Ericzon B, Groth C, Bismuth H, Calne R, McMaster P, Neuhaus P, Otto G, Pichlmayr R, Williams R
Department of Transplantation Surgery, Huddinge Hospital, Sweden.
Transpl Int. 1994;7 Suppl 1:S11-4. doi: 10.1111/j.1432-2277.1994.tb01302.x.
From September 1990 to January 1992, 545 liver transplant patients were randomised to treatment with either FK506 and prednisolone or a conventional cyclosporin-based immunosuppressive regimen (CBIR). Eight European centres participated in the study. Adverse events were reported as defined by each centre. Hyperglycaemia was reported as an adverse event in 30.7% of patients receiving FK 506 compared with 20.5% in the CBIR group (P < 0.01). Diabetes mellitus was reported in 17.2% of patients treated with FK 506 and 9.5% of CBIR-treated patients (P < 0.05). Treatment with insulin was required in 12.0% of patients in the DK 506 treatment group and in 5% in the CBIR group at 6 months. Initially, higher doses of FK 506 were used. During the study, the protocol was changed to allow a lower dose of FK 506. When the early and late cohorts of patients were compared, the incidence of diabetes mellitus fell from 23.9% to 10.5% in FK 506-treated patients but remained relatively constant in the CBIR group (10.4% to 8.7%). The median cumulative doses of i.v. and p.o. corticosteroids were significantly greater in the CBIR group. Thus, in the overall series, the incidence of diabetes mellitus was significantly greater in the FK 506 group as compared with the CBIR group. However, when a lower FK 506 dose was used during the second half of the study, the difference in the incidence of diabetes mellitus disappeared.
1990年9月至1992年1月,545例肝移植患者被随机分为接受FK506和泼尼松龙治疗组或传统的基于环孢素的免疫抑制方案(CBIR)治疗组。八个欧洲中心参与了该研究。不良事件按照各中心定义进行报告。接受FK506治疗的患者中有30.7%报告发生高血糖,而CBIR组为20.5%(P<0.01)。接受FK506治疗的患者中有17.2%报告发生糖尿病,接受CBIR治疗的患者为9.5%(P<0.05)。在6个月时,FK506治疗组12.0%的患者和CBIR组5%的患者需要胰岛素治疗。最初使用了较高剂量的FK506。在研究期间,方案改为允许使用较低剂量的FK506。当比较早期和晚期患者队列时,FK506治疗患者的糖尿病发生率从23.9%降至10.5%,而CBIR组保持相对稳定(10.4%至8.7%)。CBIR组静脉和口服皮质类固醇的累积中位剂量显著更高。因此,在整个系列中,FK506组糖尿病的发生率显著高于CBIR组。然而,在研究后半期使用较低剂量的FK506时,糖尿病发生率的差异消失了。