No excess risk of follicular lymphoma in kidney transplant and HIV-related immune deficiency
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Open Access
Type
ArticleAuthor/s
Vajdic, Claire M.van Leeuwen, Marina T.
Turner, Jennifer J.
McDonald, Ann M.
Webster, Angela C.
McDonald, Stephen P.
Chapman, Jeremy R.
Kaldor, John M.
Grulich, Andrew E.
Abstract
Subtype‐specific incidence patterns in populations at high risk of lymphoma offer insight into lymphomagenesis. The incidence profiles for the 2 most common non‐Hodgkin lymphoma subtypes were compared for 2 immunodeficient populations, adults receiving a kidney transplant 1982–2003 ...
See moreSubtype‐specific incidence patterns in populations at high risk of lymphoma offer insight into lymphomagenesis. The incidence profiles for the 2 most common non‐Hodgkin lymphoma subtypes were compared for 2 immunodeficient populations, adults receiving a kidney transplant 1982–2003 (n = 7,730) or diagnosed with human immunodeficiency virus (HIV) infection 1982–2004 (n = 17,175). National, population–based registries were linked and standardized incidence ratios (SIRs) were computed for each cohort and lymphoma subtype. Risk of diffuse large B‐cell lymphoma was significantly increased after transplantation (SIR 17.83, 95% CI: 13.61–22.95) and after HIV infection (SIR 58.81, 95% CI: 52.59–65.56). Rates of follicular lymphoma (FL) were neither significantly increased nor decreased in transplant recipients (SIR 0.82, 95% CI: 0.10–2.96) and in people with HIV (SIR 1.25, 95% CI: 0.41–2.91). The findings argue against an infectious or other immunodeficiency‐related etiology for FL and clearly differentiate it from diffuse large B‐cell lymphoma.
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See moreSubtype‐specific incidence patterns in populations at high risk of lymphoma offer insight into lymphomagenesis. The incidence profiles for the 2 most common non‐Hodgkin lymphoma subtypes were compared for 2 immunodeficient populations, adults receiving a kidney transplant 1982–2003 (n = 7,730) or diagnosed with human immunodeficiency virus (HIV) infection 1982–2004 (n = 17,175). National, population–based registries were linked and standardized incidence ratios (SIRs) were computed for each cohort and lymphoma subtype. Risk of diffuse large B‐cell lymphoma was significantly increased after transplantation (SIR 17.83, 95% CI: 13.61–22.95) and after HIV infection (SIR 58.81, 95% CI: 52.59–65.56). Rates of follicular lymphoma (FL) were neither significantly increased nor decreased in transplant recipients (SIR 0.82, 95% CI: 0.10–2.96) and in people with HIV (SIR 1.25, 95% CI: 0.41–2.91). The findings argue against an infectious or other immunodeficiency‐related etiology for FL and clearly differentiate it from diffuse large B‐cell lymphoma.
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Date
2010-02-22Publisher
WileyLicence
OtherRights statement
This is the peer reviewed version of the following article: [Vajdic CM, van Leeuwen MT, Turner JJ, McDonald AM, Webster AC, McDonald SP, Chapman JR, Kaldor JM, Grulich AE. No excess risk of follicular lymphoma in kidney transplant and HIV-related immune deficiency. International Journal of Cancer. 2010; 127:2732-5], which has been published in final form at [https://doi.org/10.1002/ijc.25272]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.Faculty/School
Faculty of Medicine and Health, Sydney Medical SchoolCitation
Vajdic CM, van Leeuwen MT, Turner JJ, McDonald AM, Webster AC, McDonald SP, Chapman JR, Kaldor JM, Grulich AE. No excess risk of follicular lymphoma in kidney transplant and HIV-related immune deficiency. International Journal of Cancer. 2010; 127:2732-5Share