On-treatment serum albumin level can guide long-term treatment in patients with cirrhosis and uncomplicated ascites.
Ascites
/ etiology
Biological Products
/ administration & dosage
Biomarkers, Pharmacological
/ analysis
Drug Monitoring
/ methods
Female
Humans
Intention to Treat Analysis
Liver Cirrhosis
/ blood
Long-Term Care
/ methods
Male
Middle Aged
Predictive Value of Tests
Serum Albumin
/ analysis
Serum Albumin, Human
/ administration & dosage
Survival Analysis
Treatment Outcome
Ascites
Cirrhosis
Complications
Serum albumin
Survival
Journal
Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
28
01
2020
revised:
10
07
2020
accepted:
17
08
2020
pubmed:
28
8
2020
medline:
21
1
2022
entrez:
28
8
2020
Statut:
ppublish
Résumé
The ANSWER study reported that long-term albumin administration in patients with cirrhosis and uncomplicated ascites improves survival. During treatment, serum albumin increased within a month and remained stable thereafter. In this post hoc analysis, we aimed to determine whether on-treatment serum albumin levels could guide therapy. Logistic regression was used to assess the association between baseline serum albumin and mortality, as well as to determine on-treatment factors associated with mortality and to predict the achievement of a given on-treatment serum albumin level. Survival was assessed by Kaplan-Meier estimates and second-order polynomial regression. Patients whose on-treatment serum albumin remained below normal were compared with a subset of patients from the control arm matched by principal score. Baseline serum albumin was closely associated with 18-month mortality in untreated patients; albumin treatment almost effaced this relationship. On-treatment serum albumin and MELD-Na at month 1 were the sole independent variables associated with mortality. Second-order polynomial regression revealed that survival improved in parallel with increased 1-month on-treatment serum albumin. Kaplan-Meier estimations showed that any value of 1-month on-treatment serum albumin (0.1 g/dl intervals) in the range 2.5-4.5 g/dl discriminated patient survival. In the normal range of serum albumin, the best discriminant value was 4.0 g/dl. Compared to untreated patients, survival even improved in patients whose on-treatment serum albumin remained below normal. Baseline serum albumin per se should not guide the decision to start albumin therapy. Conversely, 1-month on-treatment serum albumin levels are strongly associated with outcomes and could guide the use of albumin - 4.0 g/dl being the target threshold. However, even patients whose serum albumin remains below normal benefit from long-term albumin administration. The ANSWER study has shown that long-term albumin administration improves survival and prevents the occurrence of major complications in patients with cirrhosis and ascites. This study shows that the achievement of these beneficial effects is related to a significant increase in serum albumin concentration. Even though the best results follow the achievement of a serum albumin concentration of 4 g/dl, a survival benefit is also achieved in patients who fail to normalise serum albumin.
Sections du résumé
BACKGROUND & AIMS
The ANSWER study reported that long-term albumin administration in patients with cirrhosis and uncomplicated ascites improves survival. During treatment, serum albumin increased within a month and remained stable thereafter. In this post hoc analysis, we aimed to determine whether on-treatment serum albumin levels could guide therapy.
METHODS
Logistic regression was used to assess the association between baseline serum albumin and mortality, as well as to determine on-treatment factors associated with mortality and to predict the achievement of a given on-treatment serum albumin level. Survival was assessed by Kaplan-Meier estimates and second-order polynomial regression. Patients whose on-treatment serum albumin remained below normal were compared with a subset of patients from the control arm matched by principal score.
RESULTS
Baseline serum albumin was closely associated with 18-month mortality in untreated patients; albumin treatment almost effaced this relationship. On-treatment serum albumin and MELD-Na at month 1 were the sole independent variables associated with mortality. Second-order polynomial regression revealed that survival improved in parallel with increased 1-month on-treatment serum albumin. Kaplan-Meier estimations showed that any value of 1-month on-treatment serum albumin (0.1 g/dl intervals) in the range 2.5-4.5 g/dl discriminated patient survival. In the normal range of serum albumin, the best discriminant value was 4.0 g/dl. Compared to untreated patients, survival even improved in patients whose on-treatment serum albumin remained below normal.
