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CA19-9水平与血清γ-谷氨酰转移酶作为胰头癌患者潜在的预后生物标志物

CA19-9 Level to Serum γ-Glutamyltransferase as a Potential Prognostic Biomarker in Patients with Pancreatic Head Carcinoma.

作者信息

Lyu Shao-Cheng, Wang Jing, Huang Mengxiu, Wang Han-Xuan, Zhou Lin, He Qiang, Lang Ren

机构信息

Department of Hepatobiliary and Pancreaticosplenic Surgery, Beijing ChaoYang Hospital, Capital Medical University, Beijing, 100020, People's Republic of China.

出版信息

Cancer Manag Res. 2021 Jun 21;13:4887-4898. doi: 10.2147/CMAR.S313517. eCollection 2021.

DOI:10.2147/CMAR.S313517
PMID:34188542
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8232842/
Abstract

BACKGROUND

The aim of this study was to reduce the influence of biliary obstruction on carbohydrate antigen 19-9 level (CA19-9) by introducing the CA19-9 level to serum γ-glutamyltransferase (GGT) ratio as an indicator, and ultimately to reveal the correlation between CA19-9/GGT and the prognosis of patients with pancreatic head carcinoma (PHC).

METHODS

A total of 339 enrolled patients who underwent pancreatoduodenectomy for PHC in Beijing ChaoYang Hospital from January 2010 to December 2019 were analyzed retrospectively. The optimal cut-off value, according to which patients were divided into a low-ratio group (Group 1, n=179) and a high-ratio group (Group 2, n=160), was determined by the ROC curve obtained from preoperative CA19-9/GGT and 1-year survival. Through univariate and multivariate analyses, risk factors for postoperative tumor recurrence and long-term survival were screened out among PHC patients.

RESULTS

The best cut-off value of CA19-9/GGT was 2.07 (area under the curve=0.567, 95% CI 0.498-0.636). Compared with Group 2, Group 1 had lower CA19-9, and higher GGT, total bilirubin (TB) and lymph-node metastasis rate (<0.05). The 1-, 2- and 3-year disease-free survival rates of patients in Groups 1 and 2 were 68.2%, 42.5% and 28.2%, and 42.2%, 19.3% and 18.3%, respectively (=0.000), and the 1-, 2- and 3-year overall survival rates were 79.1%, 50.7% and 29.1%, and 56.7%, 22.2% and 17.2%, respectively (=0.000). Multivariate analysis showed that CA19-9/GGT, portal system invasion and lymph-node metastasis were independent risk factors for postoperative tumor recurrence and long-term survival among patients with PHC.

CONCLUSION

Compared with CA19-9 level alone, CA19-9/GGT plays a more precise role in the evaluation of postoperative tumor recurrence and the long-term prognosis of PHC patients. The lower the ratio, the better the long-term prognosis. The CA19-9/GGT ratio may prove to be a useful biomarker for identifying PHC patients at high risk of early recurrence and unfavorable prognosis.

摘要

背景

本研究旨在通过引入血清γ-谷氨酰转移酶(GGT)与糖类抗原19-9(CA19-9)水平的比值作为指标,降低胆道梗阻对CA19-9水平的影响,并最终揭示CA19-9/GGT与胰头癌(PHC)患者预后之间的相关性。

方法

回顾性分析2010年1月至2019年12月在北京朝阳医院接受胰十二指肠切除术治疗PHC的339例入组患者。根据术前CA19-9/GGT与1年生存率的ROC曲线确定最佳截断值,据此将患者分为低比值组(第1组,n = 179)和高比值组(第2组,n = 160)。通过单因素和多因素分析,筛选出PHC患者术后肿瘤复发和长期生存的危险因素。

结果

CA19-9/GGT的最佳截断值为2.07(曲线下面积 = 0.567,95% CI 0.498 - 0.636)。与第2组相比,第1组的CA19-9水平较低,GGT、总胆红素(TB)水平及淋巴结转移率较高(P < 0.05)。第1组和第2组患者的1年、2年和3年无病生存率分别为68.2%、42.5%和28.2%,以及42.2%、19.3%和18.3%(P = 0.000),1年、2年和3年总生存率分别为79.1%、50.7%和29.1%,以及56.7%、22.2%和17.2%(P = 0.000)。多因素分析显示,CA19-9/GGT、门静脉系统侵犯和淋巴结转移是PHC患者术后肿瘤复发和长期生存的独立危险因素。

结论

与单独的CA19-9水平相比,CA19-9/GGT在评估PHC患者术后肿瘤复发和长期预后方面发挥着更精确的作用。比值越低,长期预后越好。CA19-9/GGT比值可能是识别早期复发和预后不良高风险PHC患者的有用生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/cbacebdc7402/CMAR-13-4887-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/7399dce3c9d6/CMAR-13-4887-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/35a69f4e2f23/CMAR-13-4887-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/0dfa113f664c/CMAR-13-4887-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/cbacebdc7402/CMAR-13-4887-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/7399dce3c9d6/CMAR-13-4887-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/35a69f4e2f23/CMAR-13-4887-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/0dfa113f664c/CMAR-13-4887-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc54/8232842/cbacebdc7402/CMAR-13-4887-g0004.jpg

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