Mukherjee Aparna, McGarrity Thomas J, Ruggiero Francesca, Koltun Walter, McKenna Kevin, Poritz Lisa, Baker Maria J
Department of Medicine, Penn State Hershey Cancer Institute, Penn State Milton S, Hershey Medical Center, Hershey, USA.
Hered Cancer Clin Pract. 2010 Nov 22;8(1):9. doi: 10.1186/1897-4287-8-9.
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.
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.
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.
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.
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。
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。
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。
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。