CONCLUSION
Baseline serum albumin per se should not guide the decision to start albumin therapy. Conversely, 1-month on-treatment serum albumin levels are strongly associated with outcomes and could guide the use of albumin - 4.0 g/dl being the target threshold. However, even patients whose serum albumin remains below normal benefit from long-term albumin administration.
LAY SUMMARY
The ANSWER study has shown that long-term albumin administration improves survival and prevents the occurrence of major complications in patients with cirrhosis and ascites. This study shows that the achievement of these beneficial effects is related to a significant increase in serum albumin concentration. Even though the best results follow the achievement of a serum albumin concentration of 4 g/dl, a survival benefit is also achieved in patients who fail to normalise serum albumin.
Identifiants
pubmed: 32853747
pii: S0168-8278(20)33551-0
doi: 10.1016/j.jhep.2020.08.021
pii:
doi:
Substances chimiques
Biological Products
0
Biomarkers, Pharmacological
0
Serum Albumin
0
Serum Albumin, Human
ZIF514RVZR
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
340-349Investigateurs
Marco Domenicali
(M)
Ferdinando A Giannone
(FA)
Agnese Antognoli
(A)
Manuela Merli
(M)
Chiara Pasquale
(C)
Stefania Gioia
(S)
Silvano Fasolato
(S)
Antonietta Sticca
(A)
Daniela Campion
(D)
Alessandro Risso
(A)
Giorgio M Saracco
(GM)
Loredana Prestianni
(L)
Federica Fidone
(F)
Daniela Maiorca
(D)
Agostino Rizzotto
(A)
Federica Mirici Cappa
(FM)
Arianna Lanzi
(A)
Elga Neri
(E)
Anna Visani
(A)
Antonio Mastroianni
(A)
Giovanni Perricone
(G)
Alberto B Alberti
(AB)
Lucia Cesarini
(L)
Chiara Mazzarelli
(C)
Marcello Vangeli
(M)
Raffaella Viganò
(R)
Marco Marzioni
(M)
Francesca Capretti
(F)
Alba Kostandini
(A)
Giulia Magini
(G)
Maria Colpani
(M)
Tommaso Gabbani
(T)
Maria Marsico
(M)
Marianna Zappimbulso
(M)
Josè Petruzzi
(J)
Vincenza Calvaruso
(V)
Giovanni Parrella
(G)
Nicola Caporaso
(N)
Francesco Auriemma
(F)
Maria Guarino
(M)
Fabio Pugliese
(F)
Annalisa Tortora
(A)
Pietro Leo
(P)
Mario Angelico
(M)
Francesco De Leonardis
(F)
Alessandra Pecchioli
(A)
Piera Rossi
(P)
Giovanni Raimondo
(G)
Irene Cacciola
(I)
Gianfranco Elia
(G)
Elisa Negri
(E)
Marcello Dallio
(M)
Carmelina Loguercio
(C)
Alessandro Federico
(A)
Dario Conte
(D)
Sara Massironi
(S)
Giorgio Ballardini Natascia Celli
(GB)
Maria Rendina
(M)
Roberto Bringiotti
(R)
Nicola Maurizio Castellaneta
(NM)
Francesco Salerno
(F)
Sergio Boccia
(S)
Riccardo Guarisco
(R)
Alessandra Galioto
(A)
Marta Cavallin
(M)
Alida Andrealli
(A)
Informations de copyright
Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of interest PC is part of the speakers' bureau for Grifols SA, Octapharma AG, Baxalta, and Kedrion Biopharma, is consultant for Kedrion Biopharma, is on the advisory board for Grifols SA, and has a research grant from Octapharma AG. MT is part of the speakers' bureau for Grifols SA and Octapharma AG. GZ is part of the speakers' bureau for Octapharma. OR is part of speakers' bureau for Baxalta. PA is part of the speakers' bureau for Baxalta and Kedrion Biopharma. PT is part of the speakers' bureau for Grifols and Kedrion Biopharma. MBa is part of the speakers' bureau Octapharma AG. MBe is part of the speakers' bureau for Grifols SA, Octapharma AG, Baxalta, CLS Behring GmbH, and PPTA, and is a consultant for CLS Behring GmbH, Grifols SA and Baxalta. All other authors have no competing interests. Please refer to the accompanying ICMJE disclosure forms for further details.