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奥马珠单抗治疗哮喘患者的效果与过敏原的数量和类型有关。

Omalizumab response in patients with asthma by number and type of allergen.

机构信息

Alabama Allergy and Asthma Center, Homewood, Alabama.

Genentech, Inc., South San Francisco, California.

出版信息

Ann Allergy Asthma Immunol. 2021 Aug;127(2):223-231. doi: 10.1016/j.anai.2021.04.002. Epub 2021 Apr 8.

Abstract

BACKGROUND

The anti-immunoglobulin E therapy, omalizumab, improves asthma control and reduces exacerbations in patients with moderate-to-severe allergic asthma. However, it has been suggested that omalizumab should be reserved for highly allergic patients with multiple allergen sensitivities or perennial-only sensitivities.

OBJECTIVE

To examine impact of allergy burden, including number and type of allergen sensitivities, on omalizumab response in a real-world setting.

METHODS

This post hoc analysis evaluated a subset of omalizumab-treated patients from the Prospective Observational Study to Evaluate Predictors of Clinical Effectiveness in Response to Omalizumab (NCT01922037) who had completed 13 allergen assessments (N=478). Patients were classified by allergen burden (nonsensitized, 1, 2-4, or ≥5 allergen sensitivities) and type of allergen (nonsensitized, seasonal, perennial, or both). Outcome measures included exacerbation rate vs previous year and improvements in lung function and Asthma Quality of Life Questionnaire (AQLQ).

RESULTS

Comparable adjusted exacerbation rates were observed after omalizumab initiation, regardless of number or type of allergen sensitizations (0.56-0.85/y). Improvements in forced expiratory volume in 1 second from baseline at months 6 (0.03-0.09 L) and 12 (-0.08 to 0.08 L) were also similar across subgroups. Least squares mean change in AQLQ from baseline at months 6 (1.0-1.2) and 12 (1.1-1.4) was comparable across patient subgroups, and similar percentages of patients achieved AQLQ minimal clinically important difference of at least a 0.5-point improvement at month 6 (71%-75%), which was maintained or improved to month 12 (71%-89%). In all analyses, 95% confidence intervals overlapped.

CONCLUSION

Overall findings suggest that patients with allergic asthma achieved comparable improvements across distinct outcome measures after omalizumab therapy in a real-world setting, regardless of number and type of allergen sensitizations.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT01922037.

摘要

背景

抗免疫球蛋白 E 疗法奥马珠单抗可改善中重度过敏性哮喘患者的哮喘控制并减少恶化。然而,有研究建议,奥马珠单抗应保留给具有多种过敏原敏感性或仅常年过敏原敏感性的高过敏患者。

目的

在真实环境中,研究过敏原负担(包括过敏原敏感性的数量和类型)对奥马珠单抗应答的影响。

方法

这项事后分析评估了 Prospective Observational Study to Evaluate Predictors of Clinical Effectiveness in Response to Omalizumab(NCT01922037)中接受奥马珠单抗治疗并完成 13 项过敏原评估的亚组患者(N=478)。患者按过敏原负担(未致敏、1、2-4 或≥5 种过敏原敏感性)和过敏原类型(未致敏、季节性、常年性或两者兼有)进行分类。主要观察指标为与前一年相比的恶化率和肺功能以及哮喘生活质量问卷(AQLQ)的改善。

结果

奥马珠单抗起始后,无论过敏原敏感性的数量或类型如何,调整后的恶化率均无显著差异(0.56-0.85/年)。6 个月(0.03-0.09 L)和 12 个月(0.08-0.08 L)时与基线相比,用力呼气量第一秒的改善也相似。6 个月(1.0-1.2)和 12 个月(1.1-1.4)时,AQLQ 与基线相比的最小二乘均值变化在患者亚组中相似,且有相似比例的患者在第 6 个月(71%-75%)和第 12 个月(71%-89%)达到 AQLQ 最小临床重要差异至少提高 0.5 分。所有分析中,95%置信区间均有重叠。

结论

总体而言,这些发现表明,在真实环境中,接受奥马珠单抗治疗的过敏性哮喘患者在不同的结局指标方面均取得了相似的改善,无论其过敏原敏感性的数量和类型如何。

临床试验注册号

NCT01922037。

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