| Literature DB >> 30586230 |
Maura Faraci1, Alice Bertaina2,3, Arnaud Dalissier4, Marianne Ifversen5, Ansgar Schulz6, Andrew Gennery7, Birgit Burkhardt8, Isabel Badell Serra9, Cristina Diaz-de-Heredia10, Edoardo Lanino1, Arjan C Lankester11, Bernd Gruhn12, Susanne Matthes-Martin13, Joern S Kühl14, Stefania Varotto15, Catherine Paillard16, Audrey Guilmatre17, Ana Sastre18, Manuel Abecasis19, Birgit Garwer20, Petr Sedlacek21, Jaap J Boelens22,23, Eric Beohou4, Peter Bader24.
Abstract
We report data obtained from a retrospective multicenter pediatric survey on behalf of the European Society for Blood and Marrow Transplantation (EBMT). Information on solid organ transplantation (SOT) performed in pediatric recipients of either autologous or allogeneic hematopoietic stem cell transplantation (HSCT) between 1984 and 2016 was collected in 20 pediatric EBMT Centers (25.6%). Overall, we evaluated data on 44 SOTs following HSCT including 20 liver (LTx), 12 lung (LuTx), 6 heart (HTx), and 6 kidney (KTx) transplantations. The indication for SOT was organ failure related to intractable graft-vs-host disease in 16 children (36.3%), acute or chronic HSCT-related toxicity in 18 (40.9%), and organ dysfunction related to the underlying disease in 10 (22.8%). The median follow-up was 10.9 years (95% confidence interval: 1.7-29.5). The overall survival rate at 1 and 5 years after SOT was 85.7% and 80.4%, respectively: it was 74% and 63.2% after LTx, 83.2% after HTx, and 100% equally after LuTx and KTx. This multicenter survey confirms that SOT represents a promising option in children with severe organ failure occurring after HSCT. Additional studies are needed to further establish the effectiveness of SOT after HSCT and to better understand the mechanism underlying this encouraging success.Entities:
Keywords: bone marrow/hematopoietic stem cell transplantation; clinical research/practice; graft-vs-host disease (GVHD); heart failure/injury; kidney failure/injury; liver disease; lung (allograft) function/dysfunction; organ transplantation in general; pediatrics
Year: 2019 PMID: 30586230 DOI: 10.1111/ajt.15240
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086