根据左甲状腺素剂量确定甲状腺癌幸存者罹患后续原发性癌症的风险:一项全国队列研究。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-04-01 Epub Date: 2024-03-04 DOI:10.3803/EnM.2023.1815
Min-Su Kim, Jang Won Lee, Min Kyung Hyun, Young Shin Song
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引用次数: 0

摘要

背景:目前的研究尚未调查使用左甲状腺素抑制促甲状腺激素治疗对罹患后续原发性癌症(SPC)风险的影响。本研究旨在调查左甲状腺素用量与甲状腺癌患者罹患 SPCs 风险之间的关系:我们利用韩国国民健康保险数据库开展了一项基于全国人口的回顾性队列研究。该队列包括2004年至2018年间的342 920名甲状腺癌患者。患者被分为非左甲状腺素组和左甲状腺素组,后者根据四分位数分为四个剂量亚组。通过调整包括放射性碘(RAI)治疗累积剂量在内的变量,采用 Cox 比例危险模型评估 SPC 风险:结果:在中位 7.3 年的随访中,共观察到 17,410 例 SPC。与非左甲状腺素组相比,高剂量左甲状腺素亚组(Q3和Q4)发生SPC的风险更高(调整后危险比[HR]分别为1.14和1.27;95%置信区间[CI]分别为1.05-1.24和1.17-1.37;)。特别是,在 Q4 亚组中,胃癌(1.31)、结直肠癌(1.60)、肝癌和胆道癌(1.95)以及胰腺癌(2.48)的调整后 HR 均有所增加。即使在调整了各种混杂变量后,我们仍然观察到按体重计算的高左旋甲状腺素用量与 SPC 风险之间存在正相关。此外,在根据甲状腺切除术类型和 RAI 治疗进行的分层分析中,以及在对依从性良好的患者进行的亚组分析中,也发现了类似的结果:结论:无论接受何种 RAI 治疗,甲状腺癌患者使用大剂量左甲状腺素都会增加 SPC 的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Subsequent Primary Cancers in Thyroid Cancer Survivors according to the Dose of Levothyroxine: A Nationwide Cohort Study.

Backgruound: Current research has not investigated the effect of thyroid-stimulating hormone suppression therapy with levothyroxine on the risk for developing subsequent primary cancers (SPCs). This study aimed to investigate the association between levothyroxine dosage and the risk for SPCs in thyroid cancer patients.

Methods: We conducted a nationwide population-based retrospective cohort study form Korean National Health Insurance database. This cohort included 342,920 thyroid cancer patients between 2004 and 2018. Patients were divided into the non-levothyroxine and the levothyroxine groups, the latter consisting of four dosage subgroups according to quartiles. Cox proportional hazard models were performed to evaluate the risk for SPCs by adjusting for variables including cumulative doses of radioactive iodine (RAI) therapy.

Results: A total of 17,410 SPC cases were observed over a median 7.3 years of follow-up. The high-dose levothyroxine subgroups (Q3 and Q4) had a higher risk for SPC (adjusted hazard ratio [HR], 1.14 and 1.27; 95% confidence interval [CI], 1.05-1.24 and 1.17- 1.37; respectively) compared to the non-levothyroxine group. In particular, the adjusted HR of stomach (1.31), colorectal (1.60), liver and biliary tract (1.95), and pancreatic (2.48) cancers were increased in the Q4 subgroup. We consistently observed a positive association between high levothyroxine dosage per body weight and risk of SPCs, even after adjusting for various confounding variables. Moreover, similar results were identified in the stratified analyses according to thyroidectomy type and RAI therapy, as well as in a subgroup analysis of patients with good adherence.

Conclusion: High-dose levothyroxine use was associated with increased risk of SPCs among thyroid cancer patients regardless of RAI therapy.

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