TY - JOUR
T1 - Current practices on diagnosis, prevention and treatment of post-transplant lymphoproliferative disorder in pediatric patients after solid organ transplantation
T2 - Results of ern transplantchild healthcareworking group survey
AU - Baker, Alastair
AU - Remacha, Esteban Frauca
AU - Canizales, Juan Torres
AU - Bravo-Gallego, Luz Yadira
AU - Fitzpatrick, Emer
AU - Melgar, Angel Alonso
AU - Bartolo, Gema Muñoz
AU - Guereta, Luis Garcia
AU - Boluda, Esther Ramos
AU - Mozo, Yasmina
AU - Broniszczak, Dorota
AU - Jarmużek, Wioletta
AU - Kalicinski, Piotr
AU - Maecker-Kolhoff, Britta
AU - Carlens, Julia
AU - Baumann, Ulrich
AU - Roy, Charlotte
AU - Chardot, Christophe
AU - Benetti, Elisa
AU - Cananzi, Mara
AU - Calore, Elisabetta
AU - Dello Strologo, Luca
AU - Candusso, Manila
AU - Lopes, Maria Francelina
AU - Brito, Manuel João
AU - Gonçalves, Cristina
AU - Do Carmo, Carmen
AU - Stephenne, Xavier
AU - Wennberg, Lars
AU - Stone, Rosário
AU - Rascon, Jelena
AU - Lindemans, Caroline
AU - Turkiewicz, Dominik
AU - Giraldi, Eugenia
AU - Nicastro, Emanuele
AU - D’Antiga, Lorenzo
AU - Ackermann, Oanez
AU - Vega, Paloma Jara
N1 - Funding Information:
Funding: This study has been supported by the European Reference Network on pediatric Transplantation (ERN TransplantChild), which is partly cofounded by the European Union within the framework of the Third Health Programme ERN. Specific Agreement Number: 847103.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/8
Y1 - 2021/8
N2 - (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.
AB - (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.
KW - Epstein-Barr virus
KW - Immunosuppression
KW - Pediatric
KW - Post-transplant lymphoproliferative disorder
KW - PTLD
KW - Solid organ transplantation
UR - http://www.scopus.com/inward/record.url?scp=85112779549&partnerID=8YFLogxK
U2 - 10.3390/children8080661
DO - 10.3390/children8080661
M3 - Article
AN - SCOPUS:85112779549
SN - 2227-9067
VL - 8
JO - Children
JF - Children
IS - 8
M1 - 661
ER -