Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Department of Dermatology, Venereology, and Leprology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Mycoses. 2023 Jul;66(7):576-584. doi: 10.1111/myc.13583. Epub 2023 Mar 26.
Itraconazole capsules have variable and unpredictable bioavailability.
Whether the generic brands are as effective as the innovator itraconazole in treating subjects with chronic pulmonary aspergillosis (CPA) remains unclear.
In this retrospective study, we treated CPA subjects with 6-month itraconazole capsule and measured itraconazole levels at 2 weeks, 3 months and 6 months. Our primary outcome was to compare the proportion of subjects achieving therapeutic drug levels (≥0.5 mg/L) with the generic and the innovator itraconazole after 2 weeks. We performed a multivariate logistic regression analysis to ascertain whether trough itraconazole levels affected treatment outcomes. We categorised treatment response as favourable or unfavourable based on improvement (or worsening) in clinical symptoms, microbiology and imaging. We also performed morphometric analysis of different brands of itraconazole by video-dermoscopy.
We included 193 (generic brands [n = 94] and innovator itraconazole [n = 99]) CPA subjects. A higher proportion of subjects achieved therapeutic levels at 2 weeks with the innovator than with the generic brands (72/99 [73%] vs. 27/94 [29%], p < .0001). The median trough level at 2 weeks was higher with the innovator than the generic brands (0.8 vs. 0 mg/L). The mean trough itraconazole levels achieved (average of three values measured over 6 months) independently predicted a favourable treatment response after adjusting for age, gender and CPA severity. On morphometric analysis, the generic brands had variable pellet numbers and sizes, and dummy pellets.
At 2 weeks, a significantly higher proportion of CPA subjects achieved therapeutic drug levels with the innovator than the generic itraconazole. The mean serum itraconazole levels independently predicted a favourable treatment response in CPA.
伊曲康唑胶囊的生物利用度具有可变性和不可预测性。
仿制药与创新型伊曲康唑治疗慢性肺曲霉病(CPA)患者的疗效是否相当仍不清楚。
在这项回顾性研究中,我们使用伊曲康唑胶囊治疗 6 个月的 CPA 患者,并在 2 周、3 个月和 6 个月时测量伊曲康唑水平。我们的主要结局是比较 2 周后仿制药和创新型伊曲康唑达到治疗药物水平(≥0.5mg/L)的患者比例。我们进行了多变量逻辑回归分析,以确定谷浓度伊曲康唑水平是否影响治疗结果。我们根据临床症状、微生物学和影像学的改善(或恶化)将治疗反应分类为有利或不利。我们还通过视频皮肤镜对不同品牌的伊曲康唑进行形态计量分析。
我们纳入了 193 例(仿制药品牌 [n=94] 和创新型伊曲康唑 [n=99])CPA 患者。在 2 周时,使用创新型伊曲康唑的患者达到治疗水平的比例高于仿制药品牌(72/99[73%] vs. 27/94[29%],p<0.0001)。在 2 周时,创新型伊曲康唑的谷浓度中位数高于仿制药品牌(0.8 对 0mg/L)。调整年龄、性别和 CPA 严重程度后,平均伊曲康唑谷浓度(6 个月内测量的三个值的平均值)独立预测治疗反应良好。在形态计量分析中,仿制药品牌的丸粒数量和大小以及假丸粒存在差异。
在 2 周时,与仿制药相比,创新型伊曲康唑治疗的 CPA 患者有更高比例达到治疗药物水平。血清伊曲康唑的平均水平独立预测了 CPA 的良好治疗反应。