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成人血液透析患者从聚乙二醇化促红细胞生成素β转换为达贝泊汀α后贫血控制情况及每周促红细胞生成素活性药物剂量的维持:TRANSFORM研究

Preservation of anemia control and weekly ESA dosage after conversion from PEG-Epoetin beta to darbepoetin alfa in adult hemodialysis patients: the TRANSFORM study.

作者信息

Donck Jan, Gonzalez-Tabares Lourdes, Chanliau Jacques, Martin Heike, Stamatelou Kyriaki, Manamley Nick, Farouk Mourad, Addison Janet

机构信息

Algemeen Ziekenhuis Sint Lucas, Groenebriel 1, 9000, Ghent, Belgium,

出版信息

Adv Ther. 2014 Nov;31(11):1155-68. doi: 10.1007/s12325-014-0161-5. Epub 2014 Nov 1.

Abstract

INTRODUCTION

There is scant real-world information on switching treatment for anemia associated with chronic kidney disease (CKD) from methoxy polyethylene glycol-epoetin beta (PEG-Epo) to darbepoetin alfa (DA). TRANSFORM was a multi-center, observational study designed to describe the time course of hemoglobin (Hb) concentration (primary outcome measure) and other parameters of clinical management of anemia in European hemodialysis patients in clinical practice before and after a switch from PEG-Epo to DA.

METHODS

Eligible subjects were adult patients with CKD dialyzed at European dialysis centers for ≥26 weeks and treated with PEG-Epo for ≥14 weeks immediately prior to being switched to DA and no earlier than January 2011. Erythropoiesis-stimulating agent doses and Hb values were recorded for the 14-week pre-switch and 26-week post-switch periods.

RESULTS

Of the 1,027 eligible patients enrolled at 42 hemodialysis centers in 7 European countries, 785 were included in analyses. Mean (95% confidence interval [CI]) Hb was generally stable: 11.19 (11.11, 11.26), 11.48 (11.40, 11.57), and 11.29 (11.20, 11.37) g/dL at month -1 pre-switch and months 3 and 6 post-switch, respectively. The geometric mean (95% CI) PEG-Epo dose at month -1 was 27.4 (26.0, 28.8) µg/week; DA dose was 29.4 (27.9, 30.9), 23.3 (21.9, 24.9), and 25.6 (24.1, 27.1) µg/week at months 1, 4, and 6, respectively. The geometric mean (95% CI) dose ratio at switching was 1.06 (1.01, 1.11). When stratifying by dose-ratio categories <0.8, 0.8-1.2, and >1.2 at switching, mean DA dose and Hb converged within narrow ranges by month 6 post-switch: 23.9-27.0 µg/week and 11.1-11.5 g/dL, respectively. Hb excursions <10 g/dL were less frequent post-switch versus pre-switch.

CONCLUSION

Mean Hb values remained within a narrow range following switching from PEG-Epo to DA in this population of hemodialysis patients. Time trends of mean Hb and DA dose indicate that physicians titrated DA doses post-switch, to attain Hb concentrations comparable to those attained pre-switch with PEG-Epo.

摘要

引言

关于慢性肾脏病(CKD)相关性贫血的治疗从甲氧基聚乙二醇化促红细胞生成素β(PEG-Epo)转换为达贝泊汀α(DA),现实世界中的信息较少。TRANSFORM是一项多中心观察性研究,旨在描述欧洲血液透析患者从PEG-Epo转换为DA之前和之后血红蛋白(Hb)浓度(主要结局指标)的时间进程以及贫血临床管理的其他参数。

方法

符合条件的受试者为在欧洲透析中心接受透析≥26周的成年CKD患者,在转换为DA之前,接受PEG-Epo治疗≥14周,且不早于2011年1月。记录转换前14周和转换后26周的促红细胞生成素刺激剂剂量和Hb值。

结果

在欧洲7个国家的42个血液透析中心登记的1027例符合条件的患者中,785例纳入分析。平均(95%置信区间[CI])Hb总体稳定:转换前-1个月、转换后3个月和6个月时分别为11.19(1,11,11.26)、11.48(11.40,11.57)和11.29(11.20,11.37)g/dL。转换前-1个月时PEG-Epo的几何平均(95%CI)剂量为27.4(26.0,28.8)μg/周;DA剂量在转换后1个月、4个月和6个月时分别为29.4(27.9,30.9)、23.3(21.9,24.9)和25.6(24.1,27.1)μg/周。转换时的几何平均(95%CI)剂量比为1.06(1.01,1.11)。当按转换时剂量比类别<0.8、0.8 -

1.2和>1.2分层时,转换后6个月时平均DA剂量和Hb在狭窄范围内趋于一致:分别为23.9 - 27.0μg/周和11.1 - 11.5g/dL。转换后Hb波动<10g/dL的情况比转换前更少。

结论

在这群血液透析患者中,从PEG-Epo转换为DA后,平均Hb值保持在狭窄范围内。平均Hb和DA剂量的时间趋势表明,医生在转换后调整了DA剂量,以达到与转换前使用PEG-Epo时相当的Hb浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5b/4245491/3cdf5e9ebf73/12325_2014_161_Fig1_HTML.jpg

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