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Biomarker Predictors of Clinical Efficacy of the Anti-IgE Biologic, Omalizumab, in Severe Asthma in Adults: Results of the SoMOSA Study.

Ratko DjukanovićPaul BrinkmanJohan KolmertCristina GomezJames SchofieldJoost BrandsmaAndy ShapanisPaul J S SkippAnthony PostleCraig E WheelockSven-Erik DahlénPeter J SterkThomas BrownDavid J JacksonAdel Hasan MansurIan PavordMitesh PatelChristopher BrightlingSalman SiddiquiPeter BraddingIan SabroeDinesh SaralayaLivingstone ChishimbaJoanna C PorterDouglas RobinsonStephen J FowlerPeter H HowarthLouisa LittleThomas OliverKayleigh HillLouise StantonAlexander AllenDeborah EllisGareth GriffithsTim HarrisonAyobami T AkenroyeJessica Lasky-SuLiam HeaneyRekha ChaudhuriRamesh Kurukulaaratchy
Published in: American journal of respiratory and critical care medicine (2024)
191 patients completed phase 1; 63% had early improvement. Of 173 who completed phase 2, 69% had reduced exacerbations by ≥50%, while 57% (37/65) on mOCS reduced their dose by ≥50%. The primary outcome 2, 3-dinor-11-β-PGF2α, GETE and standard clinical biomarkers (blood and sputum eosinophils, exhaled nitric oxide, serum IgE) did not predict either clinical response. Five breathomics (GC-MS) and 5 plasma lipid biomarkers strongly predicted the ≥50% reduction in exacerbations (receiver operating characteristic area under the curve (AUC): 0.780 and 0.922, respectively) and early responses (AUC:0.835 and 0.949, respectively). In independent cohorts, the GC-MS biomarkers differentiated between severe and mild asthma. Conclusions This is the first discovery of omics biomarkers that predict improvement to a biologic for asthma. Their prospective validation and development for clinical use is justified. This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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