通过内镜筛查识别 CDH1 基因致病变异携带者的标志环细胞胃癌病灶

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Lady Katherine Mejia Perez, Margaret O’Malley, Arjun Chatterjee, Ruishen Lyu, Qijun Yang, Michael W. Cruise, Lisa LaGuardia, David Liska, Carole Macaron, R. Matthew Walsh, Carol A. Burke
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引用次数: 0

摘要

确定接受胃切除术的 CDH1 致病变异型(PV)患者术前通过上消化道内窥镜(EGD)发现标志环癌细胞(SRC)的情况。评估选择监测的患者发展为晚期弥漫性胃癌(DGC)的情况。指南建议对 18 至 40 岁之间有 DGC 家族史的 CDH1 PV 携带者进行预防性全胃切除术 (pTG)。对于无 SRC 且无 DGC 家族史的携带者,建议每年按照既定方案进行胃食管造影和活检,并考虑进行 pTG。对无症状的 CDH1 PV 患者进行回顾性分析,并进行≥1 次监测性胃肠道造影。结果包括术前经胃食管造影检查发现的 SRC、手术分期,以及选择经胃食管造影监测的患者进展为晚期 DGC 的情况。48 例 CDH1 PV 患者接受了≥ 1 次胃肠造影检查。24/48(50%)例患者接受了胃切除术,其中 7 例患者接受了 pTG。21/24(87.5%)例患者的胃切除术标本中检测到 SRCC。17/21例胃切除术标本中有SRCC的患者通过胃肠道造影发现了SRC(灵敏度为81%,17/21例)。所有癌症均为pT1a期。其余 17 名患者(50% 有胃癌家族史)继续接受每年一次的胃肠道造影监测,中位随访时间为 34.6 个月。未诊断出 SRCC 或晚期 DGC。在中位随访 3 年的内镜项目中,随机活检中未发现 SRCC 的 CDH1 PV 携带者发展为晚期 DGC。从短期来看,在转诊中心有经验的医生手中,EGD 监测可能是立即进行 pTG 的安全替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Endoscopic screening for identification of signet ring cell gastric cancer foci in carriers of germline pathogenic variants in CDH1

Endoscopic screening for identification of signet ring cell gastric cancer foci in carriers of germline pathogenic variants in CDH1

To determine the preoperative detection of signet ring cancer cells (SRC) on upper endoscopy (EGD) in patients with CDH1 pathogenic variant (PV) undergoing gastrectomy. To evaluate the development of advanced diffuse gastric cancer (DGC) in patients choosing surveillance. Guidelines recommend prophylactic total gastrectomy (pTG) in CDH1 PV carriers with family history of DGC between 18 and 40 years. Annual EGD with biopsies according to established protocols is recommended in carriers with no SRC and no family history of DGC, with consideration of pTG. Retrospective analysis of asymptomatic patients with CDH1 PVs with ≥ 1 surveillance EGD. Outcomes included pre-operative EGD detection of SRC, surgical stage, and progression to advanced DGC in those electing surveillance with EGD. 48 patients with CDH1 PVs who had ≥ 1 EGD were included. 24/ 48 (50%) underwent gastrectomy, including pTG in 7 patients. SRCC were detected on gastrectomy specimen in 21/24 (87.5%). SRCs were identified by EGD in 17/21 patients who had SRCC on gastrectomy specimens (sensitivity 81%, 17/21). All cancers were stage pT1a. The remaining 17 patients (50% with a family history of gastric cancer) continue in annual EGD surveillance with a median follow-up of 34.6 months. No SRCC or advanced DGC have been diagnosed. No CDH1 PV carriers without SRCC on random biopsies followed in an endoscopic program developed advanced DGC over a median follow up of 3 years. In the short term, EGD surveillance might be a safe alternative to immediate pTG in experienced hands in referral centers.

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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.
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