Robert H Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL 60611, USA.
Br J Cancer. 2010 Feb 16;102(4):658-64. doi: 10.1038/sj.bjc.6605552. Epub 2010 Jan 26.
In a randomised phase III trial, sunitinib significantly improved efficacy over interferon-alpha (IFN-alpha) as first-line therapy for metastatic renal cell carcinoma (mRCC). We report the final health-related quality of life (HRQoL) results.
Patients (n=750) received oral sunitinib 50 mg per day in 6-week cycles (4 weeks on, 2 weeks off treatment) or subcutaneous IFN-alpha 9 million units three times weekly. Health-related quality of life was assessed with nine end points: the Functional Assessment of Cancer Therapy-General and its four subscales, FACT-Kidney Symptom Index (FKSI-15) and its Disease-Related Symptoms subscale (FKSI-DRS), and EQ-5D questionnaire's EQ-5D Index and visual analogue scale. Data were analysed using mixed-effects model (MM), supplemented with pattern-mixture models (PMM), for the total sample and the US and European Union (EU) subgroups.
Patients receiving sunitinib reported better scores in the primary end point, FKSI-DRS, across all patient populations (P<0.05), and in nine, five, and six end points in the total sample, in the US and EU groups respectively (P<0.05). There were no significant differences between the US and EU groups for all end points with the exception of the FKSI item 'I am bothered by side effects of treatment' (P=0.02). In general, MM and PMM results were similar.
Patients treated with sunitinib in this study had improved HRQoL, compared with patients treated with IFN-alpha. Treatment differences within the US cohort did not differ from those within the EU cohort.
在一项随机 III 期试验中,舒尼替尼作为转移性肾细胞癌(mRCC)的一线治疗药物,其疗效明显优于干扰素-α(IFN-α)。我们报告了最终的健康相关生活质量(HRQoL)结果。
患者(n=750)接受舒尼替尼 50 mg 口服,每日一次,6 周为一个周期(4 周治疗,2 周停药)或皮下 IFN-α 900 万单位,每周 3 次。使用 9 个终点评估健康相关生活质量:癌症治疗功能评估-一般量表及其 4 个亚量表、FACT-肾脏症状指数(FKSI-15)及其疾病相关症状亚量表(FKSI-DRS)、EQ-5D 问卷的 EQ-5D 指数和视觉模拟量表。使用混合效应模型(MM)分析数据,对总样本和美国及欧盟(EU)亚组补充模式混合模型(PMM)。
接受舒尼替尼治疗的患者在所有患者人群中报告了更好的 FKSI-DRS 主要终点评分(P<0.05),并且在总样本、美国和欧盟亚组中分别有 9 个、5 个和 6 个终点的评分更好(P<0.05)。除了 FKSI 项目“我被治疗的副作用所困扰”(P=0.02)外,美国和欧盟亚组的所有终点之间均无显著差异。一般而言,MM 和 PMM 结果相似。
与接受 IFN-α治疗的患者相比,接受舒尼替尼治疗的患者具有更好的 HRQoL。美国队列内的治疗差异与欧盟队列内的差异没有不同。