Evidence map›Paper›PMID 39424649›Full record

SynthesisArchives of dermatological research2024

Short term efficacy of biological treatment for moderate-to-severe plaque psoriasis: a systematic review and network meta-analysis.

Omar Ismail, Kamel Jaber, Yazan Jaber, Ubadah Froukh, Ahmad Younis, Karam Albdour, Yazan Momani, Noor Almaani

Abstract readSystematic ReviewNetwork Meta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Archives of dermatological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Omar IsmailSchool of Medicine, University of Jordan, Amman, 11972, Jordan. omar.moh.isml@gmail.com.
Kamel JaberSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Yazan JaberSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Ubadah FroukhSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Ahmad YounisSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Karam AlbdourSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Yazan MomaniSchool of Medicine, University of Jordan, Amman, 11972, Jordan.
Noor AlmaaniDepartment of Dermatology, School of Medicine, University of Jordan, Amman, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic inflammatory disease that is debilitating, particularly in its more severe forms. Multiple systemic therapies are used in moderate-to-severe psoriasis, but the development of biological interventions has revolutionized its management and improved its outcomes. To compare the effectiveness and safety of the different biological interventions approved for use in moderate-to-severe plaque psoriasis. Multiple databases were searched for relevant articles and a prospectively planned network meta-analysis was conducted on randomized controlled trials that assessed biological treatments in moderate-to-severe psoriasis. The search yielded 84 trials that encompassed 39,798 patients. Infliximab 5 mg/kg had the highest probability of achieving 75% reduction on PASI scale in comparison to placebo (RR = 18.76, 95% CI [12.31; 28.57], high certainty), while Ixekizumab 80 mg and Brodalumab 210 mg had the highest probability at achieving PASI90 and PASI100 (37.81, [28.57; 50.03] and 81.04, [26.16; 251.01], respectively, with moderate certainty) On the other hand, Risankizumab 150 mg and Ustekinumab 90 mg were the only regimens with significantly less withdrawal rates due to adverse events (0.41, [0.18-0.96], and 0.57, [0.35-0.91], respectively with High certainty) compared to placebo. Anti-IL17 and Infliximab were among the most effective in ameliorating the symptoms of psoriasis, however, anti-IL17 were better at achieving full or almost full improvement on the PASI scale. Real life decision-making is not so clear-cut and should remain patient centered, taking into consideration factors such as safety, comorbidities, biologic naivety, dosing preferences and insurance considerations.

Indexed as

Antibodies, Monoclonal, HumanizedBiological ProductsInfliximabPsoriasisAntibodies, MonoclonalDermatologic AgentsHumansRandomized Controlled Trials as TopicSeverity of Illness IndexTreatment OutcomeUstekinumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBiological ProductsbrodalumabDermatologic AgentsInfliximabixekizumabrisankizumabUstekinumabBiologicalMonoclonal antibodiesNetwork meta-analysisPsoriasisTherapeutics

Identifiers

PMID39424649

What OpenQuestion holds

Textmetadata
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.