Vega Jorge, Goecke Helmuth, Tapia Héctor, Labarca Eduardo, Santamarina Mario, Martínez Gonzalo
Departamento de Medicina Interna, Sección Nefrología, Hospital Naval Almirante Nef, Viña del Mar, Chile.
Am J Kidney Dis. 2009 Apr;53(4):628-37. doi: 10.1053/j.ajkd.2008.09.025. Epub 2008 Dec 31.
Idiopathic retroperitoneal fibrosis (IRPF) is an uncommon, but increasingly recognized, disease. Autoimmune mechanisms probably participate in its pathogenesis. Patients have been treated with high-dose steroids and sometimes immunosuppressive drugs, resulting in toxicity risk during prolonged treatments; thus, it would be wise to look for safer drugs. Colchicine has antifibrotic, anti-inflammatory, and immunosuppressive effects. Hence, it is a potential therapeutic resource.
Case series.
SETTING & PARTICIPANTS: 7 consecutives patients with IRPF diagnosed since 1993 at a navy hospital were prescribed colchicine plus prednisone or deflazacort. After reaching a clinical response, the steroid dose was tapered, maintaining daily colchicine therapy.
OUTCOMES & MEASUREMENTS: Symptomatic improvement was defined as time to relief of symptoms; clinical improvement, time to normalization of inflammatory parameters with symptomatic improvement; radiological changes, percentage of decrease in retroperitoneal mass; recurrence, as the need to increase steroid dose or add immunosuppressors because of reactivation of inflammation; and treatment failure, as persistence of signs of active inflammation and/or decrease in retroperitoneal mass less than 50% and/or deterioration in kidney function at the last visit.
At month 3 of treatment, all patients had symptomatic improvement and 67% had clinical improvement. Between 8 and 12 months, 67% of patients had a decrease in retroperitoneal mass greater than 50%. No recurrence or treatment failure was observed during follow-up (mean, 72.5 months). At the last visit, all patients had a significant decrease in retroperitoneal mass (mean, 79.8% +/- 19.7%). One patient died of septic shock on day 21 of treatment.
This series did not have a control group.
Colchicine in association with a low induction dose of steroids (<0.5 mg/kg/d) produced remission rates in patients with IRPF similar to those for regimens using greater steroid doses alone or in combination with immunosuppressive drugs. In addition, colchicine may have contributed to recurrence prevention.
特发性腹膜后纤维化(IRPF)是一种不常见但越来越被认识到的疾病。自身免疫机制可能参与其发病过程。患者一直使用大剂量类固醇治疗,有时还使用免疫抑制药物,这导致长期治疗期间存在毒性风险;因此,寻找更安全的药物是明智的。秋水仙碱具有抗纤维化、抗炎和免疫抑制作用。因此,它是一种潜在的治疗资源。
病例系列。
自1993年以来在一家海军医院确诊的7例连续IRPF患者被给予秋水仙碱加泼尼松或地夫可特。在达到临床反应后,逐渐减少类固醇剂量,维持每日秋水仙碱治疗。
症状改善定义为症状缓解时间;临床改善定义为炎症参数正常化且症状改善的时间;放射学变化定义为腹膜后肿块减少的百分比;复发定义为因炎症重新激活而需要增加类固醇剂量或添加免疫抑制剂;治疗失败定义为在最后一次就诊时仍存在活动性炎症体征和/或腹膜后肿块减少小于50%和/或肾功能恶化。
在治疗第3个月时,所有患者症状均有改善,67%患者有临床改善。在8至12个月之间,67%患者的腹膜后肿块减少超过50%。随访期间(平均72.5个月)未观察到复发或治疗失败。在最后一次就诊时,所有患者的腹膜后肿块均显著减少(平均79.8%±19.7%)。1例患者在治疗第21天死于感染性休克。
本系列没有对照组。
秋水仙碱联合低诱导剂量类固醇(<0.5mg/kg/d)在IRPF患者中产生的缓解率与单独使用更大剂量类固醇或与免疫抑制药物联合使用的方案相似。此外,秋水仙碱可能有助于预防复发。