Kuijper T Martijn, Lamers-Karnebeek Femke B G, Jacobs Johannes W G, Hazes Johanna M W, Luime Jolanda J
From the Department of Rheumatology, Erasmus Medical Center, Rotterdam; Department of Rheumatology, Radboud University Medical Center, Nijmegen; Department of Rheumatology and Clinical Immunology, University Medical Center, Utrecht, the Netherlands.T.M. Kuijper, MD, MSc, Department of Rheumatology, Erasmus Medical Center; F.B. Lamers-Karnebeek, MD, Department of Rheumatology, Radboud University Medical Center; J.W. Jacobs, MD, PhD, Department of Rheumatology and Clinical Immunology, University Medical Center; J.M. Hazes, MD, PhD, Department of Rheumatology, Erasmus Medical Center; J.J. Luime, PhD, Department of Rheumatology, Erasmus Medical Center.
J Rheumatol. 2015 Nov;42(11):2012-22. doi: 10.3899/jrheum.141520. Epub 2015 Oct 1.
To evaluate the risk of having a disease flare in patients with rheumatoid arthritis (RA) with low disease activity (LDA) or in remission when deescalating (tapering or stopping) disease-modifying antirheumatic drug (DMARD) therapy.
A search in medical databases including publications from January 1950 to February 2015 was performed. Included were trials and observational studies in adults with RA who were in LDA or remission, evaluating ≥ 20 patients tapering or stopping DMARD. Flare rates had to have been reported. A metaanalysis was performed on studies deescalating tumor necrosis factor (TNF) blockers.
Four studies evaluated synthetic DMARD. Flare rates ranged from 8% at 24 weeks to 63% at 4 months after deescalation. Fifteen studies reported on TNF blockers. Estimated flare rates by metaanalysis on studies tapering or stopping TNF blockers were 0.26 (95% CI 0.17-0.39) and 0.49 (95% CI 0.27-0.73) for good-quality and moderate-quality studies, respectively. Flare rates in 3 studies stopping tocilizumab were 41% after 6 months, 55% at 1 year, and 87% at 1 year. Flare rates in 3 studies deescalating abatacept were 34% at 1 year, 41% at 1 year, and 72% at 6 months. Five studies evaluating radiographic progression in patients deescalating treatment all found limited to no progression.
Results suggest that more than one-third of patients with RA with LDA or in remission may taper or stop DMARD treatment without experiencing a disease flare within the first year. Dose reduction of TNF blockers results in lower flare rates than stopping and may be noninferior to continuing full dose. Radiological progression after treatment deescalation remains low, but may increase slightly.
评估疾病活动度低(LDA)或处于缓解期的类风湿关节炎(RA)患者在减停改善病情抗风湿药物(DMARD)治疗时疾病复发的风险。
检索医学数据库,纳入1950年1月至2015年2月发表的文献。纳入对象为处于LDA或缓解期的成年RA患者,评估≥20例减停DMARD的试验和观察性研究。必须报告复发率。对减停肿瘤坏死因子(TNF)阻滞剂的研究进行荟萃分析。
四项研究评估了合成DMARD。减停后24周的复发率为8%,4个月时为63%。十五项研究报告了TNF阻滞剂。对减停TNF阻滞剂的研究进行荟萃分析,高质量和中等质量研究的估计复发率分别为0.26(95%CI 0.17 - 0.39)和0.49(95%CI 0.27 - 0.73)。三项停用托珠单抗的研究中,6个月后的复发率为41%,1年时为55%,1年时为87%。三项减停阿巴西普的研究中,1年时的复发率为34%,1年时为41%,6个月时为72%。五项评估减停治疗患者影像学进展的研究均发现进展有限或无进展。
结果表明,超过三分之一的LDA或处于缓解期的RA患者在第一年减停DMARD治疗时可能不会出现疾病复发。TNF阻滞剂减量导致的复发率低于停药,且可能不劣于继续全剂量治疗。减停治疗后的影像学进展仍然较低,但可能略有增加。