Factors affecting responsiveness of vadadustat in patients with anemia associated with chronic kidney disease: a post-hoc subgroup analysis of Japanese phase 3 randomized studies.

IF 2.2 4区 医学 Q2 UROLOGY & NEPHROLOGY
Clinical and Experimental Nephrology Pub Date : 2024-05-01 Epub Date: 2024-03-26 DOI:10.1007/s10157-023-02432-z
Masaomi Nangaku, Kiichiro Ueta, Kenichi Nishimura, Kazuyo Sasaki, Takafumi Hashimoto
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引用次数: 0

Abstract

Background: Vadadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor developed for treating anemia in chronic kidney disease (CKD). The purpose of this post-hoc analysis was to investigate the factors affecting the responsiveness to vadadustat in anemia patients with nondialysis-dependent (NDD) or hemodialysis-dependent (HDD) CKD in two Japanese phase 3 studies.

Methods: Of 151 and 162 patients enrolled in NDD-CKD and HDD-CKD studies, 136 and 140 patients, respectively, were included and divided into subgroups for the analysis. To assess vadadustat responsiveness, the resistance index was defined as the mean body weight-adjusted dose of vadadustat (mg/kg) at weeks 20-24 divided by the mean hemoglobin (g/dL) at weeks 20-24. Multivariate analysis was performed to identify the variables affecting the resistance index.

Results: Independent factors identified as determinants for better response to vadadustat were as follows: high baseline hemoglobin, low baseline eGFR, high week-20-24 ferritin, and CKD not caused by autoimmune disease/glomerulonephritis/vasculitis in NDD-CKD; and male sex, high baseline C-reactive protein, and low baseline erythropoiesis-stimulating agent resistance index (ERI) in HDD-CKD.

Conclusions: In this post-hoc analysis, several factors were identified as affecting the response to vadadustat. These results may provide useful information leading to an appropriate dose modification for vadadustat.

Clinical trial registration: NCT03329196 (MT-6548-J01) and NCT03439137 (MT-6548-J03).

影响伐地司他(Vadadustat)对慢性肾病伴贫血患者疗效的因素:日本三期随机研究的事后分组分析。
背景:伐杜司他是一种口服低氧诱导因子脯氨酰羟化酶抑制剂,用于治疗慢性肾病(CKD)贫血。这项事后分析的目的是调查影响两项日本三期研究中非透析依赖型(NDD)或血液透析依赖型(HDD)CKD 贫血患者对伐杜司他反应性的因素:在 NDD-CKD 和 HDD-CKD 两项研究的 151 名和 162 名患者中,分别纳入了 136 名和 140 名患者,并将其分成亚组进行分析。为评估伐杜司他的反应性,耐药指数被定义为第20-24周伐杜司他的平均体重调整剂量(毫克/千克)除以第20-24周的平均血红蛋白(克/分升)。为确定影响耐药指数的变量,进行了多变量分析:结果:在NDD-CKD中,被确定为对伐杜司他反应较好的决定因素的独立因素如下:高基线血红蛋白、低基线eGFR、高第20-24周铁蛋白和非自身免疫性疾病/肾小球肾炎/血管炎引起的CKD;在HDD-CKD中,男性性别、高基线C反应蛋白和低基线促红细胞生成素抵抗指数(ERI):结论:在这项事后分析中,确定了几个影响对伐杜司他反应的因素。这些结果可能为伐杜司他的适当剂量调整提供有用信息:临床试验注册:NCT03329196(MT-6548-J01)和NCT03439137(MT-6548-J03)。
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来源期刊
Clinical and Experimental Nephrology
Clinical and Experimental Nephrology UROLOGY & NEPHROLOGY-
CiteScore
4.10
自引率
4.30%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Clinical and Experimental Nephrology is a peer-reviewed monthly journal, officially published by the Japanese Society of Nephrology (JSN) to provide an international forum for the discussion of research and issues relating to the study of nephrology. Out of respect for the founders of the JSN, the title of this journal uses the term “nephrology,” a word created and brought into use with the establishment of the JSN (Japanese Journal of Nephrology, Vol. 2, No. 1, 1960). The journal publishes articles on all aspects of nephrology, including basic, experimental, and clinical research, so as to share the latest research findings and ideas not only with members of the JSN, but with all researchers who wish to contribute to a better understanding of recent advances in nephrology. The journal is unique in that it introduces to an international readership original reports from Japan and also the clinical standards discussed and agreed by JSN.
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