转移性乳腺癌患者单一和联合化疗药物的评价

Martanty Aditya, Godeliva Adriani Hendra, Suhul Raos Kumawula Ing Gustyas
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引用次数: 0

摘要

背景:治疗乳腺癌有几种方法,其中之一是使用化疗药物。化疗药物具有抑制细胞周期的活性。这将影响治疗的有效性和化疗药物的副作用。目的:本研究旨在评价单药和联合化疗药物的疗效和副作用。方法:本研究设计采用观察性队列研究,回顾性收集2019年1 - 12月的数据。从医疗记录中获得的患者在玛琅的Panti Nirmala医院被诊断为乳腺癌转移期。在第一和第三周期检测癌胚抗原(CEA)和癌抗原15-3 (CA15-3),并采用Wilcoxon和U-Mann Whitney试验分析化疗药物的有效性。对化疗药物的副作用进行描述性分析。结果:经Wilcoxon检验分析,两组化疗药物CEA、CA15-3含量差异有统计学意义(p0.05)。CA15-3在两组间差异有统计学意义(p<0.05)。两种化疗药物均表现出最常见的副作用,如疼痛、恶心、呕吐和脱发。结论:联合化疗组患者CA15-3水平低于单一化疗组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of single and combination chemotherapy agents in patients with metastatic breast cancer
Background: There are several ways to treat breast cancer, one of which is administering chemotherapy agents. Chemotherapy agents have activity in inhibiting the cell cycle. That will affect the effectiveness of therapy and the side effects of chemotherapy agents. Objective: This study aimed to evaluate single and combination chemotherapy agent therapeutic efficacy and side effects Method: The design of this study used an observational cohort study with retrospective data collection from January to December 2019. Patients obtained from medical records were diagnosed with metastatic stage of breast cancer at Panti Nirmala Hospital, Malang. The effectiveness of the chemotherapy agent was seen from the carcinoembryonic antigen (CEA) and cancer antigen 15-3 (CA15-3), which were carried out in the first and third cycles, then analyzed using the Wilcoxon and U-Mann Whitney tests. Side effects of chemotherapy agents were analyzed descriptively. Results: Analysis of the Wilcoxon test showed differences between the two groups of chemotherapeutic agents in CEA and CA15-3 (p<0.05). U-Mann Whitney test analysis showed no difference after administration of the two groups of chemotherapy agents at CEA (p>0.05). However, there was a difference in CA15-3 (p<0.05). Both chemotherapy agents showed most common side effects such as pain, nausea,  vomiting, and alopecia. Conclusion: Patients who received a combination of chemotherapy agents had lower CA15-3 levels than single chemotherapy agents.
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