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Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence

OBJECTIVES: To estimate the cancer risk of HIV-infected patients in the HAART era with respect to a general reference population and to determine risk factors for malignancy. METHODS: Long term (1996-2009) cancer incidence of the Bonn single centre HIV cohort was compared to the incidence of the ref...

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Autores principales: Vogel, M, Friedrich, O, Lüchters, G, Holleczek, B, Wasmuth, JC, Anadol, E, Schwarze-Zander, C, Nattermann, J, Oldenburg, J, Sauerbruch, T, Rockstroh, JK, Spengler, U
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352206/
https://www.ncbi.nlm.nih.gov/pubmed/21486722
http://dx.doi.org/10.1186/2047-783X-16-3-101
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author Vogel, M
Friedrich, O
Lüchters, G
Holleczek, B
Wasmuth, JC
Anadol, E
Schwarze-Zander, C
Nattermann, J
Oldenburg, J
Sauerbruch, T
Rockstroh, JK
Spengler, U
author_facet Vogel, M
Friedrich, O
Lüchters, G
Holleczek, B
Wasmuth, JC
Anadol, E
Schwarze-Zander, C
Nattermann, J
Oldenburg, J
Sauerbruch, T
Rockstroh, JK
Spengler, U
author_sort Vogel, M
collection PubMed
description OBJECTIVES: To estimate the cancer risk of HIV-infected patients in the HAART era with respect to a general reference population and to determine risk factors for malignancy. METHODS: Long term (1996-2009) cancer incidence of the Bonn single centre HIV cohort was compared to the incidence of the reference population of Saarland using standardized incidence ratios (SIR). Poisson regression analysis was used to identify predictors of cancer risk. RESULTS: 1,476 patients entered the cohort, enabling 8,772 person years of observation. 121 tumours in 114 patients, 7 in-situ and 114 invasive cancers, were identified. Malignancies associated with infectious agents such as Kaposi sarcoma (SIRs: male: 5,683; female: 277), non-Hodgkin lymphoma (SIRs male: 35; female: 18), anal cancer (SIRs male: 88; female: 115) as well a cervical carcinoma (SIR female: 4) and Hodgkin's disease (SIR male: 39) and liver cancer (SIR male: 18) were substantially more frequent in HIV-infected patients than in the general population (p < 0.001, each), whereas all other types of cancer were not increased. Poisson regression identified HAART (incidence rate ratio IRR (95% CI): 0.28 (0.19-0.41), p < 0.001), CD4 count (IRR per 100 cells/μl increase: 0.66 (0.57-0.76), p < 0.001), hepatitis B (IRR: 2.15 (1.10-4.20), p = 0.046) and age (IRR per 10 year increase: 1.23 (1.03 - 1.46), p = 0.023) as independent predictors for the occurrence of any type of cancer. CONCLUSIONS: HAART and preserved CD4 cells preferentially reduce the risk of malignancies associated with oncogenic infections.
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spelling pubmed-33522062012-05-16 Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence Vogel, M Friedrich, O Lüchters, G Holleczek, B Wasmuth, JC Anadol, E Schwarze-Zander, C Nattermann, J Oldenburg, J Sauerbruch, T Rockstroh, JK Spengler, U Eur J Med Res Research OBJECTIVES: To estimate the cancer risk of HIV-infected patients in the HAART era with respect to a general reference population and to determine risk factors for malignancy. METHODS: Long term (1996-2009) cancer incidence of the Bonn single centre HIV cohort was compared to the incidence of the reference population of Saarland using standardized incidence ratios (SIR). Poisson regression analysis was used to identify predictors of cancer risk. RESULTS: 1,476 patients entered the cohort, enabling 8,772 person years of observation. 121 tumours in 114 patients, 7 in-situ and 114 invasive cancers, were identified. Malignancies associated with infectious agents such as Kaposi sarcoma (SIRs: male: 5,683; female: 277), non-Hodgkin lymphoma (SIRs male: 35; female: 18), anal cancer (SIRs male: 88; female: 115) as well a cervical carcinoma (SIR female: 4) and Hodgkin's disease (SIR male: 39) and liver cancer (SIR male: 18) were substantially more frequent in HIV-infected patients than in the general population (p < 0.001, each), whereas all other types of cancer were not increased. Poisson regression identified HAART (incidence rate ratio IRR (95% CI): 0.28 (0.19-0.41), p < 0.001), CD4 count (IRR per 100 cells/μl increase: 0.66 (0.57-0.76), p < 0.001), hepatitis B (IRR: 2.15 (1.10-4.20), p = 0.046) and age (IRR per 10 year increase: 1.23 (1.03 - 1.46), p = 0.023) as independent predictors for the occurrence of any type of cancer. CONCLUSIONS: HAART and preserved CD4 cells preferentially reduce the risk of malignancies associated with oncogenic infections. BioMed Central 2011-03-28 /pmc/articles/PMC3352206/ /pubmed/21486722 http://dx.doi.org/10.1186/2047-783X-16-3-101 Text en Copyright ©2011 I. Holzapfel Publishers
spellingShingle Research
Vogel, M
Friedrich, O
Lüchters, G
Holleczek, B
Wasmuth, JC
Anadol, E
Schwarze-Zander, C
Nattermann, J
Oldenburg, J
Sauerbruch, T
Rockstroh, JK
Spengler, U
Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title_full Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title_fullStr Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title_full_unstemmed Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title_short Cancer risk in HIV-infected individuals on HAART is largely attributed to oncogenic infections and state of immunocompetence
title_sort cancer risk in hiv-infected individuals on haart is largely attributed to oncogenic infections and state of immunocompetence
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352206/
https://www.ncbi.nlm.nih.gov/pubmed/21486722
http://dx.doi.org/10.1186/2047-783X-16-3-101
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