Evidence map›Paper›PMID 37298514›Full record

ReviewInternational journal of molecular sciences2023

Switching Biological Therapies in Severe Asthma.

Giulia Scioscia, Santi Nolasco, Raffaele Campisi, Carla Maria Irene Quarato, Cristiano Caruso, Corrado Pelaia, Andrea Portacci, Claudia Crimi

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Eosinophilia and the Heart: Evolving Concepts.Current cardiology reports · 2026
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  11. An overview of switching biological therapies for chronic rhinosinusitis with nasal polyposis (CRSwNP).European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2025
    Review
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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.

Giulia SciosciaDepartment of Medical and Surgical Sciences, University of Foggia, 71121 Foggia, Italy.ORCID 0000-0002-2667-077X
Santi NolascoDepartment of Clinical and Experimental Medicine, University of Catania, 95124 Catania, Italy.ORCID 0000-0003-3995-7662
Raffaele CampisiDepartment of Clinical and Experimental Medicine, University of Catania, 95124 Catania, Italy.ORCID 0000-0001-9305-6748
Carla Maria Irene QuaratoInstitute of Respiratory Diseases, Policlinico Foggia, 71121 Foggia, Italy.ORCID 0000-0003-4299-7403
Cristiano CarusoDepartment of Medical and Surgical Sciences, Digestive Disease Center, Fondazione Policlinico A. Gemelli IRCCS, 00168 Rome, Italy.ORCID 0000-0001-7631-029X
Corrado PelaiaDepartment of Health Sciences, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.ORCID 0000-0002-4236-7367
Andrea PortacciDepartment of Basic Medical Sciences, Neuroscience and Sense Organs, Section of Respiratory Disease, University "Aldo Moro" of Bari, 70121 Bari, Italy.ORCID 0000-0002-6127-2486
Claudia CrimiDepartment of Clinical and Experimental Medicine, University of Catania, 95124 Catania, Italy.ORCID 0000-0002-9088-5214

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, three classes of monoclonal antibodies targeting type 2 inflammation pathways are available in Italy for the treatment of severe asthma: anti-IgE (Omalizumab), anti-IL-5/anti-IL-5Rα (Mepolizumab and Benralizumab), and anti-IL-4Rα (Dupilumab). Numerous randomized controlled trials (RCTs) and real-life studies have been conducted to define their efficacy and identify baseline patients' characteristics potentially predictive of favorable outcomes. Switching to another monoclonal antibody is recommended in case of a lack of benefits. The aim of this work is to review the current knowledge on the impact of switching biological therapies in severe asthma as well as on predictors of treatment response or failure. Almost all of the information about switching from a previous monoclonal antibody to another comes from a real-life setting. In the available studies, the most frequent initial biologic was Omalizumab and patients who were switched because of suboptimal control with a previous biologic therapy were more likely to have a higher baseline blood eosinophil count and exacerbation rate despite OCS dependence. The choice of the most suitable treatment may be guided by the patient's clinical history, biomarkers of endotype (mainly blood eosinophils and FeNO), and comorbidities (especially nasal polyposis). Due to overlapping eligibility, larger investigations characterizing the clinical profile of patients benefiting from switching to different monoclonal antibodies are needed.

Indexed as

Anti-Asthmatic AgentsAsthmaAntibodies, MonoclonalBiological TherapyEosinophilsHumansOmalizumabAnti-Asthmatic AgentsAntibodies, MonoclonalOmalizumabbiologicsbiomarkersefficacyrandomized clinical trialsreal-life studiessevere asthma

Identifiers

PMID37298514
PMCPMC10253346

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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.