早发性胰腺和胆道癌症的负担日益加重:危险因素综述

A. Boilève , M. Brugel , M. Rémond , M. Valéry , M. Ducreux , A. Turpin , C. Smolenschi
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引用次数: 0

摘要

早发性胰腺和胆道癌症(pbtc)发病率的上升挑战了这些恶性肿瘤主要影响老年人的传统假设。尽管早发性pbtc的预后与晚发性病例相似,但新出现的证据表明,独特或混合的遗传、环境和生活方式因素导致了其独特的病因。本文综述了早发性(50岁以上)胰腺导管腺癌和胆道癌的流行病学、危险因素和分子特征。最近的研究表明,早发性PBTC发病率显著增加,随性别、地理区域和遗传易感性而变化。遗传因素,包括BRCA1/2、CDKN2A和错配修复基因突变,有助于家族聚类,而其他非遗传风险因素,如肥胖、吸烟、胰腺炎和糖尿病,似乎不成比例地影响年轻患者。此外,环境暴露,包括空气污染、农药和内分泌干扰化学物质,被认为有助于致癌,而微生物群的变化可能导致炎症、免疫调节和治疗耐药性。随着早发性pbtc负担的增加,完善筛查策略并将基于微生物组的风险评估整合到生物库策略中将至关重要。未来的研究应该集中在年龄分层的遗传风险分析、微生物群驱动的干预和个性化的治疗方法上,以提高早期发现和患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The increasing burden of early-onset pancreatic and biliary tract cancers: a review of risk factors
The rising incidence of early-onset pancreatic and biliary tract cancers (PBTCs) challenges conventional assumptions that these malignancies primarily affect older populations. Although early-onset PBTCs have a similarly poor prognosis to later-onset cases, emerging evidence suggests that unique or mixed genetic, environmental, and lifestyle factors contribute to their distinct etiologies. This review synthesizes current data on the epidemiology, risk factors, and molecular features of early-onset (in individuals <50 years of age) pancreatic ductal adenocarcinoma and biliary tract cancers. Recent studies indicate a significant increase in early-onset PBTC incidence, with variations by sex, geographic region, and genetic predisposition. Hereditary factors, including BRCA1/2, CDKN2A, and mismatch repair gene mutations, contribute to familial clustering, while other nonhereditary risk factors such as obesity, smoking, pancreatitis, and diabetes seem to disproportionately impact younger patients.
Additionally, environmental exposures, including air pollution, pesticides, and endocrine-disrupting chemicals, are suggested to contribute to carcinogenesis, while changes in microbiota may cause inflammation, immune modulation, and treatment resistance. As the burden of early-onset PBTCs grows, refining screening strategies and integrating microbiome-based risk assessment into biobanking strategies will be critical. Future research should focus on age-stratified genetic risk profiling, microbiota-driven interventions, and personalized therapeutic approaches to improve early detection and patient outcomes.
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