Abdelazeem Basel, Abbas Kirellos Said, Shehata Joseph, El-Shahat Nahla Ahmed, Baral Nischit, Savarapu Pramod, Kunadi Arvind
Department of Internal Medicine, McLaren Health Care, Flint, MI, USA.
Michigan State University, Flint, MI, USA.
Ann Transl Med. 2021 Dec;9(23):1714. doi: 10.21037/atm-21-4357.
Anemia is a common complication in chronic kidney disease (CKD) with increased morbidity and mortality. Recently published RCTs were conducted to compare the effect of the new medication roxadustat (ROX) with erythropoiesis-stimulating agent (ESA) in dialysis-dependent CKD (DD-CKD) patients. Our article aimed to meta-analyze published RCTs to investigate the efficacy and safety of ROX for anemia in DD-CKD patients and update the effect of the new studies on overall analysis with subsequent impact on management.
Electronic databases (PubMed, EMBASE, Scopus, Web of Science, Cochrane Central, and Google Scholar) were searched systematically from inception to July 2021 by using this search term (Roxadustat OR ASP1517 OR FG4592 OR "FG-4592") AND (kidney OR renal) AND (Anemia). We only included randomized control trials (RCTs) that reported the primary outcome of change in hemoglobin (Hb) level and iron utilization parameters, including ferritin, serum iron, TSAT, TIBC, transferrin, and hepcidin.
Ten RCTs were finally included with 3031 patients in the ROX group and 2737 patients in the control group. ROX was associated with increase in Hb level (SMD: 0.2; 95% CI: 0.02, 0.39; P=0.03), TIBC (SMD: 0.79; 95% CI: 0.61, 0.98; P<0.00001), serum iron (SMD: 0.27; 95% CI: 0.18, 0.36; P<0.00001), transferrin (SMD: 0.98; 95% CI: 0.81, 1.15; P<0.00001) and decrease in hepcidin (SMD: -15.53; 95% CI: -28.07, -3.00; P<0.02) when compared with control group. There was no difference between ROX and the control group regarding ferritin level and TSAT. Sensitivity analysis by removing the most recent studies, Chen . or Hou . did not show significant difference in regard to change in Hb level. There was no difference between both groups regarding the serious side effects. However, ROX showed higher TEAEs when compared to the control group (RR: 1.03; 95% CI: 1.01, 1.05; P=0.002).
Our updated meta-analysis concluded that ROX increased Hb level and improved iron utilization parameters in DD-CKD patients, but ROX was associated with higher TEAEs. Our results support the use of ROX for DD-CKD patients with anemia. However, higher-quality RCTs are still needed to confirm the results of our review.
贫血是慢性肾脏病(CKD)的常见并发症,其发病率和死亡率均有所增加。最近发表的随机对照试验(RCT)比较了新型药物罗沙司他(ROX)与促红细胞生成素(ESA)对依赖透析的CKD(DD-CKD)患者的疗效。我们的文章旨在对已发表的RCT进行荟萃分析,以研究ROX治疗DD-CKD患者贫血的疗效和安全性,并更新新研究对总体分析的影响及其对治疗管理的后续影响。
从创刊至2021年7月,通过使用搜索词(罗沙司他或ASP1517或FG4592或“FG-4592”)以及(肾脏或肾)和(贫血),对电子数据库(PubMed、EMBASE、Scopus、Web of Science、Cochrane Central和谷歌学术)进行系统检索。我们仅纳入报告了血红蛋白(Hb)水平变化以及铁利用参数(包括铁蛋白、血清铁、转铁蛋白饱和度、总铁结合力、转铁蛋白和铁调素)等主要结局的随机对照试验(RCT)。
最终纳入10项RCT,ROX组有3031例患者,对照组有2737例患者。与对照组相比,ROX可使Hb水平升高(标准化均数差:0.2;95%置信区间:0.02,0.39;P = 0.03)、总铁结合力升高(标准化均数差:0.79;95%置信区间:0.61,0.98;P < 0.00001)、血清铁升高(标准化均数差:0.27;95%置信区间:0.18,0.36;P < 0.00001)、转铁蛋白升高(标准化均数差:0.98;95%置信区间:0.81,1.15;P < 0.00001),铁调素降低(标准化均数差:-15.53;95%置信区间:-28.07,-3.00;P < 0.02)。ROX与对照组在铁蛋白水平和转铁蛋白饱和度方面无差异。通过剔除最新研究(Chen...或Hou...)进行的敏感性分析显示,Hb水平变化方面无显著差异。两组在严重副作用方面无差异。然而,与对照组相比,ROX的治疗期间出现的不良事件更高(风险比:1.03;95%置信区间:1.01,1.05;P = 0.002)。
我们更新的荟萃分析得出结论,ROX可提高DD-CKD患者的Hb水平并改善铁利用参数,但ROX与更高的治疗期间出现的不良事件相关。我们的结果支持ROX用于治疗DD-CKD贫血患者。然而,仍需要更高质量的RCT来证实我们综述的结果。