调强放疗和PD⁃1抑制剂治疗局部晚期鼻咽癌后甲状腺功能障碍。

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics
Therapeutics and Clinical Risk Management Pub Date : 2025-01-06 eCollection Date: 2025-01-01 DOI:10.2147/TCRM.S489899
Kai Shang, Qianyong He, Xinyu Xu, Xunyan Luo, Chaofen Zhao, Lina Liu, Zhuoling Li, Yuanyuan Li, Feng Jin
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引用次数: 0

摘要

目的:分析调强放疗(IMRT)和PD⁃1抑制剂治疗后晚期鼻咽癌(LA-NPC)患者甲状腺功能障碍的发生率、危险因素及其与治疗疗效和预后的关系。方法:回顾性收集2019年3月1日至2022年5月30日接受IMRT和PD-1抑制剂治疗的85例LA-NPC患者。分析联合治疗后甲状腺功能障碍的发生率。应用Kaplan-Meier法分析甲状腺功能障碍与患者预后的关系。采用Logistic回归分析筛选甲状腺功能障碍的独立危险因素。结果:截至数据截止日期(2024年5月31日),中位随访时间为27.8个月(25.6 ~ 32.0个月)。甲状腺功能障碍的中位发病时间为8.26个月。甲状腺功能障碍发生率为47.06%(40/85),其中以临床甲状腺功能减退为主,发生率为28.24%(24/85),临床甲状腺功能亢进发生率为3.53%(3/85)。1级甲状腺免疫相关不良事件(irAEs)发生率为29.41%(25/85),2级甲状腺irAEs发生率为17.65%(15/85)。与甲状腺功能正常患者相比,甲状腺功能障碍患者的1年和2年总生存期、无进展生存期和远处转移生存期均更长,但差异无统计学意义(p < 0.05)。多因素logistic回归分析显示,预处理乳酸脱氢酶(LDH) (p = 0.079)是LA-NPC放疗联合免疫治疗后甲状腺功能障碍的独立预测因子。结论:本研究发现,在LA-NPC患者行放化疗后,加入免疫治疗可增加甲状腺功能障碍的发生风险,缩短其发病时间。LDH预处理可能是LA-NPC患者甲状腺功能障碍的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thyroid Dysfunction After Intensity-Modulated Radiotherapy and PD⁃1 Inhibitor Treatment for Locally Advanced Nasopharyngeal Carcinoma.

Purpose: Analyze the incidence and risk factors of thyroid dysfunction in patients with advanced nasopharyngeal carcinoma (LA-NPC) after intensity-modulated radiotherapy (IMRT) and PD⁃1 inhibitor treatment and their relationship with treatment efficacy and prognosis.

Methods: Eighty-five LA-NPC patients treated with IMRT and PD-1 inhibitors were retrospectively collected from March 1, 2019, to May 30, 2022. The incidence of thyroid dysfunction after combination therapy was analyzed. The Kaplan-Meier method was used to analyze the relationship between thyroid dysfunction and patient prognosis. Logistic regression analysis was used to screen independent risk factors for thyroid dysfunction.

Results: As of data cutoff (May 31, 2024), the median follow-up time was 27.8 months (range: 25.6 to 32.0 months). The median time of onset of thyroid dysfunction was 8.26 months. The incidence of thyroid dysfunction is 47.06% (40/85), with clinical hypothyroidism being the main cause at an incidence rate of 28.24% (24/85) and clinical hyperthyroidism at an incidence rate of 3.53% (3/85). The incidence of grade 1 thyroid immune-related adverse events (irAEs) was 29.41% (25/85), and the incidence of grade 2 thyroid irAEs was 17.65% (15/85). Patients with thyroid dysfunction had longer overall survival, progression-free survival, and distant metastasis-free survival at both one and two years compared to patients with normal thyroid function, but the difference was not statistically significant (p > 0.05). Multivariate logistic regression analysis showed that pretreatment lactate dehydrogenase (LDH) (p = 0.079) is an independent predictor of thyroid dysfunction after radiotherapy in combination with immunotherapy for LA-NPC.

Conclusion: The study found that the addition of immunotherapy increases the risk and shortens the onset time of thyroid dysfunction in LA-NPC patients treated with chemoradiotherapy. Pretreatment LDH may serve as an independent risk factor for thyroid dysfunction for LA-NPC patients.

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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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