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阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析
BACKGROUND AND OBJECTIVE: Chemotherapy is the most important method for cancer treatment. However, chemotherapy induced nausea and vomiting (CINV) has a profound effect on patients. In recent years, there have been new antiemetic drugs, such as aprepitant. We review the curative effect of aprepitant...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189028/ https://www.ncbi.nlm.nih.gov/pubmed/30309434 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.10.12 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Chemotherapy is the most important method for cancer treatment. However, chemotherapy induced nausea and vomiting (CINV) has a profound effect on patients. In recent years, there have been new antiemetic drugs, such as aprepitant. We review the curative effect of aprepitant with tropisetron and dexamethasone for prevention of nausea and vomiting in patients receiving Cisplatin chemotherapy. METHODS: Observation is divided into three stages. Whole study phase (0-120 h after chemotherapy administration), acute phases (0-24 h), and delayed phase (24 h-120 h). The primary endpoints were complete response (CR) and complete prevention (CP) during the three different study phase. RESULTS: In the whole study phase, 86.02% of patients achieved CR; in acute phases and delayed phases were 89.25%, 87.1%, respectively. CP were 46.22%, 83.87%, 45.16%, respectively. Anti-CINV effect was significantly associated with age distribution (P=0.008). CONCLUSION: Aprepitant with tropisetron and dexamethasone prevented effectively CNIV for patients receiving Cisplatin chemotherapy. This combination could improve the quality of life and the compliance of patient with chemotherapy. |
format | Online Article Text |
id | pubmed-6189028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-61890282018-11-02 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Chemotherapy is the most important method for cancer treatment. However, chemotherapy induced nausea and vomiting (CINV) has a profound effect on patients. In recent years, there have been new antiemetic drugs, such as aprepitant. We review the curative effect of aprepitant with tropisetron and dexamethasone for prevention of nausea and vomiting in patients receiving Cisplatin chemotherapy. METHODS: Observation is divided into three stages. Whole study phase (0-120 h after chemotherapy administration), acute phases (0-24 h), and delayed phase (24 h-120 h). The primary endpoints were complete response (CR) and complete prevention (CP) during the three different study phase. RESULTS: In the whole study phase, 86.02% of patients achieved CR; in acute phases and delayed phases were 89.25%, 87.1%, respectively. CP were 46.22%, 83.87%, 45.16%, respectively. Anti-CINV effect was significantly associated with age distribution (P=0.008). CONCLUSION: Aprepitant with tropisetron and dexamethasone prevented effectively CNIV for patients receiving Cisplatin chemotherapy. This combination could improve the quality of life and the compliance of patient with chemotherapy. 中国肺癌杂志编辑部 2018-10-20 /pmc/articles/PMC6189028/ /pubmed/30309434 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.10.12 Text en 版权所有©《中国肺癌杂志》编辑部2018 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | 临床研究 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title_full | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title_fullStr | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title_full_unstemmed | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title_short | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
title_sort | 阿瑞匹坦预防化疗诱导恶心呕吐的疗效分析 |
topic | 临床研究 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189028/ https://www.ncbi.nlm.nih.gov/pubmed/30309434 http://dx.doi.org/10.3779/j.issn.1009-3419.2018.10.12 |
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