Evidence map›Paper›PMID 37308847›Full record

ArticleBMC infectious diseases2023

Treatment persistence of bictegravir/emtricitabine/tenofovir alafenamide and efavirenz + lamivudine + tenofovir disoproxil among HIV-1 patients newly starting treatment in Hunan Province in China.

Cao Jing, Tang Wei, Wang Ning, Zheng Fang, Xiao Gang, Wang Xingzhi, Zhou Guoqiang, Wang Min

Abstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Cao JingDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.
Tang WeiDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.
Wang NingDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.
Zheng FangDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.
Xiao GangDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.
Wang XingzhiYidu Cloud Technology, Shanghai, China.
Zhou GuoqiangDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China. Cqc5262@126.com.
Wang MinDivision of Infectious Diseases, the First Hospital of Changsha, Changsha, Hunan, China.

Funding

Special Foundation for Innovation Development in Hunan Province 2020SK21362the National Major Infectious Prevention and Treatment Program in the 13th Five-Year Plan 2018zx10302104-001
6 · The paper itself

Abstract

backgroundThough bictegravir/emtricitabine/tenofovir (BIC/FTC/TAF) have been regulatory approved and included in the National Reimbursement Drug List in China, due to the affordability concern, generic version of efavirenz + lamivudine + tenofovir (EFV + 3TC + TDF) is still recommended as the first-line therapy in the clinical guideline and widely used in clinical practice. The aim of the study is to assess the persistence with first-line BIC/TAF/TAF and EFV + 3TC + TDF in newly treated HIV-1 patients in the real-world setting in Hunan Province in China.

methodsA retrospective analysis of the medical records of HIV patients initiating first-line antiretroviral therapy in the First Hospital of Changsha in January 1st, 2021-July 31st, 2022 was conducted. Persistence was assessed as the number of days on the therapy from the index until treatment discontinuation or end of data availability. Kaplan-Meier Curves and Cox Proportional Hazard models were used to evaluate the discontinuation rates. Subgroup analysis was performed excluding BIC/FTC/TAF patients with treatment discontinuation due to economic reason, and EFV + 3TC + TDF patients with a viral load > 500,000 copies/mL.

resultsA total of 310 eligible patients were included in the study, with 244 and 66 patients in the BIC/FTC/TAF group and EFV + 3TC + TDF group, respectively. Compared with EFV + 3TC + TDF patients, BIC/FTC/TAF patients were older, more living in the capital city currently, and had significantly higher total cholesterol and low-density level (all p < 0.05). No significant difference was shown in the time to discontinuation between BIC/FTC/TAF patients and EFV + 3TC + TDF patients. After excluding BIC/FTC/TAF patients with treatment discontinuation due to economic reason, EFV + 3TC + TDF group were shown to have a significantly higher risk of discontinuation than BIC/FTC/TAF group (hazard ratio [HR] = 11.1, 95% confidence interval [CI] = 1.3-93.2). After further removing the EFV + 3TC + TDF patients with a viral load > 500,000 copies/mL, the analysis showed similar results (HR = 10.1, 95% CI = 1.2-84.1). 79.4% of the EFV + 3TC + TDF patients discontinued treatment due to clinical reasons, while 83.3% of the BIC/FTC/TAF patients discontinued treatment due to economic reasons.

conclusionsCompared with BIC/FTC/TAF, EFV + TDF + 3TC patients were significantly more likely to discontinue the first-line treatment in Hunan Province in China.

Indexed as

HIV-1HIV InfectionsAlanineAlkynesAmidesBenzoxazinesChinaCyclopropanesDrug CombinationsHeterocyclic Compounds, 3-RingHeterocyclic Compounds, 4 or More RingsHumansLamivudinePiperazinesPyridonesRetrospective StudiesAlanineAlkynesAmidesBenzoxazinesbictegravirCyclopropanesDrug CombinationsefavirenzHeterocyclic Compounds, 3-RingHeterocyclic Compounds, 4 or More RingsLamivudinePiperazinesPyridonesTenofovirtenofovir alafenamideBIC/FTA/TAFChinaEFV + TDF + 3TCFirst-line therapyPersistenceTreatment discontinuation

Identifiers

PMID37308847
PMCPMC10258991

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Registered trials

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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.