Second-Line Treatment Outcomes After First-Line Sunitinib Therapy in Metastatic Renal Cell Carcinoma

被引:20
|
作者
Chen, Chi-Chang [1 ]
Hess, Gregory P. [1 ,2 ]
Liu, Zhimei [3 ]
Gesme, Dean H. [4 ]
Agarwala, Sanjiv S. [5 ]
Garay, Carlos C. [3 ]
Hill, Jerrold W. [1 ]
Guo, Amy [3 ]
机构
[1] IMS Hlth, Hlth Econ & Outcomes Res, Plymouth Meeting, PA 19462 USA
[2] Univ Penn, Philadelphia, PA 19104 USA
[3] Novartis Pharmaceut, Oncol US Hlth Econ & Outcomes Res, E Hanover, NJ USA
[4] Minnesota Oncol, Minneapolis, MN USA
[5] Temple Univ, Sch Med Oncol & Hematol, St Lukes Canc Ctr, Bethlehem, PA USA
关键词
Everolimus; Metastatic renal cell carcinoma; Sorafenib; Temsirolimus; Tyrosine kinase inhibitor; TARGETED THERAPIES; INTERFERON-ALPHA; DOUBLE-BLIND;
D O I
10.1016/j.clgc.2012.04.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study evaluated the treatment outcomes associated with common second-line targeted therapies given after first-line sunitinib to help inform decision making in this setting. The sample comprised patients with metastatic renal cell carcinoma (n = 257) who were receiving second-line everolimus, sorafenib, or temsirolimus. The results appeared to suggest that the risk of second-line treatment failure after first-line sunitinib was significantly higher with temsirolimus and sorafenib compared with everolimus. This study was conducted to evaluate the treatment outcomes associated with common second-line targeted therapies given after first-line sunitinib for metastatic renal cell carcinoma (mRCC). The sample comprised patients with mRCC (n = 257) who were receiving second-line everolimus, sorafenib, or temsirolimus between April 1, 2008, and February 29, 2011, after first-line sunitinib treatment. The patients were followed-up from the start of second-line treatment until treatment failure (defined as advancement to a third-line therapy or to mortality) or the last observation in the medical and pharmacy databases. Treatment failure was observed in 38.5% (n = 99) of cases: 20.2% of patients (n = 52) advanced a line of treatment; and 18.3% of patients (n = 47) died. Kaplan-Meier analysis indicated a statistical difference in time to treatment failure among the 3 second-line targeted therapies (log-rank test, P = .045). The estimated 1-year cumulative probabilities of treatment failure were 49.9% for everolimus, 68.4% for sorafenib, and 71.4% for temsirolimus. In a multivariate Cox proportional hazards model, a higher adjusted risk of treatment failure vs. everolimus was observed for both temsirolimus (hazard ratio [HR] 2.05 [95% CI, 1.26-3.35]; P = .004) and sorafenib (HR 1.77 [95% CI, 1.02-3.07]; P = .043). The results of this real-world data analysis suggest that the risk of second-line treatment failure after first-line sunitinib was significantly higher with temsirolimus and sorafenib compared with everolimus.
引用
收藏
页码:256 / 261
页数:6
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