Lane Andrew P, Mullol Joaquim, Hopkins Claire, Fokkens Wytske J, Lee Stella E, Msihid Jerome, Nash Scott, Sacks Harry, Borsos Kinga, Kamat Siddhesh, Rowe Paul J, Deniz Yamo, Jacob-Nara Juby A
Division of Rhinology, Sinus and Skull Base Surgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Hospital Clínic, IDIBAPS, Universitat de Barcelona, CIBERES, Barcelona, Spain.
Curr Med Res Opin. 2025 Jan;41(1):53-59. doi: 10.1080/03007995.2024.2434083. Epub 2024 Dec 14.
Loss of sense of smell is a cardinal symptom of chronic rhinosinusitis with nasal polyps (CRSwNP) and significantly impacts health-related quality-of-life. Dupilumab significantly improved smell outcomes (loss of smell [LoS] score; University of Pennsylvania Smell Identification Test [UPSIT]) versus placebo in the phase 3 SINUS-24/-52 studies (clinicaltrials.gov, NCT02898454/NCT02912468) in patients with severe CRSwNP. This post hoc analysis investigated the effect of dupilumab on olfaction using UPSIT smell impairment categories.
Patients with baseline smell impairment (UPSIT ≤34/≤33 [women/men; score range 0-40] AND LoS score ≥1 [0-3] AND smell/taste item of the 22-item Sinonasal Outcome Test >0 [SNOT-22; 0-5]) treated with dupilumab 300 mg or placebo once every 2 weeks on background intranasal corticosteroids were analyzed.
Of 724 patients, 665 (91.9%) had smell impairment at baseline; most had anosmia (UPSIT 0-18) (dupilumab/placebo: 80.9%/79.8%). At week 24, the proportion of dupilumab-treated patients with anosmia decreased to 28.5%, while 14.9% achieved normosmia; most placebo-group patients (79.2%) remained anosmic and only 1.2% achieved normosmia (odds ratio = 17.3; 95% confidence interval = 5.1-59.0; <.0001); results were similar at week 52. Improvements in Nasal Polyp Score, nasal congestion, and SNOT-22 total score were moderately correlated with improvements in UPSIT at weeks 24 and 52 (r = -.38 to -.50).
Most patients with severe CRSwNP had anosmia at baseline. Dupilumab treatment significantly improved smell versus placebo, with 14.9% achieving normosmia by week 24. There was a trend for better clinical outcomes in patients with greater smell improvement.
嗅觉丧失是伴鼻息肉的慢性鼻-鼻窦炎(CRSwNP)的主要症状,对健康相关生活质量有显著影响。在3期SINUS-24/-52研究(clinicaltrials.gov,NCT02898454/NCT02912468)中,与安慰剂相比,度普利尤单抗显著改善了重度CRSwNP患者的嗅觉结果(嗅觉丧失[LoS]评分;宾夕法尼亚大学嗅觉识别测试[UPSIT])。这项事后分析使用UPSIT嗅觉损害类别研究了度普利尤单抗对嗅觉的影响。
分析了接受300mg度普利尤单抗或安慰剂治疗的患者,这些患者在鼻内使用糖皮质激素的基础上,每2周接受一次治疗,基线时有嗅觉损害(UPSIT≤34/≤33[女性/男性;评分范围0-40]且LoS评分≥1[0-3]以及22项鼻鼻窦结局测试中的嗅觉/味觉项目>0[SNOT-22;0-5])。
724例患者中,665例(91.9%)基线时有嗅觉损害;大多数为嗅觉缺失(UPSIT 0-18)(度普利尤单抗/安慰剂:80.9%/79.8%)。在第24周时,接受度普利尤单抗治疗的嗅觉缺失患者比例降至28.5%,而14.9%达到嗅觉正常;大多数安慰剂组患者(79.2%)仍为嗅觉缺失,只有1.2%达到嗅觉正常(优势比=17.3;95%置信区间=5.1-59.0;P<.0001);第52周时结果相似。在第24周和第52周时,鼻息肉评分、鼻充血和SNOT-22总分的改善与UPSIT的改善中度相关(r=-0.38至-0.50)。
大多数重度CRSwNP患者基线时存在嗅觉缺失。与安慰剂相比,度普利尤单抗治疗显著改善了嗅觉,到第24周时14.9%的患者达到嗅觉正常。嗅觉改善程度越大的患者临床结局有更好的趋势。