Predictors of neoplastic progression in gastroesophageal lesions indefinite for dysplasia.

IF 3.9 2区 医学 Q2 CELL BIOLOGY
Histopathology Pub Date : 2025-03-25 DOI:10.1111/his.15449
Valentina Angerilli, Francesca Galuppini, Stefano Brignola, Gianluca Businello, Beatrice Filippin, Gianmaria Pennelli, Jessica Gasparello, Paola Parente, Angelo Paolo Dei Tos, Stefano Realdon, Alberto Fantin, Edoardo Vincenzo Savarino, Matteo Fassan
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引用次数: 0

Abstract

Aims: Current understanding of the risk of neoplastic progression in patients with Barrett's esophagus with indefinite for dysplasia (BE-IND) and gastric indefinite for dysplasia (G-IND) remains limited. This study aims to identify prognostic histological and clinicopathological factors for IND progression in the upper gastrointestinal tract.

Methods and results: Patients with confirmed BE-IND and G-IND, no previous evidence of dysplasia/cancer and follow-up of ≥ 6 months were included. The rate of neoplastic progression was calculated and the multivariate Cox regression model adjusted for demographic and histological features was used to identify risk factors for progression. A total of 719 patients diagnosed with IND (158 BE-IND and 561 G-IND) were identified, 395 of whom were excluded. Progression rates were 4.4 per 100 person-year for BE-IND and 1.6 per 100 person-year for G-IND patients. Progression was observed only in IND of hyperproliferative intestinal metaplasia (HIM) type. Operative link for gastritis assessment (OLGA) stage (III-IV versus 0-II) was the only significant predictor of G-IND progression [hazard ratio (HR) = 47.82, confidence interval (CI) = 5%: 6.24-366.37, P < 0.001]. In BE-IND patients, lack of interval endoscopy significantly increased the risk for BE-IND (HR = 13.45, CI = 95%: 1.24-145.75, P = 0.032).

Conclusion: IND is a challenging diagnosis for pathologists and implies an increased risk for neoplasia, especially in BE patients, without providing definitive information for patient management. This study highlights that neoplastic progression of IND lesions is primarily associated with HIM type. For BE-IND, interval endoscopy significantly reduces progression risk, while in G-IND, OLGA staging (III-IV) is a strong predictor of progression. These findings emphasise the importance of identifying HIM and using OLGA staging in G-IND for better risk stratification and follow-up strategies.

胃食管病变肿瘤进展的预测因素不确定的不典型增生。
目的:目前对Barrett食管不明确不典型增生(BE-IND)和胃不明确不典型增生(G-IND)患者肿瘤进展风险的了解仍然有限。本研究旨在确定IND在上胃肠道进展的预后组织学和临床病理因素。方法和结果:纳入确诊BE-IND和G-IND患者,既往无发育不良/癌症证据,随访≥6个月。计算肿瘤进展率,并使用调整人口统计学和组织学特征的多变量Cox回归模型来确定进展的危险因素。共发现719例IND患者(158例BE-IND和561例G-IND),其中395例被排除在外。BE-IND患者的进展率为4.4 / 100人/年,G-IND患者为1.6 / 100人/年。仅在HIM型的IND中观察到进展。胃炎评估(OLGA)阶段(III-IV vs 0-II)的手术联系是G-IND进展的唯一显著预测因素[风险比(HR) = 47.82,置信区间(CI) = 5%: 6.24-366.37, P]结论:IND对病理学家来说是一个具有挑战性的诊断,意味着肿瘤发生的风险增加,特别是在BE患者中,没有为患者管理提供明确的信息。本研究强调,IND病变的肿瘤进展主要与HIM类型有关。对于BE-IND,间隔内窥镜检查可显著降低进展风险,而对于G-IND, OLGA分期(III-IV)是进展的有力预测因子。这些发现强调了在G-IND中识别HIM和使用OLGA分期对于更好的风险分层和随访策略的重要性。
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来源期刊
Histopathology
Histopathology 医学-病理学
CiteScore
10.20
自引率
4.70%
发文量
239
审稿时长
1 months
期刊介绍: Histopathology is an international journal intended to be of practical value to surgical and diagnostic histopathologists, and to investigators of human disease who employ histopathological methods. Our primary purpose is to publish advances in pathology, in particular those applicable to clinical practice and contributing to the better understanding of human disease.
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