Comparison of darbepoetin alpha and recombinant human erythropoietin for treatment of anemia in pediatric chronic kidney disease: a non-inferiority trial from India (October, 10.1007/s00431-022-04650-1, 2022)

被引:0
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作者
Mazahir, Rufaida [1 ,2 ]
Anand, Kanav [2 ]
Pruthi, P. K. [2 ]
机构
[1] TMU, Teerthanker Mahaveer Med Coll & Res Ctr, Dept Pediat, Moradabad, Uttar Pradesh, India
[2] Sir Ganga Ram Hosp, Inst Child Hlth, Dept Pediat, Div Pediat Nephrol, New Delhi, India
关键词
Anemia; Chronic kidney disease; Darbepoetin alpha; Erythropoietin; Pediatrics;
D O I
10.1007/s00431-022-04669-4
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To determine whether or not Darbepoetin alpha (DA) was non-inferior to recombinant human erythropoietin (rHuEPO) in the treatment of anemia in children with chronic kidney disease (CKD) stage 3–5 (on or not on dialysis). This was a randomized, open-label, two-arm, parallel group, active-controlled, non-inferiority trial conducted at a tertiary care center in New Delhi, India. Fifty patients of either gender (aged 1–18 years) with CKD stage 3–5 (on or not on dialysis) who had baseline hemoglobin (Hb) between 9 and 12 g/dL and were on stable erythropoietin therapy for at least 8 weeks were randomized (1:1) to either continue rHuEPO or switch to DA therapy for a period of 28 weeks. Doses were titrated in the initial 23 weeks to maintain the Hb between 11 and 12 g/dL, and efficacy was assessed between weeks 24 and 28. The primary efficacy outcome was the mean change in Hb between baseline and the evaluation period. In the intention-to-treat population (n = 50), the adjusted between-group difference in mean Hb change between the baseline and the evaluation period was 0.131 g/dL (95% CI: − 0.439 to 0.719, p = 0.629). The lower limit of the two-sided 95% CI for the difference in the mean change in Hb between the two treatment groups was well above the pre-specified non-inferiority margin of − 1.0 g/dL. Similar pattern of non-inferiority was seen for per protocol population. The safety profile of DA and rHuEPO was also comparable (injection site pain:rHuEPO-3, DA-7; p-0.296). Conclusion: DA is non-inferior to rHuEPO for the treatment of anemia of CKD (stage 3–5) in pediatric population with a comparable safety profile. Trial registration: ClinicalTrials.gov Identifier: NCT04959578 (retrospectively registered), Date: July 13, 2021.What is Known:• Limited studies showing darbepoetin alpha is effective in children as an erythropoiesis stimulating agent.• No RCT from Indian subcontinent addressing this topic.What is New:• Darbepoetin alpha is non inferior to recombinant human erythropoietin for treatment of anemia in children with CKD stage 3-5 (on or not on dialysis) with safety comparable to recombinant human erythropoietin.• A cost reduction of approximately 8.6% per patient by shifting to darbepoetin alpha. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
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页码:111 / 112
页数:2
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