Alexis Andrew, McMichael Amy, Vashi Neelam, Bhutani Tina, Rodriguez Adrian O, Yeung Jensen, Choi Olivia, Chan Daphne, Alkousakis Theodore, Bronner Denise N, Park-Wyllie Laura, Gao Long-Long, Grimes Pearl, Shahriari Mona, Yadav Geeta, Kindred Chesahna, Taylor Susan C, Desai Seemal R
Department of Dermatology, Weill Cornell Medicine, New York, New York.
Department of Dermatology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
JAMA Dermatol. 2025 Mar 1;161(3):256-264. doi: 10.1001/jamadermatol.2024.5103.
Diverse racial and ethnic representation in clinical trials has been limited, not representative of the US population, and the subject of pending US Food and Drug Administration guidance. Psoriasis presentation and disease burden can vary by skin pigmentation, race and ethnicity, and socioeconomic differences. Overall, there are limited primary data on clinical response, genetics, and quality of life in populations with psoriasis and skin of color (SoC). The Varying Skin Tones in Body and Scalp Psoriasis: Guselkumab Efficacy and Safety trial (VISIBLE) is underway and uses strategies aimed at addressing this persistent gap.
To assess the innovative strategies used in the VISIBLE trial to recruit and retain diverse participants in a randomized clinical trial of psoriasis in participants with SoC.
DESIGN, SETTING, AND PARTICIPANTS: This was an ad hoc quality improvement assessment of participant recruitment and retention approaches used by the VISIBLE trial. VISIBLE enrolled and randomized 211 participants (mean [SD] age, 43 [13] years; 75 females [36%] and 136 males [64%]) with SoC and moderate to severe plaque psoriasis from August 2022 to March 2023 to evaluate guselkumab treatment. The self-identified race and ethnicity of the participants was: 1 American Indian/Alaska Native (0.5%), 63 Asian (29.9%), 24 Black (11.4%), 94 Hispanic/Latino (44.5%), 13 Middle Eastern (6.2%), 1 Pacific Islander/Native Hawaiian (0.5%), 12 multiracial (5.7%), and 3 of other race and/or ethnicity (1.4%). Using a combination of objective (colorimetry to determine Fitzpatrick skin type) and self-reported (race and ethnicity consistent with SoC) parameters, VISIBLE sought to broaden inclusion of participants from various backgrounds.
Observed improvements were that participant enrollment occurred approximately 7 times faster than anticipated (vs historical recruitment data for psoriasis studies); 211 participants (100%) self-identified themselves as a race or ethnicity other than White; and more than 50% had skin tone in the darker half of the Fitzpatrick skin type spectrum (type IV-VI). Innovations implemented by VISIBLE were (1) assessment of the natural history of postinflammatory pigment alteration and improvements over time using combined objective colorimetry and clinician- and patient-reported outcomes; (2) evaluation of genetic and comorbidity biomarkers relevant to participants with SoC; (3) a diverse demographic-driven approach to site selection (emphasizing investigator and staff diversity and experience with populations with SoC); (4) provision of cultural competency training to enhance participant enrollment and retention; (5) collection of patient-reported outcomes data in participants' primary language; and (6) periodic, blinded central review and feedback on investigator efficacy scoring to promote consistency and accuracy in evaluating psoriasis in participants with SoC.
VISIBLE is a unique study focused on addressing important knowledge and data gaps in populations of patients with psoriasis and SoC, with the goal of generating data to help improve clinical care and inform future best practices in diversity within dermatology research. The rapid study enrollment demonstrates that intentional and strategic approaches to clinical trial design and conduct can speed recruitment and bolster participation and retention of diverse populations in a dermatologic setting.
ClinicalTrials.gov Identifier: NCT05272150.
临床试验中不同种族和族裔的代表性有限,不能代表美国人口,且是美国食品药品监督管理局待发布指南的主题。银屑病的表现和疾病负担可能因皮肤色素沉着、种族和族裔以及社会经济差异而有所不同。总体而言,关于银屑病患者和有色人种(SoC)人群的临床反应、遗传学和生活质量的原始数据有限。“身体和头皮银屑病中不同肤色:古塞库单抗的疗效和安全性试验(VISIBLE)”正在进行中,该试验采用了旨在解决这一长期存在差距的策略。
评估VISIBLE试验中用于招募和留住SoC参与者参加银屑病随机临床试验的创新策略。
设计、背景和参与者:这是对VISIBLE试验所采用的参与者招募和留住方法进行的临时质量改进评估。VISIBLE在2022年8月至2023年3月期间招募并随机分配了211名SoC且患有中度至重度斑块状银屑病的参与者(平均[标准差]年龄,43[13]岁;75名女性[36%]和136名男性[64%])以评估古塞库单抗治疗效果。参与者自我认定的种族和族裔为:1名美洲印第安人/阿拉斯加原住民(0.5%)、63名亚洲人(29.9%)、24名黑人(11.4%)、94名西班牙裔/拉丁裔(44.5%)、13名中东人(6.2%)、1名太平洋岛民/夏威夷原住民(0.5%)、12名多种族(5.7%)以及3名其他种族和/或族裔(1.4%)。VISIBLE使用客观(比色法确定菲茨帕特里克皮肤类型)和自我报告(与SoC一致的种族和族裔)参数相结合的方法,力求扩大来自不同背景参与者的纳入范围。
观察到的改进包括:参与者入组速度比预期快约7倍(与银屑病研究的历史招募数据相比);211名参与者(100%)自我认定为非白人种族或族裔;超过50%的人皮肤色调处于菲茨帕特里克皮肤类型谱较深的一半(IV - VI型)。VISIBLE实施的创新措施包括:(1)使用客观比色法与临床医生和患者报告的结果相结合,评估炎症后色素改变的自然史及其随时间的改善情况;(2)评估与SoC参与者相关的遗传和合并症生物标志物;(3)采用由不同人口统计学驱动的地点选择方法(强调研究者和工作人员的多样性以及对SoC人群的经验);(4)提供文化能力培训以提高参与者的招募和留存率;(5)以参与者的母语收集患者报告的结果数据;(6)定期进行盲法中心审查并反馈研究者疗效评分,以促进在评估SoC参与者的银屑病时的一致性和准确性。
VISIBLE是一项独特的研究,专注于解决银屑病患者和SoC人群中重要的知识和数据空白,目标是生成数据以帮助改善临床护理,并为皮肤病学研究中的多样性未来最佳实践提供参考。快速的研究入组表明,临床试验设计和实施中有意且有策略的方法可以加快招募速度,并增强皮肤科环境中不同人群的参与度和留存率。
ClinicalTrials.gov标识符:NCT05272150。