Sinclair Rodney, Law Ernest H, Zhang Xingqi, Zhang Fan, Napatalung Lynne, Zwillich Samuel H, King Brett, Mesinkovska Natasha
Sinclair Dermatology, Melbourne, Victoria, Australia.
Pfizer Inc., New York, New York, USA.
Dermatology. 2024;240(5-6):767-777. doi: 10.1159/000539536. Epub 2024 Jun 27.
Patients with alopecia areata (AA) report high levels of dissatisfaction with commonly used treatments. Patient-reported outcomes are essential to understanding patients' experiences with AA treatments. The objective of this study was to evaluate patient-reported satisfaction with hair growth among patients with AA receiving ritlecitinib or placebo and the correlation between clinician-assessed efficacy and patient-reported satisfaction.
In the ALLEGRO-2b/3 (NCT03732807) trial, patients with AA and ≥50% scalp hair loss were randomized to daily ritlecitinib or placebo for 24 weeks, with a 24-week extension of continued ritlecitinib or switch from placebo to ritlecitinib. The Patient Satisfaction with Hair Growth (P-Sat) measure evaluated patients' satisfaction with hair growth in 3 domains: amount, quality, and overall satisfaction with hair growth. The prespecified analysis evaluated the proportion of patients who were slightly, moderately, or very satisfied with hair growth. Several post hoc analyses assessed the proportion of patients who were moderately/very satisfied and moderately/very dissatisfied and calculated polyserial correlations between change from baseline (CFB) in Severity of Alopecia Tool (SALT) and P-Sat scores at weeks 24 and 48.
At week 24, the proportion of patients (N = 718) reporting satisfaction (slightly, moderately, or very satisfied) overall with their hair growth ranged from 36.4% in the ritlecitinib 10-mg group (evaluated for dose ranging only) to 67.5% in the 200/50-mg group versus 22.6% in the placebo groups. In patients randomized to ritlecitinib, the proportion who were satisfied increased or was maintained at week 48. A substantially greater proportion of placebo patients who switched to ritlecitinib reported satisfaction at week 48 than at week 24. Similar results were observed for patient satisfaction with the amount and quality of hair growth. In the post hoc analyses defining satisfaction as moderately/very satisfied and dissatisfaction as moderately/very dissatisfied, the benefit of ritlecitinib was also observed. All P-Sat domain scores strongly correlated with CFB-SALT scores at weeks 24 (range 0.73-0.76; p < 0.05) and 48 (0.74-0.77; p < 0.05).
Patients receiving active ritlecitinib doses reported favorable results versus placebo in satisfaction with hair growth up to week 48. High concordance was observed between improvement in scalp hair growth evaluated by clinicians and patient-reported satisfaction.
斑秃(AA)患者对常用治疗方法的满意度较低。患者报告的结果对于了解患者接受AA治疗的体验至关重要。本研究的目的是评估接受利特昔替尼或安慰剂治疗的AA患者对头发生长的患者报告满意度,以及临床医生评估的疗效与患者报告满意度之间的相关性。
在ALLEGRO-2b/3(NCT03732807)试验中,头皮脱发≥50%的AA患者被随机分为每日服用利特昔替尼或安慰剂,为期24周,随后继续服用利特昔替尼24周或从安慰剂转换为利特昔替尼。患者对头发生长的满意度(P-Sat)测量评估了患者在三个方面对头发生长的满意度:数量、质量和对头发生长的总体满意度。预先设定的分析评估了对头发增长略有、中度或非常满意的患者比例。几项事后分析评估了中度/非常满意和中度/非常不满意的患者比例,并计算了第24周和第48周脱发严重程度工具(SALT)基线变化(CFB)与P-Sat评分之间的多系列相关性。
在第24周,报告对头发增长总体满意(略有、中度或非常满意)的患者比例(N = 718),在利特昔替尼10 mg组(仅评估剂量范围)为36.4%,在200/50 mg组为67.5%,而安慰剂组为22.6%。在随机接受利特昔替尼治疗的患者中,第48周时满意的患者比例增加或保持不变。在第48周时,从安慰剂转换为利特昔替尼的患者中,报告满意的比例比第24周时大幅增加。在患者对头发生长的数量和质量的满意度方面也观察到了类似的结果。在将满意度定义为中度/非常满意,不满意定义为中度/非常不满意的事后分析中,也观察到了利特昔替尼的益处。所有P-Sat领域评分在第24周(范围0.73-0.76;p < 0.