Evidence map›Paper›PMID 39104870›Full record

ArticleClinical kidney journal2024

Prospective study of the effect of rituximab on kidney function in membranous nephropathy.

Durga A K Kanigicherla, Angie A Kehagia, Babak Jamshidi, Lina Manounah, Anna Barnes, Hannah Patrick, Helen Powell, Catrin Austin, Stephen Norton, Lisa Willcocks and 5 more

Abstract read
In one paragraph

Article in Clinical kidney journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

15 authors.

Durga A K KanigicherlaManchester Institute of Nephrology and Transplantation, Manchester, UK.ORCID https://orcid.org/0000-0003-3011-7878
Angie A KehagiaKing's College Technology Evaluation Centre (KiTEC), UK.
Babak JamshidiKing's College Technology Evaluation Centre (KiTEC), UK.
Lina ManounahKing's College Technology Evaluation Centre (KiTEC), UK.
Anna BarnesKing's College Technology Evaluation Centre (KiTEC), UK.
Hannah PatrickNational Institute for Health and Care Excellence, UK.ORCID https://orcid.org/0000-0001-8674-9108
Helen PowellNational Institute for Health and Care Excellence, UK.
Catrin AustinNational Institute for Health and Care Excellence, UK.
Stephen NortonNational Institute for Health and Care Excellence, UK.
Lisa WillcocksCambridge University Hospital NHS Trust, UK.
Megan GriffithImperial College Healthcare NHS Trust Renal Unit, UK.
Fiona BraddonUK Kidney Association & UK National Registry of Rare Kidney Diseases, UK.
Retha SteenkampUK Kidney Association & UK National Registry of Rare Kidney Diseases, UK.
William S McKaneSheffield Kidney Institute, UK.
Arif KhwajaSheffield Kidney Institute, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with membranous nephropathy (MN) and poor kidney function or active disease despite previous immunosuppression are underrepresented in clinical trials. It is unknown how effective rituximab is in this population. Methods: This prospective, multi-centre, single-arm, real-world study of patients with active MN [urine protein-creatinine ratio (uPCR) >350 mg/mmol and serum albumin <30 g/L, or a fall in estimated glomerular filtration rate (eGFR) of at least 20% or more over at least 3 months] evaluated rituximab in those with contraindications to calcineurin inhibitors and cytotoxic therapy. The primary outcome was change in rate of eGFR decline before and after rituximab. Complete or partial remission were defined as uPCR <30 mg/mmol or uPCR <350 mg/mmol with a ≥50% fall from baseline, respectively. Results: A total of 180 patients [median age 59 years, interquartile range (IQR) 48-68] received rituximab and were followed up for a median duration of 17 months. Seventy-seven percent had prior immunosuppression. Median eGFR and uPCR at baseline were 49.2 mL/min/1.73 m Conclusion: Rituximab significantly reduced the rate of eGFR decline in active MN including those who had received prior immunosuppression or with poor baseline kidney function.

Indexed as

eGFRmembranous nephropathyremissionrituximab

Identifiers

PMID39104870
PMCPMC11299108

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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.