Park Gyerim, Park Se Jun, Kim Younghoon
Department of Hospital Pathology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Division of Medical Oncology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Front Oncol. 2024 Nov 20;14:1453906. doi: 10.3389/fonc.2024.1453906. eCollection 2024.
Claudin18.2 has been established as a putative therapeutic target in human solid malignancies. The aim of this study is to determine claudin18.2 expression as a clinicopathological and prognostic factor in human solid tumors through a systematic review and meta-analysis. Articles were systematically reviewed for studies that included the correlation between claudin18.2 expression and clinicopathological features and prognosis in solid tumors. Meta-analysis was conducted to estimate either odds ratio and 95% confidence intervals (CIs) of clinicopathological factors or hazard ratio and 95% CIs of survival outcomes for claudin18.2 expression in all available solid tumors.
21 studies including 5,331 patients were identified. Overall proportion of claudin18.2 positivity was 29.7%. Analyses of clinicopathological features demonstrated that claudin18.2 positivity correlated with male predominance, lower T stage, more frequent MUC5AC positivity when all primary tumors included. In subgroup analysis, gastric cancer showed significant correlation between high claudin18.2 expression and frequent EBV infection, male predominance and lower T stage. In lung cancer, claudin18.2 expression was associated with favorable overall survival. However, analyses of survival outcomes in all solid tumors showed that claudin18.2 expression was not associated with overall survival and pooled disease-free survival, tumor-specific survival, progression-free survival and relapse-free survival.
Our study emphasizes evaluation of claudin18.2 expression as a potential prognostic factor in lung adenocarcinoma and further exploration in other solid tumors as well.
https://www.crd.york.ac.uk/prospero/, identifier CRD42023468651.
Claudin18.2已被确立为人类实体恶性肿瘤的一个潜在治疗靶点。本研究的目的是通过系统评价和荟萃分析,确定Claudin18.2表达作为人类实体瘤的临床病理和预后因素。系统检索了包括Claudin18.2表达与实体瘤临床病理特征及预后之间相关性的研究。进行荟萃分析以估计所有可用实体瘤中Claudin18.2表达的临床病理因素的优势比和95%置信区间(CIs)或生存结局的风险比和95% CIs。
确定了21项研究,共5331例患者。Claudin18.2阳性的总体比例为29.7%。临床病理特征分析表明,当纳入所有原发性肿瘤时,Claudin18.2阳性与男性占优势、较低的T分期、更频繁的MUC5AC阳性相关。在亚组分析中,胃癌显示Claudin18.2高表达与频繁的EBV感染、男性占优势和较低的T分期之间存在显著相关性。在肺癌中,Claudin18.2表达与良好的总生存期相关。然而,对所有实体瘤生存结局的分析表明,Claudin18.2表达与总生存期、合并的无病生存期、肿瘤特异性生存期、无进展生存期和无复发生存期无关。
我们的研究强调评估Claudin18.2表达作为肺腺癌潜在预后因素的作用,并在其他实体瘤中进一步探索。