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首页> 外文期刊>Journal of Clinical Oncology >Determinants of postchemotherapy nausea and vomiting in patients with cancer. Quality of Life and Symptom Control Committees of the National Cancer Institute of Canada Clinical Trials Group.
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Determinants of postchemotherapy nausea and vomiting in patients with cancer. Quality of Life and Symptom Control Committees of the National Cancer Institute of Canada Clinical Trials Group.

机译:癌症患者化疗后恶心和呕吐的决定因素。加拿大国家癌症研究所临床试验小组的生活质量和症状控制委员会。

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PURPOSE: To assess whether prechemotherapy health-related quality-of-life (HQL) variables are associated with postchemotherapy nausea and vomiting (PCNV), and to determine their relationship to patient and treatment variables. PATIENTS AND METHODS: Eight hundred thirty-two chemotherapy-naive patients scheduled to receive antiemetic regimens containing a 5-hydroxytryptamine (5-HT3) antagonist with or without dexamethasone for moderately or highly emetogenic chemotherapy were enrolled. HQL was measured by the self-report European Organization for Research and Treatment of Cancer (EORTC) Care Quality of Life Questionnaire (QLQ-C30) within 7 days before chemotherapy. Prechemotherapy HQL scores, as well as other patient, disease, and treatment variables were compared in the groups of patients who had PCNV and those who did not have PCNV. All variables were assessed initially in a univariate analysis and then together in a multivariate analysis using step-wise logistic regression. The final model generated by the multivariate analyses was used in a risk factor analysis to predict PCNV. RESULTS: Univariate analyses identified 10 HQL variables and five patient and treatment characteristics that were associated with PCNV. In the multivariate analysis, the variables remaining in the final model included low social functioning, prechemotherapy nausea, female gender, highly emetogenic chemotherapy, and the lack of maintenance antiemetics (5-HT3 antagonists with or without dexamethasone) after chemotherapy. A history of low alcohol use was also associated with PCV, whereas increased fatigue and lower performance status were associated with PCN. In the risk factor analysis, the incidence of PCV increased from 20% in those having no risk factors to 76% in those having any four of the six risk factors. CONCLUSION: Several pretreatment HQL, patient, and treatment characteristics are associated with the occurrence of PCNV. Patients about to receive moderately or highly emetogenic chemotherapy should be screened for these factors and additional measures, such as behavior modification and modification of antiemetic therapy, should be considered in attempts to improve the control of PCNV.
机译:目的:评估化疗前与健康相关的生活质量(HQL)变量是否与化疗后恶心和呕吐(PCNV)相关,并确定它们与患者和治疗变量的关系。患者和方法:招募了322名未接受化疗的未接受化疗的患者,这些患者计划接受包含5-羟色胺(5-HT3)拮抗剂的地塞米松或不使用地塞米松的中度或高度致呕性化疗。 HQL由自我报告的欧洲癌症研究和治疗组织(EORTC)护理生活质量调查表(QLQ-C30)在化疗前7天内进行了测量。在患有PCNV和未患有PCNV的患者组中比较了化疗前HQL得分以及其他患者,疾病和治疗变量。首先在单变量分析中评估所有变量,然后使用逐步逻辑回归在多变量分析中一起评估所有变量。由多变量分析生成的最终模型用于风险因素分析中以预测PCNV。结果:单因素分析确定了与PCNV相关的10个HQL变量以及5个患者和治疗特征。在多变量分析中,最终模型中剩余的变量包括社交功能低下,化疗前恶心,女性,高致呕性化疗以及化疗后缺乏维持性止吐药(5-HT3拮抗剂(含或不含地塞米松))。低度饮酒的历史也与PCV相关,而疲劳度增加和低下的运动状态与PCN相关。在危险因素分析中,PCV的发生率从无危险因素的20%增加到有六个危险因素中的任何四个的76%。结论:若干治疗前HQL,患者和治疗特点与PCNV的发生有关。应筛选将要接受中度或高度致呕性化学疗法的患者这些因素,并应考虑采取其他措施,例如行为改变和止吐疗法改变,以改善对PCNV的控制。

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