Connelly Kathryn, Koelmeyer Rachel, Ayton Darshini, May John, Gregory Kate, Eades Laura E, Barallon Raychel, Kandane-Rathnayake Rangi, Golder Vera, Anzum Afia, Mydin Maisarah, Akther Munni, Friedman Alan, Askanase Anca D, Aranow Cynthia, Vital Edward, Pons-Estel Guillermo, Brunner Hermine, Kalunian Kenneth, Dantata Khadija, Arnaud Laurent, Burke Laurie, Simon Lee S, Zuraw Qing, Garces Sandra, Werth Victoria P, Sun Ying B, Tanaka Yoshiya, Lahoud Youmna, Cornet Alain, Sorrentino Alessandro, Rahman Anisur, Stevens Anna, Barbey Catherine, Dey Ida Dzifa, Karis Elaine, Bonfá Eloisa, Noss Erika, Smith Eve M D, Stojan George, Andersen Jeanette, Merola Joseph F, Ross Terres Jorge A, Buie Joy, Maller Justine, Mosca Marta, Hojnik Maja, Dall'Era Maria, Furie Richard A, van Vollenhoven Ronald F, Banerjee Subhashis, Morand Eric
Centre for Inflammatory Diseases, Monash University, Melbourne, Victoria, Australia.
Centre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia.
Lupus Sci Med. 2025 May 6;12(1):e001484. doi: 10.1136/lupus-2024-001484.
To achieve consensus on domains of active disease for inclusion in a novel outcome measure for SLE randomised controlled trials (RCTs), the Treatment Response Measure for SLE (TRM-SLE).
Domains nominated by TRM-SLE Taskforce members were rated in a two-stage modified Delphi study. Each stage comprised two online survey rounds separated by a structured discussion meeting. In Stage 1, expert lupus clinicians and patient representatives rated domain 'importance' (impact on symptoms, function or survival). In Stage 2, clinicians rated 'important' domains on three characteristics relevant to RCT utility: 'appropriateness' for evaluating change in disease activity, 'representation' in patients with active SLE and 'measurability' in an RCT context. Consensus for domain inclusion was prespecified as all four characteristics achieving a rating ≥7 on a 1-9 scale by ≥70% of participants.
Domain nominations from 36/59 (61%) TRM-SLE Taskforce members yielded 34 potential domains which were rated in the modified Delphi study. At least one Delphi round was completed by 87 clinicians and 13 patient representatives. In Stage 1, 14 domains met consensus on 'importance' in both clinician and patient groups, and 11 domains met consensus among patients only. After Stage 2, eight of these domains also reached consensus on 'appropriateness', 'representation' and 'measurability': alopecia, arthritis, haemolytic anaemia, nephritis, mucosal ulcers, rash, serositis and thrombocytopenia.
Considering patient and clinician perspectives, we reached consensus to include eight disease activity domains for future development into the novel TRM-SLE clinical trial outcome measure, aiming to improve trial interpretability and success.
就纳入系统性红斑狼疮(SLE)随机对照试验(RCT)新型疗效指标“系统性红斑狼疮治疗反应指标”(TRM - SLE)的活动性疾病领域达成共识。
TRM - SLE工作组成员提名的领域在两阶段改良德尔菲研究中进行评分。每个阶段包括两轮在线调查,中间间隔一次结构化讨论会。在第1阶段,狼疮专家临床医生和患者代表对领域的“重要性”(对症状、功能或生存的影响)进行评分。在第2阶段,临床医生根据与RCT效用相关的三个特征对“重要”领域进行评分:评估疾病活动度变化的“适宜性”、活动性SLE患者中的“代表性”以及RCT背景下的“可测量性”。纳入领域的共识预先设定为所有四个特征在1 - 9分制中,≥70%的参与者评分≥7分。
59名TRM - SLE工作组成员中的36名(61%)提名的领域产生了34个潜在领域,在改良德尔菲研究中进行了评分。87名临床医生和13名患者代表至少完成了一轮德尔菲调查。在第1阶段,14个领域在临床医生和患者组中均就“重要性”达成共识,11个领域仅在患者中达成共识。在第2阶段之后,其中8个领域在“适宜性”、“代表性”和“可测量性”方面也达成了共识:脱发、关节炎、溶血性贫血、肾炎、黏膜溃疡、皮疹、浆膜炎和血小板减少症。
综合考虑患者和临床医生的观点,我们达成共识,纳入八个疾病活动领域,以便未来开发新型TRM - SLE临床试验疗效指标,旨在提高试验的可解释性和成功率。