Evidence map›Paper›PMID 38730460›Full record

SynthesisArthritis research & therapy2024

Efficacy and safety study of targeted small-molecule drugs in the treatment of systemic lupus erythematosus.

Shiheng Wang, Wanling Ning, Hanqing Tang, Chaochao Mu, Xiaosong Huang

Abstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in Arthritis research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 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, 1 synthesis or guideline pooled it.

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

5 authors.

Shiheng Wang *China Institute for History of Medicine and Medical Literature, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Wanling Ning *Hunan University of Chinese Medicine, Changsha Hunan, 410005, China.
Hanqing TangSchool of Basic Medicine, Youjiang Medical University for Nationalities, Youjiang Guangxi, Baise, 533000, China.
Chaochao MuTraditional Chinese Medicine Department, Tianjin Nankai District Bainian Renyitang Traditional Chinese Medicine Clinic, Tianjin, 301700, China. 13114950328@163.com.
Xiaosong HuangHunan Provincial Brain Hospital, Changsha Hunan, 410021, China. Huangxs-0819@163.com.

Funding

2016 Hunan Provincial Health and Family Planning Commission Research Program Project C2016019
6 · The paper itself

Abstract

backgroundTargeted small-molecule drugs in the treatment of systemic lupus erythematosus (SLE) have attracted increasing attention from clinical investigators. However, there is still a lack of evidence on the difference in the efficacy and safety of different targeted small-molecule drugs. Therefore, this study was conducted to assess the efficacy and safety of different targeted small-molecule drugs for SLE.

methodsRandomized controlled trials (RCTs) on targeted small-molecule drugs in the treatment of SLE in PubMed, Web of Science, Embase, and Cochrane Library were systematically searched as of April 25, 2023. Risk of bias assessment was performed for included studies using the Cochrane's tool for evaluating the risk of bias. The primary outcome indicators were SRI-4 response, BICLA response, and adverse reaction. Because different doses and courses of treatment were used in the included studies, Bayesian network meta-regression was used to investigate the effect of different doses and courses of treatment on efficacy and safety.

resultsA total of 13 studies were included, involving 3,622 patients and 9 targeted small-molecule drugs. The results of network meta-analysis showed that, in terms of improving SRI-4, Deucravacitinib was significantly superior to that of Baricitinib (RR = 1.32, 95% CI (1.04, 1.68), P < 0.05). Deucravacitinib significantly outperformed the placebo in improving BICLA response (RR = 1.55, 95% CI (1.20, 2.02), P < 0.05). In terms of adverse reactions, targeted small-molecule drugs did not significantly increase the risk of adverse events as compared to placebo (P > 0.05).

conclusionBased on the evidence obtained in this study, the differences in the efficacy of targeted small-molecule drugs were statistically significant as compared to placebo, but the difference in the safety was not statistically significant. The dose and the course of treatment had little impact on the effect of targeted small-molecule drugs. Deucravacitinib could significantly improve BICLA response and SRI-4 response without significantly increasing the risk of AEs. Therefore, Deucravacitinib is very likely to be the best intervention measure. Due to the small number of included studies, more high-quality clinical evidence is needed to further verify the efficacy and safety of targeted small-molecule drugs for SLE.

Indexed as

Lupus Erythematosus, SystemicRandomized Controlled Trials as TopicAzetidinesHumansMolecular Targeted TherapyPurinesPyrazolesSulfonamidesTreatment OutcomeAzetidinesbaricitinibPurinesPyrazolesSulfonamidesBayesian network meta-analysisSafetySLESystem evaluationTargeted small-molecule drugs

Identifiers

PMID38730460
PMCPMC11083747

What OpenQuestion holds

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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.