Ideguchi Haruko, Ohno Shigeru, Ishigatsubo Yoshiaki
Chronic Intractable Disease Center, Yokohama City University Medical Center, Yokohama, Kanagawa, Japan.
J Clin Rheumatol. 2007 Apr;13(2):73-8. doi: 10.1097/01.rhu.0000260526.29331.a8.
Methotrexate (MTX) has become the most commonly prescribed disease-modifying antirheumatic drug (DMARD) for the treatment of rheumatoid arthritis (RA). In the Western countries, the MTX dosage is safely increased to a maximum of 25 mg/wk until a significant response is observed. On the contrary, in Japan, MTX has been approved only as a second-line agent, and the approved maximum MTX dosage is only 8 mg/wk. This suboptimal dosage may affect MTX survival in Japanese RA patients.
To study risk factors associated with the cumulative survival of MTX in Japanese RA patients.
Data on 273 patients (male 44, female 229) with RA treated with MTX between January 1, 2000 and September 30, 2004 in our center were studied.
Two hundred seventy-three patients were followed for 437 person-years of MTX exposure. Mean MTX dosage was 5.5 +/- 1.9 mg/wk. The cumulative MTX survival probability after 5 years was 61.9%. Univariate Cox regression analysis showed a significant correlation between MTX survival probability and use of fewer previous DMARDs, higher dose of MTX, inclusion of folate supplementation, and shorter disease duration. In the multivariate Cox regression model, use of fewer previous DMARDs remained significantly related to MTX survival. Reasons for discontinuation included adverse effects in 34 patients (12.5%) and inefficacy in 6 patients (2.2%).
Cumulative survival was the same or slightly better than those in reports from Western countries, with less withdrawals reported due to adverse events or inefficacy. Whether these results are due to different MTX needs in Japanese or to acceptance of less clinical efficacy will require further studies. The use of fewer previous DMARDs was associated with longer MTX survival.
甲氨蝶呤(MTX)已成为治疗类风湿关节炎(RA)最常用的改善病情抗风湿药(DMARD)。在西方国家,MTX剂量可安全增加至最大25mg/周,直至观察到明显疗效。相反,在日本,MTX仅被批准作为二线药物,批准的最大MTX剂量仅为8mg/周。这种次优剂量可能会影响日本RA患者使用MTX的持续时间。
研究与日本RA患者MTX累积持续时间相关的危险因素。
对2000年1月1日至2004年9月30日在本中心接受MTX治疗的273例RA患者(男性44例,女性229例)的数据进行研究。
273例患者接受MTX治疗的总人年数为437人年。MTX平均剂量为5.5±1.9mg/周。5年后MTX累积持续概率为61.9%。单因素Cox回归分析显示,MTX持续概率与既往使用较少的DMARDs、较高剂量的MTX、补充叶酸以及较短的病程显著相关。在多因素Cox回归模型中,既往使用较少的DMARDs仍与MTX持续时间显著相关。停药原因包括34例(12.5%)出现不良反应和6例(2.2%)治疗无效。
累积持续时间与西方国家的报道相同或略好,因不良事件或治疗无效而停药的情况较少。这些结果是由于日本人对MTX的需求不同,还是由于对较低临床疗效的接受程度,需要进一步研究。既往使用较少的DMARDs与MTX更长的持续时间相关。