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Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy (CROSBI ID 309359)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

(D:A:D Study Group) Chammartin, Frédérique ; Lodi, Sara ; Logan, Roger ; Ryom, Lene ; Mocroft, Amanda ; Kirk, Ole ; d’Arminio Monforte, Antonella ; Reiss, Peter ; Phillips, Andrew ; El-Sadr, Wafaa et al. Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy // Annals of internal medicine, 174 (2021), 6; 768-776. doi: 10.7326/m20-5226

Podaci o odgovornosti

Chammartin, Frédérique ; Lodi, Sara ; Logan, Roger ; Ryom, Lene ; Mocroft, Amanda ; Kirk, Ole ; d’Arminio Monforte, Antonella ; Reiss, Peter ; Phillips, Andrew ; El-Sadr, Wafaa ; Hatleberg, Camilla I. ; Pradier, Christian ; Bonnet, Fabrice ; Law, Matthew ; De Wit, Stéphane ; Sabin, Caroline ; Lundgren, Jens D. ; Bucher, Heiner C.

D:A:D Study Group

engleski

Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy

ackground: Immediate initiation of antiretroviral therapy (ART) regardless of CD4 cell count reduces risk for AIDS and non-AIDS-related events in asymptomatic, HIV-positive persons and is the standard of care. However, most HIV-positive persons initiate ART when their CD4 count decreases below 500 × 109 cells/L. Consequences of delayed ART on risk for non-AIDS-defining and AIDS-defining cancer, one of the most common reasons for death in HIV, are unclear. Objective: To estimate the long-term risk difference for cancer with the immediate ART strategy. Design: Multinational prospective cohort study. Setting: The D:A:D (Data collection on Adverse events of anti-HIV Drugs) study, which included HIV-positive persons from Europe, Australia, and the United States. Participants: 8318 HIV-positive persons with at least 1 measurement each of CD4 cell count and viral load while ART-naive (study period, 2006 to 2016). Measurements: The parametric g-formula was used, with adjustment for baseline and time- dependent confounders (CD4 cell count and viral load), to assess the 10-year risk for non-AIDS- defining and AIDS-defining cancer of immediate versus deferred (at CD4 counts < 350 and < 500 × 109 cells/L) ART initiation strategies. Results: During 64 021 person-years of follow-up, 231 cases of non-AIDS-defining cancer and 272 of AIDS- defining cancer occurred among HIV-positive persons with a median age of 36 years (interquartile range, 29 to 43 years). With immediate ART, the 10-year risk for non-AIDS- defining cancer was 2.97% (95% CI, 2.37% to 3.50%) and that for AIDS-defining cancer was 2.50% (CI, 2.37% to 3.38%). Compared with immediate ART initiation, the 10-year absolute risk differences when deferring ART to CD4 counts less than 500 × 109 cells/L and less than 350 × 109 cells/L were 0.12 percentage point (CI, -0.01 to 0.26 percentage point) and 0.29 percentage point (CI, -0.03 to 0.73 percentage point), respectively, for non-AIDS-defining cancer and 0.32 percentage point (CI, 0.21 to 0.44 percentage point) and 1.00 percentage point (CI, 0.67 to 1.44 percentage points), respectively, for AIDS-defining cancer. Limitation: Potential residual confounding due to observational study design. Conclusion: In this young cohort, effects of immediate ART on 10-year risk for cancer were small, and further supportive data are needed for non-AIDS-defining cancer. Primary Funding Source: Highly Active Antiretroviral Therapy Oversight Committee.

adult ; anti-HIV agents ; CD4 lymphocyte count ; female ; HIV infections ; humans ; incidence ; male ; middle aged ; neoplasms ; prospective studies ; risk factors ; time-to-treatment ; viral load

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Podaci o izdanju

174 (6)

2021.

768-776

objavljeno

0003-4819

1539-3704

10.7326/m20-5226

Povezanost rada

Kliničke medicinske znanosti

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