Sakhiya Jagdish, Sakhiya Dhruv, Khambhati Ravi, Patel Mehul, Darji Piyush, Gajjar Trusha, Daruwala Feral, Dudhatra Nimish
Dr. J. Sakhiya and Drs. Khambhati, Patel, Darji, and Gajjar are with the Sakhiya Skin Clinic in Gujarat, India.
Mrs. Daruwala and Mr. Dudhatra are with the Sakhiya Skin Clinic in Gujarat, India.
J Clin Aesthet Dermatol. 2020 Feb;13(2):47-52. Epub 2020 Feb 1.
Rituximab, an anticluster of differentation 20 antibody, has been shown in open series studies to be effective in treating pemphigus. In the literature, lymphoma (dose of 375mg/m, four-week infusion) and rheumatoid arthritis (two infusions of 1,000mg each, 15 days apart) are two protocols extensively used for rituximab treatment in pemphigus. We investigated whether a modified rheumatoid arthritis protocol, in which the patient received a single treatment course ranging from 2 to 5 infusions of 1,000mg of rituximab during an interval of four weeks is safe and effective in pemphigus management. Patients with pemphigus were treated with a single treatment course ranging from 2 to 5 infusions of 1,000mg of rituximab during an interval of four weeks. Clinical consensus late endpoints and desmoglein 1 and desmoglein 3 indices were monitored. We enrolled 32 patients in the study: four with pemphigus foliaceus (PF) and 28 with pemphigus vulgaris (PV). The follow-up period was 98.22±20.65 weeks (range: 40-140 weeks). All 32 patients responded to therapy. Nineteen patients achieved complete remission during a median period of 46 weeks (8 on minimal therapy, 11 off therapy). Thirteen patients achieved partial remission during a median period of 46 weeks (8 on minimal therapy, 5 off therapy). Relapses were seen in five (15.63%) patients between 72 and 96 weeks (median: 96 weeks) after the start of therapy. The antidesmoglein index correlated well with clinical improvement in PV or PF. Modified rheumatic arthritis protocol for rituximab was shown to be effective and safe in treating patients with pemphigus.
利妥昔单抗是一种抗分化簇20抗体,开放系列研究表明其在治疗天疱疮方面有效。在文献中,淋巴瘤(剂量为375mg/m²,四周输注)和类风湿关节炎(两次输注,每次1000mg,间隔15天)是利妥昔单抗治疗天疱疮广泛使用的两种方案。我们研究了一种改良的类风湿关节炎方案,即患者在四周的间隔期内接受2至5次1000mg利妥昔单抗的单次治疗疗程,在天疱疮治疗中是否安全有效。天疱疮患者在四周的间隔期内接受2至5次1000mg利妥昔单抗的单次治疗疗程。监测临床共识晚期终点以及桥粒芯糖蛋白1和桥粒芯糖蛋白3指标。我们招募了32名患者进行研究:4例落叶型天疱疮(PF)患者和28例寻常型天疱疮(PV)患者。随访期为98.22±20.65周(范围:40 - 140周)。所有32例患者对治疗均有反应。19例患者在中位时间46周时达到完全缓解(8例接受最小剂量治疗,11例停止治疗)。13例患者在中位时间46周时达到部分缓解(8例接受最小剂量治疗,5例停止治疗)。在治疗开始后72至96周(中位时间:96周)之间,5例(15.63%)患者出现复发。抗桥粒芯糖蛋白指标与PV或PF的临床改善情况相关性良好。利妥昔单抗的改良风湿性关节炎方案在治疗天疱疮患者方面显示出有效且安全。