Genetic and other risk factors for pancreatic ductal adenocarcinoma (PDAC)

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2024-04-04 DOI:10.1007/s10689-024-00372-5
Michelle F. Jacobs, Elena M. Stoffel
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Abstract

Pancreatic ductal adenocarcinoma (PDAC) is often diagnosed at an advanced stage, resulting in poor prognosis and low 5-year survival rates. While early evidence suggests increased long-term survival in those with screen-detected resectable cancers, surveillance imaging is currently only recommended for individuals with a lifetime risk of PDAC ≥ 5%. Identification of risk factors for PDAC provides opportunities for early detection, risk reducing interventions, and targeted therapies, thus potentially improving patient outcomes. Here, we summarize modifiable and non-modifiable risk factors for PDAC. We review hereditary cancer syndromes associated with risk for PDAC and their implications for patients and their relatives. In addition, other biologically relevant pathways and environmental and lifestyle risk factors are discussed. Future work may focus on elucidating additional genetic, environmental, and lifestyle risk factors that may modify PDAC risk to continue to identify individuals at increased risk for PDAC who may benefit from surveillance and risk reducing interventions.

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胰腺导管腺癌 (PDAC) 的遗传因素和其他风险因素
胰腺导管腺癌(PDAC)通常在晚期才被确诊,因此预后较差,5 年生存率较低。虽然早期证据表明,通过筛查发现的可切除癌症患者的长期生存率有所提高,但目前只推荐终生罹患 PDAC 风险≥ 5%的患者进行监测成像。PDAC风险因素的识别为早期检测、降低风险干预和靶向治疗提供了机会,从而有可能改善患者的预后。在此,我们总结了 PDAC 的可改变和不可改变的风险因素。我们回顾了与 PDAC 风险相关的遗传性癌症综合征及其对患者及其亲属的影响。此外,我们还讨论了其他生物相关途径以及环境和生活方式风险因素。未来的工作可能侧重于阐明可能改变 PDAC 风险的其他遗传、环境和生活方式风险因素,以继续识别 PDAC 风险增加的个体,这些个体可能会从监测和降低风险的干预措施中获益。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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