Cardiology and Rheumatology Clinic, University of Sarajevo Clinics Centre, Bolnicka 25, Sarajevo, Bosnia and Herzegovina.
Bosn J Basic Med Sci. 2010 May;10(2):121-4. doi: 10.17305/bjbms.2010.2706.
The open prospective combined cytogenetic and clinical study investigated the impact of biological therapy Rituximab on number and structure of chromosomes in Rheumatoid arthritis patients. The purpose of this study was to investigate safety of Rituximab on chromosomes as well as cytotoxic therapy Methotrexate. A total of 8 seropositive Rheumatoid arthritis patients were analyzed for primary end point of eventual cytotoxic effect of Rituximab. Assessment was done before and 1 month later, actually 2 weeks after the administration of full course of Rituximab in infusion. Patients suffering from active Rheumatoid arthritis were randomly assigned according to established protocol to receive infusion of Rituximab in a full dose of 2.0 grams divided in a two doses of 1.0 gram on days 1 and 15. The lymphocytes from peripheral blood were cultured according to Moorhead method. The results obtained from this investigation showed that normal male and female karyogram was found after the full therapy of Rituximab. The results from this study, that was done on a rather small number of subjects, indicate that Rituximab does not express either clastogenic or aneugenic effects. But, co-finding of this study was that Methotrexate had a side effect on chromosomal aberration in one female RA patient, and after discontinuation of this treatment the normal karyogram was observed.
这项开放前瞻性的细胞遗传学和临床联合研究旨在探讨生物疗法利妥昔单抗对类风湿关节炎患者染色体数量和结构的影响。本研究的目的是调查利妥昔单抗对染色体的安全性以及细胞毒性药物甲氨蝶呤的安全性。对 8 例血清阳性的类风湿关节炎患者进行了分析,以评估利妥昔单抗最终的细胞毒性作用这一主要终点。评估在治疗前和治疗后 1 个月进行,实际上是在全疗程利妥昔单抗输注后 2 周进行。根据既定方案,患有活动期类风湿关节炎的患者被随机分配接受全剂量 2.0 克利妥昔单抗输注,分为 1.0 克剂量,在第 1 天和第 15 天各 1 次。外周血淋巴细胞按 Moorhead 法培养。这项研究的结果表明,在完成利妥昔单抗的全疗程治疗后,发现了正常的男性和女性核型。这项在数量相对较少的受试者中进行的研究结果表明,利妥昔单抗既没有表现出致裂作用,也没有表现出变倍作用。但是,这项研究的共同发现是,甲氨蝶呤对 1 例女性 RA 患者的染色体畸变有副作用,并且在停止该治疗后观察到正常核型。