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舒尼替尼治疗转移性肾细胞癌患者的真实世界经验:根据风险评分的临床结果

Real-world Experience With Sunitinib Treatment in Patients With Metastatic Renal Cell Carcinoma: Clinical Outcome According to Risk Score.

作者信息

Schmidinger Manuela, Porta Camillo, Oudard Stephane, Denechere Gwenael, Brault Yves, Serfass Lucile, Costa Nuno, Larkin James

机构信息

Clinical Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Department of Internal Medicine, University of Pavia and I.R.C.C.S. Istituti Clinici Scientifici Maugeri, Pavia, Italy.

出版信息

Clin Genitourin Cancer. 2020 Oct;18(5):e588-e597. doi: 10.1016/j.clgc.2020.02.013. Epub 2020 Mar 6.

Abstract

BACKGROUND

ADONIS is an ongoing observational study in 9 European countries, designed to evaluate treatment patterns/outcomes in patients with metastatic renal cell carcinoma (mRCC) treated with first-line sunitinib and/or second-line axitinib post sunitinib. We present an evaluation of sunitinib efficacy by risk group, in the real-world setting examined in ADONIS.

PATIENTS AND METHODS

Patients were enrolled at the start of first-line sunitinib treatment or second-line axitinib post sunitinib treatment. Evaluation of sunitinib efficacy was assessed by International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) and Memorial Sloan Kettering Cancer Center risk criteria.

RESULTS

For all patients in this analysis (N = 467), the median progression-free survival was 23.8 months (95% confidence interval [CI], 16.5-28.5 months), 11.8 months (95% CI, 8.1-17.4 months), and 4.6 months (95% CI, 2.5-7.7 months) for IMDC favorable-, intermediate-, and poor-risk groups, respectively. The median overall survival was 97.1 months (95% CI, 46.3 months-not evaluable [NE]), 33.5 months (95% CI, 20.5-46.6 months), and 10.0 months (95% CI, 4.5-19.8 months) for the respective risk groups. Data on individual risk factors were available for a subgroup of patients, allowing analysis by intermediate risk by 1 versus 2 risk factors. When including this subgroup (n = 120), the median overall survival for IMDC favorable-, intermediate-1, and intermediate-2 risk factors was 21.6 months (95% CI, 16.3 months-NE), 20.5 months (15.5 months-NE), and 15.1 months (4.1 months-NE), respectively.

CONCLUSIONS

For patients overall and by risk-group stratification, survival estimates were aligned with previously published data. In patients with intermediate-1 risk, overall survival was very similar to patients with favorable risk. However, further exploration of outcome data from different sources is needed to confirm these observations.

摘要

背景

ADONIS是一项正在9个欧洲国家开展的观察性研究,旨在评估一线使用舒尼替尼和/或舒尼替尼治疗后二线使用阿昔替尼治疗的转移性肾细胞癌(mRCC)患者的治疗模式/结局。我们在ADONIS所研究的真实世界环境中,按风险组对舒尼替尼的疗效进行了评估。

患者与方法

患者在一线舒尼替尼治疗开始时或舒尼替尼治疗后二线阿昔替尼治疗开始时入组。舒尼替尼疗效的评估采用国际转移性肾细胞癌数据库联盟(IMDC)和纪念斯隆凯特琳癌症中心的风险标准。

结果

在本次分析的所有患者(N = 467)中,IMDC低危、中危和高危组的无进展生存期(PFS)中位数分别为23.8个月(95%置信区间[CI],16.5 - 28.5个月)、11.8个月(95% CI,8.1 - 17.4个月)和4.6个月(95% CI,2.5 - 7.7个月)。各风险组的总生存期(OS)中位数分别为97.1个月(95% CI,46.3个月 - 不可评估[NE])、33.5个月(95% CI,20.5 - 46.6个月)和10.0个月(95% CI,4.5 - 19.8个月)。部分患者亚组可获得个体风险因素数据,从而能够按1个与2个风险因素的中危情况进行分析。纳入该亚组(n = 120)后,IMDC低危、中危1和中危2风险因素患者的总生存期中位数分别为21.6个月(95% CI,16.3个月 - NE)、20.5个月(15.5个月 - NE)和15.1个月(4.1个月 - NE)。

结论

对于总体患者以及按风险组分层的患者,生存估计与先前发表的数据一致。中危1风险患者的总生存期与低危患者非常相似。然而,需要进一步探索来自不同来源的结局数据以证实这些观察结果。

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