Evidence map›Paper›PMID 40367375›Full record

Trial reportThe New England journal of medicine2025

Second-Line Antiretroviral Therapy for Children Living with HIV in Africa.

Victor Musiime, Mutsa Bwakura-Dangarembizi, Alexander J Szubert, Vivian Mumbiro, Hilda A Mujuru, Cissy M Kityo, Abbas Lugemwa, Katja Doerholt, Chishala Chabala, Shafic Makumbi and 28 more

Abstract readClinical Trial, Phase IIIComparative StudyEquivalence Trial
In one paragraph

Trial report in The New England journal of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Trial
  2. Observational
  3. HIV Resistance to Dolutegravir Varies With Coadministered Agents.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  4. Article
  5. EU-Africa partnerships in health research from 2014 to 2023: Outputs and lessons learnt.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2026
    Article
  6. Review
  7. Article
  8. Review
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

38 authors.

Victor MusiimeMakerere University, College of Health Sciences, School of Medicine, Department of Paediatrics and Child Health, Kampala, Uganda.
Mutsa Bwakura-DangarembiziFaculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Alexander J SzubertMedical Research Council Clinical Trials Unit at University College London, London.
Vivian MumbiroUniversity of Zimbabwe Clinical Research Center, Harare, Zimbabwe.
Hilda A MujuruFaculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Cissy M KityoJoint Clinical Research Centre, Kampala, Uganda.
Abbas LugemwaJoint Clinical Research Centre, Mbarara, Uganda.
Katja DoerholtMedical Research Council Clinical Trials Unit at University College London, London.
Chishala ChabalaUniversity of Zambia, School of Medicine, Lusaka, Zambia.
Shafic MakumbiInfectious Diseases Research Collaboration, Kampala, Uganda.
Veronica MulengaUniversity of Zambia, School of Medicine, Lusaka, Zambia.
Helen McIlleronDepartment of Medicine, University of Cape Town, Cape Town, South Africa.
David BurgerRadboudumc Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, the Netherlands.
Eva NatukundaJoint Clinical Research Centre, Kampala, Uganda.
Clare ShakeshaftMedical Research Council Clinical Trials Unit at University College London, London.
Kyomuhendo Jovia LindaJoint Clinical Research Centre, Kampala, Uganda.
Kusum NathooUniversity of Zimbabwe Clinical Research Center, Harare, Zimbabwe.
Lara MonkiewiczMedical Research Council Clinical Trials Unit at University College London, London.
Ibrahim YaweJoint Clinical Research Centre, Fort Portal, Uganda.
Monica KapasaUniversity Teaching Hospitals Children's Hospital, Lusaka, Zambia.
Mary NyathiMpilo Central Hospital, Bulawayo, Zimbabwe.
Joyce LunguUniversity of Zambia, School of Medicine, Lusaka, Zambia.
Bwendo NdunaArthur Davison Children's Hospital, Ndola, Zambia.
Wedu NdebeleNational University of Science and Technology (NUST), NUST Mpilo Hospital Complex, Bulawayo, Zimbabwe.
Annabelle SouthMedical Research Council Clinical Trials Unit at University College London, London.
Mwate MwamabaziArthur Davison Children's Hospital, Ndola, Zambia.
Godfrey MusoroUniversity of Zimbabwe Clinical Research Center, Harare, Zimbabwe.
Anna GriffithsMedical Research Council Clinical Trials Unit at University College London, London.
Khozya ZyamboUniversity Teaching Hospitals Children's Hospital, Lusaka, Zambia.
Rashidah NazzindaJoint Clinical Research Centre, Kampala, Uganda.
Kevin ZimbaUniversity Teaching Hospitals Children's Hospital, Lusaka, Zambia.
Yingying ZhangCentre for Health Economics, University of York, York, United Kingdom.
Simon WalkerCentre for Health Economics, University of York, York, United Kingdom.
Anna TurkovaMedical Research Council Clinical Trials Unit at University College London, London.
A Sarah WalkerMedical Research Council Clinical Trials Unit at University College London, London.
Alasdair BamfordMedical Research Council Clinical Trials Unit at University College London, London.
Diana M GibbMedical Research Council Clinical Trials Unit at University College London, London.
CHAPAS-4 Trial Team

