Publications

Journal Article Ahead of print

PubMed: 41967904 DOI: 10.1093/cid/ciag232

Predictors of treatment failure in children living with HIV starting first-line antiretroviral therapy in the ODYSSEY trial.

Clin Infect Dis

Authors: James Wyncoll, Rujirek Kamolrattana, Moherndran Archary, Hilda A Mujuru, Adeodata R Kekitiinwa, Avy Violari, Sathaporn Na-Rajsima, Abbas Lugemwa, Ebrahim Variava, Mark Cotton, Cissy M Kityo, Christoph Königs, Ngundu Osee Behuhuma, Steve Welch, Yacine Saïdi, Laura Marques, Grace M Ahimbisibwe, Lily Houlden, Carlo Giaquinto, Pablo Rojo, Diana M Gibb, Thanyawee Puthanakit, Anna Turkova, Ellen White, Deborah Ford

Affiliations

  • MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London, United Kingdom.
  • Department of Pediatrics, Nakornping Hospital, Chiang Mai, Thailand.
  • Enhancing Care Foundation, Victoria Mxenge Hospital, Durban, South Africa.
  • University of Zimbabwe, Harare, Zimbabwe.
  • Baylor College of Medicine Children's Foundation, Uganda.
  • Perinatal HIV Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
  • Pediatric Department, Mahasarakam Hospital, Maha Sarakham, Thailand.
  • Joint Clinical Research Centre (JCRC), Mbarara, Uganda.
  • Family Center for Research with Ubuntu, Department of Paediatrics & Child Health, Stellenbosch University, Tygerberg, South Africa.
  • Joint Clinical Research Centre (JCRC), Kampala, Uganda.
  • Goethe University Frankfurt, Department of Paediatrics and Adolescent Medicine, Germany.
  • Africa Health Research Institute (AHRI), Kwazulu-Natal, South Africa.
  • University Hospitals Birmingham NHS Foundation Trust, Birmingham.
  • INSERM/ANRS SC10-US19, Essais thérapeutiques et maladies Infectieuses, Villejuif, France.
  • Centro Materno-infantil do Norte, ULSSA, Porto, Portugal.
  • Makerere University-Johns Hopkins University (MU-JHU) Research Collaboration, Kampala, Uganda.
  • University of Padova, Department of Women and Child Health, Padova, Italy.
  • Pediatric Infectious Diseases Unit, Hospital 12 de Octubre, Madrid, Spain.
  • HIVNAT, Thai Red Cross AIDS Research Center, Bangkok, Thailand.

Abstract

BACKGROUND

Data on predictors of treatment failure in children starting antiretroviral therapy (ART) are limited, particularly on dolutegravir-based regimens (DTG).

METHODS

ODYSSEY demonstrated superior efficacy of DTG versus standard-of-care (SOC). We assessed predictors at ART initiation of treatment failure by 96 weeks.

RESULTS

381 children started first-line ART (82% African). At ART-initiation, median age was 10.5 years (IQR:6.5,14.0, 67<3 years), CD4% 20% (IQR:12, 28), BMI-for-age Z-score -0.58 (IQR:-1.48,+0.25). 189 children started DTG, 192 started SOC (91%≥3 years started efavirenz; 79%<3 years started lopinavir). 75 children experienced treatment failure (24 DTG, 51 SOC). Failure risk was lower on DTG than SOC (HR=0.47, 95%CI:0.29-0.77, p=0.002). Lower BMI-for-age Z-score (HR=0.82 for each unit gain, 95%CI:0.70-0.96, p=0.01) and being at an African site (HR=2.09, 95%CI:0.82-5.31, p=0.09) were associated with higher failure risk. Risk was also higher at younger ages with the steepest increase in the youngest children, and increased at lower CD4%, with a stronger CD4% effect at younger ages. At CD4%=20, hazard ratios relative to age 10 years were 2.40 (95%CI: 1.58-3.65) at age 1 year, 1.30 (95%CI: 1.15-1.48) at age 5 years and 0.80 (95%CI: 0.72-0.89) at age 18 years. At age 1 year, hazard ratios relative to CD4%=20 were 1.39 (95%CI: 1.16-1.66) at CD4%=15, and 0.52 (95%CI: 0.36-0.75) at CD4%=30; at age 10 corresponding estimates were 1.07 (95%CI: 0.94-1.20) at CD4%=15, and 0.88 (95%CI: 0.69-1.13) at CD4%=30.

CONCLUSIONS

Young age, low BMI-for-age and low CD4% at ART initiation predicted higher risk of treatment failure and can guide targeted support.

MeSH

Treatment Failure, Hiv, Therapeutics, Communicable Diseases, Child, Dolutegravir