Evidence map›Paper›PMID 40416945›Full record

ArticleClinical, cosmetic and investigational dermatology2025

Efficacy and Safety of Apremilast in Oncological Patients with Moderate-to-Severe Plaque Psoriasis: A 5 years Retrospective Observational Study.

Caterina Lanna, Antonia Rivieccio, Martina Vultaggio, Ruslana Gaeta Shumak, Francesco Maria Bonacci, Fabio Artosi, Cristiana Borselli, Gaetana Costanza, Luca Bianchi, Elena Campione

Abstract read
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Article in Clinical, cosmetic and investigational dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Caterina LannaDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.ORCID 0000-0002-3485-6275
Antonia RivieccioDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Martina VultaggioDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Ruslana Gaeta ShumakDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Francesco Maria BonacciDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Fabio ArtosiDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Cristiana BorselliDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Gaetana CostanzaVirology Unit, Department of Experimental Medicine, Università di Roma Tor Vergata, Roma, Italia.
Luca BianchiDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.
Elena CampioneDermatology Unit, Department of Systems Medicine, Università di Roma Tor Vergata, Roma, Italia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Psoriasis and psoriatic arthritis are chronic autoimmune inflammatory conditions frequently associated with a range of comorbidities, including oncological diseases. Managing these conditions in patients with a history of cancer requires careful consideration of treatment efficacy and safety. Apremilast, an oral phosphodiesterase 4 (PDE4) inhibitor, has shown promise in the treatment of psoriasis and psoriatic arthritis. However, data on its use in oncological patients remain limited. Methods: This retrospective observational study evaluated the efficacy and safety of Apremilast in 79 patients with a history of cancer who were treated for psoriasis and/or psoriatic arthritis over a period of approximately five years. Clinical outcomes were assessed using the Psoriasis Area Severity Index (PASI), Dermatology Life Quality Index (DLQI), and Visual Analog Scale for pain (PAIN VAS) to monitor disease severity, quality of life, and articular involvement, respectively. Regular oncological assessments were conducted concurrently with Apremilast therapy to ensure patient safety and identify potential interactions. Results: Over the five-year treatment period, significant improvements were observed in PASI, DLQI, and PAIN VAS scores, indicating effective management of both dermatological and articular symptoms. Patients reported enhanced quality of life and reduced pain levels, reflecting the therapeutic benefits of Apremilast. Oncological evaluations revealed no significant adverse interactions between Apremilast and the patients' cancer history or treatments, underscoring the drug's safety profile in this population. Conclusion: This study highlights the efficacy and safety of Apremilast as a treatment option for psoriasis and psoriatic arthritis in oncological patients. The findings support its role in improving disease outcomes and quality of life, emphasizing the importance of personalized treatment strategies in managing complex cases involving a history of cancer. Further research is warranted to validate these results in larger patient cohorts.

Indexed as

apremilastcancerpsoriasistumors

Identifiers

PMID40416945
PMCPMC12103192

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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.