Validation of a scoring algorithm for the clinician‐reported outcome tool ‘prurigo activity and severity (PAS)’ based on clinical studies of dupilumab in adults with prurigo Nodularis

Author:

Zeidler Claudia1ORCID,Stander Sonja1ORCID,Rhoten Stephanie2,Wratten Samantha3,Zhang Dian4,Msihid Jerome5,Brookes Ella6,Thomas Ryan7,Bahloul Donia5ORCID

Affiliation:

1. Center for Chronic Pruritus University Hospital Münster Münster Germany

2. IQVIA San Francisco USA

3. IQVIA Manchester UK

4. IQVIA Falls Church Virginia USA

5. Sanofi Gentilly France

6. Sanofi Reading UK

7. Regeneron Tarrytown New York USA

Abstract

AbstractBackgroundPrurigo nodularis (PN) also known as chronic prurigo, is a chronic inflammatory skin disease characterized by intensely itchy nodules/lesions which occur due to intensive scratching. PN management is, in part, based on clinician evaluations of PN lesions, which can be supported by clinician‐reported outcomes (ClinRO) such as the Prurigo Activity and Severity (PAS) instrument. A 5‐item version of PAS was included in recent phase‐3 dupilumab PN trials (PRIME [NCT04183335]/PRIME2 [NCT04202679]). The PAS score was derived using the unweighted sum of 3‐items of the 5‐item PAS (range, 0–11; higher score indicates worse activity and severity): Item 2 (number of lesions), Item 5a (percentage of lesions with excoriations/crusts) and Item 5b (percentage of healed lesions) for use in clinical practice and for communication of treatment benefit to physicians.ObjectivesTo evaluate the measurement properties of PAS score and derive within‐patient (responder definition) and between‐group improvement thresholds for interpreting changes in PAS score in patients with PN.MethodsThe data source was the pooled treatment group, intention‐to‐treat (ITT) data from the phase‐3 PRIME (NCT04183335) and PRIME2 (NCT04202679) studies evaluating the efficacy of dupilumab in adult patients with PN with ≥20 nodules and severe itch uncontrolled with topical therapies. PAS score reliability, validity and sensitivity to change were evaluated, and anchor‐ and distribution‐based methods were applied to derive meaningful change thresholds.ResultsThe pooled ITT population included 311 patients (mean age 49.5 years, 65.3% female). Adequate to good psychometric properties were demonstrated for PAS score. The within‐patient meaningful improvement threshold was estimated as 3.0 points (absolute change) and 37% (per cent change). A 1.7‐point (absolute change) and 20% (per cent change) improvement were estimated to reflect a between‐group meaningful change in PAS score.ConclusionsPAS score is a simple, clinically relevant indicator of PN lesion activity and severity supported by suitable psychometric performance.

Funder

Sanofi

Regeneron Pharmaceuticals

Publisher

Wiley

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