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Casual effect of methotrexate+etanercept/infliximab on survival of?patients with?rheumatoid arthritis

机译:甲氨蝶呤+依那西普/英夫利昔单抗对类风湿关节炎患者生存的偶然影响

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Background and objectives: Following the discovery of new drugs, physicians and pharmaceutical companies have become interested in examining patients’ mortality and morbidity rates. In this respect, the effects of methotrexate (MTX)+etanercept/infliximab (ETA/INF) therapy on the survival of rheumatoid arthritis patients (RA) were evaluated in this study using marginal structural piecewise constant baseline hazard model. Patients and methods: According to the standard protocol, MTX is considered as the first-line treatment for RA patients. If there is no adequate response to MTX, biologic drugs will be added. To compare the survival rates of RA patients in MTX- and MTX+ETA/INF-treated groups, the piecewise constant baseline hazard model was fitted. Then, due to the existence of the time-dependent confounder (VAS) which was affected by previous treatment, the weight for each person-time was calculated via the inverse probability treatment weighting method. These weights were then used by marginal structural piecewise constant baseline hazard model. Finally, these models were compared. Results: The median (IQR) of the follow-up period in patients receiving MTX+ETN/INF and MTX was 11 (15.25) and 11 (31), respectively, and the 8-year survival rate was reported by 70% versus 68%, respectively. First, the piece-wise constant baseline hazard model was fitted. Fitting the given model showed that MTX+ETA/INF had a significant effect on patients’ survival (HR=0.789, 95% CI [0.634, 0.983]). Second, marginal structural piecewise constant baseline hazard model was fitted. But, the results of this model revealed that MTX+ETA/INF did not have a significant impact on patients’ survival (HR=0.968, 95% CI [0.860, 1.090]). Conclusion: Adjusting the pain score over time as a time-dependent confounder via marginal structural piecewise constant baseline hazard model, it has been demonstrated that MTX+ETA/INF does not have a significant effect on patients’ survival rates. Therefore, a significant difference can be found between survival rates of these groups using longitudinal studies.
机译:背景和目的:随着新药的发现,医生和制药公司对检查患者的死亡率和发病率变得很感兴趣。在这方面,本研究使用边缘结构分段恒定基线风险模型评估了甲氨蝶呤(MTX)+依那西普/英夫利昔单抗(ETA / INF)治疗对类风湿关节炎患者(RA)生存的影响。患者和方法:根据标准方案,MTX被认为是RA患者的一线治疗。如果对MTX没有足够的反应,将添加生物药物。为了比较MTX和MTX + ETA / INF治疗组中RA患者的存活率,拟合了分段恒定基线风险模型。然后,由于存在时间依赖性混杂因素(VAS),该混杂因素受到先前治疗的影响,因此通过逆概率治疗加权方法计算每个人次的权重。然后将这些权重用于边际结构分段恒定基线危害模型。最后,对这些模型进行了比较。结果:接受MTX + ETN / INF和MTX的患者的随访期中位数(IQR)分别为11(15.25)和11(31),据报道8年生存率分别为70%和68 %, 分别。首先,拟合分段恒定基线危害模型。拟合给定模型表明,MTX + ETA / INF对患者的生存有显着影响(HR = 0.789,95%CI [0.634,0.983])。其次,拟合了边际结构分段恒定基线危害模型。但是,该模型的结果表明,MTX + ETA / INF对患者的存活率没有显着影响(HR = 0.968,95%CI [0.860,1.090])。结论:通过边际结构分段恒定基线危险模型随时间变化的混杂因素来调整疼痛评分,已证明MTX + ETA / INF对患者的生存率没有显着影响。因此,使用纵向研究可以发现这些组的存活率之间存在显着差异。

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