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甲巯咪唑/氢化可的松软膏与口服甲巯咪唑治疗格雷夫斯病患者的比较:一项前瞻性、随机、开放标签、平行组、为期18个月的研究。

Comparison of methimazole/hydrocortisone ointment with oral methimazole in patients with graves disease: A prospective, randomized, open-label, parallel-group, 18-month study.

作者信息

Chen Ling, Wang Hong-Qing, Gao Yan-Yan, Liang Jun, Wang Men, Bai Jie, Qi Wen-Bo, Zhang Jun-Sheng, Zhang Jian, Ren Juan-Qing, Li Hui-Qing

机构信息

Division of Endocrinology, Provincial Hospital Affiliated to Shandong University, Jinan, China.

Gynecology and Obstetrical Department, Provincial Hospital Affiliated to Shandong University, Jinan, China.

出版信息

Curr Ther Res Clin Exp. 2008 Aug;69(4):305-17. doi: 10.1016/j.curtheres.2008.08.004.

Abstract

BACKGROUND

Thionamide antithyroid drugs (ATDs) have certain disadvantages and are associated with some adverse events (AEs). To overcome the problems associated with ATDs, a compound antithyroid ointment (CATO) containing methimazole (MMI) and hydrocortisone has been developed for use as a local thyroid treatment (LTT).

OBJECTIVE

The aim of this study was to assess the clinical effectiveness and tolerability of CATO LTT in patients with Graves disease (GD).

METHODS

This was a prospective, randomized, open-label, parallel-group clinical trial conducted at the Provincial Hospital Affiliated to Shandong University (Jinan, China). Patients with GD aged 19 to 65 years were randomized to receive either CATO LTT 0.3 g/d or oral MMI 37.5 mg/d (control group) treatment for 18 months, with a 4-year follow-up period. Hyperthyroid symptoms, thyroid function, granulocyte count, liver function, and AEs were assessed at baseline and every 2 weeks until serum thyroid hormone (TH) concentration normalized, at which point patients were assessed monthly. The primary efficacy end points were the duration of treatment required for serum TH concentration to normalize and the remission rate after completing the 18-month treatment regimen.

RESULTS

A total of 154 patients (133 women, 21 men; mean [SD] age, 39.6 [11.8] years; all Han Chinese) participated in the study; all patients completed the 18-month treatment period. Compared with the MMI group (n 76), the CATO- treated group (n 78) had a significantly shorter median (range) time to restoration of normal serum thyroid hormone concentration (43 [12-150] vs 22 [7-60] days; P < 0.001), a significantly lower rate of recurrence of hyperthyroidism (309/1520 [20.3%] vs 193/1368 [14.1%] person-time; P < 0.001), a significantly lower drug hypothyroidism rate (185/1520 [12.2%] vs 54/1368 [3.9%] person-time; P < 0.001), and a higher remission rate (year 1:46/69 [66.7%] vs 65/72 [90.3%] patients, P 0.001; year 2:40/69 [58.0%] vs 60/72 [83.3%] patients, P - 0.001; year 3:34/69 [49.3%] vs 57/72 [79.2%] patients, P < 0.001; and year 4:30/69 [43.5%] vs 55/72 [76.4%] patients, P < 0.001). Systemic AEs occurred in 6 patients (7.9%) in the MMI group (drug neutropenia, 2 patients [2.6%]; epistaxis, 1 [1.3%]; hepatopathy, 1 [1.3%]; and other systemic AEs, 2 [2.6%]), while no systemic AEs were observed/reported in the CATO group.

CONCLUSION

This study suggests that CATO LTT was well tolerated and more effective than oral MMI treatment in controlling thyrotoxicosis and promoting remission of GD in these Han Chinese patients.

摘要

背景

硫酰胺类抗甲状腺药物(ATD)存在一定缺点且与一些不良事件(AE)相关。为克服与ATD相关的问题,已研发出一种含甲巯咪唑(MMI)和氢化可的松的复方抗甲状腺软膏(CATO),用于局部甲状腺治疗(LTT)。

目的

本研究旨在评估CATO局部甲状腺治疗(LTT)对格雷夫斯病(GD)患者的临床有效性和耐受性。

方法

这是一项在山东大学附属省立医院(中国济南)进行的前瞻性、随机、开放标签、平行组临床试验。19至65岁的GD患者被随机分为接受CATO LTT 0.3 g/d或口服MMI 37.5 mg/d(对照组)治疗18个月,并进行4年随访。在基线时以及每2周评估一次甲状腺功能亢进症状、甲状腺功能、粒细胞计数、肝功能和AE,直至血清甲状腺激素(TH)浓度恢复正常,此后每月对患者进行评估。主要疗效终点为血清TH浓度恢复正常所需的治疗持续时间以及完成18个月治疗方案后的缓解率。

结果

共有154例患者(133例女性,21例男性;平均[标准差]年龄,39.6[11.8]岁;均为汉族)参与研究;所有患者均完成了18个月的治疗期。与MMI组(n = 76)相比,CATO治疗组(n = 78)血清甲状腺激素浓度恢复正常的中位(范围)时间显著缩短(43[12 - 150]天对22[7 - 60]天;P < 0.001),甲状腺功能亢进复发率显著降低(309/1520[20.3%]对193/1368[14.1%]人时;P < 0.001),药物性甲状腺功能减退率显著降低(185/1520[12.2%]对54/1368[3.9%]人时;P < 0.001),缓解率更高(第1年:46/69[66.7%]对65/72[90.3%]例患者,P = 0.001;第2年:40/69[58.0%]对60/72[83.3%]例患者,P = 0.

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