Lindor K D, Jorgensen R A, Anderson M L, Gores G J, Hofmann A F, LaRusso N F
Division of Gastroenterology and Internal Medicine, Mayo Foundation, Rochester, Minnesota, USA.
Am J Gastroenterol. 1996 Mar;91(3):511-5.
Ursodeoxycholic acid (UDCA) and methotrexate (MTX) are both undergoing evaluation for the treatment of patients with primary sclerosing cholangitis (PSC). In this pilot study, we sought to study the safety and estimate of efficacy of a combination of these two drugs administered over a 2-yr period in patients with PSC.
Nineteen patients with well defined PSC were entered prospectively into a pilot study with anticipation of 2-yr follow-up. The patients received UDCA (13-15 mg/kg/day)in divided doses in conjunction with MTX (0.25 mg/kg/wk). The results of treatment were compared with a concurrently studied, but not randomized, group of 10 patients receiving UDCA alone. At entry, the two groups were comparable with respect to age, sex, liver biochemistries, and histological stage when available.
During this period, five patients treated with the combination of UDCA and MTX were severed from the study (three referred for transplantation, one death from small bowel cancer, and one with pre-existing, high ileostomy output who withdrew voluntarily). MTX was discontinued by the investigators in an additional five patients (hair loss in three, pulmonary problems in two). There was no change in fatigue or itching compared with baseline in the group receiving the UDCA/MTX combination. Changes in biochemistries from baseline values were not different in the group receiving UDCA and MTX compared with the group receiving UDCA alone. Furthermore, after MTX was withdrawn and UDCA was continued, there was no clear evidence of further biochemical change. The use of MTX in combination with UDCA was associated with toxicity without any further improvement in liver biochemistries compared with the use of UDCA alone.
This pilot study found no evidence to support the use of MTX in combination with UDCA for patients with PSC.
熊去氧胆酸(UDCA)和甲氨蝶呤(MTX)均在接受治疗原发性硬化性胆管炎(PSC)患者的评估。在这项初步研究中,我们试图研究这两种药物联合应用2年对PSC患者的安全性及疗效评估。
19例确诊为PSC的患者前瞻性地进入一项预期进行2年随访的初步研究。患者接受分剂量的UDCA(13 - 15mg/kg/天)联合MTX(0.25mg/kg/周)治疗。将治疗结果与同期研究的10例仅接受UDCA治疗(未随机分组)的患者进行比较。入组时,两组在年龄、性别、肝脏生化指标以及可获取的组织学分期方面具有可比性。
在此期间,5例接受UDCA和MTX联合治疗的患者退出研究(3例转至移植治疗,1例死于小肠癌,1例因既往存在的高回肠造口输出量而自愿退出)。研究人员又让另外5例患者停用MTX(3例因脱发,2例因肺部问题)。接受UDCA/MTX联合治疗组的疲劳或瘙痒与基线相比无变化。接受UDCA和MTX联合治疗组与仅接受UDCA治疗组相比,生化指标相对于基线值的变化并无差异。此外,在停用MTX并继续使用UDCA后,没有明确证据表明生化指标有进一步变化。与单独使用UDCA相比,MTX与UDCA联合使用会产生毒性,且肝脏生化指标并无进一步改善。
这项初步研究未发现证据支持PSC患者联合使用MTX和UDCA。