Dawson Nancy, Payne Heather, Battersby Clare, Taboada Maria, James Nick
Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
University College Hospital, London, UK.
J Cancer Res Clin Oncol. 2011 Jan;137(1):99-113. doi: 10.1007/s00432-010-0864-1. Epub 2010 Apr 14.
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.
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.
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.
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.
齐考诺肽(ZD4054)是一种特异性内皮素A受体拮抗剂,正处于治疗激素抵抗性前列腺癌(HRPC)的临床开发阶段。在一项针对无症状或症状轻微的转移性HRPC患者的II期试验中,与安慰剂相比,齐考诺肽耐受性良好,在延长总生存期方面有显著信号。作为该试验的一部分,评估了齐考诺肽与安慰剂相比对健康相关生活质量(HRQoL)的影响。
患者被随机分配接受每日一次口服10或15mg齐考诺肽,或匹配的安慰剂。患者被分配到两份问卷中的一份;癌症治疗功能评估-前列腺(FACT-P)问卷或欧洲癌症研究与治疗组织生活质量问卷(EORTC QLQ-C30),并辅以针对前列腺癌的PR25问卷。问卷在基线时以及每4周完成一次,直至疾病进展时停止研究治疗。
在基线时,符合问卷完成要求的人数占意向性治疗人群的>90%(312例患者中的286例)。在可进行评估(即未出现临床进展)的基线完成者中,分别有89%(184例中的164例)和83%(88例中的73例)在12周和24周完成了问卷。两份问卷的HRQoL评分在基线时都很高,并且在整个研究过程中保持较高水平,齐考诺肽组和安慰剂组的评分相似。然而,在EORTC QLQ-C30问卷中观察到了一些地板效应和天花板效应。
在整个齐考诺肽治疗过程中,高基线HRQoL评分得以维持。在III期临床试验项目中,选择FACT-P工具进一步评估齐考诺肽对HRQoL的影响。