唾液皮质醇取样反映头颈癌放化疗患者痛苦的可行性和价值:一项概念验证研究

Karishma Chhabria, Mark Bonnen, Joshua Asper, Giselle D Carnaby
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摘要

背景:接受化疗/放疗的头颈癌(HNC)患者通常会经历与治疗相关的恐惧和身体副作用(如口干、吞咽困难和口干)相关的严重和持续的痛苦。皮质醇是一种压力敏感激素,可以很容易地在唾液中测量,以反映对这种压力源的生物行为反应。不幸的是,由于担心与放化疗(C/RT)相关的口干症,它尚未在这一人群中使用。方法:在一项概念验证研究中,我们探讨了收集唾液皮质醇作为HNC患者恐惧和痛苦标志物的可行性。10名接受C/RT治疗的HNC受试者在治疗前、治疗后3周和治疗后1个月三个时间点连续3天提供唾液样本,并同时完成抑郁、焦虑和吞咽相关恐惧测量。结果:唾液皮质醇采集依从性在80-60%之间。它没有受到口干症的影响。62%的受试者在预处理时表现出皮质醇的昼夜模式失调,50%的受试者在3周或更长时间内持续出现平坦的异常斜坡。结论:我们的研究支持了HNC患者在整个治疗过程中唾液皮质醇测量的可行性和实用性。在这一人群中,每日皮质醇测量可能是检测和监测C/RT期间治疗窘迫的有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Feasibility and value of salivary cortisol sampling to reflect distress in head and neck cancer patients undergoing chemoradiation: A proof-of-concept study.

Background: Head and neck cancer (HNC) patients undergoing chemo/radiation commonly experience severe and persistent distress associated with treatment related fear and physical side effects such as xerostomia, dysphagia, and dryness of mouth. Cortisol, a stress sensitive hormone, can be easily measured in saliva to reflect biobehavioral responses to such stressors. Unfortunately, it has not been used in this population due to concerns associated with chemoradiation (C/RT) related xerostomia.

Methods: In a proof-of-concept study, we explored the feasibility of collecting salivary cortisol as a marker of fear and distress in HNC patients. Ten HNC subjects undergoing C/RT provided saliva samples for 3 consecutive days across three timepoints (pre-treatment, 3-weeks and 1-month post-treatment) and completed concurrent depression, anxiety and swallowing related fear measures.

Results: Salivary cortisol collection adherence was between 80-60%. It was not impacted by xerostomia. Diurnal cortisol pattern demonstrated dysregulation at pretreatment in 62%, and flattened aberrant slopes continued at 3-weeks and beyond in 50% of subjects.

Conclusions: Our study supports the feasibility and utility of salivary cortisol measurement in HNC patients across the treatment trajectory. Diurnal cortisol measures may be a valuable tool to detect and monitor treatment distress during C/RT in this population.

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