Kitchen Helen, Wyrwich Kathleen W, Carmichael Chloe, Deal Linda S, Lukic Tatjana, Al-Zubeidi Tamara, Marshall Chris, Pegram Hannah, Hamzavi Iltefat H, King Brett
Clinical Outcomes Assessment, Clarivate, UK.
Pfizer Inc, NYC, New York, NY, USA.
Dermatol Ther (Heidelb). 2022 Jul;12(7):1623-1637. doi: 10.1007/s13555-022-00752-8. Epub 2022 Jun 30.
This study explored patients' and dermatologists' priority outcomes for treatment to address, clinical outcome assessments (COA) for use in vitiligo clinical trials, and perceptions of within-patient meaningful change in facial and total body vitiligo.
Semistructured, individual, qualitative interviews were conducted with patients living with non-segmental vitiligo in the USA and with expert dermatologists in vitiligo. Concept elicitation discussions included open-ended questions to identify patient priority outcomes. Vitiligo COAs were reviewed by dermatologists. Tasks were completed by patients to explore their perceptions of meaningful changes in vitiligo outcomes; dermatologists' opinions were elicited. Data were analyzed using thematic methods; meaningful change tasks were descriptively summarized.
Individuals with vitiligo (N = 60) included adults (n = 48, 63% female) and adolescents (n = 12, 67% female). All Fitzpatrick Skin Types were represented. Eight (13%) were first- or second-generation immigrants to the USA. Expert dermatologists (N = 14) participated from the USA (n = 8), EU (n = 4), India (n = 1), and Egypt (n = 1). All individuals with vitiligo reported experiencing skin depigmentation; an observable clinical sign of vitiligo. Most confirmed that lesion surface area (n = 59/60, 98%) and level of pigmentation (n = 53/60, 88%) were important to include in disease assessments. Following an explanation, participants (n = 49/60, 82%) felt that the Facial Vitiligo Area Scoring Index (F-VASI) measurement generally made sense and understood that doctors would use it to assess facial vitiligo. Most participants felt that a 75% (n = 47/59, 80%) or 9 0% improvement in their facial vitiligo would be indicative of treatment success (n = 55/59, 93%). In the context of evaluating a systemic oral treatment for vitiligo, dermatologists perceived a 75% improvement on the F-VASI as successful (n = 9/14, 64%). Regarding the Total VASI (T-VASI) score, n = 30 participants considered 33% improvement as treatment success; an additional n = 10 endorsed 50% improvement and a further n = 5 endorsed 75% improvement. Clinicians most frequently identified 50% (n = 6/14, 43%) or 75% (n = 4/14, 29%) improvement in T-VASI as successful.
Repigmentation is a priority outcome for patients. The VASI was considered an appropriate tool to assess the extent of vitiligo. A minimum 75% improvement from baseline in the F-VASI and minimum 50% improvement from baseline in the T-VASI were identified as within-patient clinically meaningful thresholds.
本研究探讨了患者和皮肤科医生对于白癜风治疗的首要结局、白癜风临床试验中使用的临床结局评估(COA),以及患者对面部和全身白癜风自身有意义变化的认知。
对美国非节段型白癜风患者和白癜风领域的专家皮肤科医生进行了半结构化的个人定性访谈。概念引出讨论包括开放式问题,以确定患者的首要结局。皮肤科医生对白癜风COA进行了评估。患者完成任务以探索他们对白癜风结局有意义变化的认知;并征求了皮肤科医生的意见。使用主题分析法对数据进行分析;对有意义变化任务进行了描述性总结。
白癜风患者(N = 60)包括成年人(n = 48,63%为女性)和青少年(n = 12,67%为女性)。涵盖了所有菲茨帕特里克皮肤类型。8人(13%)是美国的第一代或第二代移民。专家皮肤科医生(N = 14)来自美国(n = 8)、欧盟(n = 4)、印度(n = 1)和埃及(n = 1)。所有白癜风患者均报告有皮肤色素脱失,这是白癜风的一个可观察到的临床体征。大多数人确认病变表面积(n = 59/60,98%)和色素沉着水平(n = 53/60,88%)对于疾病评估很重要。经过解释后,参与者(n = 49/60,82%)认为面部白癜风面积评分指数(F-VASI)测量总体上有意义,并理解医生会用它来评估面部白癜风。大多数参与者认为面部白癜风改善75%(n = 47/59,80%)或90%将表明治疗成功(n = 55/59,93%)。在评估一种白癜风全身口服治疗方法时,皮肤科医生认为F-VASI改善75%即为成功(n = 9/14,64%)。关于总VASI(T-VASI)评分,30名参与者认为改善33%即为治疗成功;另有10人认可改善50%,还有5人认可改善75%。临床医生最常认为T-VASI改善50%(n = 6/14,43%)或75%(n = 4/14,29%)即为成功。
色素再生是患者的首要结局。VASI被认为是评估白癜风程度的合适工具。F-VASI自基线至少改善75%以及T-VASI自基线至少改善50%被确定为患者自身临床上有意义的阈值。