Grebe S K, Feek C M, Ford H C, Fagerström J N, Cordwell D P, Delahunt J W, Toomath R J
Department of Pathology, Wellington School of Medicine, New Zealand.
Clin Endocrinol (Oxf). 1998 May;48(5):585-92. doi: 10.1046/j.1365-2265.1998.00446.x.
The optimal treatment regimen with thionamide drugs remains a matter for debate. We have investigated whether high doses of carbimazole, when compared with low doses, reduce relapse rates of Graves' disease.
In an open label, randomized, prospective trial of treatment of Graves' disease we compared high doses of carbimazole (6 months of 100 mg carbimazole per day plus thyroxine) to low-dose carbimazole treatment (starting at 25 mg and titrating the carbimazole dose with the aim to maintain serum thyroid function test results within the normal reference range).
Thirty-seven patients with a first episode of Graves' disease were enrolled.
During the 6 months of treatment we evaluated the rate of normalization of serum thyroid function tests, changes in serum thyroid auto-antibody levels and the rate of side-effects during treatment. After completion of the 6-month treatment course patients were observed for 2 years for evidence of relapse of Graves' disease.
There were no differences between the two groups either in the rate of normalization of serum thyroid function tests or in serum thyroid auto-antibody levels during treatment. Of the 17 patients randomized to high-dose treatment seven suffered treatment side-effects, compared to only one of the 20 patients receiving low-dose treatment (P < 0.006). There was no significant difference in 2-year post-treatment remission rates on an intention-to-treat basis between the two treatment groups (18.7% vs. 5.9%, P = NS). However, for those patients who completed 6 months of treatment (high-dose group = 9, low-dose group = 16), multivariate survival analysis demonstrated a significantly longer median relapse-free interval (P < 0.04) in the high-dose group (27 weeks; 25th percentile: 9.6 weeks, 75th percentile: 75 weeks) versus the low-dose group (6 weeks; 25th percentile: 4.8 weeks, 75th percentile: 13.1 weeks).
High-dose carbimazole treatment delays, but does not prevent, relapse from Graves' disease in those patients able to tolerate the treatment. However, it leads to more frequent side-effects than conventional dose treatment.
硫代酰胺类药物的最佳治疗方案仍存在争议。我们研究了与低剂量相比,高剂量卡比马唑是否能降低格雷夫斯病的复发率。
在一项开放标签、随机、前瞻性的格雷夫斯病治疗试验中,我们将高剂量卡比马唑(每天100毫克卡比马唑,持续6个月加甲状腺素)与低剂量卡比马唑治疗(起始剂量25毫克,滴定卡比马唑剂量以维持血清甲状腺功能测试结果在正常参考范围内)进行了比较。
纳入了37例首次发作格雷夫斯病的患者。
在6个月的治疗期间,我们评估了血清甲状腺功能测试的正常化率、血清甲状腺自身抗体水平的变化以及治疗期间的副作用发生率。在完成6个月的治疗疗程后,对患者进行了2年的观察,以寻找格雷夫斯病复发的证据。
两组在治疗期间血清甲状腺功能测试的正常化率或血清甲状腺自身抗体水平方面均无差异。随机接受高剂量治疗的17例患者中有7例出现治疗副作用,而接受低剂量治疗的20例患者中只有1例出现副作用(P < 0.006)。在意向性治疗基础上,两个治疗组之间的2年治疗后缓解率无显著差异(18.7%对5.9%,P = 无统计学意义)。然而,对于那些完成6个月治疗的患者(高剂量组 = 9例,低剂量组 = 16例),多变量生存分析显示高剂量组(27周;第25百分位数:9.6周,第75百分位数:75周)的无复发间隔中位数明显长于低剂量组(6周;第25百分位数:4.8周,第75百分位数:13.1周)(P < 0.04)。
高剂量卡比马唑治疗可延迟但不能预防格雷夫斯病在能够耐受该治疗的患者中的复发。然而,与传统剂量治疗相比,它会导致更频繁的副作用。