Evidence map›Paper›PMID 31628802›Full record

Observational studyRheumatology (Oxford, England)2020

Treatment with cyclophosphamide i.v. pulse therapy is an option for effective treatment of skin fibrosis in patients with early systemic sclerosis.

Brigit E Kersten, Nathan den Broeder, Frank H J van den Hoogen, Hanneke A K Knaapen-Hans, Cornelia H M van den Ende, Madelon C Vonk

Erratum issuedOpen access · hybridAbstract readObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Brigit E KerstenDepartment of Rheumatic Diseases, Radboud University Medical Center.
Nathan den BroederDepartment of Rheumatology, Sint Maartenskliniek, Nijmegen, The Netherlands.
Frank H J van den HoogenDepartment of Rheumatic Diseases, Radboud University Medical Center.
Hanneke A K Knaapen-HansDepartment of Rheumatic Diseases, Radboud University Medical Center.
Cornelia H M van den EndeDepartment of Rheumatic Diseases, Radboud University Medical Center.
Madelon C VonkDepartment of Rheumatic Diseases, Radboud University Medical Center.
Radboud University Medical Center · NLRadboud University Nijmegen · NLSint Maartenskliniek · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSSc is a autoimmune disease characterized by fibrosis of the skin and internal organs. There is a lack of evidence for the efficacy of i.v. CYC pulse therapy on skin thickening. We aimed to examine the response of i.v. CYC pulse therapy on skin thickening in our cohort of SSc patients and analysed factors that predict this response.

methodsWe retrospectively evaluated the data for 143 patients with SSc from baseline to 12, 24 and 36 months. All patients were treated with at least 6 i.v. CYC pulses (750 mg/m2/month). We applied the modified Rodnan Skin Score (mRSS) to assess skin thickening. A clinically relevant response was defined as a decrease in mRSS of 5 points and 25% from baseline. Different baseline variables for predicting response on month 12 were tested in logistic regression analyses.

resultsBaseline characteristics of the patients with dcSSc and lcSSc were collected. Forty-three percent (n = 42) of dcSSc patients had a clinically relevant response on month 12. Non-responding on month 6 predicts non-response on month 12 (odds ratio 37.1; 95% CI 4.5, 306.4).

conclusionWe concluded that i.v. CYC pulse therapy should be considered as an effective treatment option for skin thickening in dcSSc patients, because 43% of this group of patients were found to have a clinically relevant response. Of the dcSSC patients who did not respond by month 6, only 29% had a response by month 12. This finding can help the physician and patient in shared decision making about whether or not to continue therapy.

Indexed as

SkinAdultAgedCyclophosphamideFemaleHumansImmunosuppressive AgentsInfusions, IntravenousLogistic ModelsLongitudinal StudiesLung Diseases, InterstitialMaleMiddle AgedPrognosisPulse Therapy, DrugRetrospective StudiesCyclophosphamideImmunosuppressive Agentscyclophosphamideskin fibrosissystemic sclerosis

Identifiers

PMID31628802
PMCPMC7310100
OpenAlexW2980834915

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.