Your browser doesn't support javascript.
loading
Risk for Non-AIDS-Defining and AIDS-Defining Cancer of Early Versus Delayed Initiation of Antiretroviral Therapy : A Multinational Prospective Cohort Study.
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.
Afiliación
  • Chammartin F; University Hospital Basel and University of Basel, Basel, Switzerland (F.C., H.C.B.).
  • Lodi S; Boston University School of Public Health, Boston, Massachusetts (S.L.).
  • Logan R; Harvard T.H. Chan School of Public Health, Boston, Massachusetts (R.L.).
  • Ryom L; Rigshospitalet, University of Copenhagen, Copenhagen, Denmark (L.R., O.K., C.I.H., J.D.L.).
  • Mocroft A; University College London, London, United Kingdom (A.M., A.P., C.S.).
  • Kirk O; Rigshospitalet, University of Copenhagen, Copenhagen, Denmark (L.R., O.K., C.I.H., J.D.L.).
  • d'Arminio Monforte A; Azienda Ospedaliera-Polo, Universitario San Paolo, Milan, Italy (A.D.M.).
  • Reiss P; Amsterdam University Medical Centers, University of Amsterdam, and HIV Monitoring Foundation, Amsterdam, the Netherlands (P.R.).
  • Phillips A; University College London, London, United Kingdom (A.M., A.P., C.S.).
  • El-Sadr W; ICAP at Columbia University and Harlem Hospital, New York, New York (W.E.).
  • Hatleberg CI; Rigshospitalet, University of Copenhagen, Copenhagen, Denmark (L.R., O.K., C.I.H., J.D.L.).
  • Pradier C; Nice University Hospital, Nice, France (C.P.).
  • Bonnet F; Hôpital Saint-André and Université de Bordeaux, Bordeaux, France (F.B.).
  • Law M; University of New South Wales Sydney, Sydney, Australia (M.L.).
  • De Wit S; Saint Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium (S.D.).
  • Sabin C; University College London, London, United Kingdom (A.M., A.P., C.S.).
  • Lundgren JD; Rigshospitalet, University of Copenhagen, Copenhagen, Denmark (L.R., O.K., C.I.H., J.D.L.).
  • Bucher HC; University Hospital Basel and University of Basel, Basel, Switzerland (F.C., H.C.B.).
Ann Intern Med ; 174(6): 768-776, 2021 06.
Article en En | MEDLINE | ID: mdl-33721519
ABSTRACT

BACKGROUND:

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 DAD (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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Fármacos Anti-VIH / Tiempo de Tratamiento / Neoplasias Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Intern Med Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / Fármacos Anti-VIH / Tiempo de Tratamiento / Neoplasias Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Intern Med Año: 2021 Tipo del documento: Article