Maric Leyla, Castaneda Daniel, Singh Harjinder, Bejarano Pablo, Jimenez Cantisano Brenda, Castro Fernando J
Digestive Disease Institute, Cleveland Clinic Florida, 2950 Cleveland Clinic Blvd, 2nd Floor, Weston, FL, 33331, USA.
Department of Pathology, Cleveland Clinic Florida, Weston, FL, 33331, USA.
Dig Dis Sci. 2022 Aug;67(8):4092-4099. doi: 10.1007/s10620-021-07212-x. Epub 2021 Aug 18.
Gastric cancer is a leading cause of morbidity and mortality worldwide. Gastric intestinal metaplasia (GIM) has been described as a key histologic step in the development of gastric adenocarcinoma. However, not all people with GIM develop malignancy. We studied the factors associated with progression to dysplasia and advanced gastric neoplasia (aGN) in patients with baseline GIM.
Retrospective cohort analysis of patients with baseline GIM and subsequent endoscopic evaluation at Cleveland Clinic Florida and Ohio Main Campus between 2005 and 2017. Demographic and exposure risk factors, as well as Kimura-Takemoto classification (KTc), were used as variables for hazards ratio (HR) and Kaplan-Meier survival-free analysis for aGN and any form of dysplasia progression.
There were 708 patients identified with GIM; 29 patients (4.1%) progressed to any degree of dysplasia. From these, LGD was present in 12 cases (1.7%), HGD in 4 cases (0.6%), and gastric cancer in 13 cases (1.8%), for a total of 17 aGN cases. KTc was associated with dysplasia and aGN progression (p < 0.001), and no cases progressed if KTc findings were absent. Open-type KTc was associated with aGN (HR 6.36, p < 0.001) and any dysplasia progression (HR 13.34, p < 0.001) compared to closed-type or absent KTc features. No other factors were associated with aGN or dysplasia progression. Open-type KTc was also associated with shorter cancer survival-free progression.
Patients with baseline GIM present a higher progression risk to aGN, dysplasia, or cancer if concomitant KTc findings are present, particularly an open-type KTc pattern.
胃癌是全球发病和死亡的主要原因。胃小肠化生(GIM)被认为是胃腺癌发生过程中的关键组织学步骤。然而,并非所有GIM患者都会发生恶性病变。我们研究了基线GIM患者进展为发育异常和晚期胃肿瘤(aGN)的相关因素。
对2005年至2017年在佛罗里达克利夫兰诊所和俄亥俄州主校区接受基线GIM检查及后续内镜评估的患者进行回顾性队列分析。人口统计学和暴露风险因素,以及木村 - 竹本分类(KTc),被用作风险比(HR)以及aGN和任何形式发育异常进展的Kaplan - Meier无生存分析的变量。
共识别出708例GIM患者;29例(4.1%)进展为任何程度的发育异常。其中,低级别上皮内瘤变(LGD)12例(1.7%),高级别上皮内瘤变(HGD)4例(0.6%),胃癌13例(1.8%),aGN病例共17例。KTc与发育异常和aGN进展相关(p < 0.001),若KTc检查结果为阴性则无病例进展。与闭合型或无KTc特征相比,开放型KTc与aGN(HR 6.36,p < 0.001)和任何发育异常进展(HR 13.34,p < 0.001)相关。没有其他因素与aGN或发育异常进展相关。开放型KTc也与较短的无癌生存进展相关。
如果同时存在KTc检查结果,特别是开放型KTc模式,基线GIM患者进展为aGN、发育异常或癌症的风险更高。