Masikane Sphelele, Mkhiz Thokozani, Harry Lerwine, Gabela Lerato, Nxasana Thembelihle, Ndlovu Nontobeko, Patel Maryam, Pillay Venesen, Hadebe Bawinile, Nyakale Nozipho, Vorster Mariza
Department of Nuclear Medicine, College of Health Sciences, University of KwaZulu Natal, Private Bag X54001, Durban 4001, South Africa.
Hell J Nucl Med. 2024 Sep-Dec;27(3):176-180. doi: 10.1967/s002449912751. Epub 2024 Dec 9.
Graves' disease represents 60%-90% of all causes of thyrotoxicosis in different regions of the world. Thyrotoxicosis contributes approximately 66% to thyroid disorders in South Africa and of those Graves' disease contributes about 34%. In most Sub-Saharan African countries, Graves' disease is managed mainly with medical treatment, due to a lack of or poor access to other means of treatment. Despite the primary use of anti-thyroid drugs (ATD) in the management of Graves' disease, the use of radioactive iodine (RAI) is required in many patients, especially in cases where ATD are contraindicated, or in patients who have failed ATD treatment and are poor surgical candidates. There is no consensus on the best method for deciding on how much activity of radioiodine to administer to patients with Graves' disease, that is, whether to use a calculated dose, or an empirical or fixed dose for RAI. The standardized fixed dose is particularly helpful in under-resourced areas or centres with few nuclear physicians and high patient loads. However, little is known about the efficacy of the fixed dose compared to the calculated or empirical dose methods. The purpose of this retrospective observational study was to assess the efficacy of a fixed low dose of radioiodine-131 (I) in the treatment of Graves' disease.
Patients treated with a fixed dose of 10mCi between the periods of 2014 to 2017 were evaluated for treatment response after each dose of RAI. Outcome of therapy was evaluated at 3 monthly follow-up using biochemical markers: thyroid stimulating hormone (TSH), total free thyroxine (fT4), and or triiodothyronine (T3), and the presence or absence of clinical symptoms of thyrotoxicosis. According to their response to RAI therapy, patients were classified as responders (if they became euthyroid or hypothyroid), non-responders (if they failed to achieve euthyroidism or hypothyroidism at 6 months) and complete treatment failure (if no response was present within 18 months after two or three fixed low doses of RAI). Percentage uptake, baseline fT4 and patient age were compared according to treatment response.
Our cohort included 111 patients, 95 (86%) females and 16 (14%) males, with a mean age of 41.9 years. Treatment was successful after the first dose in 89.2% of cases (27.0% euthyroid; 62.2% hypothyroid), with 10.8% requiring a second dose, and only a single patient who remained hyperthyroid after that second empiric dose. Statistical analysis demonstrated that a high percentage thyroid uptake was associated with treatment failure, whereas a low percent thyroid uptake was associated with a good treatment response (P=0.0048). We found no significant difference in FT4 levels or age, between hyperthyroid and non-hyperthyroid (euthyroid or hypothyroid) groups post initial RAI therapy (P=0.5 and P=0.96, respectively).
The use of a low fixed/empiric radioiodine activity for hyperthyroidism due to Graves' disease performed well in our setting with a nearly 90% response rate achieved after a single dose of 10mCi. Justification for higher activity should be specified, and this method of determining the optimal dose of RAI therapy may be beneficial in resource constrained settings with high patient volumes.
在世界不同地区,格雷夫斯病占所有甲状腺毒症病因的60%-90%。在南非,甲状腺毒症约占甲状腺疾病的66%,其中格雷夫斯病约占34%。在大多数撒哈拉以南非洲国家,由于缺乏其他治疗手段或难以获得这些手段,格雷夫斯病主要通过药物治疗。尽管抗甲状腺药物(ATD)是格雷夫斯病治疗的主要手段,但许多患者仍需要使用放射性碘(RAI),特别是在ATD禁忌的情况下,或在ATD治疗失败且不适合手术的患者中。对于给格雷夫斯病患者使用多少放射性碘活度的最佳方法尚无共识,即对于RAI是使用计算剂量、经验剂量还是固定剂量。标准化固定剂量在资源匮乏地区或核医学医生少、患者量大的中心特别有用。然而,与计算剂量或经验剂量方法相比,固定剂量的疗效鲜为人知。这项回顾性观察研究的目的是评估固定低剂量放射性碘-131(I)治疗格雷夫斯病的疗效。
对2014年至2017年期间接受10mCi固定剂量治疗的患者,在每次RAI给药后评估治疗反应。在3个月的随访中,使用生化指标:促甲状腺激素(TSH)、总游离甲状腺素(fT4)和/或三碘甲状腺原氨酸(T3)以及甲状腺毒症临床症状的有无来评估治疗结果。根据患者对RAI治疗的反应,将患者分为反应者(如果变为甲状腺功能正常或甲状腺功能减退)、无反应者(如果在6个月时未实现甲状腺功能正常或甲状腺功能减退)和完全治疗失败(如果在两或三次固定低剂量RAI后18个月内无反应)。根据治疗反应比较摄取百分比、基线fT4和患者年龄。
我们的队列包括111名患者,95名(86%)女性和16名(14%)男性,平均年龄41.9岁。89.2%的病例在首次给药后治疗成功(27.0%甲状腺功能正常;62.2%甲状腺功能减退),10.8%的患者需要第二次给药,只有一名患者在第二次经验性给药后仍为甲状腺功能亢进。统计分析表明,高百分比的甲状腺摄取与治疗失败相关,而低百分比的甲状腺摄取与良好的治疗反应相关(P=0.0048)。我们发现,初始RAI治疗后,甲状腺功能亢进组与非甲状腺功能亢进组(甲状腺功能正常或甲状腺功能减退)之间的FT4水平或年龄无显著差异(分别为P=0.5和P=0.96)。
在我们的研究中,使用低固定/经验性放射性碘活度治疗格雷夫斯病所致甲状腺功能亢进效果良好,单次10mCi剂量后实现了近90%的反应率。应明确更高活度的理由,这种确定RAI治疗最佳剂量的方法可能对患者量大的资源受限环境有益。