Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy: A multinational prospective cohort study

For the D:A:D Study Group

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

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 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.

Original languageEnglish
Pages (from-to)768-776
Number of pages9
JournalAnnals of Internal Medicine
Volume174
Issue number6
DOIs
StatePublished - 1 Jun 2021
Externally publishedYes

Funding

FundersFunder number
Merck
Boehringer Ingelheim
Providence/Boston Center for AIDS Research
CHIP
Danmarks Grundforskningsfond
Cilag
Gilead Sciences
National Institutes of Health
Swiss Cancer League/Swiss Cancer Research
Ministerie van Volksgezondheid, Welzijn en Sport
National Institute of Allergy and Infectious Diseases
Centre of Excellence for Health, Immunity and Infections
Seventh Framework Programme260694
Janssen Pharmaceuticals
Janssen Research and Development
National Institute for Public Health
Swiss HIV Cohort Research Foundation
Bristol-Myers Squibb
U.S. Food and Drug Administration
Personalized Medicine of Infectious Complications
ViiV Healthcare
Pfizer
Highly Active Anti-retroviral Therapy Oversight Committee
Fondo de Investigación SanitariaFIPSE 3171/00
Agence Nationale de Recherches sur le Sida et les Hépatites ViralesFIS 99/0887
Stiftung Institut fu€r klinische EpidemiologieP30AI042853
GlaxoSmithKline108787
Fundación para la Investigación y la Prevención del SIDA en España5U01AI046362-03, 5U01AI042170-10
University of New South WalesKFS-4106-02-2017
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung148522
amfAR, The Foundation for AIDS ResearchU01-AI069907

    Fingerprint

    Dive into the research topics of 'Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy: A multinational prospective cohort study'. Together they form a unique fingerprint.

    Cite this