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Primary post-transplant lymphoproliferative disorder of the central nervous system: characteristics, management and outcome in 25 paediatric patients
MM. Taj, B. Maecker-Kolhoff, R. Ling, S. Bomken, B. Burkhardt, AKS. Chiang, M. Csoka, A. Füreder, S. Haouy, J. Lazic, N. Miakova, V. Minard-Colin, SD. Turner, A. Uyttebroeck, A. Attarbaschi, European Intergroup for Childhood Non-Hodgkin's...
Language English Country Great Britain
Document type Clinical Trial, Journal Article, Multicenter Study
PubMed
33764500
DOI
10.1111/bjh.17398
Knihovny.cz E-resources
- MeSH
- Allografts MeSH
- Child MeSH
- Adult MeSH
- Infant MeSH
- Humans MeSH
- Lymphoproliferative Disorders * drug therapy etiology mortality MeSH
- Survival Rate MeSH
- Adolescent MeSH
- Brain Neoplasms * drug therapy etiology mortality MeSH
- Child, Preschool MeSH
- Disease-Free Survival MeSH
- Rituximab administration & dosage MeSH
- Injections, Spinal MeSH
- Hematopoietic Stem Cell Transplantation adverse effects MeSH
- Organ Transplantation adverse effects MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Multicenter Study MeSH
Primary central nervous system (CNS) post-transplant lymphoproliferative disorder (PTLD) in childhood is rare. Twenty-five patients were retrieved from nine European Intergroup for Childhood Non-Hodgkin's Lymphoma and/or international Berlin-Frankfurt-Münster Study Group members. Types of allografts included kidney (n = 11), liver (n = 4), heart (n = 5), bowel (n = 1) and haematopoietic stem cells (n = 4). Eighteen were male, 16 ≥ 10 years old, 21 had monomorphic disease and 24 solid intracranial tumour masses. Four-year event-free and overall survival rates were 50% ± 10% and 74% ± 9% respectively. This report represents the largest paediatric series of CNS PTLD reported to date, showing favourable survival odds following systemic and intrathecal chemotherapy and rituximab administration.
2nd Department of Pediatrics Semmelweis University Budapest Hungary
Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Pediatric Hematology and Oncology Hannover Medical School Hannover Germany
Department of Pediatric Hematology and Oncology University Hospital Leuven Leuven Belgium
Department of Pediatric Hematology and Oncology University of Münster Münster Germany
References provided by Crossref.org
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- $a Primary central nervous system (CNS) post-transplant lymphoproliferative disorder (PTLD) in childhood is rare. Twenty-five patients were retrieved from nine European Intergroup for Childhood Non-Hodgkin's Lymphoma and/or international Berlin-Frankfurt-Münster Study Group members. Types of allografts included kidney (n = 11), liver (n = 4), heart (n = 5), bowel (n = 1) and haematopoietic stem cells (n = 4). Eighteen were male, 16 ≥ 10 years old, 21 had monomorphic disease and 24 solid intracranial tumour masses. Four-year event-free and overall survival rates were 50% ± 10% and 74% ± 9% respectively. This report represents the largest paediatric series of CNS PTLD reported to date, showing favourable survival odds following systemic and intrathecal chemotherapy and rituximab administration.
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