Excellent outcomes in children after haematopoietic stem cell transplantation for hepatitis‐associated aplastic anaemia following liver transplantation

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Authors: Satish Kumar Meena, Adarsh Kancharla, Amany Ihab Mohamed, Beki James, Anna-Maria Ewins, Shahzya Chaudhury, Wing Roberts, Juliana Silva, Robert Chiesa, Persis Jal Amrolia, Susan E. Height, Nedim Hadžić
+1 more Kanchan Rao
Cited by: 0
References: 25

Abstract

Hepatitis-associated aplastic anaemia is a rare entity that can sometimes be life-threatening due to its rapid progression to liver failure, necessitating an urgent liver transplantation (LT). Treating severe aplastic anaemia following an LT can be very challenging. While immunosuppressive therapy (IST) has been reported to have some success, the vulnerable state of these patients in addition to the time taken for IST to work makes this a less suitable option for the majority of patients. Haematopoietic stem cell transplantation (HSCT) with matched related donors has been reported as a curative option; there has been less success using alternate donors. Here, we present our experience of predominantly alternate donor HSCT following liver transplantation in an extremely high-risk group of 10 children. Overall survival was 90% at a median of 38 months post-LT. Surviving children have normal blood counts, normal liver function and performance status. No liver-related complications or significant graft versus host disease were encountered. Multiple infective and non-infective post-HSCT complications were successfully treated with excellent multidisciplinary input. Upfront HSCT, even with alternate donors, can be lifesaving if performed in a timely manner, following close liaison between liver transplantation and HSCT teams and with the appropriate multidisciplinary support.

Fields of Study & Subjects

Hematopoietic Stem Cell Transplantation Organ Transplantation Techniques and Outcomes Blood disorders and treatments

Publication details

Journal / source
British Journal of Haematology
Volume
208
Issue
3
Pages
1009–1016
Publication date
12 January 2026
Language
EN