then MRI. Biospecimens are collected at pragmatic intervals with first sampling at registration to support future biomarker development to detect pancreatic cancer early. Detection of early-stage pancreatic cancer and actionable lesions will be evaluated.
The EUROPAC study has been reviewed and approved by the Yorkshire and Humber Research Ethics Committee (Ref 19/YH/0250). Study results will be disseminated through national and international symposium presentations and published in peer-reviewed, open-access journals. All participants provided informed consent prior to entering the study.
ISRCTN62546421.
胰腺癌是一种极具破坏性的疾病,是全球癌症死亡的主要原因之一。超过30%的病例是潜在可避免的,虽然对这种疾病进行筛查应该是可行的,但目前的方法没有对高危人群进行风险分层,不太可能检测出这些个体。一种量身定制的筛查途径可应用于具有胰腺癌种系遗传病因的个体,这类个体约占病例的10%。
欧洲胰腺癌前瞻性筛查研究(EUROPAC)虽然具有国际影响力,但本文仅就其在英国的情况进行描述。这项全国性前瞻性观察性研究已开展数十年,但在2019年改为当前的试验,旨在招募和筛查10000名患有家族性胰腺癌或遗传性胰腺炎(HP)的个体。通过生成个体家系并赋予家族风险评分(FR)来评估申请人的资格。根据年龄评估个体风险。FR>30且年龄超过40岁的个体接受基线成像检查,然后每三年进行一次年度内镜超声(EUS)和MRI检查(第三年)。FR>60的个体每年接受EUS和MRI检查。HP患者根据是否存在糖尿病、吸烟或饮酒情况进行风险分层,通过CT和/或MRI进行筛查。低风险(不存在这些因素)患者每两年进行一次CT检查,高风险(存在上述一个或多个因素)患者每年交替进行CT和MRI筛查。在实际可行的时间间隔收集生物样本,首次采样在登记时进行,以支持未来生物标志物的开发,以便早期检测胰腺癌。将评估早期胰腺癌和可采取行动的病变的检测情况。
EUROPAC研究已得到约克郡和亨伯赛德研究伦理委员会的审查和批准(参考编号19/YH/0250)。研究结果将通过国内和国际研讨会报告进行传播,并发表在同行评审的开放获取期刊上。所有参与者在进入研究前均提供了知情同意书。
ISRCTN62546421。