Salliot C, van der Heijde D
Paris Descartes University, Medicine Faculty, Rheumatology B Department, Cochin Hospital, Paris, France.
Ann Rheum Dis. 2009 Jul;68(7):1100-4. doi: 10.1136/ard.2008.093690. Epub 2008 Dec 5.
To perform a systematic literature review of the long-term safety of methotrexate (MTX) monotherapy in rheumatoid arthritis (RA).
A search was performed in Medline, Cochrane and EMBASE. Adults with RA who had received MTX monotherapy for more than 2 years were studied.
88 published studies were included. Over 12 years of treatment, the termination rate of MTX due to toxicity was less than for sulfasalazine, gold, d-penicillamine and higher than for hydroxychloroquine (level of evidence 2a-2b). Long-term use of MTX does not appear to be a risk factor for serious infections, including herpes zoster (2b-4), and could provide a survival benefit by reducing cardiovascular mortality (2b). The prevalence of raised liver enzymes (more than twice the upper limit of normal) is close to 13% of patients; 3.7% of patients stopped MTX permanently owing to liver toxicity (2b). Data on the risk for liver fibrosis/cirrhosis are conflicting: a meta-analysis showed an incidence of fibrosis of 2.7% after 4 years of MTX (2a). However, two other studies on sequential liver biopsies did not show evidence for developing severe damage (2b). Insufficient data are available to fully assess the risk of lymphoma and malignancies, although there is no strong evidence of increased risk (2b-4).
This systematic literature search on MTX monotherapy with relatively low-dose use during at least 2 years shows favourable long-term safety.
对甲氨蝶呤(MTX)单药治疗类风湿关节炎(RA)的长期安全性进行系统的文献综述。
在Medline、Cochrane和EMBASE数据库进行检索。研究对象为接受MTX单药治疗超过2年的成年RA患者。
纳入88项已发表研究。在超过12年的治疗期间,MTX因毒性导致的停药率低于柳氮磺吡啶、金制剂、青霉胺,高于羟氯喹(证据级别2a - 2b)。长期使用MTX似乎不是包括带状疱疹在内的严重感染的危险因素(2b - 4),并且通过降低心血管死亡率可能带来生存获益(2b)。肝酶升高(超过正常上限两倍)的患者患病率接近13%;3.7%的患者因肝毒性永久停用MTX(2b)。关于肝纤维化/肝硬化风险的数据存在矛盾:一项荟萃分析显示MTX治疗4年后纤维化发生率为2.7%(2a)。然而,另外两项关于序贯肝活检的研究未显示出现严重损害的证据(2b)。虽然没有有力证据表明风险增加,但现有数据不足以全面评估淋巴瘤和恶性肿瘤的风险(2b - 4)。
这项关于至少2年使用相对低剂量MTX单药治疗的系统文献检索显示其长期安全性良好。