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Risk of lymphoma subtypes after solid organ transplantation in the United States
BACKGROUND: Solid organ transplant recipients have high risk of lymphomas, including non-Hodgkin lymphoma (NHL) and Hodgkin lymphoma (HL). A gap in our understanding of post-transplant lymphomas involves the spectrum and associated risks of their many histologic subtypes. METHODS: We linked nationwi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708563/ https://www.ncbi.nlm.nih.gov/pubmed/23756857 http://dx.doi.org/10.1038/bjc.2013.294 |
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author | Clarke, C A Morton, L M Lynch, C Pfeiffer, R M Hall, E C Gibson, T M Weisenburger, D D Martínez-Maza, O Hussain, S K Yang, J Chang, E T Engels, E A |
author_facet | Clarke, C A Morton, L M Lynch, C Pfeiffer, R M Hall, E C Gibson, T M Weisenburger, D D Martínez-Maza, O Hussain, S K Yang, J Chang, E T Engels, E A |
author_sort | Clarke, C A |
collection | PubMed |
description | BACKGROUND: Solid organ transplant recipients have high risk of lymphomas, including non-Hodgkin lymphoma (NHL) and Hodgkin lymphoma (HL). A gap in our understanding of post-transplant lymphomas involves the spectrum and associated risks of their many histologic subtypes. METHODS: We linked nationwide data on solid organ transplants from the US Scientific Registry of Transplant Recipients (1987–2008) to 14 state and regional cancer registries, yielding 791 281 person-years of follow-up for 19 distinct NHL subtypes and HL. We calculated standardised incidence ratios (SIRs) and used Poisson regression to compare SIRs by recipient age, transplanted organ, and time since transplantation. RESULTS: The risk varied widely across subtypes, with strong elevations (SIRs 10–100) for hepatosplenic T-cell lymphoma, Burkitt's lymphoma, NK/T-cell lymphoma, diffuse large B-cell lymphoma, and anaplastic large-cell lymphoma (both systemic and primary cutaneous forms). Moderate elevations (SIRs 2–4) were observed for HL and lymphoplasmacytic, peripheral T-cell, and marginal zone lymphomas, but SIRs for indolent lymphoma subtypes were not elevated. Generally, SIRs were highest for younger recipients (<20 years) and those receiving organs other than kidneys. CONCLUSION: Transplant recipients experience markedly elevated risk of a distinct spectrum of lymphoma subtypes. These findings support the aetiologic relevance of immunosuppression for certain subtypes and underscore the importance of detailed haematopathologic workup for transplant recipients with suspected lymphoma. |
format | Online Article Text |
id | pubmed-3708563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37085632014-07-09 Risk of lymphoma subtypes after solid organ transplantation in the United States Clarke, C A Morton, L M Lynch, C Pfeiffer, R M Hall, E C Gibson, T M Weisenburger, D D Martínez-Maza, O Hussain, S K Yang, J Chang, E T Engels, E A Br J Cancer Epidemiology BACKGROUND: Solid organ transplant recipients have high risk of lymphomas, including non-Hodgkin lymphoma (NHL) and Hodgkin lymphoma (HL). A gap in our understanding of post-transplant lymphomas involves the spectrum and associated risks of their many histologic subtypes. METHODS: We linked nationwide data on solid organ transplants from the US Scientific Registry of Transplant Recipients (1987–2008) to 14 state and regional cancer registries, yielding 791 281 person-years of follow-up for 19 distinct NHL subtypes and HL. We calculated standardised incidence ratios (SIRs) and used Poisson regression to compare SIRs by recipient age, transplanted organ, and time since transplantation. RESULTS: The risk varied widely across subtypes, with strong elevations (SIRs 10–100) for hepatosplenic T-cell lymphoma, Burkitt's lymphoma, NK/T-cell lymphoma, diffuse large B-cell lymphoma, and anaplastic large-cell lymphoma (both systemic and primary cutaneous forms). Moderate elevations (SIRs 2–4) were observed for HL and lymphoplasmacytic, peripheral T-cell, and marginal zone lymphomas, but SIRs for indolent lymphoma subtypes were not elevated. Generally, SIRs were highest for younger recipients (<20 years) and those receiving organs other than kidneys. CONCLUSION: Transplant recipients experience markedly elevated risk of a distinct spectrum of lymphoma subtypes. These findings support the aetiologic relevance of immunosuppression for certain subtypes and underscore the importance of detailed haematopathologic workup for transplant recipients with suspected lymphoma. Nature Publishing Group 2013-07-09 2013-06-11 /pmc/articles/PMC3708563/ /pubmed/23756857 http://dx.doi.org/10.1038/bjc.2013.294 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Epidemiology Clarke, C A Morton, L M Lynch, C Pfeiffer, R M Hall, E C Gibson, T M Weisenburger, D D Martínez-Maza, O Hussain, S K Yang, J Chang, E T Engels, E A Risk of lymphoma subtypes after solid organ transplantation in the United States |
title | Risk of lymphoma subtypes after solid organ transplantation in the United States |
title_full | Risk of lymphoma subtypes after solid organ transplantation in the United States |
title_fullStr | Risk of lymphoma subtypes after solid organ transplantation in the United States |
title_full_unstemmed | Risk of lymphoma subtypes after solid organ transplantation in the United States |
title_short | Risk of lymphoma subtypes after solid organ transplantation in the United States |
title_sort | risk of lymphoma subtypes after solid organ transplantation in the united states |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708563/ https://www.ncbi.nlm.nih.gov/pubmed/23756857 http://dx.doi.org/10.1038/bjc.2013.294 |
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