Replacement Dose for Overt Hypothyroidism Induced by Programmed Cell Death Protein 1 Antibodies May Be Higher than Recommended.

IF 2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Endocrine, metabolic & immune disorders drug targets Pub Date : 2024-01-01 DOI:10.2174/1871530323666230821102730
Qian Zhang, Yao Zhang, Huijuan Zhu, Kuanzhi Liu, Pingping Lou, Peixuan Kong, Lei Su, Shuchang Wang
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Abstract

Background: The present recommendations, consensus, or guidelines for the replacement dosage for hypothyroidism induced by programmed cell death protein 1 (PD-1) therapy are not uniform, and there are very few special clinical trials that have examined the replacement dosage for it.

Objectives: This article illustrates the clinical characteristics of hypothyroidism induced by PD-1 antibodies (Abs) and reports the recommended replacement dosage for hypothyroidism.

Methods: Eighteen patients with overt primary hypothyroidism induced by PD-1 Abs (group 1) were selected from 655 patients with different tumor types. Retrospective analysis was performed on patients in group 1 and 18 patients with natural courses of overt primary hypothyroidism who were age- and sex-matched with the patients in group 1 (group 2). The replacement dosages required for the patients in the two groups were compared.

Results: Thyroid dysfunction occurred in group 1 after approximately 3.0 ± 1.4 cycles of PD-1 therapy (1-6 stages), with a median time of 61.5 days. The median time of onset of hypothyroidism among all patients was 87.5 days (30-240 days). Most of the patients with hypothyroidism were asymptomatic, and the onset of hypothyroidism was independent of age, sex, TPOAb, TgAb and TSH in group 1 (P>0.05). The average replacement dosage for patients in group 1 was 1.8 ± 0.6 μg/kg/d (0.6-3.2 μg/kg/d). Multiple linear regression analysis showed that sex, age, TPOAb, TgAb and TSH were not correlated with drug dosage.

Conclusion: It seemed that the average maintenance dosage of levothyroxine might need to be 1.8 μg/kg/day for patients with overt hypothyroidism induced by PD-1 Abs.

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程序性细胞死亡蛋白 1 抗体诱发的明显甲状腺功能减退症的替代剂量可能高于建议剂量。
背景:目前关于程序性细胞死亡蛋白1(PD-1)治疗诱发的甲状腺功能减退症的替代剂量的建议、共识或指南并不统一,而且很少有专门的临床试验研究其替代剂量:本文阐述了PD-1抗体(Abs)诱导的甲状腺功能减退症的临床特点,并报告了甲状腺功能减退症的推荐替代剂量:从655例不同肿瘤类型的患者中筛选出18例PD-1抗体诱发的明显原发性甲状腺功能减退症患者(第1组)。对第1组患者和18名与第1组患者年龄和性别相匹配的原发性甲减自然病程患者(第2组)进行回顾性分析。对两组患者所需的替代剂量进行了比较:第1组患者在接受PD-1治疗(1-6期)约3.0±1.4个周期后出现甲状腺功能障碍,中位时间为61.5天。所有患者出现甲减的中位时间为87.5天(30-240天)。大多数甲减患者无症状,第 1 组患者的甲减发病与年龄、性别、TPOAb、TgAb 和 TSH 无关(P>0.05)。第 1 组患者的平均替代剂量为 1.8 ± 0.6 μg/kg/d(0.6-3.2 μg/kg/d)。多元线性回归分析表明,性别、年龄、TPOAb、TgAb 和 TSH 与药物剂量无关:PD-1抗体诱发的明显甲状腺功能减退症患者的左旋甲状腺素平均维持剂量可能需要1.8 μg/kg/天。
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来源期刊
Endocrine, metabolic & immune disorders drug targets
Endocrine, metabolic & immune disorders drug targets ENDOCRINOLOGY & METABOLISMIMMUNOLOGY-IMMUNOLOGY
CiteScore
4.60
自引率
5.30%
发文量
217
期刊介绍: Aims & Scope This journal is devoted to timely reviews and original articles of experimental and clinical studies in the field of endocrine, metabolic, and immune disorders. Specific emphasis is placed on humoral and cellular targets for natural, synthetic, and genetically engineered drugs that enhance or impair endocrine, metabolic, and immune parameters and functions. Moreover, the topics related to effects of food components and/or nutraceuticals on the endocrine-metabolic-immune axis and on microbioma composition are welcome.
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