Evidence map›Paper›PMID 40873141›Full record

ArticleYonsei medical journal2025

Real-World Effectiveness of Omalizumab Treatment in Adult Asthma Patients.

Jae-Hyuk Jang, ChulHyoung Park, Chungsoo Kim, Youngsoo Lee, Eunyoung Lee, Rae Woong Park, Hae-Sim Park

Abstract read
In one paragraph

Article in Yonsei medical journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jae-Hyuk Jang *Department of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.ORCID https://orcid.org/0000-0002-4225-7117
ChulHyoung Park *Department of Biomedical Informatics, Ajou University School of Medicine, Suwon, Korea.ORCID https://orcid.org/0000-0003-0531-9144
Chungsoo KimDepartment of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT, USA.ORCID https://orcid.org/0000-0003-1802-1777
Youngsoo LeeDepartment of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.ORCID https://orcid.org/0000-0001-8918-9353
Eunyoung LeeDepartment of Neurology, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.ORCID https://orcid.org/0000-0002-9440-9119
Rae Woong ParkDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon, Korea.ORCID https://orcid.org/0000-0003-4989-3287
Hae-Sim ParkDepartment of Allergy & Clinical Immunology, Ajou University School of Medicine, Suwon, Korea. hspark@ajou.ac.kr.ORCID https://orcid.org/0000-0003-2614-0303

Funding

Korea Health Industry Development Institute HR16C0001Ministry of Health & Welfare HG22C0024
6 · The paper itself

Abstract

purposeOmalizumab improves clinical outcomes for patients with severe asthma (SA), but its long-term effectiveness and potential biomarkers for predicting patient response require further investigation. This study aimed to evaluate the real-world effectiveness of omalizumab in treating SA and to identify potential biomarkers for predicting a favorable treatment response. MATERIALS AND

methodsClinical outcomes were compared between asthma patients receiving omalizumab (omalizumab group) and those on inhaled corticosteroid with long-acting beta-agonist (ICS-LABA) alone (ICS-LABA group). Propensity score matching and Cox proportional hazards model were used to calculate hazard ratios (HRs). Study outcomes included severe asthma exacerbation (SAE), incompletely controlled asthma, intravenous (IV) corticosteroid use, and asthma-related hospitalization. Incompletely controlled asthma was defined by blood eosinophil counts ≥150 cells/µL, fractional exhaled nitric oxide (FeNO) ≥25 ppb, forced expiratory volume in one second (FEV1%) <80%, or SAE occurrence.

resultsThe omalizumab group had significantly lower risks of SAE (HR 0.17,

conclusionOmalizumab treatment effectively reduces SAE and improves lung function and asthma control. Blood neutrophil counts and serum total IgE may be potential biomarkers for predicting favorable responses to omalizumab treatment.

Indexed as

Anti-Asthmatic AgentsAsthmaOmalizumabAdrenal Cortex HormonesAdultAgedEosinophilsFemaleForced Expiratory VolumeHumansImmunoglobulin EMaleMiddle AgedNitric OxideProportional Hazards ModelsRetrospective StudiesAdrenal Cortex HormonesAnti-Asthmatic AgentsImmunoglobulin ENitric OxideOmalizumabAsthmaIgEneutrophilsomalizumab

Identifiers

PMID40873141
PMCPMC12394757

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.