From the Division of Rheumatology, and the Nuclear Medicine Unit, Ospedale Pediatrico Bambino Gesù IRCCS, Rome, Italy.
M. Pardeo, MD, Division of Rheumatology, Ospedale Pediatrico Bambino Gesù IRCCS; D. Pires Marafon, MD, Division of Rheumatology, Ospedale Pediatrico Bambino Gesù IRCCS; V. Messia, MD, Division of Rheumatology, Ospedale Pediatrico Bambino Gesù IRCCS; M.C. Garganese, MD, Nuclear Medicine Unit, Ospedale Pediatrico Bambino Gesù IRCCS; F. De Benedetti, MD, PhD, Division of Rheumatology, Ospedale Pediatrico Bambino Gesù IRCCS; A. Insalaco, MD, Division of Rheumatology, Ospedale Pediatrico Bambino Gesù IRCCS.
J Rheumatol. 2017 Aug;44(8):1231-1238. doi: 10.3899/jrheum.160690. Epub 2017 Jun 15.
To report efficacy and safety in patients with chronic nonbacterial osteomyelitis (CNO) unresponsive to nonsteroidal antiinflammatory drugs (NSAID) and bisphosphonates and/or glucocorticoids treated with anakinra.
Nine patients (6 females) with refractory CNO were treated with anakinra for at least 6 months. We recorded, at baseline and after 6 months of treatment, clinical and laboratory features, and number and distribution of bone lesions detected by 99mTc-MDP bone scintigraphy. Disease activity was evaluated using a physician's global assessment (PGA).
At baseline, 9/9 patients had mild to severe PGA. After 6 months of treatment, in 5 patients the PGA score was graded from none to minimal. At baseline, erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were elevated in 8 out of 9 patients. After 6 months, 5/9 patients had normalized CRP and ESR and in all except 1, CRP and ESR decreased. Before starting anakinra, a total of 77 bone lesions were detected by bone scintigraphy. After 6 months of treatment of the 77 lesions, 42 had resolved and 35 were stable. In 7/9 patients, 20 new lesions appeared during treatment; 2 of these 7 patients were symptomatic. At the last followup visit (median 1.7 yrs, range 0.8-2.8), 6/9 patients maintained a PGA graded as none to minimal.
Anakinra is a possible therapeutic alternative in patients with refractory CNO. The practical significance of clinically silent bone lesions detected by bone scintigraphy remains to be established.
报告对非甾体抗炎药(NSAID)和双膦酸盐和/或糖皮质激素治疗无反应的慢性非细菌性骨髓炎(CNO)患者使用阿那白滞素的疗效和安全性。
9 名(6 名女性)对难治性 CNO 的患者接受阿那白滞素治疗至少 6 个月。我们记录了基线时和治疗 6 个月后的临床和实验室特征,以及 99mTc-MDP 骨闪烁显像检测到的骨病变的数量和分布。使用医生整体评估(PGA)评估疾病活动度。
基线时,9/9 例患者的 PGA 评分均为轻度至重度。治疗 6 个月后,5 例患者的 PGA 评分从无到轻度。基线时,8/9 例患者的红细胞沉降率(ESR)和 C 反应蛋白(CRP)升高。治疗 6 个月后,5/9 例患者 CRP 和 ESR 正常化,除 1 例外,所有患者的 CRP 和 ESR 均降低。在开始使用阿那白滞素之前,骨闪烁显像总共检测到 77 个骨病变。在治疗 77 个病变的 6 个月后,42 个病变已消退,35 个病变稳定。在 7/9 例患者中,在治疗期间出现 20 个新病变;其中 2 例有症状。在最后一次随访时(中位数 1.7 年,范围 0.8-2.8 年),6/9 例患者保持 PGA 评为无至轻度。
阿那白滞素可能是难治性 CNO 患者的一种治疗选择。骨闪烁显像检测到的临床无症状骨病变的实际意义仍有待确定。