Funding

European and Developing Countries Clinical Trials Partnership RIA2019PD-2882European and Developing Countries Clinical Trials Partnership TRIA2015-1078European & Developing Countries Clinical Trials Partnership (EDCTP) RIA2019PD-2882European & Developing Countries Clinical Trials Partnership (EDCTP) TRIA2015-1078Gilead Sciences CO-EU-311-4461Janssen Pharmaceuticals 2094259Medical Research Council MC_UU_00004/03Medical Research Council MC_UU_0004/03
6 · The paper itself

Abstract

backgroundChildren living with human immunodeficiency virus (HIV) have limited options for second-line antiretroviral therapy (ART).

methodsIn this open-label trial with a 2-by-4 factorial design, we randomly assigned children with HIV who had first-line treatment failure to receive second-line therapy with tenofovir alafenamide fumarate (TAF)-emtricitabine or standard care (abacavir or zidovudine, plus lamivudine) as the backbone and dolutegravir or ritonavir-boosted darunavir, atazanavir, or lopinavir as the anchor drug. The primary outcome was a viral load of less than 400 copies per milliliter at 96 weeks. We hypothesized that TAF-emtricitabine would be noninferior to standard care, that dolutegravir and ritonavir-boosted darunavir would each be superior to ritonavir-boosted lopinavir and atazanavir analyzed in combination, and that ritonavir-boosted atazanavir would be noninferior to ritonavir-boosted lopinavir. Safety was also assessed.

resultsA total of 919 children underwent randomization; 458 were assigned to receive TAF-emtricitabine, and 461 to receive standard care. Assigned anchor drugs were dolutegravir (229 participants), ritonavir-boosted darunavir (232), ritonavir-boosted atazanavir (231), and ritonavir-boosted lopinavir (227). The median age of participants was 10 years, and 497 (54.1%) were male. The median viral load at baseline was 17,573 copies per milliliter. At week 96, TAF-emtricitabine was superior to standard care: the adjusted difference in the percentage of participants with a viral load of less than 400 copies per milliliter was 6.3 percentage points (95% confidence interval [CI], 2.0 to 10.6; P = 0.004). Dolutegravir was superior to ritonavir-boosted lopinavir and atazanavir analyzed in combination (adjusted difference, 9.7 percentage points; 95% CI, 4.8 to 14.5; P<0.001), but ritonavir-boosted darunavir was not (adjusted difference, 5.6 percentage points; 95% CI, 0.3 to 11.0; P = 0.04 [prespecified threshold, P = 0.03]). Ritonavir-boosted atazanavir was noninferior to ritonavir-boosted lopinavir. One child died, and 29 (3.2%) had serious adverse events, with no significant between-group differences.

conclusionsSecond-line ART regimens including TAF-emtricitabine and dolutegravir were effective for children, with no evidence of safety concerns. Ritonavir-boosted darunavir was also effective. (Funded by the European and Developing Countries Clinical Trials Partnership and others; CHAPAS-4 ISRCTN Registry number, ISRCTN22964075.).

Indexed as

Anti-HIV AgentsHIV InfectionsAdolescentAfricaAtazanavir SulfateCD4 Lymphocyte CountChildChild, PreschoolDarunavirDolutegravirDrug Therapy, CombinationEmtricitabineFemaleHeterocyclic Compounds, 3-RingHumansLopinavirAnti-HIV AgentsAtazanavir SulfateDarunavirDolutegravirEmtricitabineHeterocyclic Compounds, 3-RingLopinavirOxazinesPiperazinesPyridonesRitonavirTenofovir

Identifiers

PMID40367375
PMCPMC7617794

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.