Ozguler Yesim, Hatemi Gulen, Ugurlu Serdal, Seyahi Emire, Melikoglu Melike, Borekci Sermin, Atahan Ersan, Ongen Gul, Hamuryudan Vedat
Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, Istanbul University, Fatih, Istanbul, 34098, Turkey.
Department of Pulmonary Diseases, Cerrahpasa Medical Faculty, Istanbul University, Fatih, Istanbul, 34098, Turkey.
Rheumatol Int. 2016 Dec;36(12):1719-1725. doi: 10.1007/s00296-016-3575-3. Epub 2016 Oct 3.
The use of anti-TNF agents is associated with an increased risk of tuberculosis (TB) and anti-TNF agents are stopped when active TB develops. However, discontinuation of treatment can result in flare of the underlying disease. The charts of 22 patients who developed active TB among a cohort of 2754 patients using anti-TNF agents between 2001 and 2013 were reviewed retrospectively. Patients restarting biologics during further follow-up were identified. One patient with miliary TB died within 1 month. A biologic agent was restarted in 16 of the remaining 21 patients (76 %). The most frequently re-initiated biologic agent was etanercept (n = 6) followed by rituximab (n = 5) and interferon-alpha (n = 3). Biologic treatment was re-initiated during anti-TB treatment in four patients and after completing TB treatment in 12 patients. The median follow-up after restarting biologics was 53 (IQR: 40-75) months. TB re-occurred in one patient with Behçet's syndrome, who initially received etanercept due to severe sight-threatening uveitis at the third month of anti-TB treatment followed by canakinumab 15 months later along with methotrexate, cyclosporine and corticosteroids. After a second course of 9 months TB therapy this patient is currently stable on interferon-alpha for 33 months. Restarting of anti-TNF agents and other biologic agents, even during TB treatment, seems to be possible among patients who had previously developed TB under anti-TNF treatment. However, the risk of re-development of TB infection mandates careful follow-up.
使用抗TNF药物与结核病(TB)风险增加相关,当发生活动性结核病时会停用抗TNF药物。然而,停止治疗可能导致基础疾病复发。对2001年至2013年间使用抗TNF药物的2754名患者队列中22例发生活动性结核病的患者病历进行了回顾性分析。确定了在进一步随访期间重新开始使用生物制剂的患者。1例粟粒性结核病患者在1个月内死亡。其余21例患者中有16例(76%)重新开始使用生物制剂。最常重新开始使用的生物制剂是依那西普(n = 6),其次是利妥昔单抗(n = 5)和干扰素-α(n = 3)。4例患者在抗结核治疗期间重新开始生物治疗,12例患者在完成抗结核治疗后重新开始。重新开始使用生物制剂后的中位随访时间为53(四分位间距:40 - 75)个月。1例白塞病患者结核病复发,该患者最初因严重威胁视力的葡萄膜炎在抗结核治疗第3个月时接受依那西普治疗,15个月后接受卡那单抗治疗,并联合甲氨蝶呤、环孢素和皮质类固醇。在进行第二个疗程9个月的抗结核治疗后,该患者目前使用干扰素-α稳定治疗33个月。对于先前在抗TNF治疗下发生过结核病的患者,即使在抗结核治疗期间重新开始使用抗TNF药物和其他生物制剂似乎也是可行的。然而,结核病再次发生的风险要求进行仔细随访。