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乳酸脱氢酶是索拉非尼治疗的肝细胞癌患者的预后指标:乙肝流行地区的真实临床实践结果

Lactate dehydrogenase is a prognostic indicator in patients with hepatocellular carcinoma treated by sorafenib: results from the real life practice in HBV endemic area.

作者信息

Li Mu-Xing, Zhao Hong, Bi Xin-Yu, Li Zhi-Yu, Yao Xue-Song, Li Huai, Huang Zhen, Han Yue, Zhou Jian-Guo, Zhao Jian-Jun, Zhang Ye-Fan, Zhao Dong-Bin, Cai Jian-Qiang

机构信息

Department of Abdominal Surgical Oncology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing 100021, P. R. China.

Department of Interventional Therapies, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing 100021, P. R. China.

出版信息

Oncotarget. 2016 Dec 27;7(52):86630-86647. doi: 10.18632/oncotarget.13428.

DOI:10.18632/oncotarget.13428
PMID:27880930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5349941/
Abstract

PURPOSE

Lactate dehydrogenase (LDH), which was an indirect marker of hypoxia, was a potentially prognostic factor in several malignancies. There is a lack of evidence about the prognostic value of serum LDH level in patients with hepatocellular carcinoma (HCC) receiving sorafenib treatment from hepatitis B virus endemic areas.

MATERIALS AND METHODS

A total of 119 HBV-related HCC patients treated by sorafenib from a Chinese center were included into the study. They were categorized into 2 groups according to the cut-off value of pre-treatment LDH, which was determined by the time dependent receiver operating characteristics (ROC) curve for the overall survival. The prognostic value of LDH was evaluated. The relationships between LDH and other clinicopathological factors were also assessed.

RESULTS

The cut-off value was 221 U/L. With a median follow up of 15 (range, 3-73) months, 91 patients reached the endpoint. Multivariate analysis proved that pre-treatment serum LDH level was an independent prognostic factor for both overall survival (OS) and progression-free survival (PFS). For patients whose pre-treatment LDH ≥ 221 U/L, increased LDH value after 3 months of sorafenib treatment predicted inferior OS and PFS. And patients with elevated pre-treatment LDH level predisposed to be featured with lower serum albumin, presence of macroscopic vascular invasion, advanced Child-Pugh class, advanced T category, higher AFP, and higher serum total bilirubin.

CONCLUSIONS

Serum LDH level was a potentially prognostic factor in HCC patients treated by sorafenib in HBV endemic area. More relevant studies with reasonable study design are needed to further strengthen its prognostic value.

摘要

目的

乳酸脱氢酶(LDH)作为缺氧的间接标志物,是多种恶性肿瘤潜在的预后因素。对于来自乙肝病毒流行地区、接受索拉非尼治疗的肝细胞癌(HCC)患者,血清LDH水平的预后价值尚缺乏证据。

材料与方法

本研究纳入了来自中国某中心的119例接受索拉非尼治疗的HBV相关HCC患者。根据治疗前LDH的临界值将他们分为两组,该临界值由总生存时间依赖性受试者工作特征(ROC)曲线确定。评估LDH的预后价值,并分析LDH与其他临床病理因素之间的关系。

结果

临界值为221 U/L。中位随访时间为15(3 - 73)个月,91例患者达到终点。多因素分析表明,治疗前血清LDH水平是总生存(OS)和无进展生存(PFS)的独立预后因素。对于治疗前LDH≥221 U/L的患者,索拉非尼治疗3个月后LDH值升高预示着较差的OS和PFS。治疗前LDH水平升高的患者更容易出现血清白蛋白降低、存在肉眼可见的血管侵犯、Child-Pugh分级 advanced、T分期 advanced、甲胎蛋白升高以及血清总胆红素升高。

结论

在HBV流行地区,血清LDH水平是接受索拉非尼治疗的HCC患者潜在的预后因素。需要更多设计合理的相关研究来进一步强化其预后价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/614eb96f5f6a/oncotarget-07-86630-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/7220ce170fbb/oncotarget-07-86630-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/cc257b91a9fb/oncotarget-07-86630-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/6bdc848b228a/oncotarget-07-86630-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/2e96abca63fe/oncotarget-07-86630-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/e7e75f3641a6/oncotarget-07-86630-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/e9ede2fc23d4/oncotarget-07-86630-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/614eb96f5f6a/oncotarget-07-86630-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/7220ce170fbb/oncotarget-07-86630-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/cc257b91a9fb/oncotarget-07-86630-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/6bdc848b228a/oncotarget-07-86630-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/2e96abca63fe/oncotarget-07-86630-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/e7e75f3641a6/oncotarget-07-86630-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/e9ede2fc23d4/oncotarget-07-86630-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27d3/5349941/614eb96f5f6a/oncotarget-07-86630-g007.jpg

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