Evidence map›Paper›PMID 40281525›Full record

ArticleBMC infectious diseases2025

INSTIs-centered antiviral regimens for first-line treatment of HIV/AIDS: a network meta-analysis and cost-effectiveness analysis.

Jian Yang, Xuejuan Zhao, Fan Li

Abstract readNetwork Meta-Analysis
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
–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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. 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

3 authors.

Jian Yang *School of Pharmaceutical Sciences & Yunnan Provincial Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming, Yunnan, 650500, People's Republic of China.
Xuejuan Zhao *School of Pharmaceutical Sciences & Yunnan Provincial Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming, Yunnan, 650500, People's Republic of China.
Fan LiYunnan Provincial Center for Drug Policy Research, Kunming, Yunnan, 650500, People's Republic of China. ywzxyjzx@163.com.

Funding

Research Project on Education and Teaching of Kunming Medical University, 2023 Project No. 2023-JY-Y-090The First-Class Discipline Team of Kunming Medical University (Research and Practice Team of Pharmaceutical Policy) No. 2024XKTDPY21Undergraduate Teaching Quality and Reform Project of Kunming Medical University, 2024 (Course: Clinical Pharmacokinetics) Project No. 2024KCSZSFXM022Yunnan Provincial Department of Education Science Research Fund Project 2025J0227
6 · The paper itself

Abstract

objectiveThis study evaluates the efficacy, safety, and cost-effectiveness of INSTI-based antiretroviral regimens compared to the national standard first-line treatment EFV/3TC/TDF for HIV/AIDS in China. The aim is to guide clinical decision-making and improve HIV/AIDS prevention and treatment.

methodsA network meta-analysis was conducted using ADDIS software on data from domestic and international randomized controlled trials comparing INSTI-based regimens with EFV/3 TC/TDF. Additionally, a Markov model assessed the cost-effectiveness of the representative INSTI regimen B/F/TAF (Bictegravir/Emtricitabine/Tenofovir Alafenamide) against EFV/3 TC/TDF. Costs and health outcomes were measured in US Dollars ($) and Quality-Adjusted Life Years (QALYs), respectively, evaluating incremental cost-utility ratios (ICERs) against a willingness-to-pay threshold of 1.5 times GDP per capita.

resultsSeventeen trials involving 12,620 patients were analyzed. INSTI regimens showed no significant efficacy or safety advantages over EFV/3 TC/TDF but offered better drug resistance, adherence, and quality of life improvements. Economic analysis from the patient perspective showed that B/F/TAF had an ICER of $12,714.29/QALY, which is below the willingness-to-pay threshold, indicating cost-effectiveness. From the healthcare system perspective, B/F/TAF's ICER was $23,052.77/QALY, which is above the threshold, suggesting it is not cost-effective from this perspective. Sensitivity analyses confirmed these findings, with drug costs for B/F/TAF and the probability of CD4 count increase post-EFV/3TC/TDF treatment being the largest influencing factors. Additionally, probabilistic sensitivity analysis indicated that B/F/TAF has a varying probability of economic viability depending on the willingness-to-pay threshold, highlighting its potential value in specific economic contexts.

conclusionINSTI-based regimens are as effective and safe as the national standard but offer additional benefits in drug resistance and patient compliance. B/F/TAF is economically viable from the patient perspective but does not present a cost-utility advantage from the healthcare system perspective. This study underscores the need for considering both clinical and economic factors in selecting first-line HIV/AIDS treatments in China.

Indexed as

Anti-HIV AgentsHIV InfectionsChinaCost-Benefit AnalysisCost-Effectiveness AnalysisHumansQuality-Adjusted Life YearsRandomized Controlled Trials as TopicTreatment OutcomeAnti-HIV AgentsCost-effectiveness analysisHealthcare resource allocationHIV/AIDS treatmentINSTI-based regimensNetwork meta-analysis

Identifiers

PMID40281525
PMCPMC12032712

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.