Vergidis Paschalis, Avery Robin K, Wheat L Joseph, Dotson Jennifer L, Assi Maha A, Antoun Smyrna A, Hamoud Kassem A, Burdette Steven D, Freifeld Alison G, McKinsey David S, Money Mary E, Myint Thein, Andes David R, Hoey Cynthia A, Kaul Daniel A, Dickter Jana K, Liebers David E, Miller Rachel A, Muth William E, Prakash Vidhya, Steiner Frederick T, Walker Randall C, Hage Chadi A
Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pennsylvania.
Division of Infectious Disease, Johns Hopkins Hospital, Baltimore, Maryland.
Clin Infect Dis. 2015 Aug 1;61(3):409-17. doi: 10.1093/cid/civ299. Epub 2015 Apr 13.
Histoplasmosis may complicate tumor necrosis factor (TNF)-α blocker therapy. Published case series provide limited guidance on disease management. We sought to determine the need for long-term antifungal therapy and the safety of resuming TNF-α blocker therapy after successful treatment of histoplasmosis.
We conducted a multicenter retrospective review of 98 patients diagnosed with histoplasmosis between January 2000 and June 2011. Multivariate logistic regression was used to evaluate risk factors for severe disease.
The most commonly used biologic agent was infliximab (67.3%). Concomitant corticosteroid use (odds ratio [OR], 3.94 [95% confidence interval {CI}, 1.06-14.60]) and higher urine Histoplasma antigen levels (OR, 1.14 [95% CI, 1.03-1.25]) were found to be independent predictors of severe disease. Forty-six (47.4%) patients were initially treated with an amphotericin B formulation for a median duration of 2 weeks. Azole treatment was given for a median of 12 months. TNF-α blocker therapy was initially discontinued in 95 of 98 (96.9%) patients and later resumed in 25 of 74 (33.8%) patients at a median of 12 months (range, 1-69 months). The recurrence rate was 3.2% at a median follow-up period of 32 months. Of the 3 patients with recurrence, 2 had restarted TNF-α blocker therapy, 1 of whom died. Mortality rate was 3.2%.
In this study, disease outcomes were generally favorable. Discontinuation of antifungal treatment after clinical response and an appropriate duration of therapy, probably at least 12 months, appears safe if pharmacologic immunosuppression has been held. Resumption of TNF-α blocker therapy also appears safe, assuming that the initial antifungal therapy was administered for 12 months.
组织胞浆菌病可能使肿瘤坏死因子(TNF)-α阻滞剂治疗复杂化。已发表的病例系列对疾病管理的指导有限。我们试图确定长期抗真菌治疗的必要性以及组织胞浆菌病成功治疗后恢复TNF-α阻滞剂治疗的安全性。
我们对2000年1月至2011年6月期间诊断为组织胞浆菌病的98例患者进行了多中心回顾性研究。采用多因素逻辑回归评估重症疾病的危险因素。
最常用的生物制剂是英夫利昔单抗(67.3%)。发现同时使用皮质类固醇(比值比[OR],3.94[95%置信区间{CI},1.06 - 14.60])和较高的尿组织胞浆菌抗原水平(OR,1.14[95%CI,1.03 - 1.25])是重症疾病的独立预测因素。46例(47.4%)患者最初接受两性霉素B制剂治疗,中位疗程为2周。唑类治疗的中位时间为12个月。98例患者中有95例(96.9%)最初停用了TNF-α阻滞剂治疗,74例患者中有25例(33.8%)后来恢复使用,中位时间为12个月(范围,1 - 69个月)。中位随访期32个月时复发率为3.2%。在3例复发患者中,2例重新开始了TNF-α阻滞剂治疗,其中1例死亡。死亡率为3.2%。
在本研究中,疾病结局总体良好。如果已经停止了药物免疫抑制,在临床缓解和适当疗程(可能至少12个月)的治疗后停止抗真菌治疗似乎是安全的。假设最初的抗真菌治疗持续了12个月,恢复TNF-α阻滞剂治疗似乎也是安全的。