C. P. Mondéjar, C. I. Navalón, I. Valverde, Amelia Soto, P. Fernández, M. Candel, L. R. Redondo, M. Candela, M. Coronel, Mdc Caballero Requejo, E. U. Sanz
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Material and methods A retrospective study was performed in which all patients diagnosed with these pathologies who initiated treatment with adalimumab from January 2007 to December 2016 were included. Data for start date, date of discontinuation of treatment if suspension occurred, sex and age of the patients were collected. Adalimumab’s persistence was calculated in months from the beginning of treatment to the last dispensation register. We collected dispensation data from January 2007 to May 2019 to calculate adalimumab’s persistence until this date. The drug’s survival was calculated using the Kaplan–Meier method and the log rank test to compare survival in each of the pathologies. A significant difference was considered with a p value Results 125 patients started treatment with adalimumab between January 2007 and December 2016; 48 patients (38.4%) were diagnosed with rheumatoid arthritis, 43 (34.4%) with ankylosing spondylitis and 34 (27.2%) with psoriasis arthritis. 52.1% of all patients were naive for biological drug treatments. 83.3%, 48.8% and 52.9% were women aged 57.6±43.8, 47.1±10.1 and 55.6 ±14.0 years in the rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis groups, respectively. After analysing the data using the Kaplan–Meier method, we obtained an overall survival of adalimumab in each pathology, which was greatest in psoriatic arthritis with 59.9 months (95% CI 39.6 to 80,2), followed by 46.8 months in rheumatoid arthritis (95% CI 31.5 to 62.0) and 38.8 months (95% CI 25.1 to 52.4) in ankylosing spondylitis. When we compared the different pathologies by the log rank test, adalimumab’ s persistence was statistically significant for rheumatoid arthritis and ankylosing spondylitis (p Conclusion and relevance Adalimumab is a biologic drug with proven therapeutic efficacy in the treatment of theses pathologies. According to our data, adalimumab showed considerable persistence, which was greatest in psoriatic arthritis. References and/or acknowledgements Conflict of interest No conflict of interest","PeriodicalId":11998,"journal":{"name":"European Journal of Hospital Pharmacy","volume":"19 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"4CPS-326 Adalimumab’s persistence in rheumatological diseases\",\"authors\":\"C. P. Mondéjar, C. I. Navalón, I. Valverde, Amelia Soto, P. Fernández, M. Candel, L. R. Redondo, M. Candela, M. Coronel, Mdc Caballero Requejo, E. U. Sanz\",\"doi\":\"10.1136/EJHPHARM-2021-EAHPCONF.158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background and importance Adalimumab is a human monoclonal recombinant antibody whose mechanism of action is mediated by binding specifically to tumour necrosis factor (TNF), neutralising its function. Adalimumab is indicated for the treatment of progression of pathologies such as rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis. Aim and objectives To calculate the overall survival of adalimumab in patients diagnosed with rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis in our hospital. Material and methods A retrospective study was performed in which all patients diagnosed with these pathologies who initiated treatment with adalimumab from January 2007 to December 2016 were included. Data for start date, date of discontinuation of treatment if suspension occurred, sex and age of the patients were collected. Adalimumab’s persistence was calculated in months from the beginning of treatment to the last dispensation register. We collected dispensation data from January 2007 to May 2019 to calculate adalimumab’s persistence until this date. The drug’s survival was calculated using the Kaplan–Meier method and the log rank test to compare survival in each of the pathologies. A significant difference was considered with a p value Results 125 patients started treatment with adalimumab between January 2007 and December 2016; 48 patients (38.4%) were diagnosed with rheumatoid arthritis, 43 (34.4%) with ankylosing spondylitis and 34 (27.2%) with psoriasis arthritis. 52.1% of all patients were naive for biological drug treatments. 