阿霉素和环磷酰胺联合化疗治疗浸润性导管乳腺癌的血液毒性和功能影响:临床记录研究

S. Kameo, M. Ramos, R. Lima, B. Amorim, Jéssica dos Santos Costa, Pabliane Matias Lordelo Marinho, N. Sawada, Glebson Moura Silva
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引用次数: 1

摘要

目的:探讨多柔比星与环磷酰胺联合化疗对乳腺浸润性导管癌患者血液学及功能的影响。方法:采用描述性、横断面和定量研究方法,收集2014年2月至2015年2月在某肿瘤科门诊接受乳腺浸润性导管癌化疗的119例女性患者的临床资料。结果:多柔比星和环磷酰胺暴露患者的毒副作用及其发生率分别为血红蛋白血症(26.5%)、白细胞减少症(21.6%)、中性粒细胞减少症(10.8%)、血小板减少症(无)和红细胞压积降低(28.4%),此外还有疲劳(93.1%)、发热(20.6%)、体重增加(35.3%)和体重减轻(22.5%)。在这些变量中,暴露和未暴露的患者之间没有显着差异。与紫杉烷相关的红细胞压积值显著降低(p=0.019),暴露组内不同年龄组的毒性分布不显著。结论:暴露于阿霉素和环磷酰胺与乳腺导管浸润性癌女性血液毒性和功能影响发生率的增加无关,除非与紫杉烷类药物相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hematotoxicity and functional impacts related to chemotherapy with doxorubicin and cyclophosphamide for invasive ductal breast carcinoma: a study in clinical records
Objective: To evaluate the occurrence of hematological and functional toxicities during chemotherapy with doxorubicin and cyclophosphamide in women with breast invasive ductal carcinoma. Methods: This was a descriptive, cross-sectional and quantitative study, involving the data collection in clinical records of 119 women undergoing chemotherapy for breast invasive ductal carcinoma in an oncology outpatient clinic, carried out between February 2014 and February 2015. Results: The investigated toxicities and their respectively occurrences in patients exposed to doxorubicin and cyclophosphamide were hemoglobinemia (26,5%), leukopenia (21,6%), neutropenia (10,8%), thrombocytopenia (none) and reduced hematocrit (28,4%), in addition to fatigue (93,1%), fever (20,6%), gain (35,3%) and weight loss (22,5%). In these variables, there were no significant differences between the exposed and not exposed patients. The association with taxanes showed a significant reduction in hematocrit values (p=0.019) and the toxicities distributed by age group were not significant within the exposed group. Conclusions: Exposure to doxorubicin and cyclophosphamide was not associated with an increase in the occurrence of hematotoxicities and functional impacts in women with breast ductal invasive carcinoma, except when associated with taxane agents.
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