Evidence map›Paper›PMID 35230560›Full record

ArticleClinical rheumatology2022

Low dosage use of cyclophosphamide improves the survival of patients with systemic lupus erythematosus.

Yoosuf Ali Ashraf Muhammad Hussenbocus, Ziyi Jin, Wenyou Pan, Lin Liu, Min Wu, Huaixia Hu, Xiang Ding, Hua Wei, Yaohong Zou, Xian Qian and 9 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2022. 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. Article
  3. [A multicenter study on the tolerance of intravenous low-dose cyclophosphamide in systemic lupus erythematosus].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2022
    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

19 authors.

Yoosuf Ali Ashraf Muhammad HussenbocusNanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, China.
Ziyi JinDepartment of Rheumatology and Immunology, the Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, China. jzy-327@163.com.ORCID http://orcid.org/0000-0002-8091-2266
Wenyou PanDepartment of Rheumatology, Huai'an First People's Hospital, Huai'an, China.
Lin LiuDepartment of Rheumatology, Xuzhou Central Hospital, Xuzhou, China.
Min WuDepartment of Rheumatology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Huaixia HuDepartment of Rheumatology, Lianyungang Second People's Hospital, Lianyungang, China.
Xiang DingDepartment of Rheumatology, Lianyungang First People's Hospital, Lianyungang, China.
Hua WeiDepartment of Rheumatology, Northern Jiangsu People's Hospital, Yangzhou, China.
Yaohong ZouDepartment of Rheumatology, Wuxi People's Hospital, Wuxi, China.
Xian QianDepartment of Rheumatology, Jiangsu Province Hospital of TCM, Nanjing, China.
Meimei WangDepartment of Rheumatology, Southeast University Zhongda Hospital, Nanjing, China.
Jian WuDepartment of Rheumatology, the First Affiliated Hospital of Soochow University, Suzhou, China.
Juan TaoDepartment of Rheumatology, Wuxi TCM Hospital, Wuxi, China.
Jun TanDepartment of Rheumatology, Zhenjiang First People's Hospital, Zhenjiang, China.
Zhanyun DaDepartment of Rheumatology, Affiliated Hospital of Nantong University, Nantong, China.
Miaojia ZhangDepartment of Rheumatology, Jiangsu Province Hospital, Nanjing, China.
Jing LiDepartment of Rheumatology, Affiliated Hospital of Jiangsu University, Jiangsu, China.
Xuebing FengDepartment of Rheumatology and Immunology, the Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, China.
Lingyun SunNanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, China. lingyunsun@nju.edu.cn.

Funding

Jiangsu Provincial Key Research and Development Program BE2020621Key Program of National Natural Science Foundation of China 81930043Major International (Regional) Joint Research Project 81720108020
6 · The paper itself

Abstract

objectiveTo investigate the effect of cyclophosphamide (CYC) on organ involvement and SLE patients' overall and cause-specific mortality.

methodsInformation about CYC prescription was taken from the Jiangsu Lupus database, which was set up to collect medical records from SLE patients since their first admission during 1999-2009 in Jiangsu province, China. Follow-up studies were carried out in 2010 and 2015 to check the survival status of the patients. Cox regression models were used to estimate the hazard ratio (HR) and 95% CI. Kaplan-Meier model was used to assess the effect of CYC on mortality between organ involvement and non-involvement.

resultsThere were 221 deaths observed out of 2446 SLE patients. CYC users decreased overall mortality of SLE (8.4%) with adjusted HR (95% CI) of 0.74 (0.56-0.97), as compared to non-users. A decrease in overall mortality of SLE was found in the low dosage (< 600 mg) of CYC users, with adjusted HR (95% CI) of 0.54 (0.36-0.81). The protection of CYC on mortality of SLE was further observed in subgroups, such as female; SLEDAI score ≥ 15 group; and those with neuropsychiatric, renal, and hematological involvements, and low serum C3. In addition, CYC could eliminate the differences in mortality between organ involvement and non-involvement, including renal, neuropsychiatric, cardiopulmonary, gastrointestinal, and hematological involvement, but not for mucocutaneous and musculoskeletal involvement.

conclusionLow dosage use of CYC decreased the risk of overall mortality of SLE. CYC might improve the survival of SLE patients with renal, neuropsychiatric, cardiopulmonary, gastrointestinal, and hematological involvements. Key Points • Cyclophosphamide decreases overall mortality of SLE patients. • Decreased mortality is mainly observed from low dosage use of cyclophosphamide. • Cyclophosphamide improves the survival of SLE patients when major systems such as renal, neuropsychiatric, cardiopulmonary, gastrointestinal, and hematological are involved.

Indexed as

Lupus Erythematosus, SystemicCyclophosphamideFemaleFollow-Up StudiesHospitalizationHumansImmunosuppressive AgentsKidneyCyclophosphamideImmunosuppressive AgentsCyclophosphamideDosageOrgan involvementSurvivalSystemic lupus erythematosus

Identifiers

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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.