83.3%, 48.8% and 52.9% were women aged 57.6±43.8, 47.1±10.1 and 55.6 ±14.0 years in the rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis groups, respectively. After analysing the data using the Kaplan–Meier method, we obtained an overall survival of adalimumab in each pathology, which was greatest in psoriatic arthritis with 59.9 months (95% CI 39.6 to 80,2), followed by 46.8 months in rheumatoid arthritis (95% CI 31.5 to 62.0) and 38.8 months (95% CI 25.1 to 52.4) in ankylosing spondylitis. When we compared the different pathologies by the log rank test, adalimumab’ s persistence was statistically significant for rheumatoid arthritis and ankylosing spondylitis (p Conclusion and relevance Adalimumab is a biologic drug with proven therapeutic efficacy in the treatment of theses pathologies. According to our data, adalimumab showed considerable persistence, which was greatest in psoriatic arthritis. 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引用次数: 0
摘要
背景和重要性阿达木单抗是一种人单克隆重组抗体,其作用机制是通过特异性结合肿瘤坏死因子(TNF)介导,中和其功能。阿达木单抗适用于治疗疾病进展,如类风湿关节炎、强直性脊柱炎和银屑病关节炎。目的和目的计算阿达木单抗在我院诊断为类风湿关节炎、强直性脊柱炎和银屑病关节炎患者的总生存率。材料和方法回顾性研究纳入了2007年1月至2016年12月间开始接受阿达木单抗治疗的所有诊断为上述病理的患者。收集患者的起始日期、停止治疗日期(如果停止治疗)、性别和年龄等数据。阿达木单抗的持续时间以月为单位计算,从开始治疗到最后一次配药登记。我们收集了2007年1月至2019年5月的配药数据,以计算阿达木单抗在此日期之前的持续时间。使用Kaplan-Meier法和log rank检验计算药物的生存期,以比较每种病理的生存期。结果:2007年1月至2016年12月,125例患者开始使用阿达木单抗治疗;其中类风湿关节炎48例(38.4%),强直性脊柱炎43例(34.4%),银屑病关节炎34例(27.2%)。52.1%的患者未接受生物药物治疗。类风湿关节炎组、强直性脊柱炎组和银屑病关节炎组女性患病率分别为57.6±43.8岁、47.1±10.1岁和55.6±14.0岁,占83.3%、48.8%和52.9%。在使用Kaplan-Meier方法分析数据后,我们获得了阿达木单抗在每种病理中的总生存期,其中银屑病关节炎的生存期最长,为59.9个月(95% CI 39.6至802,2),其次是类风湿关节炎的46.8个月(95% CI 31.5至62.0)和强直性脊柱炎的38.8个月(95% CI 25.1至52.4)。当我们通过对数秩检验比较不同的病理时,阿达木单抗对类风湿关节炎和强直性脊柱炎的持续性具有统计学意义(p结论和相关性阿达木单抗是一种生物药物,在治疗这些病理方面已被证实有疗效。根据我们的数据,阿达木单抗显示出相当大的持久性,这在银屑病关节炎中表现最好。参考文献和/或致谢利益冲突无利益冲突
4CPS-326 Adalimumab’s persistence in rheumatological diseases
Background and importance Adalimumab is a human monoclonal recombinant antibody whose mechanism of action is mediated by binding specifically to tumour necrosis factor (TNF), neutralising its function. Adalimumab is indicated for the treatment of progression of pathologies such as rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis. Aim and objectives To calculate the overall survival of adalimumab in patients diagnosed with rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis in our hospital. Material and methods A retrospective study was performed in which all patients diagnosed with these pathologies who initiated treatment with adalimumab from January 2007 to December 2016 were included. Data for start date, date of discontinuation of treatment if suspension occurred, sex and age of the patients were collected. Adalimumab’s persistence was calculated in months from the beginning of treatment to the last dispensation register. We collected dispensation data from January 2007 to May 2019 to calculate adalimumab’s persistence until this date. The drug’s survival was calculated using the Kaplan–Meier method and the log rank test to compare survival in each of the pathologies. A significant difference was considered with a p value Results 125 patients started treatment with adalimumab between January 2007 and December 2016; 48 patients (38.4%) were diagnosed with rheumatoid arthritis, 43 (34.4%) with ankylosing spondylitis and 34 (27.2%) with psoriasis arthritis. 52.1% of all patients were naive for biological drug treatments. 83.3%, 48.8% and 52.9% were women aged 57.6±43.8, 47.1±10.1 and 55.6 ±14.0 years in the rheumatoid arthritis, ankylosing spondylitis and psoriatic arthritis groups, respectively. After analysing the data using the Kaplan–Meier method, we obtained an overall survival of adalimumab in each pathology, which was greatest in psoriatic arthritis with 59.9 months (95% CI 39.6 to 80,2), followed by 46.8 months in rheumatoid arthritis (95% CI 31.5 to 62.0) and 38.8 months (95% CI 25.1 to 52.4) in ankylosing spondylitis. When we compared the different pathologies by the log rank test, adalimumab’ s persistence was statistically significant for rheumatoid arthritis and ankylosing spondylitis (p Conclusion and relevance Adalimumab is a biologic drug with proven therapeutic efficacy in the treatment of theses pathologies. According to our data, adalimumab showed considerable persistence, which was greatest in psoriatic arthritis. References and/or acknowledgements Conflict of interest No conflict of interest