Evidence map›Paper›PMID 30076588›Full record

ArticleMolecular diagnosis & therapy2018

Treating a Multidrug-Resistant Psoriatic HLA-C*18:01 Allele Carrier with Combination Ustekinumab Apremilast Therapy.

Marco Galluzzo, Simone D'Adamio, Elena Campione, Luca Bianchi, Marina Talamonti

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Molecular diagnosis & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. CCR7Nature communications · 2025
    Article
  3. Review
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

5 authors at 1 institution in 1 country.

Marco GalluzzoDermatology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Viale Oxford, 81, 00133, Rome, Italy. marco.galluzzo83@gmail.com.ORCID http://orcid.org/0000-0002-3424-5175
Simone D'AdamioDermatology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Viale Oxford, 81, 00133, Rome, Italy.
Elena CampioneDermatology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Viale Oxford, 81, 00133, Rome, Italy.
Luca BianchiDermatology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Viale Oxford, 81, 00133, Rome, Italy.
Marina TalamontiDermatology, Department of "Medicina dei Sistemi", University of Rome "Tor Vergata", Viale Oxford, 81, 00133, Rome, Italy.
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNowadays, even though several biologic therapies are available to treat psoriasis, multidrug-resistant disease continues to be a therapeutic challenge. Combination therapy has therefore become increasingly important. In this context, apremilast, according to its safety profile, could easily be combined with biologics in patients with comorbidities and/or recalcitrant multidrug-resistant psoriasis.

objectiveOur goal is to share experience from our institution in the observation of a patient with severe chronic plaque psoriasis that was unresponsive to all anti-tumor necrosis factor-α treatment and to an anti-interleukin (IL)-17A drug and only partially responsive to ustekinumab, even in combination with apremilast. The patient carried a rare allele infrequently found in Caucasian people: human leukocyte antigen (HLA)-C*18:01. This allele has been found to be positively associated with psoriasis in Brazilian patients.

methodsThe patient was typed for the HLA-C locus at high resolution via polymerase chain reaction sequence-specific oligonucleotide probes (PCR-SSOP) using a commercial kit (LAB

resultsOur patient, previously described as having multidrug-resistant psoriasis, commenced ustekinumab and apremilast combination therapy. After 12 weeks, the Psoriasis Area Severity Index score had worsened, and we suspended combination therapy because the patient reported an absence of any benefit and was experiencing side effects from the induction therapy with apremilast.

conclusionsExpanding on the previously reported experience with this patient, we conclude that HLA-C*18:01 probably indicates a severe, recalcitrant, multidrug-resistant psoriasis phenotype for which proper therapy remains to be identified.

Indexed as

AllelesCombined Modality TherapyDermatologic AgentsDrug Resistance, MultipleFemaleHLA-C AntigensHumansMiddle AgedPsoriasisUstekinumabDermatologic AgentsHLA-C AntigensUstekinumab

Identifiers

PMID30076588
OpenAlexW2886187951

What OpenQuestion holds

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Registered trials

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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.