- Oral presentation
- Open Access
Immunodeficiency, HIV RNA plasma viral load and risk of AIDS-defining and non-AIDS-defining neoplasia, ANRS CO3 Aquitaine Cohort (1998–2006)
© Bruyand et al; licensee BioMed Central Ltd. 2009
- Published: 17 June 2009
- Viral Load
- Anal Cancer
- Limited Statistical Power
- Dependent Covariates
- Viral Load Measurement
The risk of neoplasis is increased in HIV-infected subjects. Beside traditional determinants of cancer occurrence, a specific role of HIV-related immunosuppression is strongly suspected and a more complex relationship between HIV and antiretroviral therapy (ART) cannot be excluded. Our objective was to disentangle the relationship between some frequently diagnosed cancers in HIV-infected patients and immunosuppression, HIV and ART exposure.
Patients from the ANRS CO3 Aquitaine Cohort were included in this study if they had a duration of follow-up of at least three months, at least two follow-up visits recorded within the study period (1998 to 2006) and if one HIV RNA plasma viral load (VL) was collected within the first follow-up visit. Durations of exposure were calculated as the time durations with CD4 count <200 and 500 cells/mm3 or VL >500 copies/mL. Multivariate modelling was based on extended Cox proportional hazards models for time-time dependent covariates and delayed entry (at time of first VL measurement). ART exposure was defined as the prescription of at least three antiretroviral drugs.
Among the 4,194 patients included, 61 cases of Non-Hodgkin's lymphoma, 41 Kaposi's sarcoma, 41 bronchopulmonary and upper respiratory tract cancers, 20 skin cancers, 18 cases of Hodgkin's disease, 16 hepatocarcinomas and 14 anal cancers were reported during the study period. Kaposi's sarcoma was independently associated with each year spent with CD4 <200 (Hazard ratio [HR] = 1.53; 95% CI: 1.23 – 1.90; p < 0.001), each year of ART exposure (HR = 0.74; 95% CI: 0.61 – 0.90; p < 0.003) and male gender (HR = 5.26; 95% CI: 1.66 – 16.66; p < 0.006). Non-Hodgkin's lymphoma was associated with each year spent with HIV RNA >500 (HR = 1.34; 95% CI: 1.19 – 1.51; p < 0.001), each year with CD4 <200 (HR = 1.31; 95% CI: 1.12 – 1.53; p < 0.001), and each year of ART exposure (HR = 0.86; 95% CI: 0.75 – 0.99; p < 0.03). Hepatocarcinoma was independently associated with each year spent with CD4 <500 (HR = 1.31; 95% CI: 1.06 – 1.63; p = 0.012). Anal cancer was also independently associated with each year spent with HIV RNA >500 copies/mL (HR = 1.31; 95% CI: 1.02 – 1.68; p = 0.033). Regarding the associations between skin, anal and bronchopulmonary cancers and CD4 <200, the adjusted analyses showed p-values of 0.058, 0.112 and 0.13, respectively).
Together with immunosuppression, HIV VL may be independently associated with an increased risk of some cancers, AIDS-defining or not. Due to the limited statistical power to investigate several types of cancers that are still relatively infrequent, our results need to be confirmed by further studies, possibly collaborative and including lower-income Country cohorts. Moreover, maintaining a high CD4 count, a strict control of HIV VL with fully suppressive ART could have a direct and measurable impact in preventing the currently predictable increasing occurrence of cancer in HIV-infected patients, in addition to other prevention policies.
This article is published under license to BioMed Central Ltd.