Braid Jessica, Islam Lutaf, Gugiu Cristian, Omachi Theodore A, Doll Helen
Roche Products Ltd., Welwyn Garden City, Hertfordshire, United Kingdom.
Formerly of Clinical Outcomes Solutions, Chicago, IL, United States.
World Allergy Organ J. 2023 May 13;16(5):100776. doi: 10.1016/j.waojou.2023.100776. eCollection 2023 May.
Nasal Polyp Score (NPS) and Nasal Congestion Score (NCS) are commonly used clinical trial endpoints to determine improvements in response to treatment in patients with chronic rhinosinusitis with nasal polyps (CRSwNP). However, limited information is available on within-patient meaningful change thresholds (MCTs) and between-group minimal important differences (MIDs) for NPS and NCS, which would aid interpretation of results.
Data from phase 3 placebo-controlled trials of omalizumab in patients with CRSwNP (POLYP 1 and POLYP 2) were used to estimate MCTs and MIDs for both NPS and NCS using anchor-based methods. Sino-Nasal Outcome Test-22 (SNOT-22) and SNOT-22 Sino-Nasal Symptoms Subscale (SNSS) scores were used as anchors (≥0.35 correlation with NPS and NCS). Within- and between-group differences in NPS and NCS change scores were used to estimate MCTs and MIDs, respectively. Identified MCTs were used in unblinded responder analyses to compare the proportions of patients per treatment group achieving a meaningful improvement.
MCTs and MIDs were estimated at -1.0 and -0.5 for NPS and -0.50 and -0.35 for NCS, respectively, and were consistent across studies. Overall, 57.0% of patients achieved the MCT in NPS with omalizumab vs 29.9% with placebo (p < 0.0001). Similarly, 58.9% of patients achieved the MCT in NCS with omalizumab vs 30.7% with placebo (p < 0.0001). Group differences in mean change were statistically significant and exceeded the estimated MIDs.
Meaningful change estimates for NPS and NCS could be used to assess response to treatment for patients with chronic rhinosinusitis with nasal polyps.: POLYP1: clinicaltrails.gov NCT03280550; registered September 12, 2017; https://clinicaltrials.gov/ct2/show/NCT03280550). POLYP2 (clinicaltrials.gov NCT03280537; registered September 12, 2017; https://clinicaltrials.gov/ct2/show/NCT03280537).
鼻息肉评分(NPS)和鼻阻塞评分(NCS)是常用的临床试验终点指标,用于确定鼻息肉慢性鼻窦炎(CRSwNP)患者治疗反应的改善情况。然而,关于NPS和NCS的患者内有意义变化阈值(MCT)和组间最小重要差异(MID)的信息有限,而这些信息有助于结果的解释。
使用奥马珠单抗治疗CRSwNP患者的3期安慰剂对照试验(POLYP 1和POLYP 2)的数据,采用基于锚定的方法估计NPS和NCS的MCT和MID。采用鼻窦结局测试-22(SNOT-22)和SNOT-22鼻窦症状子量表(SNSS)评分作为锚定指标(与NPS和NCS的相关性≥0.35)。NPS和NCS变化评分的组内和组间差异分别用于估计MCT和MID。确定的MCT用于非盲应答者分析,以比较每个治疗组中实现有意义改善的患者比例。
NPS的MCT和MID估计分别为-1.0和-0.5,NCS的MCT和MID估计分别为-0.50和-0.35,且各研究结果一致。总体而言,使用奥马珠单抗的患者中有57.0%达到了NPS的MCT,而使用安慰剂的患者中这一比例为29.9%(p<0.0001)。同样,使用奥马珠单抗的患者中有58.9%达到了NCS的MCT,而使用安慰剂的患者中这一比例为30.7%(p<0.0001)。平均变化的组间差异具有统计学意义且超过了估计的MID。
NPS和NCS的有意义变化估计可用于评估鼻息肉慢性鼻窦炎患者的治疗反应。:POLYP1:clinicaltrails.gov NCT03280550;2017年9月12日注册;https://clinicaltrials.gov/ct2/show/NCT03280550)。POLYP2(clinicaltrials.gov NCT03280537;2017年9月12日注册;https://clinicaltrials.gov/ct2/show/NCT03280537)。