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Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data

机译:在结直肠癌患者的检查中忽略了家族史:使用癌症登记数据进行质量评估

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摘要

In the diagnostic work-up of hereditary non-polyposis colorectal cancer (HNPCC, Lynch syndrome), high-risk patients can be identified using information from the family history on cancer (‘Amsterdam criteria’ and ‘Bethesda guidelines’). To investigate to what extent the medical specialists apply these criteria to patients with colorectal carcinoma and a suspicion of HNPCC, we collected information on diagnostic work-up of 224 patients of seven hospitals in the region of the Comprehensive Cancer Centre West in Leiden, The Netherlands. These patients were diagnosed with colorectal cancer between 1999 and 2001 and satisfied at least one of the Bethesda guidelines. A complete family history was recorded for 38 of the 244 patients (16%). Patients with a complete family history were more likely to be referred to the Clinical Genetic Centre than those with an incomplete or absent family history (53% vs. 13% and 4%, respectively; P < 0.0001), and more likely to be analyzed for microsatellite instability (MSI), which is a characteristic of HNPCC (34% vs. 6% and 1%, respectively; P < 0.0001). We conclude that the family history is neglected in the majority of patients with colorectal cancer and MSI-analysis is only performed in a small proportion of the patients that meet the guidelines for this analysis.
机译:在遗传性非息肉性大肠直肠癌(HNPCC,林奇综合征)的诊断检查中,可以使用来自癌症家族史的信息(“阿姆斯特丹标准”和“贝塞斯达指南”)来识别高危患者。为了调查医学专家在多大程度上将这些标准应用于大肠癌和HNPCC怀疑患者,我们收集了有关荷兰莱顿综合癌症中心西区七家医院的224名患者的诊断检查信息。 。这些患者在1999年至2001年之间被诊断出患有大肠癌,并且至少满足Bethesda指南之一。记录了244例患者中的38例的完整家族史(16%)。具有完整家族史的患者比没有完整家族史或不存在家族史的患者更有可能被转诊到临床遗传中心(分别为53%vs.13%和4%; P <0.0001),并且更有可能被分析微卫星不稳定性(MSI),这是HNPCC的特征(分别为34%对6%和1%; P <0.0001)。我们得出的结论是,大多数结直肠癌患者都忽略了家族史,并且仅在符合该分析指南的患者中进行了MSI分析。

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