Evidence map›Paper›PMID 40156259›Full record

Observational studyThe Journal of dermatology2025

Real-world safety and effectiveness of guselkumab in patients with psoriasis: A post-marketing surveillance study through up to week 52 in Japan.

Yayoi Tada, Yukako Sugiura, Manami Kamishima, Shoya Takahashi, Yoshihito Tanaka, Junya Masuda, Keiichi Yamanaka

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Review
  4. Article
  5. Article
  6. Observational
  7. 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

7 authors.

Yayoi TadaDepartment of Dermatology, Teikyo University, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3743-135X
Yukako SugiuraMedical Affairs Division, Johnson & Johnson, Tokyo, Japan.
Manami KamishimaJapan Safety & Surveillance Division, Johnson & Johnson, Tokyo, Japan.
Shoya TakahashiJapan Safety & Surveillance Division, Johnson & Johnson, Tokyo, Japan.
Yoshihito TanakaStatistics & Decision Sciences Division, Johnson & Johnson, Tokyo, Japan.
Junya MasudaMedical Affairs Division, Johnson & Johnson, Tokyo, Japan.
Keiichi YamanakaDepartment of Dermatology, Mie University, Mie, Japan.

Funding

Johnson & Johnson
6 · The paper itself

Abstract

Guselkumab is a monoclonal antibody that binds to the p19 subunit of interleukin-23 and inhibits its downstream signaling. The safety profile of guselkumab and its superior efficacy over placebo and adalimumab for the treatment of patients with moderate-to-severe psoriasis were reported in phase 3 studies conducted within and outside Japan. To assess the real-world safety and effectiveness of guselkumab in Japanese patients with psoriasis, we conducted a multicenter, single-arm, prospective, post-marketing surveillance study. Guselkumab was administered by subcutaneous injection at a dose of 100 mg at weeks 0 and 4, then every following 8 weeks. The patient observation period was 52 weeks after the initial guselkumab dose or until treatment withdrawal. The safety analysis set consisted of 416 patients, including 310 patients with vulgaris (PsV); and the effectiveness analysis set consisted of 251 patients, including 236 patients with PsV or psoriatic arthritis (PsA). There were more men (71.3%, 221/310) than women among the PsV group. The median age among those with PsV was 58 years, the median disease duration was 11.50 years, 50.0% (155/310) had comorbidity, and 41.3% (128/310) had previously been treated with biologic agents. During the observation period, 8.4% (35/416) of patients experienced 49 adverse drug reactions, 2.9% (12/416) experienced 13 serious adverse drug reactions, and 3.4% (14/416) experienced 16 adverse events leading to treatment discontinuation. In the effectiveness analysis set of 236 patients with PsV or PsA, the Psoriasis Area and Severity Index (PASI) 75, 90, and 100 response rates at week 52 were 69.9%, 54.5%, and 32.5%, respectively. Bio-naïve patients consistently had higher PASI 75 and 90 response rates than bio-experienced patients. This post-marketing surveillance study demonstrated that guselkumab was well-tolerated and effective in a real-world setting in Japanese patients with psoriasis.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedDermatologic AgentsPsoriasisAdultAgedFemaleHumansInjections, SubcutaneousJapanMaleMiddle AgedProduct Surveillance, PostmarketingProspective StudiesSeverity of Illness IndexTreatment OutcomeAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDermatologic Agentsguselkumabadverse drug reactioninterleukin‐23monoclonal antibodypost‐marketing product surveillancetreatment adherence

Identifiers

PMID40156259
PMCPMC12149365

What OpenQuestion holds

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LicenceCC BY
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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.