Unit of Nutrition, Environment and Cancer, Catalan Institute of Oncology (IDIBELL-ICO), Barcelona, Spain.
Int J Cancer. 2010 Dec 1;127(11):2654-60. doi: 10.1002/ijc.25273.
There are no established criteria to classify patients into high or low risk of progressing to gastric cancer (GC). The aim of the study was to identify predictors of GC occurrence among patients with gastric preneoplastic lesions. A prospective and retrospective follow-up study was carried out in a province in Spain with one of the highest risk of GC. The study included 478 patients who underwent gastric biopsy in 1988-1994 with diagnoses of normal mucosa, nonatrophic gastritis (NAG), non-metaplastic multifocal atrophic gastritis (MAG) and complete or incomplete intestinal metaplasia (IM) and who accepted to undergo a new biopsy during 2005-2007 or had an event during follow up. Inter- and intra-observer variability of histological diagnosis was assessed. Analysis was done using Cox proportional hazards risk (HR) models. The mean age of the patients was 50 years, 47% were males and the mean follow-up time was 12.8 years. During follow-up, 23 GC (4.8%) were diagnosed (21 adenocarcinomas and 2 lymphomas) with an incidence of 3.77 per 1,000 person per year. The incidence rate of GC for those with incomplete IM was 16.5 per 1,000 person years. Out the 21 adenocarcinomas, 16 had an incomplete IM in the baseline diagnosis. Incomplete IM (HR 11.3; 95% CI 3.8-33.9) and a family history of GC (HR 6.1; 95% CI 1.7-22.4) were the strongest risk factors for gastric adenocarcinoma. Subtyping of IM and family history of GC may be useful for the identification of high-risk patients who need more intensive surveillance.
目前尚无明确标准将患者分为胃癌(GC)进展的高风险或低风险人群。本研究旨在确定胃黏膜前病变患者发生 GC 的预测因素。在西班牙一个 GC 风险最高的省份进行了前瞻性和回顾性随访研究。该研究纳入了 478 名患者,他们于 1988-1994 年间接受了胃活检,诊断为正常黏膜、非萎缩性胃炎(NAG)、非化生多灶性萎缩性胃炎(MAG)和完全或不完全肠化生(IM),并同意在 2005-2007 年期间接受新的活检或在随访期间发生了事件。评估了组织学诊断的观察者间和观察者内变异性。采用 Cox 比例风险(HR)模型进行分析。患者的平均年龄为 50 岁,47%为男性,平均随访时间为 12.8 年。随访期间诊断出 23 例 GC(4.8%),包括 21 例腺癌和 2 例淋巴瘤,年发病率为每 1000 人 3.77 例。不完全 IM 的 GC 发病率为每 1000 人年 16.5 例。在 21 例腺癌中,有 16 例在基线诊断中存在不完全 IM。不完全 IM(HR 11.3;95%CI 3.8-33.9)和 GC 家族史(HR 6.1;95%CI 1.7-22.4)是胃腺癌的最强危险因素。IM 亚型和 GC 家族史可能有助于识别需要更强化监测的高危患者。