Dipartimento di Medicina Interna e Specialità Mediche - UOC di Reumatologia - Sapienza - Università di Roma, Azienda Policlinico Umberto I, Viale del Policlinico 155, 00161 Rome, Italy.
Rheumatology (Oxford). 2013 Oct;52(10):1914-9. doi: 10.1093/rheumatology/ket249. Epub 2013 Jul 22.
The primary objective of this retrospective study was to investigate the possibility of achieving partial remission (PR) in AS patients treated with anti-TNF-α antagonists, such as adalimumab (ADA), etanercept (ETA) and infliximab (INF), in a real clinical practice setting. Predictors of PR were also evaluated.
A retrospective study was conducted in patients with AS treated with ADA, ETA and INF from 2000 to 2012. Kaplan-Meier survival curves were plotted to determine the rates of PR during the treatment with anti-TNF-α drugs.
A total of 283 patients with AS were treated with ADA (18.7%), ETA (26.8%) and INF (54.4%) as first anti-TNF-α drugs, with a PR rate of 57.6%. The probability of obtaining PR with ADA, ETA or INF was not significantly different among all anti-TNF-α patients. AS patients treated with a second anti-TNF-α drug had a PR rate of 40.5%, but after switching for lack of response, the probability of obtaining PR with a second anti-TNF-α drug was significantly lower from that of the first anti-TNF-α drug (P = 0.0039). The probability of obtaining PR in patients with enthesitis (P = 0.04) or psoriasis (P = 0.0016) or low levels of CRP (P = 0.0225) was significantly lower compared with that of patients without these manifestations at baseline.
Our real-life study on PR confirmed the effectiveness of ADA, ETA or INF as first or second anti-TNF-α drugs. The presence at baseline of enthesitis or psoriasis or low CRP values yielded a lower probability of obtaining PR.
本回顾性研究的主要目的是在真实临床环境中探究接受 TNF-α 拮抗剂(如阿达木单抗[ADA]、依那西普[ETA]和英夫利昔单抗[INF])治疗的 AS 患者达到部分缓解(PR)的可能性,并评估 PR 的预测因素。
对 2000 年至 2012 年接受 ADA、ETA 和 INF 治疗的 AS 患者进行回顾性研究。绘制 Kaplan-Meier 生存曲线以确定接受 TNF-α 药物治疗期间 PR 的发生率。
共 283 例 AS 患者接受 ADA(18.7%)、ETA(26.8%)和 INF(54.4%)作为首用 TNF-α 拮抗剂,PR 率为 57.6%。所有 TNF-α 患者中,ADA、ETA 或 INF 获得 PR 的概率无显著差异。接受二线 TNF-α 药物治疗的 AS 患者 PR 率为 40.5%,但因无应答而转换后,二线 TNF-α 药物获得 PR 的概率显著低于首用 TNF-α 药物(P=0.0039)。基线时存在附着点炎(P=0.04)或银屑病(P=0.0016)或 CRP 水平较低(P=0.0225)的患者获得 PR 的概率显著低于无这些表现的患者。
本真实世界研究证实 ADA、ETA 或 INF 作为首用或二线 TNF-α 拮抗剂的有效性。基线时存在附着点炎或银屑病或 CRP 值较低与获得 PR 的概率较低相关。