Cargando…

Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial

OBJECTIVE: Impaired liver regeneration is associated with a poor outcome in patients with decompensated alcoholic liver disease (ALD). We assessed whether autologous bone marrow mononuclear cell transplantation (BMMCT) improved liver function in decompensated ALD. DESIGN: 58 patients (mean age 54 yr...

Descripción completa

Detalles Bibliográficos
Autores principales: Spahr, Laurent, Chalandon, Yves, Terraz, Sylvain, Kindler, Vincent, Rubbia-Brandt, Laura, Frossard, Jean-Louis, Breguet, Romain, Lanthier, Nicolas, Farina, Annarita, Passweg, Jakob, Becker, Christoph D., Hadengue, Antoine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544843/
https://www.ncbi.nlm.nih.gov/pubmed/23341981
http://dx.doi.org/10.1371/journal.pone.0053719
_version_ 1782255861789360128
author Spahr, Laurent
Chalandon, Yves
Terraz, Sylvain
Kindler, Vincent
Rubbia-Brandt, Laura
Frossard, Jean-Louis
Breguet, Romain
Lanthier, Nicolas
Farina, Annarita
Passweg, Jakob
Becker, Christoph D.
Hadengue, Antoine
author_facet Spahr, Laurent
Chalandon, Yves
Terraz, Sylvain
Kindler, Vincent
Rubbia-Brandt, Laura
Frossard, Jean-Louis
Breguet, Romain
Lanthier, Nicolas
Farina, Annarita
Passweg, Jakob
Becker, Christoph D.
Hadengue, Antoine
author_sort Spahr, Laurent
collection PubMed
description OBJECTIVE: Impaired liver regeneration is associated with a poor outcome in patients with decompensated alcoholic liver disease (ALD). We assessed whether autologous bone marrow mononuclear cell transplantation (BMMCT) improved liver function in decompensated ALD. DESIGN: 58 patients (mean age 54 yrs; mean MELD score 19, all with cirrhosis, 81% with alcoholic steatohepatitis at baseline liver biopsy) were randomized early after hospital admission to standard medical therapy (SMT) alone (n = 30), including steroids in patients with a Maddrey’s score ≥32, or combined with G-CSF injections and autologous BMMCT into the hepatic artery (n = 28). Bone marrow cells were harvested, isolated and reinfused the same day. The primary endpoint was a ≥3 points decrease in the MELD score at 3 months, corresponding to a clinically relevant improvement in liver function. Liver biopsy was repeated at week 4 to assess changes in Ki67+/CK7+ hepatic progenitor cells (HPC) compartment. RESULTS: Both study groups were comparable at baseline. After 3 months, 2 and 4 patients died in the BMMCT and SMT groups, respectively. Adverse events were equally distributed between groups. Moderate alcohol relapse occurred in 31% of patients. The MELD score improved in parallel in both groups during follow-up with 18 patients (64%) from the BMMCT group and 18 patients (53%) from the SMT group reaching the primary endpoint (p = 0.43 (OR 1.6, CI 0.49–5.4) in an intention to treat analysis. Comparing liver biopsy at 4 weeks to baseline, steatosis improved (p<0.001), and proliferating HPC tended to decrease in both groups (−35 and −33%, respectively). CONCLUSION: Autologous BMMCT, compared to SMT is a safe procedure but did not result in an expanded HPC compartment or improved liver function. These data suggest either insufficient regenerative stimulation after BMMCT or resistance to liver regenerative drive in patients with decompensated alcoholic cirrhosis. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN83972743.
format Online
Article
Text
id pubmed-3544843
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35448432013-01-22 Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial Spahr, Laurent Chalandon, Yves Terraz, Sylvain Kindler, Vincent Rubbia-Brandt, Laura Frossard, Jean-Louis Breguet, Romain Lanthier, Nicolas Farina, Annarita Passweg, Jakob Becker, Christoph D. Hadengue, Antoine PLoS One Research Article OBJECTIVE: Impaired liver regeneration is associated with a poor outcome in patients with decompensated alcoholic liver disease (ALD). We assessed whether autologous bone marrow mononuclear cell transplantation (BMMCT) improved liver function in decompensated ALD. DESIGN: 58 patients (mean age 54 yrs; mean MELD score 19, all with cirrhosis, 81% with alcoholic steatohepatitis at baseline liver biopsy) were randomized early after hospital admission to standard medical therapy (SMT) alone (n = 30), including steroids in patients with a Maddrey’s score ≥32, or combined with G-CSF injections and autologous BMMCT into the hepatic artery (n = 28). Bone marrow cells were harvested, isolated and reinfused the same day. The primary endpoint was a ≥3 points decrease in the MELD score at 3 months, corresponding to a clinically relevant improvement in liver function. Liver biopsy was repeated at week 4 to assess changes in Ki67+/CK7+ hepatic progenitor cells (HPC) compartment. RESULTS: Both study groups were comparable at baseline. After 3 months, 2 and 4 patients died in the BMMCT and SMT groups, respectively. Adverse events were equally distributed between groups. Moderate alcohol relapse occurred in 31% of patients. The MELD score improved in parallel in both groups during follow-up with 18 patients (64%) from the BMMCT group and 18 patients (53%) from the SMT group reaching the primary endpoint (p = 0.43 (OR 1.6, CI 0.49–5.4) in an intention to treat analysis. Comparing liver biopsy at 4 weeks to baseline, steatosis improved (p<0.001), and proliferating HPC tended to decrease in both groups (−35 and −33%, respectively). CONCLUSION: Autologous BMMCT, compared to SMT is a safe procedure but did not result in an expanded HPC compartment or improved liver function. These data suggest either insufficient regenerative stimulation after BMMCT or resistance to liver regenerative drive in patients with decompensated alcoholic cirrhosis. TRIAL REGISTRATION: Controlled-Trials.com ISRCTN83972743. Public Library of Science 2013-01-14 /pmc/articles/PMC3544843/ /pubmed/23341981 http://dx.doi.org/10.1371/journal.pone.0053719 Text en © 2013 Spahr et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Spahr, Laurent
Chalandon, Yves
Terraz, Sylvain
Kindler, Vincent
Rubbia-Brandt, Laura
Frossard, Jean-Louis
Breguet, Romain
Lanthier, Nicolas
Farina, Annarita
Passweg, Jakob
Becker, Christoph D.
Hadengue, Antoine
Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title_full Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title_fullStr Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title_full_unstemmed Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title_short Autologous Bone Marrow Mononuclear Cell Transplantation in Patients with Decompensated Alcoholic Liver Disease: A Randomized Controlled Trial
title_sort autologous bone marrow mononuclear cell transplantation in patients with decompensated alcoholic liver disease: a randomized controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544843/
https://www.ncbi.nlm.nih.gov/pubmed/23341981
http://dx.doi.org/10.1371/journal.pone.0053719
work_keys_str_mv AT spahrlaurent autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT chalandonyves autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT terrazsylvain autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT kindlervincent autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT rubbiabrandtlaura autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT frossardjeanlouis autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT breguetromain autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT lanthiernicolas autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT farinaannarita autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT passwegjakob autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT beckerchristophd autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial
AT hadengueantoine autologousbonemarrowmononuclearcelltransplantationinpatientswithdecompensatedalcoholicliverdiseasearandomizedcontrolledtrial