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Ageing and Cancer Risk in HIV+ and in Transplanted Persons
Diego Serraino*1, C Pradier2, G Rezza3, P Piselli1, L Fratino1, E Arbustini4, P Burra5, P Carrieri6, G Busnach7, F Citterio8, and Immunosuppression and Cancer Study Group
1Natl Inst of Infectious Diseases, L Spallanzani, Rome, Italy; 2Univ Hosp, Nice, France; 3Inst Superiore di Sanità, Rome, Italy; 4IRCCS Policlin San Matteo, Pavia, Italy; 5Univ Hosp, Padua, Italy; 6INSERM U379, Marseille, France; 7Niguarda Hosp, Milan, Italy; and 8Pol Gemelli, Catholic Univ, Rome, Italy
Background: Immunesuppression for
HIV-infection or anti-rejection therapies aftter organ transplantation is a
well known risk factor for cancer. This increased risk has been well documented
for young adults, whereas few data are available on older persons. In this
study, we assessed the impact of cancer in HIV-positive persons (HIV+) and in
transplant persons (TRP) aged 50 years or older.
Methods: Data from a multi-cohort study
conducted in Italy and France were analysed. Individuals >=50 years of age
were selected from the original study group constituted by 2002 HIV+
seroconverters from Italy, 6072 HIV+ from France and 2755 Italian TRP (1844
kidney, 702 heart, 159 liver and 50 lung TRP). Sex- and age-standardized
incidence ratios (SIR) and 95% confidence intervals (CI) were computed to
quantify the cancer risk as compared to the general population. Among HIV+, the
risk of cancer was also assessed according to treatment with highly active
antiretroviral therapies (HAART).
Results: This analysis was based on 94
cancers diagnosed in 833 HIV+, and on 154 cancers diagnosed in 1558 TRP >=50 years of age.
The SIRs for all cancers decreased with ageing, ranging from 5.1 (95%
CI:4.0-6.5) in HIV+ aged 50-59 to 2.1 (95% CI:1.4-3.1) in HIV+ aged 60 or
older. In TRP, the SIRs for all cancer were 2.5 (95% CI:2.0-3.1) and 1.6 (95%
CI: 1.2-2.0), respectively. In HIV+, the protective effect of HAART was more
evident in those aged 50-59 (SIR=6.8 in never treated and SIR=2.4 in ever
treated) than in HIV+ aged >=60 (SIR=2.8 and SIR=1.6, respectively). This
pattern of cancer occurrence was peculiar to virus-related cancers (e.g.,
Kaposi’s sarcoma, non-Hodgkin’s lymphoma, liver cancer). SIRs for lung cancer
in both groups were significantly increased but did not significantly differ
according to HAART and/or age. The survival of both HIV+ and TRP was
significantly reduced by the diagnosis of cancer, but the difference in
survival was not associated with ageing (p=0.20).
Conclusions: The findings of this
analysis suggest that in aged individuals with acquired immunesuppression the
spectrum of cancer pattern is similar to the one observed in younger persons
with immunosuppression. However, the burden of cancer will increase in absolute
terms in these population groups, because of the increasing proportion of older
individuals among both HIV+ and TRP calling for primary and secondary
preventive interventions.
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