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Lymphovascular space invasion in endometrial carcinoma: A prognostic factor independent from molecular signature

医学 内科学 肿瘤科 子宫内膜癌 淋巴血管侵犯 多元分析 置信区间 荟萃分析 辅助治疗 癌症 转移
作者
Antonio Raffone,Antonio Travaglino,Diego Raimondo,Daniele Neola,Manuela Maletta,Angela Santoro,Luigi Insabato,Paolo Casadio,Francesco Fanfani,Gian Franco Zannoni,Fulvio Zullo,Renato Seracchioli,Antonio Mollo
出处
期刊:Gynecologic Oncology [Elsevier]
卷期号:165 (1): 192-197 被引量:51
标识
DOI:10.1016/j.ygyno.2022.01.013
摘要

Abstract

Background

The 2020 ESGO/ESTRO/ESP guidelines stratify the prognosis of endometrial carcinoma (EC) patients combining The Cancer Genome ATLAS (TCGA) molecular signature and pathological factors, including lymphovascular space invasion (LVSI). However, little is known about the prognostic independence of LVSI from molecular signature.

Aim

To assess whether the prognostic value of LVSI is independent from the TCGA signature.

Material and methods

A systematic review and meta-analysis was performed by searching 5 electronic databases from their inception to March 2021. All peer-reviewed studies reporting assessing LVSI as a prognostic factor independent from the TCGA groups in EC were included. Multivariate HRs with 95% confidence interval (CI) were pooled separately for overall survival (OS), disease-specific survival (DSS) and disease-free survival (DFS). The absence of LVSI was considered as a reference. In DFS analyses, locoregional and distant recurrence were separately considered for one study.

Results

Six studies with 3331 patients were included in the systematic review and three studies with 2276 patients in the meta-analysis. LVSI showed a pooled multivariate HR of 1.818 (CI 95%, 1.378–2.399) for OS, 1.849 (CI 95%, 1.194–2.863) for DSS, 1.377 (CI 95%, 1.008–1.880) for DFS excluding one study, 1.651 (CI 95%, 1.044–2.611) for DFS additionally considering locoregional recurrence from one study, and 1.684 (CI 95%, 1.05–2.701) for DFS additionally considering distant recurrence from the same study.

Conclusion

LVSI has a prognostic value independent of TCGA signature, as well as age and adjuvant treatment, increasing the risk of death of any cause, death due to EC and recurrent or progressive disease by 1.5–2 times.
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