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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
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.
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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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