Association of methotrexate polyglutamates concentration with methotrexate efficacy and safety in patients with rheumatoid arthritis treated with predefined dose: results from the MIRACLE trial.

IF 20.3 1区 医学 Q1 RHEUMATOLOGY
Hiroya Tamai, Kei Ikeda, Toshiaki Miyamoto, Hiroaki Taguchi, Chang-Fu Kuo, Kichul Shin, Shintaro Hirata, Yutaka Okano, Shinji Sato, Hidekata Yasuoka, Masataka Kuwana, Tomonori Ishii, Hideto Kameda, Toshihisa Kojima, Yurie Nishi, Masahiko Mori, Hideaki Miyagishi, Genta Toshima, Yasunori Sato, Wen-Chan Tsai, Tsutomu Takeuchi, Yuko Kaneko
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Abstract

Objectives: The usefulness of methotrexate-polyglutamates (MTX-PGs) concentration for management of rheumatoid arthritis has been debated. We aimed to clarify the association of MTX-PGs concentration with efficacy and safety in MTX-naïve patients initiating MTX in a prospective interventional clinical trial.

Methods: The MIRACLE trial enrolled 300 MTX-naïve patients. Oral MTX was initiated and increased to the maximum tolerated dose by week 12. Patients who did not achieve remission according to the Simplified Disease Activity Index at week 24 were randomised to either the continued dose or reduced dose group and were started on subcutaneous adalimumab. We measured the concentrations of MTX-PGs in erythrocytes using liquid chromatography-tandem mass spectrometry and analysed the association of these concentrations with efficacy and safety.

Results: The mean concentration of total MTX-PGs increased with an increasing dose of MTX and continued to elevate for another 12 weeks after the dose was fixed. At week 24, the total MTX-PGs concentration was 110.5 (SD 43.8) nmol/L with MTX dose of 12.6 (3.0) mg/week (0.23 (0.07) mg/kg/week). During MTX monotherapy, the higher MTX-PGs concentration was an independent factor for lower disease activity; however, this association disappeared after adalimumab initiation in patients with continued MTX dose. Hepatotoxicity was related to the higher MTX-PGs concentration regardless of adalimumab use. The total MTX-PGs concentration was significantly elevated by lower estimated glomerular filtration rate, serum albumin and body mass index.

Conclusions: The MIRACLE trial demonstrated that higher total MTX-PGs concentration in erythrocytes is related to the higher efficacy and lower safety of MTX.

Trial registration number: NCT03505008.

采用预定剂量治疗的类风湿关节炎患者体内甲氨蝶呤多谷氨酸浓度与甲氨蝶呤疗效和安全性的关系:MIRACLE 试验的结果。
目的:甲氨蝶呤-聚谷氨酸(MTX-PGs)浓度对类风湿关节炎治疗的作用一直存在争议。我们旨在通过一项前瞻性干预临床试验,明确MTX-PGs浓度与MTX-naïve患者开始使用MTX时的疗效和安全性之间的关系:MIRACLE试验招募了300名MTX无效患者。患者开始口服MTX,并在第12周之前将剂量增加到最大耐受剂量。在第24周时根据简化疾病活动指数未达到缓解的患者被随机分配到继续用药组或减少用药组,并开始皮下注射阿达木单抗。我们使用液相色谱-串联质谱法测量了红细胞中MTX-PGs的浓度,并分析了这些浓度与疗效和安全性的关系:总MTX-PGs的平均浓度随着MTX剂量的增加而升高,并在剂量固定后的12周内持续升高。第24周时,MTX剂量为12.6 (3.0) mg/周(0.23 (0.07) mg/kg/周)时,MTX-PGs总浓度为110.5 (SD 43.8) nmol/L。在MTX单药治疗期间,较高的MTX-PGs浓度是降低疾病活动性的一个独立因素;然而,在持续服用MTX的患者中,阿达木单抗启动后这种关联消失了。无论是否使用阿达木单抗,肝毒性都与较高的MTX-PGs浓度有关。肾小球滤过率、血清白蛋白和体重指数越低,MTX-PGs总浓度越高:MIRACLE试验表明,红细胞中较高的MTX-PGs总浓度与MTX较高的疗效和较低的安全性有关:NCT03505008。
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来源期刊
Annals of the Rheumatic Diseases
Annals of the Rheumatic Diseases 医学-风湿病学
CiteScore
35.00
自引率
9.90%
发文量
3728
审稿时长
1.4 months
期刊介绍: Annals of the Rheumatic Diseases (ARD) is an international peer-reviewed journal covering all aspects of rheumatology, which includes the full spectrum of musculoskeletal conditions, arthritic disease, and connective tissue disorders. ARD publishes basic, clinical, and translational scientific research, including the most important recommendations for the management of various conditions.
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