Walter M A, Schindler C, Christ-Crain M, Müller-Brand J, Müller B
Institute of Nuclear Medicine, University Hospital Basel, Basel, Switzerland.
Eur J Clin Invest. 2009 Jan;39(1):51-7. doi: 10.1111/j.1365-2362.2008.02061.x.
Until now, it remains elusive which strategy - antithyroid drug withdrawal or increased radioiodine target doses - should be preferred to avoid the detrimental effect of antithyroid drugs in high- and low-dose radioiodine therapy, respectively.
We explored the effects of carbimazole on the 1-year post-radioiodine success and hypothyroidism rates by continuous dose-effect models, whereas success was defined as elimination of hyperthyroidism. Euthyroidism rates with and without carbimazole were calculated by numerical integration of the area between success and hypothyroidism curves. Target dose amplification factors for equal chance of success with and without carbimazole were calculated using logistic regression.
Two hundred and twenty-eight patients were included in this study. Radioiodine target doses between 33 and 839 Gy were applied. Overall, the euthyroidism rates were 16.5% and 64.8%, while the hypothyroidism rates were 37.6% and 14.8% in Graves' disease and toxic nodular goitre, respectively. The success rate with simultaneous carbimazole (median dose 15 mg day(-1); range 2.5-60 mg day(-1)) was reduced over the entire target dose range in Graves' disease and toxic nodular goitre. The areas between curves for euthyroidism without and with simultaneous carbimazole were 127 and 43 Gy in Graves' disease and 178 and 128 Gy in toxic nodular goitre. The estimated radioiodine target dose amplification factor was 5.5 for Graves' disease and 3.0 for toxic nodular goitre.
Simultaneous carbimazole reduces the euthyroidism rate, the aim of low-dose radioiodine therapy, over the entire target dose range in both Graves' disease and toxic nodular goitre. Therefore, antithyroid drug discontinuation should be preferred in low-dose radioiodine therapy. Conversely, escalation of the target dose should be preferred in high-dose radioiodine therapy.
迄今为止,在高剂量和低剂量放射性碘治疗中,究竟哪种策略——停用抗甲状腺药物还是增加放射性碘目标剂量——更有助于避免抗甲状腺药物的有害影响,仍不明确。
我们通过连续剂量效应模型探究了卡比马唑对放射性碘治疗后1年成功率及甲状腺功能减退发生率的影响,其中成功定义为甲状腺功能亢进症消除。通过对成功曲线和甲状腺功能减退曲线之间区域进行数值积分,计算出使用和不使用卡比马唑时的甲状腺功能正常发生率。使用逻辑回归计算出使用和不使用卡比马唑时成功率相等情况下的目标剂量放大系数。
本研究纳入了228例患者。应用的放射性碘目标剂量在33至839戈瑞之间。总体而言,在格雷夫斯病和毒性结节性甲状腺肿中,甲状腺功能正常发生率分别为16.5%和64.8%,甲状腺功能减退发生率分别为37.6%和14.8%。在格雷夫斯病和毒性结节性甲状腺肿中,同时使用卡比马唑(中位剂量15毫克/天;范围2.5 - 60毫克/天)时,在整个目标剂量范围内成功率均降低。在格雷夫斯病中,不使用和同时使用卡比马唑时甲状腺功能正常曲线之间的面积分别为127和43戈瑞,在毒性结节性甲状腺肿中分别为178和128戈瑞。格雷夫斯病的估计放射性碘目标剂量放大系数为5.5,毒性结节性甲状腺肿为3.0。
在格雷夫斯病和毒性结节性甲状腺肿中,同时使用卡比马唑会降低甲状腺功能正常发生率,而这正是低剂量放射性碘治疗的目标。因此,在低剂量放射性碘治疗中应优先停用抗甲状腺药物。相反,在高剂量放射性碘治疗中应优先增加目标剂量。