Department of Rheumatology, University of Rouen, 76031 Rouen Cedex, France.
Rheumatology (Oxford). 2011 Feb;50(2):283-92. doi: 10.1093/rheumatology/keq344. Epub 2010 Nov 8.
The overall non-response rate to biologics remains 30-40% for patients with RA resistant to MTX. The objective of this study was to predict responsiveness to the anakinra-MTX combination by peripheral blood mononuclear cell gene profiling in order to optimize treatment choice.
Thirty-two patients treated with anakinra (100 mg/day s.c.) and MTX were categorized as responders when their 28-joint DAS (DAS-28) had decreased by ≥1.2 at 3 months. Pre-treatment blood samples had been drawn.
For seven responders and seven non-responders, 52 microarray-identified mRNAs were expressed as a function of the response to treatment, and unsupervised hierarchical clustering correctly separated responders from non-responders. The levels of seven of these 52 transcripts, as assessed by real-time, quantitative RT-PCR, were able to accurately classify 15 of 18 other patients (8 responders and 10 non-responders), with 87.5% specificity and 77.8% negative-predictive value for responders. Among the 52 genes, 56% were associated with IL-1β.
This predictive gene expression profile was obtained with a non-invasive procedure. After further validation in other cohorts of patients, it could be proposed and used on a large scale to select likely RA responders to combined anakinra-MTX. Trial registration. Clinical Trials; NCT00213538 (http://www.clinicaltrials.gov).
对于对 MTX 耐药的 RA 患者,生物制剂的总体无应答率仍为 30%-40%。本研究的目的是通过外周血单核细胞基因谱预测对 anakinra-MTX 联合治疗的反应性,以优化治疗选择。
32 例接受 anakinra(100mg/天皮下注射)和 MTX 治疗的患者,当他们的 28 关节 DAS(DAS-28)在 3 个月时下降≥1.2 时被归类为应答者。在治疗前抽取了血液样本。
对于 7 名应答者和 7 名无应答者,52 个微阵列鉴定的 mRNAs 根据对治疗的反应进行了表达,无监督层次聚类正确地区分了应答者和无应答者。通过实时定量 RT-PCR 评估的这 52 个转录本中的 7 个,能够准确地将 18 名其他患者中的 15 名(8 名应答者和 10 名无应答者)进行分类,对应答者的特异性为 87.5%,阴性预测值为 77.8%。在这 52 个基因中,56%与 IL-1β 相关。
通过非侵入性程序获得了这种预测性的基因表达谱。在其他患者队列中进一步验证后,它可以被提出并大规模用于选择可能对 anakinra-MTX 联合治疗有反应的 RA 患者。试验注册。临床试验;NCT00213538(http://www.clinicaltrials.gov)。