首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Health-related quality of life in pain-free or mildly symptomatic patients with metastatic hormone-resistant prostate cancer following treatment with the specific endothelin A receptor antagonist zibotentan (ZD4054)
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Health-related quality of life in pain-free or mildly symptomatic patients with metastatic hormone-resistant prostate cancer following treatment with the specific endothelin A receptor antagonist zibotentan (ZD4054)

机译:使用特定的内皮素A受体拮抗剂Zibotentan(ZD4054)治疗的无痛或轻度症状的转移性激素抵抗性前列腺癌患者的健康相关生活质量

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Purpose Zibotentan (ZD4054) is a specific endothelin A receptor antagonist in clinical development for the treatment of hormone-resistant prostate cancer (HRPC). In a Phase II trial in patients with pain-free or mildly symptomatic metastatic HRPC, zibotentan was well tolerated with a promising signal for prolonged overall survival compared with placebo. As part of this trial, the impact of zibotentan compared with placebo on health-related quality of life (HRQoL) was assessed. Methods Patients were randomized to receive once-daily oral zibotentan 10 or 15 mg, or matching placebo. Patients were allocated to one of two questionnaires; the Functional Assessment of Cancer Therapy-Prostate (FACT-P) or the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30), supplemented by PR25, specific for prostate cancer. Questionnaires were completed at baseline and every 4 weeks until disease progression when study treatment was discontinued.Results Compliance with questionnaire completion was >90% (286 of 312 patients) of the intention-to-treat population at baseline. Of baseline completers who were available for assessment (i.e., had not clinically progressed), 89% (164 of 184) and 83% (73 of 88) completed questionnaires at 12 and 24 weeks, respectively. HRQoL scores from both questionnaires were high at baseline and remained high throughout the study, with scores being similar in the zibotentan and placebo groups. However, some floor and ceiling effects were seen in the EORTC QLQ-C30 questionnaire. Conclusions High-baseline HRQoL scores were maintained throughout treatment with zibotentan. The FACT-P instrument was selected to further assess the impact of zibotentan on HRQoL in the Phase III clinical trial program.
机译:目的Zibotentan(ZD4054)是在临床开发中用于治疗激素抵抗性前列腺癌(HRPC)的特异性内皮素A受体拮抗剂。在一项针对无痛或轻度有症状转移性HRPC的患者的II期试验中,与安慰剂相比,zibotentan具有良好的耐受性,并具有可延长总体生存期的有希望的信号。作为该试验的一部分,评估了与安慰剂相比,zibotentan对健康相关生活质量(HRQoL)的影响。方法将患者随机接受每日一次口服Zibotentan 10或15 mg或匹配的安慰剂。患者被分配到两个调查表之一。前列腺癌的功能评估(FACT-P)或欧洲癌症生活质量研究和治疗组织调查表(EORTC QLQ-C30),并辅以PR25,专门针对前列腺癌。问卷调查在基线时完成,每4周进行一次,直到研究治疗中断时疾病进展为止。结果问卷调查完成率是基线时意向治疗人群的90%(312名患者中的286名)。可供评估(即尚未临床进展)的基线完成者中,分别有89%(184人中的164人)和83%(88人中的73人)在12周和24周时完成了问卷调查。两种问卷的HRQoL得分在基线时都很高,在整个研究中仍然很高,在zibotentan和安慰剂组中得分相似。但是,在EORTC QLQ-C30调查表中看到了一些地板和天花板的影响。结论zibotentan治疗期间维持高基线HRQoL评分。选择FACT-P仪器以进一步评估zibotentan对III期临床试验计划中HRQoL的影响。

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