不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Dupilumab and lymphoma risk among patients with asthma: a population-based cohort study.
Dupilumab and lymphoma risk among patients with asthma: a population-based cohort study.
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Dupilumab 治疗与哮喘患者较低的全因死亡率相关,尽管淋巴瘤风险增加,尤其是 T 细胞和 NK 细胞淋巴瘤。这些发现凸显了长期监测以及进一步研究哮喘中 dupilumab 相关淋巴瘤免疫学机制的必要性。
Dupilumab 已获批用于治疗特应性皮炎、哮喘和其他过敏性疾病。近期研究表明,接受 dupilumab 治疗的特应性皮炎患者发生皮肤淋巴瘤的风险较高。本研究旨在探讨接受 dupilumab 治疗的哮喘患者中淋巴瘤的风险。
这项基于人群的队列研究纳入了2018年至2024年间在美国启动dupilumab或活性对照药(吸入性糖皮质激素(ICS)联合长效β2受体激动剂(LABA),即ICS/LABA)治疗的哮喘患者。采用倾向评分匹配以平衡两组间的基线特征。主要结局为新发淋巴瘤,次要结局包括其他恶性肿瘤和全因死亡率。
共纳入14 936例接受dupilumab治疗和734 126例接受ICS/LABA治疗的哮喘患者。经过倾向评分匹配后,发现接受dupilumab治疗的患者淋巴瘤风险更高(54例 vs 43例,风险比(HR)1.79,95% CI 1.19-2.71),尤其是T细胞和自然杀伤(NK)细胞淋巴瘤(19例 vs 10例,HR 4.58,95% CI 1.82-11.53)。其他恶性肿瘤的发生率无显著差异。Dupilumab还与显著更低的全因死亡率相关(328例 vs 793例死亡,HR 0.65,95% CI 0.57-0.74)。
Dupilumab is approved for the treatment of atopic dermatitis, asthma, and other allergic diseases. Recent studies suggest that patients with atopic dermatitis receiving dupilumab are at a higher risk of developing cutaneous lymphoma. This study aimed to investigate the risk of lymphoma among patients with asthma receiving dupilumab.
This population-based cohort study included patients in the United States with asthma who initiated dupilumab or the active comparator (combination therapy with inhaled corticosteroids (ICS) plus long-acting -agonists (LABA), or ICS/LABA), between 2018 and 2024. Propensity score matching was used to balance baseline characteristics between groups. The primary outcome was new-onset lymphoma, and secondary outcomes included other malignancies and all-cause mortality.
A total of 14 936 dupilumab-treated and 734 126 ICS/LABA-treated patients with asthma were included. After propensity score matching, dupilumab-treated patients were found to have a higher risk of lymphoma (54 versus 43 cases, hazard ratio (HR) 1.79, 95% CI 1.19-2.71), especially T-cell and natural killer (NK)-cell lymphomas (19 versus 10 cases, HR 4.58, 95% CI 1.82-11.53). There was no significant difference in incidence of other malignant neoplasms. Dupilumab was also associated with significantly lower all-cause mortality (328 versus 793 deaths, HR 0.65, 95% CI 0.57-0.74).
Dupilumab treatment was associated with lower all-cause mortality among patients with asthma, despite increased risk of lymphoma, particularly T-cell and NK-cell lymphomas. These findings highlight the need for long-term surveillance and further research into the immunological mechanisms underlying dupilumab-associated lymphoma in asthma.
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