Evidence map›Paper›PMID 35887866›Full record

ArticleJournal of clinical medicine2022

Rituximab in Mucous Membrane Pemphigoid: A Monocentric Retrospective Study in 10 Patients with Severe/Refractory Disease.

Maria Efenesia Baffa, Alberto Corrà, Roberto Maglie, Elena Biancamaria Mariotti, Francesca Montefusco, Carlo Pipitò, Stefano Senatore, Lavinia Quintarelli, Marzia Caproni, Emiliano Antiga

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. 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
1.0field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  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

10 authors at 2 institutions in 1 country.

Maria Efenesia BaffaDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.ORCID 0000-0001-8454-7617
Alberto CorràDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.ORCID 0000-0003-0903-4998
Roberto MaglieDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.
Elena Biancamaria MariottiDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.
Francesca MontefuscoDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.
Carlo PipitòDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.
Stefano SenatoreDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.
Lavinia QuintarelliRare Skin Diseases Unit, Azienda USL Toscana Centro, Department of Health Sciences, University of Florence, 50125 Florence, Italy.
Marzia CaproniRare Skin Diseases Unit, Azienda USL Toscana Centro, Department of Health Sciences, University of Florence, 50125 Florence, Italy.
Emiliano AntigaDepartment of Health Sciences, Section of Dermatology, University of Florence, 50125 Florence, Italy.ORCID 0000-0001-7787-4433
University of Florence · ITAzienda Usl Toscana Centro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rituximab (RTX) is a monoclonal antibody directed against CD20 antigen indicated in an increasing number of immune-mediated diseases. While its efficacy in pemphigus vulgaris has been widely investigated, only a few data about its possible role in pemphigoid diseases have been reported in the literature. Accordingly, herein we evaluated a case series of patients with mucous membrane pemphigoid (MMP) treated with RTX. We included patients with a history of severe/refractory MMP who received at least one cycle of intravenous RTX between May 2018 and December 2021 and had 6 months of follow-up time. Disease control (DC) was our early endpoint, while complete remission (CR) and partial remission (PR) were late endpoints. CR off-therapy, relapses, and adverse events were evaluated as well. Our population included 10 MMP patients. Eight out of ten patients (80%) achieved DC in a mean of 8 weeks, while two patients with ocular MMP were non-responders. Among the eight patients who achieved DC, two reached CR off therapy, two CR on minimal therapy, and two achieved PR on minimal therapy. In our case series, the addition of RTX to conventional therapies was demonstrated to be safe and effective in reaching rapid disease control in the majority of refractory MMP patients.

Indexed as

autoimmune bullous skin diseasemucous membrane pemphigoidrituximab

Identifiers

PMID35887866
PMCPMC9325091
OpenAlexW4285733236

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.