Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, 633 N. St, Clair - 19th Floor Chicago, IL 60611, USA.
Br J Cancer. 2013 Apr 30;108(8):1571-8. doi: 10.1038/bjc.2013.145. Epub 2013 Apr 11.
BACKGROUND: Axitinib demonstrated greater progression-free survival vs sorafenib in a phase III study of previously treated patients with metastatic renal cell carcinoma. Here, we report patient-reported kidney-specific symptoms and health status, measured by the Functional Assessment of Cancer Therapy (FACT) Kidney Cancer Symptom Index (FKSI) and the European Quality of Life self-report questionnaire (EQ-5D). METHODS: In all, 723 patients received axitinib (starting dose 5 mg twice daily (b.i.d.)) or sorafenib (400 mg b.i.d.). The FKSI-15, including the disease-related symptoms (FKSI-DRS) subscale, was administered on day 1 before dosing, every 4 weeks and at end of treatment (EOT)/withdrawal. Statistical methods included a mixed-effects repeated-measures model. RESULTS: At baseline, patients in both arms had relatively high mean FSKI-15 and FKSI-DRS scores, comparable to the general US population. Subsequent on-treatment overall mean scores were similar between axitinib and sorafenib, and there was no substantial decline during treatment. Scores substantially worsened at EOT, mainly due to disease progression. CONCLUSION: Patient-reported outcomes were comparable for second-line axitinib and sorafenib and were maintained at relatively high levels while on treatment, but worsened at EOT. As duration of treatment was longer with axitinib than sorafenib, time to worsening of symptoms can be delayed longer with axitinib.
背景:在一项转移性肾细胞癌既往治疗患者的 III 期研究中,阿昔替尼对比索拉非尼显示出了更长的无进展生存期。在此,我们报告了患者报告的肾脏特异性症状和健康状况,采用癌症治疗功能评估(FACT)肾脏癌症症状指数(FKSI)和欧洲生活质量自我报告问卷(EQ-5D)进行测量。
方法:总共 723 例患者接受了阿昔替尼(起始剂量为 5 mg,每日两次)或索拉非尼(400 mg,每日两次)治疗。在给药前的第 1 天、每 4 周以及治疗结束(EOT)/停药时,均进行 FKSI-15 评估,包括疾病相关症状(FKSI-DRS)子量表。统计方法包括混合效应重复测量模型。
结果:在基线时,两组患者的 FSKI-15 和 FKSI-DRS 评分均较高,与一般美国人群相当。随后的治疗期间总体平均评分在阿昔替尼和索拉非尼之间相似,且治疗期间没有明显下降。在 EOT 时评分显著恶化,主要归因于疾病进展。
结论:二线阿昔替尼和索拉非尼的患者报告结局相当,且在治疗期间保持在较高水平,但在 EOT 时恶化。由于阿昔替尼的治疗持续时间长于索拉非尼,因此阿昔替尼可以延迟症状恶化的时间。
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