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25年家族性和遗传性胰腺导管腺癌监测:历史视角与特刊引言

Twenty-five years of surveillance for familial and hereditary pancreatic ductal adenocarcinoma: Historical perspectives and introduction to the special issue.

作者信息

Vasen Hans Fa, Canto Marcia Irene, Goggins Michael

机构信息

Department of Gastroenterology & Hepatology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Medicine, Division of Gastroenterology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins Medical Institutions, Baltimore, MD, USA.

出版信息

Fam Cancer. 2024 Aug;23(3):209-215. doi: 10.1007/s10689-024-00404-0. Epub 2024 Jun 6.

DOI:10.1007/s10689-024-00404-0
PMID:38844715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11255030/
Abstract

In the 1990s, as prevention became a central strategy in the battle against cancer and the molecular genetics revolution uncovered the genetic basis of numerous hereditary cancer syndromes, there were no options available for patients at increased risk of developing pancreatic cancer. When surveillance efforts for those at familial and hereditary risk of pancreatic cancer emerged in the late 1990s, it was uncertain if early detection was achievable.In this introduction to the special issue, we offer an overview of the history of surveillance for pancreatic cancer, including the first reports of familial pancreatic cancer in the medical literature, the initial results of surveillance in the United States and the initiation of surveillance programs for hereditary pancreatic cancer in the Netherlands.This special issue features a collection of 18 articles written by prominent experts in the field, focusing specifically on refining surveillance methodologies with the primary objective of improving care of high-risk individuals. Several reviews in this collection highlight improved survival rates associated with pancreas surveillance, underlying the potential of early detection and improved management in the continuing fight against pancreatic cancer.

摘要

在20世纪90年代,随着预防成为抗癌斗争的核心策略,且分子遗传学革命揭示了众多遗传性癌症综合征的遗传基础,对于患胰腺癌风险增加的患者而言,当时没有可用的选择。当20世纪90年代末针对有胰腺癌家族和遗传风险者的监测工作出现时,早期检测是否可行尚不确定。在本期特刊的引言中,我们概述了胰腺癌监测的历史,包括医学文献中关于家族性胰腺癌的首次报道、美国监测的初步结果以及荷兰遗传性胰腺癌监测项目的启动。本期特刊收录了该领域杰出专家撰写的18篇文章,特别侧重于完善监测方法,主要目标是改善对高危个体的护理。本专辑中的几篇综述强调了与胰腺监测相关的生存率提高,突显了早期检测和改进管理在持续抗击胰腺癌中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9613/11255030/ea4e249d2a47/10689_2024_404_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9613/11255030/aaf1fdece36c/10689_2024_404_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9613/11255030/ea4e249d2a47/10689_2024_404_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9613/11255030/aaf1fdece36c/10689_2024_404_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9613/11255030/ea4e249d2a47/10689_2024_404_Fig2_HTML.jpg

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1
Twenty-five years of surveillance for familial and hereditary pancreatic ductal adenocarcinoma: Historical perspectives and introduction to the special issue.25年家族性和遗传性胰腺导管腺癌监测:历史视角与特刊引言
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本文引用的文献

1
Pancreatic Cancer Surveillance and Survival of High-Risk Individuals.高危人群的胰腺癌监测和生存情况。
JAMA Oncol. 2024 Aug 1;10(8):1087-1096. doi: 10.1001/jamaoncol.2024.1930.
2
Attitudes toward genetic testing, family planning and preimplantation genetic testing in families with a germline CDKN2A pathogenic variant.携带种系CDKN2A致病变异的家庭对基因检测、计划生育和植入前基因检测的态度。
Fam Cancer. 2024 Aug;23(3):255-265. doi: 10.1007/s10689-024-00401-3. Epub 2024 Jun 1.
3
Review of the cost-effectiveness of surveillance for hereditary pancreatic cancer.
遗传性胰腺癌监测的成本效益综述。
Fam Cancer. 2024 Aug;23(3):351-360. doi: 10.1007/s10689-024-00392-1. Epub 2024 May 25.
4
The best linear unbiased prediction (BLUP) method as a tool to estimate the lifetime risk of pancreatic ductal adenocarcinoma in high-risk individuals with no known pathogenic germline variants.最佳线性无偏预测(BLUP)方法作为一种工具,用于估计无已知致病种系变异的高危个体患胰腺导管腺癌的终生风险。
Fam Cancer. 2024 Aug;23(3):233-246. doi: 10.1007/s10689-024-00397-w. Epub 2024 May 23.
5
The Spanish Familial Pancreatic Cancer Registry (PANGENFAM): a decade follow-up of individuals at high-risk for pancreatic cancer.西班牙家族性胰腺癌登记处(PANGENFAM):对胰腺癌高危个体的十年随访
Fam Cancer. 2024 Aug;23(3):383-392. doi: 10.1007/s10689-024-00388-x. Epub 2024 May 16.
6
Familial and hereditary pancreatic cancer in Japan.日本的家族性和遗传性胰腺癌。
Fam Cancer. 2024 Aug;23(3):365-372. doi: 10.1007/s10689-024-00395-y. Epub 2024 May 11.
7
Screening for pancreatic cancer in high-risk individuals using MRI: optimization of scan techniques to detect small lesions.使用磁共振成像(MRI)对高危个体进行胰腺癌筛查:检测小病灶的扫描技术优化
Fam Cancer. 2024 Aug;23(3):295-308. doi: 10.1007/s10689-024-00394-z. Epub 2024 May 11.
8
The response of pancreatic acinar cell carcinoma to platinum and olaparib therapy in a germline BRCA2 variant carrier: case report and literature review.携带胚系 BRCA2 变异的胰腺腺泡细胞癌患者对铂类药物和奥拉帕利治疗的反应:病例报告及文献复习。
Fam Cancer. 2024 Aug;23(3):393-398. doi: 10.1007/s10689-024-00390-3. Epub 2024 May 11.
9
Expanding access to genetic testing for pancreatic cancer.扩大胰腺癌基因检测的可及性。
Fam Cancer. 2024 Aug;23(3):247-254. doi: 10.1007/s10689-024-00389-w. Epub 2024 May 11.
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The role of biomarkers in the early detection of pancreatic cancer.生物标志物在胰腺癌早期检测中的作用。
Fam Cancer. 2024 Aug;23(3):309-322. doi: 10.1007/s10689-024-00381-4. Epub 2024 Apr 25.