High pre-treatment static and dynamic alpha-fetoprotein values predict reduced overall survival in hepatocellular carcinoma.

Alpha-fetoprotein biomarker hepatocellular carcinoma prognosis survival

Journal

United European gastroenterology journal
ISSN: 2050-6414
Titre abrégé: United European Gastroenterol J
Pays: England
ID NLM: 101606807

Informations de publication

Date de publication:
23 Nov 2020
Historique:
entrez: 23 11 2020
pubmed: 24 11 2020
medline: 24 11 2020
Statut: aheadofprint

Résumé

Hepatocellular carcinoma is one of the most lethal cancers worldwide. Novel prognostic and/or predictive biomarkers are urgently needed to improve patient management. Alpha-fetoprotein is a well-established and widely used biomarker for hepatocellular carcinoma. However, diagnostic accuracy of static alpha-fetoprotein values is limited and the clinical potential is a matter of ongoing scientific discussion. We here evaluated the prognostic impact of pre-treatment static and dynamic alpha-fetoprotein variables on overall survival of hepatocellular carcinoma patients in a Western cohort. Patients with confirmed hepatocellular carcinoma ( High static and dynamic alpha-fetoprotein variables prior to therapy were associated with reduced survival rates of hepatocellular carcinoma patients. Several known clinical parameters such as Child-Pugh B ( Static and dynamic alpha-fetoprotein variables prior to therapy are predictive for overall survival of hepatocellular carcinoma patients. Addition of AFP-slope to established prognostic parameters might improve prognostic classification for a subgroup of hepatocellular carcinoma patients with preserved liver function and without portal vein tumour thrombosis.

Sections du résumé

BACKGROUND BACKGROUND
Hepatocellular carcinoma is one of the most lethal cancers worldwide. Novel prognostic and/or predictive biomarkers are urgently needed to improve patient management. Alpha-fetoprotein is a well-established and widely used biomarker for hepatocellular carcinoma. However, diagnostic accuracy of static alpha-fetoprotein values is limited and the clinical potential is a matter of ongoing scientific discussion.
OBJECTIVE OBJECTIVE
We here evaluated the prognostic impact of pre-treatment static and dynamic alpha-fetoprotein variables on overall survival of hepatocellular carcinoma patients in a Western cohort.
METHODS METHODS
Patients with confirmed hepatocellular carcinoma (
RESULTS RESULTS
High static and dynamic alpha-fetoprotein variables prior to therapy were associated with reduced survival rates of hepatocellular carcinoma patients. Several known clinical parameters such as Child-Pugh B (
CONCLUSION CONCLUSIONS
Static and dynamic alpha-fetoprotein variables prior to therapy are predictive for overall survival of hepatocellular carcinoma patients. Addition of AFP-slope to established prognostic parameters might improve prognostic classification for a subgroup of hepatocellular carcinoma patients with preserved liver function and without portal vein tumour thrombosis.

Identifiants

pubmed: 33226301
doi: 10.1177/2050640620972611
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2050640620972611

Auteurs

Carolin Czauderna (C)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.
Department of Medicine I, University Medical Centre Schleswig-Holstein - Campus Lübeck, Lübeck, Germany.

Irene Schmidtmann (I)

Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), Johannes Gutenberg University, Mainz, Germany.

Sandra Koch (S)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Lukas Pilz (L)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Sophia Heinrich (S)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Gerd Otto (G)

Department of General, Visceral and Transplant Surgery, Johannes Gutenberg University, Mainz, Germany.

Jens Mittler (J)

Department of General, Visceral and Transplant Surgery, Johannes Gutenberg University, Mainz, Germany.

Hauke Lang (H)

Department of General, Visceral and Transplant Surgery, Johannes Gutenberg University, Mainz, Germany.

Roman Kloeckner (R)

Department of Diagnostic and Interventional Radiology, Johannes Gutenberg University, Mainz, Germany.

Christoph Düber (C)

Department of Diagnostic and Interventional Radiology, Johannes Gutenberg University, Mainz, Germany.

Martin F Sprinzl (MF)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Marcus A Wörns (MA)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Peter R Galle (PR)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Jens U Marquardt (JU)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.
Department of Medicine I, University Medical Centre Schleswig-Holstein - Campus Lübeck, Lübeck, Germany.

Arndt Weinmann (A)

Department of Internal Medicine I, Johannes Gutenberg University, Mainz, Germany.

Classifications MeSH