ENT Department, Guy's and St Thomas' Hospitals, London, UK.
Department of Otorhinolaryngology, Düsseldorf University Hospital (UKD), Düsseldorf, Germany.
Int Forum Allergy Rhinol. 2021 Jul;11(7):1087-1101. doi: 10.1002/alr.22780. Epub 2021 Feb 21.
Chronic rhinosinusitis with nasal polyps (CRSwNP) is a type 2 inflammatory disease treated with sinus surgery when refractory to medical intervention. However, recurrence postsurgery is common. Dupilumab, a fully human monoclonal antibody, blocks the shared receptor for interleukin 4 (IL-4) and IL-13, key and central drivers of type 2 inflammation. We report the efficacy of dupilumab in patients with CRSwNP from the SINUS-24/SINUS-52 trials (NCT02912468/NCT02898454), by number of prior surgeries and time since last surgery.
Patients were randomized to placebo or dupilumab 300 mg every 2 weeks. Post hoc subgroup analyses were performed for patients with 0, ≥1, 1/2, or ≥3 prior surgeries, and for patients who had surgery within <3, 3 to <5, 5 to <10, or ≥10 years. Efficacy outcomes at 24 weeks included co-primary endpoints nasal polyp score (NPS) and nasal congestion (NC), and Lund-Mackay (LMK), 22-item Sino-Nasal Outcome Test (SNOT-22), and smell scores.
Of 724 patients randomized, 459 (63.4%) had ≥1 prior surgery. Baseline sinus disease (NPS, NC, LMK) and olfactory dysfunction (University of Pennsylvania Smell Identification Test [UPSIT] and loss of smell) scores were worse for patients with ≥3 prior surgeries vs no surgery. Baseline NPS and LMK were worse in patients with <3 years since last surgery than in patients with ≥5 years since last surgery. Dupilumab significantly improved all outcome measures vs placebo in all subgroups by number of surgeries and by time since last surgery. Improvements in NPS and LMK were greater in patients with <3 years since last surgery than patients with ≥5 years. Safety results were consistent with the known dupilumab safety profile.
Dupilumab improved CRSwNP outcomes irrespective of surgery history, with greater improvements in endoscopic outcomes in patients with shorter duration since last surgery.
伴有鼻息肉的慢性鼻-鼻窦炎(CRSwNP)是一种 2 型炎症性疾病,在药物治疗无效时需要鼻窦手术治疗。然而,手术后复发很常见。度普利尤单抗是一种全人源单克隆抗体,可阻断白细胞介素 4(IL-4)和白细胞介素 13(IL-13)的共同受体,这两种细胞因子是 2 型炎症的关键和中心驱动因素。我们报告了度普利尤单抗在 SINUS-24/SINUS-52 试验(NCT02912468/NCT02898454)中治疗伴有鼻息肉的慢性鼻-鼻窦炎患者的疗效,这些患者根据既往手术次数和末次手术时间进行了分层。
患者被随机分配至安慰剂或度普利尤单抗 300mg,每 2 周一次。对既往手术次数为 0、≥1、1/2 或≥3 次,以及末次手术时间<3 年、3-<5 年、5-<10 年或≥10 年的患者进行了事后亚组分析。24 周的疗效终点包括主要终点鼻息肉评分(NPS)和鼻腔堵塞(NC),以及 Lund-Mackay(LMK)评分、22 项鼻-鼻窦炎生活质量量表(SNOT-22)和嗅觉评分。
在 724 名随机患者中,459 名(63.4%)有≥1 次既往手术史。与无手术史患者相比,既往手术次数≥3 次的患者基线时鼻窦疾病(NPS、NC、LMK)和嗅觉功能障碍(宾夕法尼亚大学嗅觉识别测试[UPSIT]和嗅觉丧失)评分更差。与末次手术时间≥5 年的患者相比,末次手术时间<3 年的患者基线 NPS 和 LMK 评分更差。与末次手术时间≥5 年的患者相比,末次手术时间<3 年的患者,度普利尤单抗治疗在所有手术次数和末次手术时间亚组中均显著改善了所有终点指标。末次手术时间<3 年的患者 NPS 和 LMK 的改善程度大于末次手术时间≥5 年的患者。安全性结果与度普利尤单抗已知的安全性特征一致。
无论手术史如何,度普利尤单抗均改善了伴有鼻息肉的慢性鼻-鼻窦炎的结局,末次手术时间较短的患者内镜结局改善更为显著。