Evidence map›Paper›PMID 21399901›Full record

ArticlePediatric nephrology (Berlin, Germany)2011

Long-term follow-up after cyclophosphamide therapy in steroid-dependent nephrotic syndrome.

Alberto Zagury, Anne Louise de Oliveira, Carlos Augusto Pinheiro de Moraes, Jose Augusto de Araujo Montalvão, Regina Helena Leite Lemos Novaes, Vinicius Martins de Sá, Deise De Boni Monteiro de Carvalho, Tereza Matuck

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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Trial
  4. Challenging Clinical Practice Guideline Definitions in Childhood Nephrotic Syndrome.Clinical journal of the American Society of Nephrology : CJASN · 2025
    Article
  5. Article
  6. Review
  7. Observational
  8. Treating the idiopathic nephrotic syndrome: are steroids the answer?Pediatric nephrology (Berlin, Germany) · 2019
    Review
  9. Article
  10. Observational
  11. Article
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Alberto ZaguryDepartment of Pediatric Nephrology, Hospital Federal de Bonsucesso, Av. Londres 616 - Bonsucesso, Rio de Janeiro, CEP: 21041-030, RJ, Brazil. alberto.zagury@gmail.com
Anne Louise de Oliveira
Carlos Augusto Pinheiro de Moraes
Jose Augusto de Araujo Montalvão
Regina Helena Leite Lemos Novaes
Vinicius Martins de Sá
Deise De Boni Monteiro de Carvalho
Tereza Matuck
Hospital Geral de Bonsucesso · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclophosphamide (CP) has been used for over 40 years in patients with steroid-sensitive nephrotic syndrome (SSNS) presenting frequent relapses or steroid dependence (SD). We evaluated retrospectively and tried to identify parameters possibly associated with a prolonged and sustained remission (PSR+) ≥5 years in 108 children with steroid-dependent nephrotic syndrome (SDNS) treated with oral CP. Patients had a follow-up time ≥5 years and were divided into two groups according to achievement of PSR (+ and -). Gender, histological injury, cumulative doses of CP, age of onset of illness, and start of treatment and prednisone dose on the occasion of relapse were analyzed. The overall cumulative sustained remission for 5 and 10 years was 25 and 21.6%, respectively. The only factor that influenced a PSR was the degree of SD: the group PSR+ relapsed at prednisone dose of 0.96 ± 0.51 mg/kg vs. 1.29 ± 0.59 mg/kg in group PSR- (p = 0.01). Also, patients who relapsed in the presence of prednisone doses ≤1.4 mg/kg showed a cumulative sustained remission of 43, 35, and 32.7% at 2, 5, and 10 years, respectively, versus 22.5, 12.5, and 5% in those with prednisone >1.4 mg/kg (p = 0.001). Our findings suggest that patients with SDNS who relapse on prednisone dose >1.4 mg/kg are especially prone to an unfavorable response to CP use.

Indexed as

Administration, OralAdolescentChildChild, PreschoolCyclophosphamideFemaleFollow-Up StudiesHumansImmunosuppressive AgentsInfantKaplan-Meier EstimateMaleNephrotic SyndromeRecurrenceRemission InductionRetrospective StudiesCyclophosphamideImmunosuppressive AgentsSteroids

Identifiers

PMID21399901
OpenAlexW2021121389

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.