妇科肿瘤患者血清锌水平与紫杉醇/卡铂联合治疗诱导周围神经病变的关系

Fujita Medical Journal Pub Date : 2025-02-01 Epub Date: 2024-10-31 DOI:10.20407/fmj.2024-013
Yutaka Torii, Kana Naito, Junichi Takagi, Akira Yasue, Kazuhiko Tsukada, Takuma Fujii, Haruki Nishizawa
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引用次数: 0

摘要

目的:化疗引起的周围神经病变(CIPN)是紫杉醇/卡铂(TC)联合治疗中常见的不良事件,可引起肢体疼痛并显著降低患者的生活质量。由于锌已被报道与神经性疼痛有关,我们研究了TC治疗引起的CIPN与血清锌水平之间的关系。方法:对13例妇科肿瘤患者进行TC治疗前后血清锌水平测定。根据不良事件通用术语标准v5.0将CIPN分为严重等级。采用Pearson相关系数对TC治疗前血清锌水平(PreZn)、TC治疗期间最低血清锌水平(MinZn)、MinZn/PreZn比值、TC治疗周期数、CIPN最大分级(MaxG)之间的关系进行回顾性分析。此外,还分析了影响MaxG的临床因素,以及TC治疗各周期血清锌水平和CIPN分级的波动情况。结果:MinZn/PreZn比值与MaxG呈负相关(r=-0.557, p=0.048)。影响CIPN的临床因素尚不清楚,血清锌水平下降和CIPN加重在第三周期后趋于稳定。结论:如果TC治疗期间血清锌水平的下降幅度小于治疗前,则可能暗示存在抑制CIPN加重的因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Examination of the relationship between serum zinc levels and peripheral neuropathy induced by paclitaxel/carboplatin combination therapy in gynecological cancer patients.

Objectives: Chemotherapy-induced peripheral neuropathy (CIPN), a frequently occurring adverse event associated with paclitaxel/carboplatin (TC) combination therapy, causes limb pain and markedly reduces the patient's quality of life. Since zinc has been reported to be associated with neuropathic pain, we investigated the relationship between CIPN due to TC therapy and serum zinc levels.

Methods: The study included 13 patients with gynecological cancer whose serum zinc levels were measured before and during TC therapy. CIPN was classified into severity grades based on the Common Terminology Criteria for Adverse Events v5.0. A retrospective analysis was conducted on the relationship between the serum zinc level before TC therapy (PreZn), the minimum serum zinc level measured during TC therapy (MinZn), the MinZn/PreZn ratio, the number of TC treatment cycles, and the maximum grade of CIPN (MaxG) using Pearson's correlation coefficient. Moreover, an analysis was also conducted on clinical factors influencing MaxG, as well as fluctuations in serum zinc levels and CIPN grades for each cycle of TC therapy.

Results: A negative correlation was observed between the MinZn/PreZn ratio and MaxG (r=-0.557, p=0.048). The clinical factors influencing CIPN remained unclear, and the decrease in serum zinc levels and the aggravation of CIPN plateaued after the third cycle.

Conclusions: If a decrease in serum zinc levels during TC therapy is smaller than before therapy, it may imply the existence of a causal relationship that suppresses the aggravation of CIPN.

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