Postoperative Trends and Prognostic Values of Inflammatory and Nutritional Biomarkers after Liver Transplantation for Hepatocellular Carcinoma.
controlling nutritional status
hepatocellular carcinoma
liver transplantation
neutrophil-to-lymphocyte ratio
platelet-to-lymphocyte ratio
prognostic nutritional index
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
29 Jan 2021
29 Jan 2021
Historique:
received:
30
12
2020
revised:
24
01
2021
accepted:
26
01
2021
entrez:
12
2
2021
pubmed:
13
2
2021
medline:
13
2
2021
Statut:
epublish
Résumé
Preoperative inflammatory biomarkers such as the Platelet-to-Lymphocyte Ratio (PLR) and the Neutrophil-to-Lymphocyte Ratio (NLR) strongly predict the outcome in surgically treated patients with hepatocellular carcinoma (HCC), while nutritional biomarkers such as the Controlling Nutritional Status (CONUT) and the Prognostic Nutritional Index (PNI) show an analogue prognostic value in hepatic resection (HR) but not in liver transplant (LT) cases. Data on the impact of LT on the inflammatory and nutritional/metabolic function are heterogeneous. Therefore, we investigated the post-LT trend of these biomarkers up to postoperative month (POM) 12 in 324 HCC patients treated with LT. Inflammatory biomarkers peaked in the early post-LT period but at POM 3 leveled off at values similar (NLR) or higher (PLR) than pre-LT ones. CONUT and PNI worsened in the early post-LT period, but at POM 3 they stabilized at significantly better values than pre-LT. In LT recipients with an overall survival >1 year and no evidence of early HCC recurrence, 1 year post-LT NLR and PNI independently predicted patient overall survival, while 1 year post-LT PLR independently predicted late tumor recurrence. In conclusion, at 1 year post-LT, the nutritional status of liver-transplanted HCC patients significantly improved while their inflammatory state tended to persist. Consequently, post-LT PLR and NLR maintained a prognostic value for LT outcome while post-LT CONUT and PNI acquired it.
Identifiants
pubmed: 33572776
pii: cancers13030513
doi: 10.3390/cancers13030513
pmc: PMC7866292
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
HPB (Oxford). 2018 Oct;20(10):888-895
pubmed: 29853431
Cancer Epidemiol Biomarkers Prev. 2014 Jul;23(7):1204-12
pubmed: 24793958
J Gastrointest Surg. 2017 Oct;21(10):1626-1634
pubmed: 28523484
Transplant Rev (Orlando). 2018 Jan;32(1):69-77
pubmed: 28501338
J Am Soc Nephrol. 2018 Jan;29(1):24-34
pubmed: 28993504
J Clin Lab Anal. 2018 Feb;32(2):
pubmed: 28378887
Clin Lab. 2019 Mar 1;65(3):
pubmed: 30868857
Asian J Surg. 2018 Jul;41(4):341-348
pubmed: 28365200
Gastroenterol Res Pract. 2016;2016:4743808
pubmed: 26843858
Clin Transplant. 2020 Mar;34(3):e13786
pubmed: 31957065
J Natl Cancer Inst. 2014 May 29;106(6):dju124
pubmed: 24875653
BMC Res Notes. 2017 Jan 3;10(1):12
pubmed: 28057051
Biomed Res Int. 2018 Nov 11;2018:2703518
pubmed: 30534554
World J Hepatol. 2019 Jan 27;11(1):50-64
pubmed: 30705718
Hepatobiliary Pancreat Dis Int. 2015 Dec;14(6):582-7
pubmed: 26663005
BMC Gastroenterol. 2019 Dec 9;19(1):211
pubmed: 31818259
Clin Transplant. 2019 Apr;33(4):e13495
pubmed: 30773726
J Surg Res. 2015 Apr;194(2):464-470
pubmed: 25577142
Transpl Int. 2014 Jan;27(1):32-41
pubmed: 24118272
World J Gastroenterol. 2018 Apr 21;24(15):1658-1665
pubmed: 29686473
PLoS One. 2014 Nov 06;9(11):e112361
pubmed: 25375150
Biomed Res Int. 2019 Oct 14;2019:7284040
pubmed: 31737675
Am J Surg. 2016 Jul;212(1):122-7
pubmed: 26421412
Liver Transpl. 2014 Nov;20(11):1327-35
pubmed: 25088400
PLoS One. 2018 Oct 12;13(10):e0202987
pubmed: 30312295
Cancers (Basel). 2019 Oct 15;11(10):
pubmed: 31618961
Clin Lab Med. 2019 Mar;39(1):73-85
pubmed: 30709510
Liver Int. 2019 Aug;39(8):1545-1556
pubmed: 30903725
Am J Surg. 2014 Oct;208(4):605-18
pubmed: 25118164
Cell Physiol Biochem. 2017;44(3):967-981
pubmed: 29179180
Curr Opin Clin Nutr Metab Care. 2018 Sep;21(5):381-387
pubmed: 29927763