Zellenrath Pauline A, van Tilburg Laurelle, Pouw Roos E, Yadlapati Rena, Peters Yonne, Ujiki Michael B, Thota Prashanthi N, Ishimura Norihisa, Meltzer Stephen J, Peleg Noam, Choi Won-Tak, Reynolds John V, Polydorides Alexandros D, Koch Arjun D, Honing Judith, Spaander Manon C W
Division of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, the Netherlands.
Clin Gastroenterol Hepatol. 2025 Feb;23(2):225-235.e8. doi: 10.1016/j.cgh.2024.06.053. Epub 2024 Oct 5.
Females with Barrett's esophagus (BE) have a lower risk of neoplastic progression than males, but sufficiently powered risk analyses are lacking. This systematic review and meta-analysis of individual patient data (IPD) aimed to provide more robust evidence on neoplastic progression risk in females.
We conducted a systematic literature search of 3 electronic databases (Medline, Embase, Google Scholar) from inception until August 2023. Eligible studies (1) reported original data on progression from nondysplastic BE, indefinite for dysplasia, or low-grade dysplasia to high-grade dysplasia or esophageal adenocarcinoma; and (2) included female and male patients. IPD were quality controlled by 2 independent reviewers. The primary outcome was the association between sex and neoplastic progression risk, adjusted for risk factors using multivariable Cox regression analysis. Secondary outcomes were sex differences in time to progression and annual progression rate.
IPD were obtained from 11 of 66 eligible studies, including 2196 (31%) females. Neoplastic progression risk was lower in females (hazard ratio for males vs females, 1.44; 95% confidence interval, 1.13-1.82) after adjusting for age, smoking, medication use, hiatal hernia, BE length, and baseline pathology. The annual progression rate was 0.88% in females vs 1.29% in males. Time to progression was similar in both sexes: 3.7 years (interquartile range, 2.1-7.7 years) in females and 4.2 years (interquartile range, 2.0-8.1 years) in males.
Although females had a lower neoplastic progression risk, sex differences were smaller than previously reported, and time to progression was similar for both sexes. Future research should focus on other factors than sex to identify low- and high-risk BE patients.
患有巴雷特食管(BE)的女性发生肿瘤进展的风险低于男性,但缺乏足够有力的风险分析。这项对个体患者数据(IPD)的系统评价和荟萃分析旨在为女性肿瘤进展风险提供更有力的证据。
我们对3个电子数据库(Medline、Embase、谷歌学术)从创建到2023年8月进行了系统的文献检索。符合条件的研究:(1)报告了从无发育异常的BE、发育异常不明确或低级别发育异常进展为高级别发育异常或食管腺癌的原始数据;(2)纳入了女性和男性患者。IPD由2名独立的审阅者进行质量控制。主要结局是性别与肿瘤进展风险之间的关联,使用多变量Cox回归分析对风险因素进行校正。次要结局是进展时间和年度进展率的性别差异。
从66项符合条件的研究中的11项获得了IPD,其中包括2196名(31%)女性。在对年龄、吸烟、药物使用、食管裂孔疝、BE长度和基线病理进行校正后,女性的肿瘤进展风险较低(男性与女性的风险比,1.44;95%置信区间,1.13 - 1.82)。女性的年度进展率为0.88%,男性为1.29%。两性的进展时间相似:女性为3.7年(四分位间距,2.1 - 7.7年),男性为4.2年(四分位间距,2.0 - 8.1年)。
尽管女性的肿瘤进展风险较低,但性别差异比之前报道的要小,且两性的进展时间相似。未来的研究应关注性别以外的其他因素,以识别低风险和高风险的BE患者。