Freemantle Nick, Mollon Patrick, Meyer Tim, Cheng Ann-Lii, El-Khoueiry Anthony B, Kelley Robin K, Baron Ari D, Benzaghou Fawzi, Mangeshkar Milan, Abou-Alfa Ghassan K
University College London, London, UK.
Ipsen Pharma SAS, Boulogne-Billancourt, France.
Eur J Cancer. 2022 Jun;168:91-98. doi: 10.1016/j.ejca.2022.03.021. Epub 2022 Apr 26.
The CELESTIAL trial (NCT01908426) demonstrated overall survival benefit for cabozantinib versus placebo in patients with advanced hepatocellular carcinoma (aHCC) who had received prior sorafenib treatment. This analysis of CELESTIAL compared the impact of cabozantinib versus placebo on health-related quality of life (HRQoL).
Health status was assessed using the EuroQol five-dimension five-level (EQ-5D-5L) questionnaire over the 800-day follow-up period. EQ-5D-5L health states were mapped to health utility scores using reference values for the UK population. Quality-adjusted life years (QALYs) were calculated for each treatment group as the area under the curve for the plot of health utility score over time. The between-treatment group difference in restricted mean QALYs was calculated by generalized linear models and adjusted for baseline differences. A difference of 0.08 in health utility score (or in QALY) was deemed a minimally important difference and to be clinically significant.
At week 5, the difference in mean health utility score between cabozantinib and placebo was -0.097 (95% confidence interval [95% CI]: -0.126, -0.067; p ≤ 0.001). Between-group differences in health utility scores diminished over time and were generally non-significant. The cabozantinib group accrued more QALYs than the placebo group over follow-up. Differences in mean QALYs (cabozantinib minus placebo) were statistically and clinically significant, ranging from +0.092 (95% CI: 0.016, 0.169) to +0.185 (95% CI: 0.126, 0.243) in favour of cabozantinib, depending on the reference value set used.
These HRQoL findings support a positive benefit-risk profile for cabozantinib in previously treated patients with aHCC.
CELESTIAL试验(NCT01908426)表明,对于既往接受过索拉非尼治疗的晚期肝细胞癌(aHCC)患者,卡博替尼对比安慰剂可带来总生存获益。本CELESTIAL试验分析比较了卡博替尼与安慰剂对健康相关生活质量(HRQoL)的影响。
在800天的随访期内,使用欧洲五维健康量表(EQ-5D-5L)问卷评估健康状况。利用英国人群的参考值将EQ-5D-5L健康状态映射为健康效用分数。计算每个治疗组的质量调整生命年(QALY),即健康效用分数随时间变化曲线下的面积。通过广义线性模型计算治疗组间受限平均QALY的差异,并对基线差异进行校正。健康效用分数(或QALY)相差0.08被认为是最小重要差异且具有临床意义。
在第5周时,卡博替尼与安慰剂之间的平均健康效用分数差异为-0.097(95%置信区间[95%CI]:-0.126,-0.067;p≤0.001)。健康效用分数的组间差异随时间减小,且一般无统计学意义。在随访期间,卡博替尼组积累的QALY比安慰剂组更多。平均QALY的差异(卡博替尼减去安慰剂)在统计学和临床上均具有显著意义,根据所使用的参考值设定,有利于卡博替尼的差异范围为+0.092(95%CI:0.016,0.169)至+0.185(95%CI:0.126,0.243)。
这些HRQoL结果支持卡博替尼在既往接受治疗的aHCC患者中具有良好的获益-风险特征。