1 Department of Medicine, Brigham and Women's Hospital and Harvard Medical School , Boston, Massachusetts.
2 Thyroid Section, Brigham and Women's Hospital and Harvard Medical School , Boston, Massachusetts.
Thyroid. 2018 Apr;28(4):437-444. doi: 10.1089/thy.2017.0579.
Thyroid dysfunction during tyrosine kinase inhibitor (TKI) cancer treatment is common, but predisposing risk factors have not been determined. Recommendations for monitoring patients treated with one or multiple TKI and in conjunction with other relevant cancer therapies could be improved. The study objective was to assess the risk factors for new thyroid dysfunction in TKI-treated previously euthyroid cancer patients.
A retrospective cohort study of patients with advanced nonthyroidal cancer treated with TKI from 2000 to 2017, having available thyroid function tests showing initial euthyroid status, excluding patients with preexisting thyroid disease or lack of follow-up thyroid function tests. During TKI treatment, patients were classified as euthyroid (thyrotropin [TSH] normal), subclinical hypothyroidism (TSH 5-10 mIU/L, or higher TSH if free thyroxine normal), or overt hypothyroidism (TSH >10 mIU/L, low free thyroxine, or requiring thyroid hormone replacement). The timing of thyroid dysfunction and TKI used were assessed. Risk factors for incident hypothyroidism were evaluated using multivariate models.
In 538 adult patients included, subclinical hypothyroidism occurred in 71 (13.2%) and overt hypothyroidism occurred in 144 (26.8%) patients with TKI therapy, following a median cumulative TKI exposure of 196 days (interquartile range [IQR] 63.5-518.5 days). The odds of hypothyroidism were greatest during the first six months on a TKI. Median exposure time on the TKI concurrent with thyroid dysfunction in patients treated with only one TKI was 85 days (IQR 38-293.5 days) and was similar to the 74 days (IQR 38-133.3 days) in patients treated previously with other TKI (p = 0.41). Patients who developed hypothyroidism compared to those who remained euthyroid had greater odds of being female (odds ratio = 1.99 [confidence interval 1.35-2.93], p < 0.01), but greater cumulative TKI exposure and greater number of TKI received were not associated with thyroid dysfunction.
Thyroid dysfunction occurred in 40% of euthyroid patients. Monitoring thyroid function in TKI-treated patients is recommended, with particular attention to female patients and within the first six months of exposure to a new TKI.
酪氨酸激酶抑制剂(TKI)癌症治疗期间甲状腺功能障碍很常见,但尚未确定其易感危险因素。对于接受一种或多种 TKI 治疗并同时接受其他相关癌症治疗的患者,监测建议可能需要改进。本研究旨在评估 TKI 治疗的既往甲状腺功能正常的癌症患者新发甲状腺功能障碍的危险因素。
这是一项回顾性队列研究,纳入了 2000 年至 2017 年期间接受 TKI 治疗的晚期非甲状腺癌患者,这些患者的甲状腺功能检查显示初始甲状腺功能正常,排除了有甲状腺疾病或缺乏甲状腺功能检查随访的患者。在 TKI 治疗期间,将患者分为甲状腺功能正常(促甲状腺激素[TSH]正常)、亚临床甲状腺功能减退(TSH 5-10 mIU/L,或游离甲状腺素正常时 TSH 更高)或显性甲状腺功能减退(TSH>10 mIU/L、游离甲状腺素低或需要甲状腺激素替代)。评估甲状腺功能障碍的时间和 TKI 的使用情况。使用多变量模型评估发生甲状腺功能减退的危险因素。
在纳入的 538 名成年患者中,71 名(13.2%)患者出现亚临床甲状腺功能减退,144 名(26.8%)患者出现显性甲状腺功能减退,中位 TKI 累积暴露时间为 196 天(四分位距[IQR] 63.5-518.5 天)。在开始使用 TKI 的前 6 个月,甲状腺功能减退的可能性最大。仅接受一种 TKI 治疗的患者中,与甲状腺功能障碍同时接受 TKI 治疗的中位时间为 85 天(IQR 38-293.5 天),与先前接受其他 TKI 治疗的患者(中位时间 74 天,IQR 38-133.3 天)相似(p=0.41)。与甲状腺功能正常的患者相比,发生甲状腺功能减退的患者发生甲状腺功能减退的可能性更大,女性(优势比[OR]1.99[置信区间 1.35-2.93],p<0.01)的几率更高,但甲状腺功能减退与累积 TKI 暴露量更大和接受的 TKI 数量更多无关。
甲状腺功能正常的患者中有 40%发生了甲状腺功能障碍。建议对接受 TKI 治疗的患者监测甲状腺功能,尤其要关注女性患者,并在开始使用新的 TKI 后 6 个月内进行监测。