Evidence map›Paper›PMID 41027687›Full record

ArticleLupus science & medicine2025

Clinical characteristics and treatment response of patients with SLE complicated with thrombotic thrombocytopenic purpura.

Kai Zhang, Peng Zhao, Bo Huang, Yifan Wang, Taoran Bi, Peiliang Gao, Chunyu Wang, Xiaoyan Xing, Naidi Wang, Ruiling Feng and 8 more

Abstract read
In one paragraph

Article in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Epidemiology of immune-mediated thrombotic thrombocytopenic purpura in Germany.Research and practice in thrombosis and haemostasis · 2026
    Article
  3. 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

18 authors.

Kai Zhang *Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Peng Zhao *Peking University Institute of Hematology, Beijing, China.
Bo HuangDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Yifan WangDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Taoran BiDepartment of Respiratory and Critical Care Medicine, Peking University People's Hospital, Beijing, China.
Peiliang GaoPeking University People's Hospital, Beijing, China.
Chunyu WangPeking University People's Hospital, Beijing, China.
Xiaoyan XingDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Naidi WangDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Ruiling FengDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Gong ChengDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Haihong YaoDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Yuan AnDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Yunshan ZhouDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.ORCID 0000-0002-7448-8884
Yuebo JinDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Yuhui LiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Zhanguo LiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Jing HePeking University People's Hospital, Beijing, China hejing1105@126.com.ORCID 0000-0003-3904-8928

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSLE complicated with thrombotic thrombocytopenic purpura (SLE-TTP) is a rare but potentially fatal condition. Current studies regarding SLE-TTP are limited to case reports and literature reviews. This study presents a cohort of patients with SLE-TTP and aims to investigate their clinical characteristics and treatment outcomes, as well as to explore the efficacy of rituximab (RTX) maintenance therapy (RMT) for relapse prevention and long-term disease control.

methodsPatients with SLE-TTP were retrospectively identified in an SLE cohort. Baseline characteristics, acute-phase treatment responses and long-term outcomes were collected. All patients received RTX-containing induction therapy during the acute phase of TTP. Maintenance therapy was categorised as RMT (regular RTX infusions) or non-RMT (conventional immunosuppressants and/or biologics) regimens. TTP relapse, lupus low disease activity state (LLDAS) and infection rates were compared between groups.

resultsOf 33 patients with SLE-TTP, 31 (94%) achieved clinical remission following RTX-containing induction therapy, while 2 died during the acute phase. Fourteen patients (45%) received RMT, and 17 (55%) received non-RMT regimens. During a median follow-up of 22.9 months, TTP relapse occurred in seven (23%) patients: one (7%) in the RMT group and six (35%) in the non-RMT group. Kaplan-Meier analysis revealed significantly longer relapse-free survival with RMT (log-rank p=0.027). All patients receiving RMT achieved LLDAS, compared with 59% of patients in the non-RMT group. Infection rates were comparable between the two groups.

conclusionsRTX-containing induction regimens resulted in high rates of clinical remission in patients with SLE-TTP. RMT was associated with a significantly reduced risk of TTP relapse and superior long-term control of SLE disease activity, without an excess risk of severe infection. These findings support RMT as a potential option for long-term management of SLE-TTP.

Indexed as

Immunosuppressive AgentsLupus Erythematosus, SystemicPurpura, Thrombotic ThrombocytopenicRituximabAdultFemaleHumansMaleMiddle AgedRecurrenceRemission InductionRetrospective StudiesSecondary PreventionTreatment OutcomeYoung AdultImmunosuppressive AgentsRituximabHematologyLupus Erythematosus, SystemicThrombocytopenia

Identifiers

PMID41027687
PMCPMC12506446

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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.