The AST/ALT Ratio Is an Independent Prognostic Marker for Disease-free Survival in Stage II and III Colorectal Carcinoma.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 31 10 2020
accepted: 17 11 2020
entrez: 9 1 2021
pubmed: 10 1 2021
medline: 26 1 2021
Statut: ppublish

Résumé

The Aspartate aminotransaminase/Alanine aminotransaminase ratio (AST/ALT ratio) has been identified as a prognostic marker for several malignancies. In this study, we evaluated the prognostic value of the AST/ALT ratio in a large cohort of non-metastatic colorectal cancer patients (CRC). A total of 536 patients with stage II and III CRC, as well as available AST/ALT ratio were included in this single-center retrospective analysis. Laboratory data were measured within two weeks before histological tumor diagnosis. Co-Primary endpoints for this analysis were disease-free survival (DFS) and overall survival (OS). In univariate cox regression DFS was significantly shorter in patients with an elevated AST/ALT ratio (HR=1.568, 95%CI=1.10-2.23, p=0.012). In multivariable analysis, the prognostic association between an elevated AST/ALT ratio and a poor survival prevailed statistically significant (HR=1.53, 95%C=1.05-2.22, p=0.026). No statistically significant association between the AST/ALT ratio and OS was observed (HR=1.4, 95% CI=0.89-2.22, p=0.14). In this study, the serum AST/ALT ratio emerged as a valid prognostic marker for DFS in non-metastatic colorectal cancer patients at stage II and III.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
The Aspartate aminotransaminase/Alanine aminotransaminase ratio (AST/ALT ratio) has been identified as a prognostic marker for several malignancies. In this study, we evaluated the prognostic value of the AST/ALT ratio in a large cohort of non-metastatic colorectal cancer patients (CRC).
PATIENTS AND METHODS METHODS
A total of 536 patients with stage II and III CRC, as well as available AST/ALT ratio were included in this single-center retrospective analysis. Laboratory data were measured within two weeks before histological tumor diagnosis. Co-Primary endpoints for this analysis were disease-free survival (DFS) and overall survival (OS).
RESULTS RESULTS
In univariate cox regression DFS was significantly shorter in patients with an elevated AST/ALT ratio (HR=1.568, 95%CI=1.10-2.23, p=0.012). In multivariable analysis, the prognostic association between an elevated AST/ALT ratio and a poor survival prevailed statistically significant (HR=1.53, 95%C=1.05-2.22, p=0.026). No statistically significant association between the AST/ALT ratio and OS was observed (HR=1.4, 95% CI=0.89-2.22, p=0.14).
CONCLUSION CONCLUSIONS
In this study, the serum AST/ALT ratio emerged as a valid prognostic marker for DFS in non-metastatic colorectal cancer patients at stage II and III.

Identifiants

pubmed: 33419840
pii: 41/1/429
doi: 10.21873/anticanres.14792
doi:

Substances chimiques

Biomarkers, Tumor 0
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

429-436

Informations de copyright

Copyright© 2021, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Lukas Scheipner (L)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

Maria Anna Smolle (MA)

Department of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.

Dominik Barth (D)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

Florian Posch (F)

Division of Oncology, Department of Internal Medicine, Graz, Austria.
Center for Biomarker Research in Medicine, Graz, Austria.

Michael Stotz (M)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

Martin Pichler (M)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

Herbert StÖger (H)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

Armin Gerger (A)

Division of Oncology, Department of Internal Medicine, Graz, Austria; armin.gerger@medunigraz.at.
Center for Biomarker Research in Medicine, Graz, Austria.

Jakob Michael Riedl (JM)

Division of Oncology, Department of Internal Medicine, Graz, Austria.

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Classifications MeSH