Post-transplant lymphoproliferative disorders after solid organ and hematopoietic stem cell transplantation

Post-transplant lymphoproliferative disorders (PTLD) are a rare complication after both solid organ (SOT) and allogeneic hematopoietic stem cell transplantation (allo-HSCT). In this single center retrospective study, we compared clinical, biological, and histological features, and outcomes of PTLD a...

Full description

Saved in:
Bibliographic Details
Published in:Leukemia & lymphoma Vol. 60; no. 1; pp. 142 - 150
Main Authors: Romero, Samuel, Montoro, Juan, Guinot, Marta, Almenar, Luis, Andreu, Rafael, Balaguer, Aitana, Beneyto, Isabel, Espí, Jordi, Gómez-Codina, José, Iacoboni, Gloria, Jarque, Isidro, López-Andújar, Rafael, Mayordomo-Aranda, Empar, Montalar, Joaquín, Pastor, Amparo, Pastor, Miguel, Piñana, José L., Rojas-Ferrer, Nohelia, Sánchez-Lázaro, Ignacio, Sandoval, Jesús, Sanz, Guillermo, Sanz, Miguel Á., Solé, Amparo, Sanz, Jaime
Format: Journal Article
Language:English
Published: United States Taylor & Francis 02-01-2019
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Post-transplant lymphoproliferative disorders (PTLD) are a rare complication after both solid organ (SOT) and allogeneic hematopoietic stem cell transplantation (allo-HSCT). In this single center retrospective study, we compared clinical, biological, and histological features, and outcomes of PTLD after both types of transplant. We identified 82 PTLD (61 after SOT and 21 after allo-HSCT). The presence of B symptoms, Waldeyer ring, spleen, central nervous system, and liver involvement, and advanced Ann-Arbor stage were more frequent in allo-HSCT recipients. PTLD had an earlier onset in allo-HSCT than in SOT cohort (4 vs. 64 months, p < .0001). PTLD was EBV-positive in 100% of allo-HSCT, in contrast to 47% of SOT (p = .0002). Four years after PTLD diagnosis, median overall survival was 32% (95% CI, 22-48) and 10% (95% CI, 2-49) in SOT and allo-HSCT recipients, respectively (p = .002). In conclusion, the clinical presentation and the outcome of PTLD varies greatly depending on the type of transplant.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1042-8194
1029-2403
DOI:10.1080/10428194.2018.1474462