Evidence map›Paper›PMID 42706475›Full record

ArticleClinical rheumatology2026

Comparison of telitacicept and belimumab in systemic lupus erythematosus: a real-word retrospective study.

Mian Liu, Yirui Shi, Wen-Yi Yuan, Yun Zhu, Hui-Min Zhu, Xiao-Jing Li, Ya-Qi Zhang, Mengqing Rong, Shu Liu, Renju Xu and 4 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Mian LiuDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, China.
Yirui ShiDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Xuzhou Medical University, Xuzhou, China.
Wen-Yi YuanDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, China.
Yun ZhuDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China.
Hui-Min ZhuDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China.
Xiao-Jing LiDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China.
Ya-Qi ZhangDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, China.
Mengqing RongDepartment of Rheumatology and Immunology, Drum Tower Hospital, China Pharmaceutical University, Nanjing, Nanjing, 210008, China.
Shu LiuDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China.
Renju XuDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China.
Xuebing FengDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, China.
Wei ShenDepartment of Rheumatology and Immunology, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, Nanjing, Jiangsu, 210000, China. shenweiqh@163.com.
Dandan WangDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine, Nanjing, China. dandanwangffd@nju.edu.cn.ORCID http://orcid.org/0000-0002-9370-0668
Lingyun SunDepartment of Rheumatology and Immunology, Nanjing Drum Tower Hospital Clinical College of Xuzhou Medical University, Xuzhou, China. lingyunsun@nju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTelitacicept and belimumab are two biological agents approved for treating systemic lupus erythematosus (SLE) in China. This study mainly discusses the therapeutic efficacy of these two biological agents in SLE.

methodsSLE patients who received telitacicept or belimumab at Nanjing Drum Tower Hospital from March 2021 to March 2023 were included. Clinical characteristics were compared, and 1:1 propensity score matching (PSM) was performed. Statistical analyses included normality tests, t tests, Mann‒Whitney U tests, and chi‒square tests.

resultsBoth telitacicept and belimumab demonstrated robust clinical efficacy. Pre-matching, SLE responder index-4 (SRI-4) response rates were 42.4% (telitacicept) and 49% (belimumab), with median SLEDAI reductions of 2 and 1.5 points, respectively. Serum albumin, complement component 3 (C3), and complement component 4 (C4) levels increased significantly after treatment in both groups. Post-matching, clinically meaningful SRI-4 rates persisted (40.0% vs. 52.0%, P = 0.570), alongside median SLEDAI reductions (10 to 8 vs. 12 to 8). After PSM, although overall bias was reduced, baseline imbalances persisted for key laboratory parameters, notably serum C4 (standardized mean difference [SMD] > 0.2), necessitating cautious interpretation of between-group comparisons. Although the median absolute C4 increase was numerically higher with telitacicept (0.07 [IQR 0.01-0.11]) than belimumab (0.03 [IQR 0.01-0.10]), effect size quantification revealed a small magnitude (Hedges' g = 0.243, 95% CI: - 0.319 to 0.804) with limited precision. Exploratory analysis of the lupus nephritis subgroup revealed a more pronounced reduction in IgG levels with telitacicept versus belimumab (nominal P = 0.019; Hedges' g =  - 0.242, 95% CI: - 0.755 to 0.272), though findings remain hypothesis-generating given the limited sample size and unadjusted multiple comparisons.

conclusionBoth telitacicept and belimumab reduced disease activity in SLE. While telitacicept exhibited a numerical trend toward greater C4 elevation in SLE and a potential signal of greater IgG reduction in LN, these findings require validation in adequately powered prospective trials. Key points • This study compared the efficacy of telitacicept and belimumab treatment in SLE, presenting important reference function for clinical medication.

Indexed as

BelimumabSystemic lupus erythematosusTelitacicept

Identifiers

PMID42706475

What Socratic holds

Textmetadata
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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 Socratic graph.