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10.3727/096368917X694778

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suck abstract from ncbi


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pmid28120743
      Cell+Transplant 2017 ; 26 (6 ): 1059-1066
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  • Long-Term Follow-Up of Patients After Autologous Bone Marrow Cell Infusion for Decompensated Liver Cirrhosis #MMPMID28120743
  • Kim JK ; Kim SJ ; Kim Y ; Chung YE ; Park YN ; Kim HO ; Kim JS ; Park MS ; Sakaida I ; Kim DY ; Lee JI ; Ahn SH ; Lee KS ; Han KH
  • Cell Transplant 2017[Jun]; 26 (6 ): 1059-1066 PMID28120743 show ga
  • Although several human clinical trials using various bone marrow-derived cell types for cirrhotic or decompensated patients have reported a short-term benefit, long-term follow-up data are limited. We analyzed the long-term clinical outcomes of autologous bone marrow cell infusion (ABMI) for decompensated liver cirrhosis (LC). Patients enrolled in a pilot single-armed ABMI study were followed up more than 5 years. Bone marrow-derived mononuclear cells (BM-MNCs) from decompensated LC were harvested and after processing were infused into a peripheral vein. The laboratory test results and long-term clinical course including liver transplantation (LT), development of cancer, cause of death, and survival after ABMI were analyzed. Nineteen patients were followed up for a median of 66 months after ABMI. Liver function, including serum levels of albumin and Child-Pugh (CP) score, was improved at the 1-year follow-up. Liver volume was significantly greater, cirrhosis was sustained, and collagen content was decreased at the 6-month follow-up. Five years after ABMI, five patients (26.3%) maintained CP class A without LT or death, and five patients (26.3%) had undergone elective LT. Hepatocellular carcinoma (HCC) occurred in five patients (26.3%), and lymphoma and colon cancer occurred in one patient each. Three patients (15.8%) were lost to follow-up at months 22, 31, and 33, respectively, but maintained CP class A until their last follow-up. Five patients expired due to infection. While improved liver function was maintained in some patients for more than 5 years after ABMI, other patients developed HCC. Further studies of long-term follow-up cohorts after cell therapy for LC are warranted.
  • |Adolescent [MESH]
  • |Adult [MESH]
  • |Adult Stem Cells/cytology/physiology [MESH]
  • |Aged [MESH]
  • |Bone Marrow Cells/*cytology/physiology [MESH]
  • |Bone Marrow Transplantation/methods [MESH]
  • |Humans [MESH]
  • |Liver Cirrhosis/*therapy [MESH]
  • |Liver Regeneration/physiology [MESH]
  • |Liver/cytology/pathology [MESH]
  • |Middle Aged [MESH]
  • |Transplantation, Autologous/*methods [MESH]


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