Evidence map›Paper›PMID 19279120›Full record

SynthesisClinical journal of the American Society of Nephrology : CJASN2009

Rituximab therapy for membranous nephropathy: a systematic review.

Andrew S Bomback, Vimal K Derebail, Julie G McGregor, Abhijit V Kshirsagar, Ronald J Falk, Patrick H Nachman

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Clinical journal of the American Society of Nephrology : CJASN, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% of its field
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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-Up.Journal of the American Society of Nephrology : JASN · 2017
    Trial
  3. Rituximab in idiopathic membranous nephropathy.Journal of the American Society of Nephrology : JASN · 2012
    Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Idiopathic Membranous Nephropathy and Treatment Related Complications.Medical archives (Sarajevo, Bosnia and Herzegovina) · 2020
    Article
  11. Rituximab in kidney disease and transplant.Animal models and experimental medicine · 2019
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Andrew S BombackDepartment of Medicine, Division of Nephrology and Hypertension, University of North Carolina Kidney Center, Chapel Hill, North Carolina 27599-7155, USA. abomback@unch.unc.edu
Vimal K Derebail
Julie G McGregor
Abhijit V Kshirsagar
Ronald J Falk
Patrick H Nachman
University of North Carolina at Chapel Hill · USUniversity of North Carolina Health Care · US

Funding

RENAL EPIDEMIOLOGY TRAINING PROGRAMT32DK007750 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FALK, RONALD J · 1999 to 2022
$5.5M
NIDDK NIH HHS T32 DK007750
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe treatment of membranous nephropathy (MN) remains controversial. Rituximab, which selectively targets B cells, has emerged as a possible alternative treatment option with limited toxicity. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: The available data on rituximab therapy for MN were reviewed using the MEDLINE database (inception to August 1, 2008), Google Scholar, and selected reference lists. English-language studies investigating the use of rituximab in idiopathic and secondary MN, in native and transplanted kidneys, were included. Study design, subject number, clinical characteristics (diagnosis, previous and concomitant treatment courses, baseline proteinuria, baseline renal function), rituximab protocol, follow-up period, achievement of complete or partial remission, changes in proteinuria and renal function, and adverse effects of therapy were extracted.

resultsTwenty-one articles were included for review; all were either case reports or case series without controls. More than half of the published cases (50 of 85) came from one center where rituximab was used as primary immunosuppression for idiopathic MN. The available data suggest that rituximab, dosed either as 375 mg/m(2) once weekly for 4 wk or as 1 g on days 1 and 15, achieves a 15 to 20% rate of complete remission and a 35 to 40% rate of partial remission. The drug was well tolerated with minimal adverse events.

conclusionsAlthough rituximab may prove to be a better treatment option for MN than alkylating agents or calcineurin inhibitors, the current literature only supports using the drug in research protocols. Whether, when, how, and why to use rituximab in MN remains to be determined.

Indexed as

AdultAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedDrug Administration ScheduleGlomerular Filtration RateGlomerulonephritis, MembranousHumansImmunosuppressive AgentsKidneyMiddle AgedProteinuriaRituximabTreatment OutcomeAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedImmunosuppressive AgentsRituximab

Identifiers

PMID19279120
PMCPMC2666426
OpenAlexW2135619376

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.