Delayed initial radioiodine therapy related to incomplete response in low‐ to intermediate‐risk differentiated thyroid cancer

医学 甲状腺癌 内科学 单变量分析 甲状腺球蛋白 多元分析 胃肠病学 置信区间 放射性碘疗法 甲状腺切除术 风险因素 甲状腺 肿瘤科 内分泌学
作者
Hui Li,Y M Zhang,Chen Wang,Xin Zhang,Xin Li,Yansong Lin
出处
期刊:Clinical Endocrinology [Wiley]
卷期号:88 (4): 601-606 被引量:35
标识
DOI:10.1111/cen.13551
摘要

Summary Objective Whether the initiating time of radioiodine ( RAI ) therapy will affect the clinical outcome in differentiated thyroid cancer ( DTC ) remains controversial. The objective of this study was to evaluate the impact of RAI therapy initiating time on response to initial therapy in low‐ to intermediate‐risk DTC . Methods A total of 235 consecutive patients with low‐ to intermediate‐risk DTC were retrospectively reviewed. According to the time interval between thyroidectomy and RAI therapy, patients were divided into Group 1 (interval < 3 months, n = 187) and Group 2 (interval ≥ 3 months, n = 48). Response to RAI therapy was evaluated as excellent, indeterminate, biochemical incomplete or structural incomplete response ( ER , IDR , BIR or SIR ) with a median follow‐up of 780 days. The univariate and multivariate analyses were further conducted to identify factors associated with incomplete response ( IR , including BIR and SIR ). Results Response to initial therapy was significantly different between 2 groups ( P < .05), after excluding the impact of other risk factors (age, gender, histological type, status of T and N, RAI dose, thyrotropin, stimulated thyroglobulin and follow‐up time). A significantly higher IR rate (18.8% vs 4.3%, P = .001) and a lower ER proportion (62.5% vs 78.1%, P = .027) were observed in Group 2. By univariate analysis, both T status and N status, stimulated thyroglobulin and time interval were significant risk factors for IR ( P < .05). Multivariate analysis demonstrated that the time interval was an independent risk factor for IR ( P = .008). Conclusions Delayed initial RAI therapy (≥3 months after thyroidectomy) related to incomplete response in low‐ to intermediate‐risk DTC .
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