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本文引用的文献

1
Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.林奇综合征患者发生尿路上皮膀胱癌的风险增加,尤其是 MSH2 突变携带者。
J Med Genet. 2010 Jul;47(7):464-70. doi: 10.1136/jmg.2010.076992.
2
Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial.电子提醒有助于病理学家识别林奇综合征高危患者:整群随机对照试验
Virchows Arch. 2010 Jun;456(6):653-9. doi: 10.1007/s00428-010-0907-7. Epub 2010 Apr 9.
3
The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer.新诊断结直肠癌患者中林奇综合征遗传检测策略的成本效益。
Genet Med. 2010 Feb;12(2):93-104. doi: 10.1097/GIM.0b013e3181cd666c.
4
Health and lifestyle behaviors among persons at risk of Lynch syndrome.林奇综合征风险人群的健康和生活方式行为。
Cancer Causes Control. 2010 Apr;21(4):513-21. doi: 10.1007/s10552-009-9482-0. Epub 2009 Dec 10.
5
Germ-line mutations in mismatch repair genes associated with prostate cancer.与前列腺癌相关的错配修复基因中的种系突变。
Cancer Epidemiol Biomarkers Prev. 2009 Sep;18(9):2460-7. doi: 10.1158/1055-9965.EPI-09-0058. Epub 2009 Sep 1.
6
Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives.EGAPP工作组的建议:针对新诊断的结直肠癌患者的基因检测策略,旨在降低亲属患林奇综合征的发病率和死亡率。
Genet Med. 2009 Jan;11(1):35-41. doi: 10.1097/GIM.0b013e31818fa2ff.
7
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.由于TACSTD1基因3'外显子缺失导致的林奇综合征家族中MSH2基因的可遗传体细胞甲基化和失活。
Nat Genet. 2009 Jan;41(1):112-7. doi: 10.1038/ng.283. Epub 2008 Dec 21.
8
Population-based detection of Lynch syndrome in young colorectal cancer patients using microsatellite instability as the initial test.以微卫星不稳定性作为初始检测手段,对年轻结直肠癌患者进行基于人群的林奇综合征检测。
Int J Cancer. 2009 Mar 1;124(5):1097-102. doi: 10.1002/ijc.23863.
9
Feasibility of screening for Lynch syndrome among patients with colorectal cancer.结直肠癌患者中林奇综合征筛查的可行性
J Clin Oncol. 2008 Dec 10;26(35):5783-8. doi: 10.1200/JCO.2008.17.5950. Epub 2008 Sep 22.
10
Family and personal history in colorectal cancer patients: what are we missing?结直肠癌患者的家族史和个人史:我们遗漏了什么?
Colorectal Dis. 2006 Sep;8(7):612-4. doi: 10.1111/j.1463-1318.2006.01047.x.

修订后的贝塞斯达指南:在设有癌症遗传学项目的大学医院医疗中心的应用范围

The revised Bethesda guidelines: extent of utilization in a university hospital medical center with a cancer genetics program.

作者信息

Mukherjee Aparna, McGarrity Thomas J, Ruggiero Francesca, Koltun Walter, McKenna Kevin, Poritz Lisa, Baker Maria J

机构信息

Department of Medicine, Penn State Hershey Cancer Institute, Penn State Milton S, Hershey Medical Center, Hershey, USA.

出版信息

Hered Cancer Clin Pract. 2010 Nov 22;8(1):9. doi: 10.1186/1897-4287-8-9.

DOI:10.1186/1897-4287-8-9
PMID:21092199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2997085/
Abstract

BACKGROUND

In 1996, the National Cancer Institute hosted an international workshop to develop criteria to identify patients with colorectal cancer who should be offered microsatellite instability (MSI) testing due to an increased risk for Hereditary Nonpolyposis Colorectal Cancer (HNPCC). These criteria were further modified in 2004 and became known as the revised Bethesda Guidelines. Our study aimed to retrospectively evaluate the percentage of patients diagnosed with HNPCC tumors in 2004 who met revised Bethesda criteria for MSI testing, who were referred for genetic counseling within our institution.

METHODS

All HNPCC tumors diagnosed in 2004 were identified by accessing CoPath, an internal database. Both the Tumor Registry and patients' electronic medical records were accessed to collect all relevant family history information. The list of patients who met at least one of the revised Bethesda criteria, who were candidates for MSI testing, was then cross-referenced with the database of patients referred for genetic counseling within our institution.

RESULTS

A total of 380 HNPCC-associated tumors were diagnosed at our institution during 2004 of which 41 (10.7%) met at least one of the revised Bethesda criteria. Eight (19.5%) of these patients were referred for cancer genetic counseling of which 2 (25%) were seen by a genetics professional. Ultimately, only 4.9% of patients eligible for MSI testing in 2004 were seen for genetic counseling.

CONCLUSION

This retrospective study identified a number of barriers, both internal and external, which hindered the identification of individuals with HNPCC, thus limiting the ability to appropriately manage these high risk families.

摘要

背景

1996年,美国国立癌症研究所举办了一次国际研讨会,以制定标准来识别因遗传性非息肉病性结直肠癌(HNPCC)风险增加而应接受微卫星不稳定性(MSI)检测的结直肠癌患者。这些标准在2004年进一步修订,成为修订后的贝塞斯达指南。我们的研究旨在回顾性评估2004年被诊断为HNPCC肿瘤且符合MSI检测修订后贝塞斯达标准的患者比例,这些患者在我们机构接受了遗传咨询。

方法

通过访问内部数据库CoPath识别2004年诊断的所有HNPCC肿瘤。访问肿瘤登记处和患者的电子病历以收集所有相关家族史信息。然后将符合至少一项修订后贝塞斯达标准且为MSI检测候选者的患者名单与我们机构内接受遗传咨询的患者数据库进行交叉对照。

结果

2004年我们机构共诊断出380例与HNPCC相关的肿瘤,其中41例(10.7%)符合至少一项修订后贝塞斯达标准。这些患者中有8例(19.5%)被转介进行癌症遗传咨询,其中2例(25%)接受了遗传学专业人员的诊治。最终,2004年符合MSI检测条件的患者中只有4.9%接受了遗传咨询。

结论

这项回顾性研究确定了一些内部和外部障碍,这些障碍阻碍了HNPCC个体的识别,从而限制了对这些高危家庭进行适当管理的能力。