Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Care India Solutions for Sustainable Development, Bihar Technical Support Program, Patna, Bihar, India.
Indian J Dermatol Venereol Leprol. 2020 Jan-Feb;86(1):39-44. doi: 10.4103/ijdvl.IJDVL_848_17.
Rituximab is being increasingly used for the treatment of pemphigus. Data derived from single-center studies following a uniform treatment protocol are limited. Effect of demography and disease type on treatment response is poorly characterized.
Our aim was to assess the effectiveness of biosimilar rituximab in pemphigus patients who had received rituximab as per rheumatoid arthritis protocol (2 doses, 1g each, infused 14 days apart).
It was a retrospective review of 146 eligible patients to assess the proportion of patients achieving complete remission off treatment, time to achieve complete remission off treatment, proportion of patients who relapsed after achieving complete remission off treatment, time taken to relapse, duration and total cumulative dose of corticosteroids administered after rituximab. Additionally, we tried to find whether a correlation existed between age, gender, total duration of illness before rituximab and pemphigus disease type with the above-mentioned outcome measures.
Of 146 patients, 107 (73.3%) attained complete remission off treatment. Mean interval between first dose rituximab administration and complete remission off treatment was 6.6 ± 3.4months. Complete remission off treatment was sustained for a mean duration of 9.1 ± 8.5 months before relapse. Over a mean follow-up duration of 24.9 ± 17.1 months (median 23, maximum 68 months), 75 of 107 patients (76.5%) who had achieved complete remission after first cycle of rituximab relapsed. A mean total cumulative dose of 3496 ± 2496 mg prednisolone was prescribed over a mean duration of 7.2 ± 4.7 months after first cycle of rituximab. Time taken to achieve remission was significantly longer in pemphigus foliaceus and these patients required significantly higher cumulative dose of prednisolone over a longer duration after rituximab. No deaths and long-term complications were recorded.
Only clinical parameters were assessed. Immunological parameters including B-cell counts and enzyme-linked immunosorbent assay for anti-desmoglein antibody titers were not carried out.
This study reinforces the beneficial role of rituximab in pemphigus. Pemphigus foliaceus patients required a higher total cumulative dose of prednisolone over a longer time to achieve remission and the remission lasted longer than that in pemphigus vulgaris.
利妥昔单抗越来越多地用于治疗天疱疮。根据单一中心研究的数据,遵循统一的治疗方案,其数据有限。关于人口统计学和疾病类型对治疗反应的影响还没有很好地描述。
我们的目的是评估在类风湿关节炎方案(2 剂,每剂 1g,间隔 14 天输注)下接受利妥昔单抗治疗的天疱疮患者使用生物仿制药利妥昔单抗的效果。
这是一项对 146 名符合条件的患者进行的回顾性研究,以评估患者在停止治疗后达到完全缓解的比例、达到完全缓解的时间、达到完全缓解后复发的患者比例、复发时间、在接受利妥昔单抗治疗后皮质类固醇的持续时间和总累积剂量。此外,我们还试图确定年龄、性别、在接受利妥昔单抗之前的总疾病持续时间与天疱疮疾病类型与上述结果指标之间是否存在相关性。
在 146 名患者中,107 名(73.3%)在停止治疗后达到完全缓解。首次利妥昔单抗治疗后达到完全缓解的平均间隔时间为 6.6 ± 3.4 个月。在复发前,完全缓解的持续时间平均为 9.1 ± 8.5 个月。在平均随访时间 24.9 ± 17.1 个月(中位数 23,最长 68 个月)中,107 名患者中有 75 名(76.5%)在第一个利妥昔单抗周期后完全缓解复发。在第一个利妥昔单抗周期后,平均给予 3496 ± 2496mg 泼尼松龙,持续时间平均为 7.2 ± 4.7 个月。在天疱疮患者中,达到缓解的时间明显延长,这些患者在接受利妥昔单抗治疗后需要更长时间、更高累积剂量的泼尼松龙才能达到缓解。未记录到死亡和长期并发症。
仅评估了临床参数。未进行免疫参数检查,包括 B 细胞计数和酶联免疫吸附测定抗桥粒芯糖蛋白抗体滴度。
本研究再次证实了利妥昔单抗在天疱疮中的有益作用。与寻常型天疱疮相比,落叶型天疱疮患者需要更高的总累积泼尼松龙剂量和更长的时间来达到缓解,且缓解持续时间更长。