Northwestern University Feinberg School of Medicine, Evanston, IL 60611, USA.
Eur J Cancer. 2012 Feb;48(3):311-23. doi: 10.1016/j.ejca.2011.05.017.
In a double-blind, randomised phase III trial of advanced renal cell carcinoma patients, pazopanib 800mg QD (n=290) versus placebo (n=145) significantly prolonged progression-free survival (hazard ratio (HR)=0.46, 95% confidence interval [CI] 0.34-0.62, p-value<0.0001), without important differences in health-related quality of life (HRQoL). This post-hoc analysis evaluated time to HRQoL deterioration and whether tumour response/stabilisation was associated with HRQoL improvement.
HRQoL was assessed using EORTC QLQ-C30 and EQ-5D. Effect of pazopanib on time to ⩾20% decline from baseline in summary scores was estimated for all patients and by prior treatment. Analyses were conducted for different HRQoL deterioration thresholds. HRQoL changes were stratified by benefit and compared: complete response (CR) or partial response (PR) versus progressive disease (PD); CR/PR versus stable disease (SD), and SD versus PD.
There was a trend for pazopanib patients to be less likely than placebo patients to experience ⩾20% HRQoL deterioration in EORTC-QLQ-C-30 global health status/QOL scale (HR=0.77; 95% CI 0.57-1.03, not significant). Results by prior treatment and different HRQoL deterioration thresholds were similar. Patients with CR/PR and SD experienced significantly less HRQoL deterioration than those with PD (p<0.001, p=0.0024, respectively); mean differences between patients with CR/PR and PD exceeded the pre-determined minimally important difference (MID). Differences between patients with SD and PD did not exceed pre-determined MID. Results were generally consistent across treatment and EQ-5D summary scores.
Results support the favourable benefit-risk profile of pazopanib and suggest patients experiencing tumour response/stabilisation also may have better HRQoL compared to those without this response.
在一项晚期肾细胞癌患者的双盲、随机 III 期试验中,与安慰剂相比,帕唑帕尼 800mg QD(n=290)显著延长了无进展生存期(风险比(HR)=0.46,95%置信区间[CI]0.34-0.62,p 值<0.0001),而健康相关生活质量(HRQoL)没有显著差异。本事后分析评估了 HRQoL 恶化的时间,以及肿瘤反应/稳定是否与 HRQoL 改善相关。
使用 EORTC QLQ-C30 和 EQ-5D 评估 HRQoL。对于所有患者和既往治疗,估计帕唑帕尼对从基线下降 ⩾20%的时间的影响。对不同的 HRQoL 恶化阈值进行了分析。根据获益情况对 HRQoL 变化进行分层并进行比较:完全缓解(CR)或部分缓解(PR)与进展性疾病(PD);CR/PR 与稳定疾病(SD),SD 与 PD。
与安慰剂组相比,帕唑帕尼组患者发生 ⩾20%EORTC-QLQ-C-30 总体健康状况/生活质量量表 HRQoL 恶化的可能性呈下降趋势(HR=0.77;95%CI0.57-1.03,无统计学意义)。既往治疗和不同 HRQoL 恶化阈值的结果相似。CR/PR 和 SD 的患者与 PD 的患者相比,HRQoL 恶化程度显著降低(p<0.001,p=0.0024);CR/PR 与 PD 患者之间的平均差异超过预先确定的最小有意义差异(MID)。SD 与 PD 患者之间的差异未超过预先确定的 MID。结果在整个治疗和 EQ-5D 综合评分中基本一致。
结果支持帕唑帕尼的有利获益风险概况,并表明与无肿瘤反应/稳定的患者相比,经历肿瘤反应/稳定的患者的 HRQoL 可能更好。