Blood Cells Count Derived Inflammation Indexes as Predictors of Early Treatment Response to Dupilumab in Patients with Moderate-to-Severe Atopic Dermatitis

Author:

Zinellu Angelo1ORCID,Sucato Federica2,Piras Viviana3,Addis Gian Mario4,Biondi Gabriele2ORCID,Montesu Maria Antonia2,Mangoni Arduino A.56ORCID,Carru Ciriaco1ORCID,Pirina Pietro2ORCID,Paliogiannis Panagiotis2ORCID,Fois Alessandro G.2ORCID,Satta Rosanna2

Affiliation:

1. Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy

2. Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy

3. Dermatology Unit, Department of Medical Sciences and Public Health, AOU Cagliari, 09123 Cagliari, Italy

4. Dermatology Unit, Department of Medical Care of San Francesco Hospital, 08100 Nuoro, Italy

5. Discipline of Clinical Pharmacology, College of Medicine and Public Health, Flinders University, Adelaide 5042, Australia

6. Department of Clinical Pharmacology, Flinders Medical Centre, Southern Adelaide Local Health Network, Bedford Park, Adelaide 5042, Australia

Abstract

Derived inflammatory indexes from routine hematological parameters might be useful for predicting early-response vs. late/non-response to dupilumab, the first biological agent approved for moderate-to-severe atopic dermatitis (AD). We tested this hypothesis by retrospectively investigating the association between pre-specified baseline inflammatory indexes and dupilumab response (≥50% reduction in the Eczema Area and Severity Index, EASI 50) at 4 and 16 weeks in a consecutive series of 66 AD patients (38 males and 28 females). Forty-six patients (69.7%) were early-responders at 4 weeks, whereas the remaining twenty (30.3%) were late/non-responders at 16 weeks. In logistic regression, the platelet-to-lymphocyte ratio (PLR) was independently associated with early-response (OR = 1.0159, 95% CI 1.0005 to 1.0315, p = 0.0426). The predictive performance of PLR and other derived indexes towards early-response was further improved by their combination with serum IgE concentrations, with a maximum AUC value for the combined systemic immune inflammation index (SII)-IgE of 0.797 (95% CI = 0.677 to 0.884, p < 0.0001). Derived inflammatory indexes, particularly SII-IgE, might be useful to identify early-responders to dupilumab and develop alternative treatment protocols for late/non-responders.

Funder

Fondo di Ateneo per la Ricerca

Publisher

MDPI AG

Subject

General Medicine

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