Posttransplant lymphoproliferative disorder in pediatric patients: Survival rates according to primary sites of occurrence and a proposed clinical categorization.

Epstein-Barr Virus (EBV) cancer/malignancy/neoplasia classification systems clinical research/practice hematogenous/leukemia/lymphoma hematology/oncology infection and infectious agents - viral infectious disease patient survival pediatrics posttransplant lymphoproliferative disorder (PTLD)

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
10 2019
Historique:
received: 29 08 2018
revised: 06 03 2019
accepted: 10 03 2019
pubmed: 19 3 2019
medline: 5 9 2020
entrez: 19 3 2019
Statut: ppublish

Résumé

Posttransplant lymphoproliferative disorder (PTLD) is a devastating complication of organ transplant. In a hospital-based registry, we identified biopsy-proven cases of PTLD among children during a 15-year period and reviewed trends in PTLD rates, the sites of involvement, and the associated survival rates. Cases that were included had at least 1 year of follow-up after the diagnosis of PTLD. We studied 82 patients with first-episode PTLD. Median age at diagnosis was 6.4 years (IQR 3.2-12.3 years). The most frequent PTLD sites were tonsillar/adenoidal (T/A [34%]) and gastrointestinal (32%), followed by miscellaneous (defined as less common sites including central nervous system, kidney, lung, and soft tissue [12%]), lymph node (11%), and multisite (11%). Kaplan-Meier survival curves showed that T/A PTLD was associated with decreased all-cause mortality compared with PTLD at other sites (log-rank 0.004), even after adjustment for histological subtype (P = .047). PTLD-related mortality was also decreased among T/A PTLD (log-rank 0.012) but showed a trend toward significance only after adjustment for histological subtype (P = .09). Among first episodes of PTLD, T/A PTLD was associated with a survival advantage compared with PTLD at other sites, even after adjustment for potential confounders. Based on our observations, we propose a clinical categorization of PTLD according to anatomical site of occurrence.

Identifiants

pubmed: 30884098
doi: 10.1111/ajt.15358
pii: S1600-6135(22)09261-9
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2764-2774

Subventions

Organisme : Hospital for Sick Children
Pays : International

Informations de copyright

© 2019 The American Society of Transplantation and the American Society of Transplant Surgeons.

Références

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Auteurs

Arnaud G L'Huillier (AG)

Division of Infectious Diseases, Hospital for Sick Children, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.

Anne I Dipchand (AI)

University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Labatt Family Heart Centre, Hospital for Sick Children, Toronto, Ontario, Canada.

Vicky L Ng (VL)

University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Pediatric Gastroenterology, Hepatology and Nutrition, Hospital for Sick Children, Toronto, Ontario, Canada.

Diane Hebert (D)

University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Nephrology, Hospital for Sick Children, Toronto, Ontario, Canada.

Yaron Avitzur (Y)

University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Pediatric Gastroenterology, Hepatology and Nutrition, Hospital for Sick Children, Toronto, Ontario, Canada.

Melinda Solomon (M)

University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Respiratory Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.

Bo-Yee Ngan (BY)

University of Toronto, Toronto, Ontario, Canada.
Division of Pathology, Hospital for Sick Children, Toronto, Ontario, Canada.

Derek Stephens (D)

University of Toronto, Toronto, Ontario, Canada.
The Research Institute, Hospital for Sick Children, Toronto, Ontario.

Angela S Punnett (AS)

University of Toronto, Toronto, Ontario, Canada.
Division of Haematology/Oncology, Hospital for Sick Children, Toronto, Ontario, Canada.

Michelle Barton (M)

Division of Infectious Diseases, Hospital for Sick Children, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
Division of Infectious Diseases, London Health Sciences Centre, University of Western Ontario, London, Ontario, Canada.

Upton D Allen (UD)

Division of Infectious Diseases, Hospital for Sick Children, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.
Transplant and Regenerative Medicine Centre, Hospital for Sick Children, Toronto, Ontario, Canada.
The Research Institute, Hospital for Sick Children, Toronto, Ontario.

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