Cargando…

Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial

BACKGROUND: Mesenchymal stem cell (MSC) infusion was reported to improve liver function in patients with decompensated liver cirrhosis (DLC); however, whether the medication can improve outcome of these patients is poorly understood. METHODS: This prospective, open-labeled, randomized controlled stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Shi, Ming, Li, Yuan-Yuan, Xu, Ruo-Nan, Meng, Fan-Ping, Yu, Shuang-Jie, Fu, Jun-Liang, Hu, Jin-Hua, Li, Jing-Xin, Wang, Li-Feng, Jin, Lei, Wang, Fu-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651584/
https://www.ncbi.nlm.nih.gov/pubmed/34843069
http://dx.doi.org/10.1007/s12072-021-10199-2
_version_ 1784611429153767424
author Shi, Ming
Li, Yuan-Yuan
Xu, Ruo-Nan
Meng, Fan-Ping
Yu, Shuang-Jie
Fu, Jun-Liang
Hu, Jin-Hua
Li, Jing-Xin
Wang, Li-Feng
Jin, Lei
Wang, Fu-Sheng
author_facet Shi, Ming
Li, Yuan-Yuan
Xu, Ruo-Nan
Meng, Fan-Ping
Yu, Shuang-Jie
Fu, Jun-Liang
Hu, Jin-Hua
Li, Jing-Xin
Wang, Li-Feng
Jin, Lei
Wang, Fu-Sheng
author_sort Shi, Ming
collection PubMed
description BACKGROUND: Mesenchymal stem cell (MSC) infusion was reported to improve liver function in patients with decompensated liver cirrhosis (DLC); however, whether the medication can improve outcome of these patients is poorly understood. METHODS: This prospective, open-labeled, randomized controlled study enrolled 219 patients with HBV-related DLC who were divided into control group (n = 111) and umbilical cord-derived MSC (UC-MSC)-treated group (n = 108), then all of them received a follow-up check from October 2010 to October 2017. The treated patients received three times of UC-MSC infusions at 4-week intervals plus conventional treatment that was only used for control group. The overall survival rate and HCC-free survival rate were calculated as primary endpoints and the liver function and adverse events associated with the medication were also evaluated. RESULTS: During the follow-up check period from 13 to 75th months, there was a significantly higher overall survival rate in the treated group than the control group, while the difference of the hepatocellular carcinoma event-free survival rate between the treated and control groups was not observed during the 75-month follow-up. UC-MSC treatment markedly improved liver function, as indicated by the levels of serum albumin, prothrombin activity, cholinesterase, and total bilirubin during 48 weeks of follow-up. No significant side effects or treatment-related complications were observed in the UC-MSC group. CONCLUSIONS: Therapy of UC-MSC is not only well tolerated, but also significantly improves long-term survival rate, as well as the liver function in patients with HBV-related DLC. UC-MSC medication, therefore, might present a novel therapeutic approach for the disease. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12072-021-10199-2.
format Online
Article
Text
id pubmed-8651584
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer India
record_format MEDLINE/PubMed
spelling pubmed-86515842021-12-08 Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial Shi, Ming Li, Yuan-Yuan Xu, Ruo-Nan Meng, Fan-Ping Yu, Shuang-Jie Fu, Jun-Liang Hu, Jin-Hua Li, Jing-Xin Wang, Li-Feng Jin, Lei Wang, Fu-Sheng Hepatol Int Original Article BACKGROUND: Mesenchymal stem cell (MSC) infusion was reported to improve liver function in patients with decompensated liver cirrhosis (DLC); however, whether the medication can improve outcome of these patients is poorly understood. METHODS: This prospective, open-labeled, randomized controlled study enrolled 219 patients with HBV-related DLC who were divided into control group (n = 111) and umbilical cord-derived MSC (UC-MSC)-treated group (n = 108), then all of them received a follow-up check from October 2010 to October 2017. The treated patients received three times of UC-MSC infusions at 4-week intervals plus conventional treatment that was only used for control group. The overall survival rate and HCC-free survival rate were calculated as primary endpoints and the liver function and adverse events associated with the medication were also evaluated. RESULTS: During the follow-up check period from 13 to 75th months, there was a significantly higher overall survival rate in the treated group than the control group, while the difference of the hepatocellular carcinoma event-free survival rate between the treated and control groups was not observed during the 75-month follow-up. UC-MSC treatment markedly improved liver function, as indicated by the levels of serum albumin, prothrombin activity, cholinesterase, and total bilirubin during 48 weeks of follow-up. No significant side effects or treatment-related complications were observed in the UC-MSC group. CONCLUSIONS: Therapy of UC-MSC is not only well tolerated, but also significantly improves long-term survival rate, as well as the liver function in patients with HBV-related DLC. UC-MSC medication, therefore, might present a novel therapeutic approach for the disease. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12072-021-10199-2. Springer India 2021-11-29 /pmc/articles/PMC8651584/ /pubmed/34843069 http://dx.doi.org/10.1007/s12072-021-10199-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Shi, Ming
Li, Yuan-Yuan
Xu, Ruo-Nan
Meng, Fan-Ping
Yu, Shuang-Jie
Fu, Jun-Liang
Hu, Jin-Hua
Li, Jing-Xin
Wang, Li-Feng
Jin, Lei
Wang, Fu-Sheng
Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title_full Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title_fullStr Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title_full_unstemmed Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title_short Mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
title_sort mesenchymal stem cell therapy in decompensated liver cirrhosis: a long-term follow-up analysis of the randomized controlled clinical trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651584/
https://www.ncbi.nlm.nih.gov/pubmed/34843069
http://dx.doi.org/10.1007/s12072-021-10199-2
work_keys_str_mv AT shiming mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT liyuanyuan mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT xuruonan mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT mengfanping mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT yushuangjie mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT fujunliang mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT hujinhua mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT lijingxin mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT wanglifeng mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT jinlei mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial
AT wangfusheng mesenchymalstemcelltherapyindecompensatedlivercirrhosisalongtermfollowupanalysisoftherandomizedcontrolledclinicaltrial