Current Practices on Diagnosis, Prevention and Treatment of Post-Transplant Lymphoproliferative Disorder in Pediatric Patients after Solid Organ Transplantation: Results of ERN TransplantChild Healthcare Working Group Survey

Author:

Baker Alastair,Frauca Remacha Esteban,Torres Canizales JuanORCID,Bravo-Gallego Luz YadiraORCID,Fitzpatrick Emer,Alonso Melgar Angel,Muñoz Bartolo Gema,Garcia Guereta Luis,Ramos Boluda EstherORCID,Mozo YasminaORCID,Broniszczak Dorota,Jarmużek Wioletta,Kalicinski PiotrORCID,Maecker-Kolhoff Britta,Carlens Julia,Baumann Ulrich,Roy CharlotteORCID,Chardot ChristopheORCID,Benetti Elisa,Cananzi Mara,Calore Elisabetta,Dello Strologo LucaORCID,Candusso Manila,Lopes Maria FrancelinaORCID,Brito Manuel João,Gonçalves Cristina,Do Carmo Carmen,Stephenne Xavier,Wennberg Lars,Stone Rosário,Rascon JelenaORCID,Lindemans Caroline,Turkiewicz Dominik,Giraldi Eugenia,Nicastro EmanueleORCID,D’Antiga Lorenzo,Ackermann Oanez,Jara Vega Paloma

Abstract

(1) Background: Post-transplant lymphoproliferative disease (PTLD) is a significant complication of solid organ transplantation (SOT). However, there is lack of consensus in PTLD management. Our aim was to establish a present benchmark for comparison between international centers and between various organ transplant systems and modalities; (2) Methods: A cross-sectional questionnaire of relevant PTLD practices in pediatric transplantation was sent to multidisciplinary teams from 17 European center members of ERN TransplantChild to evaluate the centers’ approach strategies for diagnosis and treatment and how current practices impact a cross-sectional series of PTLD cases; (3) Results: A total of 34 SOT programs from 13 European centers participated. The decision to start preemptive treatment and its guidance was based on both EBV viremia monitoring plus additional laboratory methods and clinical assessment (61%). Among treatment modalities the most common initial practice at diagnosis was to reduce the immunosuppression (61%). A total of 126 PTLD cases were reported during the period 2012–2016. According to their histopathological classification, monomorphic lesions were the most frequent (46%). Graft rejection after PTLD remission was 33%. Of the total cases diagnosed with PTLD, 88% survived; (4) Conclusions: There is still no consensus on prevention and treatment of PTLD, which implies the need to generate evidence. This might successively allow the development of clinical guidelines.

Funder

Third Health Programme

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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