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DOI 10.1097/md.0000000000025330

Медицинская библиотека · Medicine · 2021

High L1CAM expression predicts poor prognosis of patients with endometrial cancer: A systematic review and meta-analysis.

Guo Min, Gong Han, Nie Dan, Li Zhengyu

СтатьяМетаанализСистематический обзорПеревод пока не подготовлен

Аннотация

BACKGROUD: Previous studies have reported that the levels of L1 cell adhesion molecule (L1CAM) indicate poor prognosis of patients with various solid tumors. However, the prognostic significance of L1CAM in endometrial cancer has remained controversial. Herein, we conducted a systematic review and meta-analysis to evaluate the prognostic value of L1CAM in endometrial cancer.

METHODS

All studies related to the association between L1CAM expression and clinical characteristics of endometrial cancer were identified by searching the PubMed, MEDLINE, EMBASE, and Web of Science databases. Primary outcomes of the meta-analysis were the hazard ratios (HRs) for overall survival (OS) and disease-free survival (DFS). Secondary outcomes were odds ratios (ORs) for clinicopathological characteristics. Publication bias and sensitivity analysis were conducted to ensure reliability of the results.

RESULTS

Overall, 17 studies encompassing 7146 patients were eligible for the meta-analysis. Results showed L1CAM overexpression to be significantly associated with decreased overall survival (HR = 2.87, 95% CI; 1.81-4.55, P < .001) and disease-free survival (HR = 3.32, 95% CI; 1.99-5.55, P < .001) in patients with endometrial cancer. High L1CAM expression was also related to adverse clinicopathological characteristics.

CONCLUSION

This systematic review demonstrated that high L1CAM expression is correlated with poor survival outcomes and adverse clinicopathological parameters in patients with endometrial cancer.

Для цитирования: Guo Min, Gong Han, Nie Dan, Li Zhengyu. High L1CAM expression predicts poor prognosis of patients with endometrial cancer: A systematic review and meta-analysis.. Medicine. 2021. DOI: 10.1097/md.0000000000025330.

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