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AKR1C4 的预后意义以及结合 EBV DNA 分层分析鼻咽癌患者局部区域复发高风险的优势。

Prognostic significance of AKR1C4 and the advantage of combining EBV DNA to stratify patients at high risk of locoregional recurrence of nasopharyngeal carcinoma.

机构信息

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.

Department of Nasopharyngeal Carcinoma, Sun Yat-Sen University Cancer Center, Guangzhou, China.

出版信息

BMC Cancer. 2022 Aug 11;22(1):880. doi: 10.1186/s12885-022-09924-3.

DOI:10.1186/s12885-022-09924-3
PMID:35953777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9373296/
Abstract

BACKGROUND

Distinguishing patients at a greater risk of recurrence is essential for treating locoregional advanced nasopharyngeal carcinoma (NPC). This study aimed to explore the potential of aldo-keto reductase 1C4 (AKR1C4) in stratifying patients at high risk of locoregional relapse.

METHODS

A total of 179 patients with locoregionally advanced NPC were grouped by different strategies; they were: (a) divided into two groups according to AKR1C4 expression level, and (b) classified into three clusters by integrating AKR1C4 and Epstein-Barr virus (EBV) DNA. The Kaplan-Meier method was used to calculate locoregional relapse-free survival (LRFS), overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival (DMFS). The Cox proportional hazards model was used to determine potential prognostic factors, and a nomogram was generated to predict 3-year and 5-year LRFS.

RESULTS

A significant difference in the 5-year LRFS was observed between the high and low AKR1C4 expression groups (83.3% vs. 92.7%, respectively; p = 0.009). After integrating AKR1C4 expression and EBV DNA, the LRFS (84.7%, 84.5%, 96.9%, p = 0.014) of high-, intermediate-, and low- AKR1C4 and EBV DNA was also significant. Multivariate analysis indicated that AKR1C4 expression (p = 0.006) was an independent prognostic factor for LRFS. The prognostic factors incorporated into the nomogram were AKR1C4 expression, T stage, and EBV DNA, and the concordance index of the nomogram for locoregional relapse was 0.718.

CONCLUSIONS

In conclusion, high AKR1C4 expression was associated with a high possibility of relapse in NPC patients, and integrating EBV DNA and AKR1C4 can stratify high-risk patients with locoregional recurrence.

摘要

背景

鉴别复发风险较高的患者对于治疗局部晚期鼻咽癌(NPC)至关重要。本研究旨在探索醛酮还原酶 1C4(AKR1C4)在分层局部区域复发高危患者中的潜在作用。

方法

共 179 例局部晚期 NPC 患者根据不同策略分组:(a)根据 AKR1C4 表达水平分为两组;(b)通过整合 AKR1C4 和 Epstein-Barr 病毒(EBV)DNA 将其分为三个聚类。采用 Kaplan-Meier 法计算局部区域无复发生存率(LRFS)、总生存率(OS)、无进展生存率(PFS)和无远处转移生存率(DMFS)。采用 Cox 比例风险模型确定潜在的预后因素,并生成预测 3 年和 5 年 LRFS 的列线图。

结果

高低 AKR1C4 表达组的 5 年 LRFS 差异有统计学意义(分别为 83.3%和 92.7%,p=0.009)。整合 AKR1C4 表达和 EBV DNA 后,高低 AKR1C4 和 EBV DNA 的 LRFS(84.7%、84.5%、96.9%,p=0.014)也具有显著差异。多因素分析表明,AKR1C4 表达(p=0.006)是 LRFS 的独立预后因素。纳入列线图的预后因素包括 AKR1C4 表达、T 分期和 EBV DNA,列线图局部区域复发的一致性指数为 0.718。

结论

高 AKR1C4 表达与 NPC 患者复发的可能性较高相关,整合 EBV DNA 和 AKR1C4 可分层局部区域复发的高危患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/fccd4381147b/12885_2022_9924_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/be5e2d16ac4e/12885_2022_9924_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/8317285de269/12885_2022_9924_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/75990fe92e63/12885_2022_9924_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/940747d2da52/12885_2022_9924_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/fccd4381147b/12885_2022_9924_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/be5e2d16ac4e/12885_2022_9924_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/8317285de269/12885_2022_9924_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/75990fe92e63/12885_2022_9924_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/940747d2da52/12885_2022_9924_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194e/9373296/fccd4381147b/12885_2022_9924_Fig5_HTML.jpg

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