癌症遗传学主流化:在爱尔兰开展由高级执业护士主导的林奇综合征结直肠癌诊断服务的可行性。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2024-11-15 DOI:10.1007/s10689-024-00427-7
Mechelle Loughrey, Lauren V O'Connell, Lynda McSorley, Sean Martin, Ann Hanly, Des C Winter, Ian M Frayling, Kieran Sheahan, Rory Kennelly
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引用次数: 0

摘要

结肠直肠癌(CRC)是爱尔兰常见的癌症。在所有 CRC 中,2%-4% 可归因于林奇综合征(Lynch Syndrome,LS),这是最常见的 CRC 易感综合征。林奇综合征是由影响错配修复(MMR)基因并导致 MMR 蛋白缺乏(dMMR)的致病变体(PVs)引起的。人们主张用 MMR 免疫组化(IHC)检测筛查所有 CRC,以提高 LS 的检出率。然而,成功实施筛查需要适当的下游管理。在爱尔兰,传统的途径包括转诊至癌症遗传学服务机构,以评估基因检测的资格。爱尔兰的癌症遗传学服务在提供统一的及时医疗服务方面面临许多挑战,目前评估等待时间超过 1 年。越来越多采用的途径是主流化,即由多学科团队成员在当地管理基因检测。因此,我们机构实施了一项由高级执业护士(ANP)领导的服务,负责 LS 诊断路径和主流基因检测。我们从前瞻性维护的数据库中提取了数据,该数据库包含了2023年1月1日至2024年5月31日期间在本机构CRC多学科会议(MDM)上讨论的所有新诊断CRC患者。在 385 例确诊为 CRC 的患者中,97.9% 进行了 MMR IHC 检测。从组织学确诊为 CRC 到获得 MMR IHC 报告的中位时间为 6 天。所有需要进行连续肿瘤检测的 51 名患者(100%)都进行了 BRAF V600 ± MLH1 启动子甲基化检测。此外,在符合主流基因检测条件的 14 名患者中,100% 都被转诊到 ANP 领导的遗传学服务机构。从最初的 MDM 讨论到开始基因检测的中位时间为 69 天,而从检测到获得结果的中位时间为 19 天。患者在 21 天内收到结果。MMR IHC检测通过识别dMMR肿瘤,提高了LS的检出率。然而,在资源有限的环境中,成功提供下游临床服务需要适当的后续管理。我们机构的经验证明了以ANP为主导的遗传性结直肠癌主流化治疗模式的可行性、效率和有效性。
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Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland.

Colorectal cancer (CRC) is a common cancer in Ireland. Of all CRCs, 2-4% are attributable to Lynch Syndrome (LS), the most common CRC predisposition syndrome. LS is caused by constitutional pathogenic variants (PVs) affecting mismatch repair (MMR) genes with resultant MMR protein deficiency (dMMR). Screening of all CRCs with MMR immunohistochemistry (IHC) testing is advocated to increase the detection of LS. However, successful implementation requires appropriate downstream management. In Ireland the traditional pathway involves referral to cancer genetics services to assess eligibility for genetic testing. Cancer genetics services in Ireland face many challenges in providing uniform access to timely healthcare with current wait times for assessment in excess of 1 year. An increasingly adopted pathway is that of mainstreaming, whereby genetic testing is managed locally by a multidisciplinary team member. Our institution therefore implemented an Advanced Nurse Practitioner (ANP)-led service with responsibility for the LS Diagnostic Pathway and mainstream genetic testing. Data was extracted from a prospectively maintained database of all newly diagnosed CRC patients discussed at our institutions CRC multidisciplinary meeting (MDM) between January 1st, 2023, and May 31st, 2024. MMR IHC testing was performed in 97.9% of the 385 patients diagnosed with CRC. The median time from histological confirmation of CRC to the availability of the MMR IHC report was 6 days. All 51 patients (100%) who required sequential tumor testing underwent BRAF V600 ± MLH1 promoter methylation testing. Additionally, 100% of the 14 patients eligible for mainstream genetic testing were referred to the ANP-led genetics service. The median time from the initial MDM discussion to the initiation of genetic testing was 69 days, while the median time from testing to the availability of results was 19 days. Patients received their results within a median of 21 days. MMR IHC testing increases the detection of LS through identification of dMMR tumours. Successful downstream delivery of clinical services, however, requires appropriate subsequent management, in a resource-limited environment. Our institutional experience demonstrates the feasibility, efficiency, and effectiveness of an ANP-led mainstreaming model of care for hereditary colorectal cancer.

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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.
期刊最新文献
A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic. Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework. Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service. BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants. Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome.
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