The evaluation of the inflammatory status and systemic antioxidant-oxidant balance of women with breast cancer during adjuvant chemotherapy.

IF 1.2 Q4 ONCOLOGY
Reports of Practical Oncology and Radiotherapy Pub Date : 2024-10-03 eCollection Date: 2024-01-01 DOI:10.5603/rpor.102130
Joanna Grupińska, Magdalena Budzyń, Jakub Janowski, Bogna Gryszczyńska, Elżbieta Kaja, Jacek J Brzeziński, Ewa Leporowska, Dorota Formanowicz, Witold Kycler
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引用次数: 0

Abstract

Background: Chemotherapy may cause systemic inflammation. Therefore, reliable markers monitoring inflammation during cancer treatment are intensively investigated. In our study, we analyzed the concentration of high-sensitivity C-reactive protein (hs-CRP) and selected oxidative stress markers, such as malondialdehyde (MDA), glutathione peroxidase activity (GPx), and total antioxidant capacity (TAC), in breast cancer women before and during adjuvant chemotherapy.

Materials and methods: The study included 90 women with breast cancer stratified according to clinicopathological and anthropometric features. Blood samples were taken before and after two cycles of adjuvant chemotherapy.

Results: During adjuvant chemotherapy, a significant increase in hs-CRP concentration was noticed in the entire group of patients with breast cancer. After division into appropriate groups, a twofold increase in hs-CRP concentration was particularly observed in patients not expressing steroid hormone receptors and those without metastases in regional lymph nodes. A significant rise in hs-CRP was observed in patients with smaller tumor sizes (2 cm ≤) and with a lower stage of disease [I-IIA according to the tumor-node-metastasis (TNM) classification]. Adjuvant chemotherapy resulted in a significant decrease in GPx activity, especially in patients diagnosed with larger (> 2 cm) and more advanced tumors (IIB-IIIC according to the TNM classification), without metastasis in regional lymph nodes, and without HER-2 expression. A significant decrease in glutathione peroxidase (GPx) activity during adjuvant chemotherapy was also observed in patients with abnormal body mass index (BMI) and body fat content. TAC and MDA values remained unchanged in the entire group of patients and individual subgroups during adjuvant chemotherapy.

Conclusion: Our study showed that adjuvant chemotherapy causes systemic inflammation, manifested by increased hs-CRP and altered markers of oxidative stress in the blood of breast cancer patients. The severity of inflammatory processes during adjuvant chemotherapy may depend on specific characteristics of breast cancer and body composition.

辅助化疗期间乳腺癌患者炎症状态及全身抗氧化平衡的评价。
背景:化疗可引起全身炎症。因此,在癌症治疗期间监测炎症的可靠标志物被深入研究。在我们的研究中,我们分析了乳腺癌妇女在辅助化疗前和化疗期间的高敏c反应蛋白(hs-CRP)浓度和氧化应激标志物,如丙二醛(MDA)、谷胱甘肽过氧化物酶活性(GPx)和总抗氧化能力(TAC)。材料和方法:本研究纳入90例乳腺癌患者,根据临床病理和人体测量学特征进行分层。在两个辅助化疗周期前后分别采集血样。结果:在辅助化疗期间,全组乳腺癌患者hs-CRP浓度均明显升高。在适当分组后,在不表达类固醇激素受体的患者和没有区域淋巴结转移的患者中,hs-CRP浓度增加了两倍。hs-CRP在肿瘤大小较小(2 cm≤)和疾病分期较低的患者中显著升高[根据肿瘤-淋巴结-转移(TNM)分类为I-IIA]。辅助化疗导致GPx活性明显降低,特别是在诊断为较大(> ~ 2cm)和晚期肿瘤(根据TNM分类为IIB-IIIC),无区域淋巴结转移,无HER-2表达的患者。在体重指数(BMI)和体脂含量异常的患者中,辅助化疗期间谷胱甘肽过氧化物酶(GPx)活性也显著降低。在辅助化疗期间,TAC和MDA值在整个患者组和单个亚组中保持不变。结论:我们的研究表明,辅助化疗引起全身炎症,表现为乳腺癌患者血液中hs-CRP升高和氧化应激标志物改变。辅助化疗期间炎症过程的严重程度可能取决于乳腺癌的特定特征和身体成分。
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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来源期刊
CiteScore
2.80
自引率
8.30%
发文量
115
审稿时长
16 weeks
期刊介绍: Reports of Practical Oncology and Radiotherapy is an interdisciplinary bimonthly journal, publishing original contributions in clinical oncology and radiotherapy, as well as in radiotherapy physics, techniques and radiotherapy equipment. Reports of Practical Oncology and Radiotherapy is a journal of the Polish Society of Radiation Oncology, the Czech Society of Radiation Oncology, the Hungarian Society for Radiation Oncology, the Slovenian Society for Radiotherapy and Oncology, the Polish Study Group of Head and Neck Cancer, the Guild of Bulgarian Radiotherapists and the Greater Poland Cancer Centre, affiliated with the Spanish Society of Radiotherapy and Oncology, the Italian Association of Radiotherapy and the Portuguese Society of Radiotherapy - Oncology.
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