Evidence map›Paper›PMID 41851731›Full record

ArticleArthritis research & therapy2026

Treatment patterns, treat-to-target goals and clinical outcomes of patients with active lupus nephritis: real-world evidence from a multicentre cohort study.

Joanna Kent, Xiaomeng Xu, Arushi Ramnarain, Worawit Louthrenoo, Vera Golder, Laniyati Hamijoyo, Shue-Fen Luo, Yeong-Jian Jan Wu, Yi-Hsing Chen, Jiacai Cho and 35 more

Abstract readMulticenter Study
In one paragraph

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

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0citing papers in PubMed
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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

45 authors.

Joanna KentDepartment of Nephrology, Monash Health, Clayton, Victoria, Australia.
Xiaomeng XuGSK, Value, Evidence & Outcomes, Singapore, Singapore.
Arushi RamnarainDepartment of Nephrology, Monash Health, Clayton, Victoria, Australia.
Worawit LouthrenooDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Vera GolderCentre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia.
Laniyati HamijoyoDivision of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Padjadjaran University/Hasan Sadikin General Hospital, Bandung, Indonesia.
Shue-Fen LuoDepartment of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Chang Gung University, Taipei, Taiwan.
Yeong-Jian Jan WuDepartment of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Chang Gung University, Keelung, Taiwan.
Yi-Hsing ChenDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Jiacai ChoRheumatology Division, Department of Medicine, National University Hospital, Singapore, Singapore.
Aisha LateefDepartment of Rheumatology, Division of Medicine, Woodlands Health, Singapore, Singapore.
Shirley ChanDivision of Rheumatology & Clinical Immunology, Department of Medicine, Queen Mary Hospital, the University of Hong Kong, Pokfulam, Hong Kong.
Chak Sing LauDivision of Rheumatology & Clinical Immunology, Department of Medicine, Queen Mary Hospital, the University of Hong Kong, Pokfulam, Hong Kong.
Sandra NavarraSection of Rheumatology, University of Santo Tomas Hospital, Manila, Philippines.
Leonid ZamoraSection of Rheumatology, University of Santo Tomas Hospital, Manila, Philippines.
Haihong YaoDepartment of Rheumatology and Immunology, People's Hospital, Peking University Health Science Center, Beijing, China.
Sargunan SockalingamDepartment of Medicine, Faculty of Medicine, Universiti Malaya Medical Center, Kuala Lumpur, Malaysia.
Bmdb BasnayakeDepartment of Nephrology, Teaching Hospital Kandy, Kandy, Sri Lanka.
Yanjie HaoDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Zhuoli ZhangRheumatology and Immunology Department, Peking University First Hospital, Beijing, China.
Madelynn ChanDepartment of Rheumatology, Tan Tock Seng Hospital, Allergy & Immunology, Singapore, Singapore.
Chuanhui XuDepartment of Rheumatology, Tan Tock Seng Hospital, Allergy & Immunology, Singapore, Singapore.
Sang-Cheol BaeDepartment of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, and Hanyang University Institute for Rheumatology Research, Hanyang Institute of Bioscience and Biotechnology, Seoul, Korea.
Yasuhiro KatsumataDivision of Rheumatology, Department of Internal Medicine, Tokyo Women's Medical University, Tokyo, Japan.
Jun KikuchiDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Yuko KanekoDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Tsutomu TakeuchiDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Shereen OonDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Sean O'NeillRheumatology Department, Liverpool Hospital, Liverpool, New South Wales, Australia.
Geraldine HassettRheumatology Department, Liverpool Hospital, Liverpool, New South Wales, Australia.
Fiona GoldblattDepartment of Rheumatology, Flinders Medical Centre, Bedford Park, South Australia, Australia.
Yih Jia PohDepartment of Rheumatology and Immunology, Singapore General Hospital, Singapore, Singapore.
Mark SapsfordHealth New Zealand Counties Manukau, Te Whatu Ora (Middlemore Hospital), Auckland, New Zealand.
Nicola TugnetHealth New Zealand Auckland, Te Whatu Ora (Greenlane Clinical Centre, Auckland, New Zealand.
Kristine Pek Ling NgHealth New Zealand Waitemata, Te Whatu Ora (North Shore Hospital), Auckland, New Zealand.
Cherica TeeDepartment of Paediatrics, College of Medicine, University of the Philippines, Manila, Philippines.
Michael TeeDepartment of Paediatrics, College of Medicine, University of the Philippines, Manila, Philippines.
Yusuke MiyazakiThe First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Naoaki OhkuboThe First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Yoshiya TanakaThe First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Mandana NikpourDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Alberta HoiCentre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia.
Aldo A Navarro RojasMedical Affairs, GSK, Greater China & Intercontinental, Singapore, Singapore.
Eric MorandCentre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia.
Rangi Kandane-RathnayakeCentre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia. rangi.kandane-rathnayake@monash.edu.ORCID http://orcid.org/0000-0001-5397-1482

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLupus nephritis (LN) is a common and severe manifestation of systemic lupus erythematosus (SLE). We sought to evaluate treatment patterns, treat-to-target state attainment, and outcomes of patients with active LN on non-biologic, conventional therapy, in a large real-world cohort from the Asia–Pacific region.

methodsAdult patients enrolled in a multinational lupus cohort were studied for evidence of active LN, defined based on the SLE Disease Activity Index-2000 (SLEDAI-2K)-proteinuria threshold (> 0.5 g/24 h or > 0.05g/mmol), ≥ 2 visits of data, and no exposure to biologics. The subset of these patients who had kidney biopsy-confirmed LN was retrospectively determined. Attainment of treatment goals, including modified versions of complete renal response (mCRR) and primary efficacy renal response (mPERR), lupus low disease activity state (LLDAS) and DORIS remission (REM), and organ damage accrual, were assessed over time following the first visit with proteinuria.

resultsOne thousand one hundred eighty patients were studied for a median 2.7 [IQR 1.0, 5.0] years, 435 (37%) of whom had biopsies (Class III/IV = 242 (56%)). mCRR, mPERR, LLDAS, and REM were attained at least once during follow-up by 46%, 55%, 60%, and 46% of patients, respectively. mCRR and mPERR attainment was highest at year 2, while LLDAS and REM attainment gradually increased over time. New organ damage accrued in 11% of patients by year 1, increasing to 33% by year 5.

conclusionIn a multinational cohort of patients with active LN receiving non-biologic conventional therapy, the attainment of renal responses, LLDAS, and REM was low, while damage accrual was prevalent.

Indexed as

Immunosuppressive AgentsLupus NephritisAdultCohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeImmunosuppressive AgentsCohort studyDisease ActivityLupus nephritisOutcomesTreat-to-target states

Identifiers

PMID41851731
PMCPMC13112692

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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.