Psychometric Validation of the QLQ-NMIBC24 in Low Grade, Intermediate Risk Non-Muscle Invasive Bladder Cancer
Rattachement africain : us. Niveau de preuve : code pays fourni par la source.
Le résumé fourni par la source
Purpose: This study aimed to evaluate the psychometric properties of the EORTC QLQ-NMIBC24 and to propose distribution-based minimal clinically important difference (MCID) thresholds in patients with low-grade, intermediate-risk NMIBC (LG-IR-NMIBC). Patients and Methods: Patients with LG-IR-NMIBC from two phase 3 trials (ATLAS, n = 270; ENVISION, n = 240) completed the EORTC QLQ-C30 (ENVISION only) and QLQ-NMIBC24 questionnaires at baseline, Week 6, and Month 3. Psychometric evaluation of the QLQ-NMIBC24 in the LG-IR-NMIBC population included internal consistency, item convergence, known-groups validity, test-retest reliability and responsiveness to clinical change. Results: Item-item (0.40–0.96) and item-scale correlations (0.44–0.96) indicated good convergent validity across most domains. Internal consistency was acceptable for all multi-item domains (Cronbach’s α 0.78–0.93) except Malaise, which showed lower reliability (Cronbach’s α 0.34–0.67). Known-groups comparisons supported the instrument’s ability to distinguish patients by physical function (effect sizes up to 1.63) and sex-related domains. Test-retest reliability was generally good for Urinary Symptoms and Sexual Function (ICC 0.79–0.82). Selected domains (Urinary Symptoms, Sexual Intimacy, Malaise) demonstrated responsiveness to clinical change. Distribution-based MCID estimates varied across domains (4.37–16.29), providing potential thresholds for meaningful changes in HRQoL scores. Anchor-based analyses using QLQ-C30 change scores were explored, but correlations with QLQ-NMIBC24 domains (r = –0.37 to 0.01) did not meet the minimum threshold (0.37). Conclusion: The QLQ-NMIBC24 demonstrates valid, reliable, and interpretable measurement properties in patients with LG-IR-NMIBC. Although sensitivity varied across domains, the findings support its use in clinical trials and potentially routine practice. Distribution-based MCID thresholds provide guidance for interpreting meaningful HRQoL changes, though further studies using anchor-based methods are warranted.
Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.
Le contrôle bibliographique ouvert
Où se fait cette recherche
-
University of North Carolina at Chapel Hill pays non établi dans la noticeUniversité ou école supérieure
University of North Carolina at Chapel Hill.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.