Fokkens Wytske J, Bachert Claus, Hopkins Claire, Marglani Osama, Praestgaard Amy, Nash Scott, Deniz Yamo, Rowe Paul J, Sacks Harry, Jacob-Nara Juby A
Department of Otorhinolaryngology Amsterdam University Medical Centres Amsterdam The Netherlands.
Department of Otorhinolaryngology - Head and Neck Surgery University Hospital of Münster Münster Germany.
Clin Transl Immunology. 2024 Jun 8;13(6):e1511. doi: 10.1002/cti2.1511. eCollection 2024.
This analysis assessed disease characteristics and response to dupilumab treatment in male and female patients with severe chronic rhinosinusitis with nasal polyps (CRSwNP) (SINUS-52 study; NCT02898454).
Patients received dupilumab 300 mg or placebo every 2 weeks for 52 weeks on background intranasal corticosteroids. Efficacy was assessed through Week 52 using nasal polyp score (NPS), nasal congestion/obstruction score, loss of smell score and University of Pennsylvania Smell Identification Test score. Disease-specific health-related quality of life (HRQoL) was assessed using the 22-item Sino-Nasal Outcome Test (SNOT-22).
The analysis included 192 male and 111 female patients. Female patients had higher mean SNOT-22 total score (56.6 vs. 49.1, < 0.01) and more coexisting asthma (78.4% vs. 46.4%, < 0.0001) and non-steroidal anti-inflammatory drug-exacerbated respiratory disease (NSAID-ERD) (38.7% vs. 18.8%, = 0.0001) than male patients, but other baseline characteristics were similar. Dupilumab significantly improved CRSwNP outcomes vs. placebo at Week 52, regardless of gender: least squares mean differences (95% confidence interval) for NPS were -2.33 (-2.80, -1.86) in male and -2.54 (-3.18, -1.90) in female patients (both < 0.0001 vs. placebo), and for SNOT-22 were -19.2 (-24.1, -14.2) in male and -24.4 (-31.5, -17.3) in female patients (both < 0.0001 vs. placebo). There were no significant efficacy-by-gender interactions.
Female patients had greater asthma, NSAID-ERD and HRQoL burden at baseline than male patients. Dupilumab treatment significantly improved objective and subjective outcomes compared with placebo, irrespective of gender.
本分析评估了患有重度慢性鼻-鼻窦炎伴鼻息肉(CRSwNP)的男性和女性患者的疾病特征以及对度普利尤单抗治疗的反应(SINUS-52研究;NCT02898454)。
患者在使用鼻内糖皮质激素的基础上,每2周接受一次300mg度普利尤单抗或安慰剂治疗,持续52周。在第52周时,使用鼻息肉评分(NPS)、鼻充血/阻塞评分、嗅觉丧失评分和宾夕法尼亚大学嗅觉识别测试评分评估疗效。使用22项鼻鼻窦结局测试(SNOT-22)评估特定疾病的健康相关生活质量(HRQoL)。
该分析纳入了192名男性患者和111名女性患者。女性患者的SNOT-22总分均值较高(56.6对49.1,P<0.01),合并哮喘(78.4%对46.4%,P<0.0001)和非甾体抗炎药诱发的呼吸道疾病(NSAID-ERD)(38.7%对18.8%,P=0.0001)的比例也高于男性患者,但其他基线特征相似。在第52周时,与安慰剂相比,度普利尤单抗显著改善了CRSwNP的结局,无论性别如何:男性患者NPS的最小二乘均值差异(95%置信区间)为-2.33(-2.80,-1.86),女性患者为-2.54(-3.18,-1.90)(两者与安慰剂相比均P<0.0001),SNOT-22的最小二乘均值差异在男性患者中为-19.2(-24.1,-14.2),女性患者为-24.4(-31.5,-17.3)(两者与安慰剂相比均P<0.0001)。不存在按性别划分的显著疗效交互作用。
女性患者在基线时的哮喘、NSAID-ERD和HRQoL负担比男性患者更重。与安慰剂相比,度普利尤单抗治疗显著改善了客观和主观结局,与性别无关。