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血浆 Epstein-Barr 病毒微小 RNA BART8-3p 作为鼻咽癌的诊断和预后生物标志物。

Plasma Epstein-Barr Virus MicroRNA BART8-3p as a Diagnostic and Prognostic Biomarker in Nasopharyngeal Carcinoma.

机构信息

Department of Radiation Oncology, Fujian Medical University Cancer Hospital & Fujian Cancer Hospital, Fuzhou, People's Republic of China.

The School of Clinical Medicine and Fujian Medical University, Fuzhou, People's Republic of China.

出版信息

Oncologist. 2022 Apr 5;27(4):e340-e349. doi: 10.1093/oncolo/oyac024.

DOI:10.1093/oncolo/oyac024
PMID:35380720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8982379/
Abstract

BACKGROUND

Nasopharyngeal carcinoma is an Epstein-Barr virus (EBV)-associated tumor that is highly common in southern China. Our previous sequencing data demonstrated that the EBV-encoded microRNA BART8-3p was most upregulated in nasopharyngeal carcinoma (NPC) and was closely associated with the metastasis of NPC. However, the values of plasma BART8-3p in NPC patients have not yet been well characterized.

MATERIAL AND METHODS

We quantified plasma BART8-3p expression by quantitative real-time PCR in 205 newly diagnosed NPC patients. Kaplan-Meier analysis was used to compare overall survival (OS), distant metastasis-free survival (DMFS), and locoregional relapse-free survival (LRRFS) between the groups.

RESULTS

Plasma pretreatment BART8-3p was highly expressed in NPC patients compared with healthy controls. Pretreatment BART8-3p yielded a 92% predictive value for detecting NPC. Importantly, BART8-3p decreased dramatically after therapy relative to pretreatment levels. High levels of pretreatment or post-treatment BART8-3p were associated with worse OS, DMFS, and LRRFS. Multivariate analysis showed that high pretreatment or post-treatment BART8-3p was an independent unfavorable prognostic marker for OS (HR 3.82, 95% CI 1.77-8.24, P = .001 or HR 2.74, 95% CI 1.27-5.91, P = .010), DMFS (HR 2.82, 95% CI 1.36-5.85, P = .005 or HR 3.27, 95% CI 1.57-6.81, P = .002), and LRRFS (HR 1.94, 95% CI 1.12-3.35, P = .018 or HR 2.03, 95% CI 1.14-3.62, P = .016) in NPC. Subgroup analysis revealed that for patients with locally advanced NPC with high levels of pretreatment BART8-3p (n = 58), more cycles of chemotherapy (≥6 cycles) tended to prolong OS (P = .070). Over 50% (6/11) patients with high levels of post-treatment BART8-3p presented distant metastasis.

CONCLUSION

Plasma BART8-3p is a promising biomarker for the detection and prognosis of NPC.

摘要

背景

鼻咽癌是一种 Epstein-Barr 病毒(EBV)相关肿瘤,在中国南方地区非常常见。我们之前的测序数据表明,EBV 编码的 microRNA BART8-3p 在鼻咽癌(NPC)中上调最为明显,并且与 NPC 的转移密切相关。然而,NPC 患者血浆 BART8-3p 的价值尚未得到很好的描述。

材料和方法

我们通过定量实时 PCR 定量了 205 例新诊断 NPC 患者的血浆 BART8-3p 表达。使用 Kaplan-Meier 分析比较了两组之间的总生存期(OS)、无远处转移生存期(DMFS)和局部区域无复发生存期(LRRFS)。

结果

与健康对照组相比,NPC 患者的血浆预处理 BART8-3p 表达水平较高。预处理 BART8-3p 对 NPC 的检测具有 92%的预测价值。重要的是,与预处理水平相比,治疗后 BART8-3p 水平显著降低。高预处理或治疗后 BART8-3p 水平与较差的 OS、DMFS 和 LRRFS 相关。多变量分析表明,高预处理或治疗后 BART8-3p 是 OS(HR 3.82,95%CI 1.77-8.24,P=0.001 或 HR 2.74,95%CI 1.27-5.91,P=0.010)、DMFS(HR 2.82,95%CI 1.36-5.85,P=0.005 或 HR 3.27,95%CI 1.57-6.81,P=0.002)和 LRRFS(HR 1.94,95%CI 1.12-3.35,P=0.018 或 HR 2.03,95%CI 1.14-3.62,P=0.016)的独立不良预后标志物。亚组分析表明,对于高水平预处理 BART8-3p(n=58)的局部晚期 NPC 患者,更多周期的化疗(≥6 个周期)可能延长 OS(P=0.070)。6/11 例高水平治疗后 BART8-3p 患者出现远处转移。

结论

血浆 BART8-3p 是 NPC 检测和预后的有前途的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/078ce98d65d1/oyac024f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/a1067546e123/oyac024f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/9f5acef6a95f/oyac024f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/836b73463b48/oyac024f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/078ce98d65d1/oyac024f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/a1067546e123/oyac024f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/9f5acef6a95f/oyac024f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/836b73463b48/oyac024f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9973/8982379/078ce98d65d1/oyac024f0004.jpg

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