Late Breaking Abstract - Benralizumab reduces eosinophils and ANCA in sputum in EGPA
<bold>Introduction:</bold> Benralizumab (30mg subcutaneous Q4W) is noninferior to mepolizumab (300mg sc Q4W) to induce clinical remission in patients with refractory EGPA (PMID: 38393328). <bold>Aims:</bold> We evaluated if treatment arms were associated with eosinophil reduction and ANCA in sputum in the randomized, double-blind, head-to-head MANDARA trial (<ext-link>NCT04157348</ext-link>). <bold>Methods:</bold> In a mechanistic sub-study (n=16) of the MANDARA trial, n=7 patients received benralizumab (52±11years, 57% female) and, n=9 received mepolizumab (58±16years, 78% female). Eosinophils, eosinophil activity (eosinophil peroxidase, EPX), T1/T2 cytokines and ANCA were assessed in blood and sputum pre- and post-treatment (PMID: 30179583). <bold>Results:</bold> Benralizumab reduced sputum eosinophils to <2.3% in 6/7 (86%) patients compared to mepolizumab (6/9, 66%) (χ2, P<0.01), but did not significantly reduce sputum EPX. At baseline, spANCA in both arms were comparable (mepo:4/9, 44%; benra: 3/7, 43%; only one sero-positive). Post-treatment, benralizumab significantly reduced spANCA levels compared to mepolizumab (P<0.05), with 2/7 (28%) remaining spANCA<sup>+</sup>. By comparison, there was an increase in the proportion of patients with spANCA on mepolizumab from baseline (6/9, 67%). Increase in spANCA correlated with spEPX (rho=0.65; P=0.01). The two patients on benralizumab who remained spANCA<sup>+</sup> had elevated spEPX and ACQ-6≥1.5 at the time-point of sampling, despite having achieved clinical remission. Reduction of T2 cytokines was comparable in both arms. However, an increase in spIL-17A post-mepolizumab (P<0.05) was noted that correlated with an increase in spANCA. <bold>Conclusions:</bold> Benralizumab has a greater effect on reducing sputum eosinophils and ANCA levels in EGPA compared to mepolizumab.
Authors
- Roma Sehmi (ORCID: https://orcid.org/0000-0003-0968-6304)
- Sofia Necander
- Carmen Venegas Garrido
- NADER A. KHALIDI (ORCID: https://orcid.org/0000-0002-8270-2617)
- Chynna Huang (ORCID: https://orcid.org/0000-0001-5179-0872)
- Michael E. Wechsler (ORCID: https://orcid.org/0000-0003-3505-2946)
- Katherine Radford (ORCID: https://orcid.org/0000-0002-9734-6213)
- Anurag Bhalla (ORCID: https://orcid.org/0000-0003-0613-0546)
- Parameswaran Nair (ORCID: https://orcid.org/0000-0002-1041-9492)
- Eva Rodríguez‐Suárez
- Julie Weidner (ORCID: https://orcid.org/0000-0002-7140-8666)
- Christopher McCrae (ORCID: https://orcid.org/0000-0001-7184-9069)
- Brandie Walker (ORCID: https://orcid.org/0000-0002-9899-0481)
- Manali Mukherjee (ORCID: https://orcid.org/0000-0002-7924-7211)
- Lena Börjesson Sjö
- Ali A. Ashkar (ORCID: https://orcid.org/0000-0003-1139-1468)
- Brian Kim (ORCID: https://orcid.org/0000-0002-8100-7161)
- Nadia Suray Tan
Institutions
- McMaster Divinity College (CA)
- University of Calgary (CA)
- McMaster University Medical Centre (CA)
- National Jewish Health (US)
- AstraZeneca (Switzerland) (CH)
- AstraZeneca (Finland) (FI)
- AstraZeneca (Spain) (ES)
- University of Colorado Denver (US)
- McMaster University (CA)
Publication Details
- Published
- 2024-09-14
- DOI
- https://doi.org/10.1183/13993003.congress-2024.pa5372
- Citations
- 1
- Primary Topic
- Eosinophilic Esophagitis
- Type
- article
- Field-Weighted Citation Impact
- 0.57