Devlin Nancy, Herdman Michael, Pavesi Marco, Phung De, Naidoo Shevani, Beer Tomasz M, Tombal Bertrand, Loriot Yohann, Ivanescu Cristina, Parli Teresa, Balk Mark, Holmstrom Stefan
Office of Health Economics, Southside, 7th Floor, 105 Victoria Street, London, SW1E 6QT, UK.
European Association for the Study of the Liver-Chronic Liver Failure (EASL-CLIF) Consortium, C/Mallorca 183, 08036, Barcelona, Spain.
Health Qual Life Outcomes. 2017 Jun 23;15(1):130. doi: 10.1186/s12955-017-0704-y.
The effect of enzalutamide on health-related quality of life (HRQoL) in the PREVAIL trial in chemotherapy-naïve men with metastatic castration-resistant prostate cancer was analyzed using the generic EQ-5D instrument.
Patients received oral enzalutamide 160 mg/day (n = 872) or placebo (n = 845). EQ-5D index and EQ-5D visual analogue scale (EQ-5D VAS) scores were evaluated at baseline, week 13, and every 12 weeks until week 61 due to sample size reduction thereafter. Changes on individual dimensions were assessed, and Paretian Classification of Health Change (PCHC) and time-to-event analyses were conducted.
With enzalutamide, EQ-5D index and EQ-5D VAS scores declined more slowly versus placebo and time to diverge from full health was prolonged. Average decline in EQ-5D index (-0.042 vs. -0.070; P < .0001) and EQ-5D VAS (-1.3 vs. -4.4; P < .0001) was significantly smaller with enzalutamide. There were significant (P < .05) between-group differences favoring enzalutamide in Pain/Discomfort to week 37, Anxiety/Depression at week 13, and Usual Activities at week 25, but no significant differences for Mobility and Self-care. The PCHC analysis showed more enzalutamide patients reporting improvement than placebo patients at weeks 13, 25, and 49 (all P < .05) and week 37 (P = .0512). Enzalutamide was superior (P ≤ .0003) to placebo for time to diverge from full health and time to first deterioration on Pain/Discomfort and Anxiety/Depression dimensions.
This in-depth post hoc analysis showed that enzalutamide delayed HRQoL deterioration and had beneficial effects on several HRQoL domains, including Pain/Discomfort and the proportion of patients in full health, compared with placebo, and may help to support future analyses of this type.
NCT01212991.
在一项针对未接受过化疗的转移性去势抵抗性前列腺癌男性患者的PREVAIL试验中,使用通用的EQ-5D工具分析了恩杂鲁胺对健康相关生活质量(HRQoL)的影响。
患者接受口服恩杂鲁胺160毫克/天(n = 872)或安慰剂(n = 845)。在基线、第13周以及之后每12周直至第61周(因样本量减少)评估EQ-5D指数和EQ-5D视觉模拟量表(EQ-5D VAS)得分。评估各个维度的变化,并进行健康变化的帕累托分类(PCHC)和事件发生时间分析。
与安慰剂相比,使用恩杂鲁胺时EQ-5D指数和EQ-5D VAS得分下降更缓慢,且偏离完全健康状态所需的时间延长。恩杂鲁胺组EQ-5D指数(-0.042对-0.070;P <.0001)和EQ-5D VAS(-1.3对-4.4;P <.0001)的平均下降幅度显著更小。在第37周的疼痛/不适、第13周的焦虑/抑郁以及第25周的日常活动方面,存在显著的组间差异(P <.05),支持恩杂鲁胺,但在活动能力和自我护理方面无显著差异。PCHC分析显示,在第13周、第25周和第49周(均P <.05)以及第37周(P =.0512),报告病情改善的恩杂鲁胺患者比安慰剂患者更多。在偏离完全健康状态所需时间以及疼痛/不适和焦虑/抑郁维度首次恶化的时间方面,恩杂鲁胺优于安慰剂(P≤.0003)。
这项深入的事后分析表明,与安慰剂相比,恩杂鲁胺延缓了HRQoL的恶化,并对多个HRQoL领域产生有益影响,包括疼痛/不适和完全健康患者的比例,可能有助于支持未来此类分析。
NCT01212991。