Evidence map›Paper›PMID 41385077›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Efficacy and safety of scheduled rituximab in children with refractory nephrotic syndrome after multi-target therapy failure.

Jing Yang, Yonghua He, Jinyun Pu, Yu Zhang, Jianhua Zhou, Liru Qiu

Abstract read
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jing YangDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China.
Yonghua HeDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China.
Jinyun PuDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China.
Yu ZhangDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China.
Jianhua ZhouDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China.
Liru QiuDepartment of Pediatrics, Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases, Hubei Provincial Clinical Research Center for Children's Growth and Development and Metabolic Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Jiefang Ave. No. 1095, Wuhan, 430030, China. liruqiutj@163.com.ORCID http://orcid.org/0000-0002-1583-7183

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with refractory nephrotic syndrome (NS) often experience frequent relapses despite combination immunosuppressive therapy. This study evaluated the efficacy and safety of scheduled rituximab (RTX) maintenance therapy in children with refractory NS who failed multi-target therapy.

methodsWe retrospectively analyzed 48 children under 18 years old with steroid-dependent or steroid-resistant NS who had ≥ 2 relapses within 6 months despite corticosteroids plus at least two other immunosuppressants (multi-target therapy failure). Relapse rates before and after RTX, medication reduction, adverse events, and kidney outcomes were assessed.

resultsOf 51 patients treated, 48 met inclusion criteria (three excluded for severe infusion reactions or loss to follow-up). RTX maintenance therapy significantly reduced the annual relapse rate from a mean of 2.1 relapses/year before RTX to 0.2 relapses/year after RTX (p < 0.0001). Over half of patients (56%) remained completely relapse-free during RTX treatment. Corticosteroids were successfully discontinued in 85% of patients (median 1 year after RTX), and all other immunosuppressants were stopped in 73% (median 0.8 years). Overall, 69% of patients were able to discontinue steroids plus two immunosuppressive drugs, maintaining remission on RTX alone. Adverse events were mostly mild: 56% had asymptomatic hypogammaglobulinemia, 8% experienced transient neutropenia (no agranulocytosis), 4% had mild infections, and 4% had infusion reactions (rash or throat discomfort) that resolved with supportive care. No patient progressed to kidney failure over a median follow-up of 2.5 years.

conclusionsScheduled RTX maintenance therapy effectively maintained remission in children with multi-target therapy-refractory NS, allowing substantial reduction or cessation of steroids and other immunosuppressants.

Indexed as

Immunosuppressive AgentsNephrotic SyndromeRituximabAdolescentAdrenal Cortex HormonesChildChild, PreschoolDrug Administration ScheduleDrug Therapy, CombinationFemaleHumansInfantMaleRecurrenceRetrospective StudiesTreatment FailureAdrenal Cortex HormonesImmunosuppressive AgentsRituximabChildrenMulti-target therapy failureRefractory nephrotic syndromeRituximabScheduled therapy

Identifiers

PMID41385077
PMCPMC13009123

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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.