Prognostic factors for survival following initiation of second-line treatment with everolimus for metastatic renal cell carcinoma: evidence from a nationwide sample of clinical practice in the United States

被引:6
作者
Wong, Michael K. [1 ]
Jonasch, Eric [2 ]
Pal, Sumanta K. [3 ]
Signorovitch, James E. [4 ]
Lin, Peggy L. [4 ]
Wang, Xufang [5 ]
Liu, Zhimei [5 ]
Culver, Ken [5 ]
Scott, Jeffrey A. [6 ]
George, Daniel J. [7 ]
Vogelzang, Nicholas J. [8 ]
机构
[1] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] City Hope Comprehens Canc Ctr, Duarte, CA USA
[4] Anal Grp Inc, Boston, MA USA
[5] Novartis Pharmaceut, E Hanover, NJ USA
[6] Cardinal Hlth, Grand Prairie, TX USA
[7] Duke Canc Inst, GU Oncol, Durham, NC USA
[8] Comprehens Canc Ctr Nevada, US Oncol Res, Las Vegas, NV USA
关键词
everolimus; metastatic renal cell carcinoma; overall survival; prognostic; second-line; targeted therapy; tyrosine kinase inhibitor; TYROSINE KINASE INHIBITORS; TARGETED THERAPY; MAMMALIAN TARGET; PROGRESSION-FREE; CANCER; MODEL; VALIDATION; IMMUNOTHERAPY; EXPERIENCE; SUNITINIB;
D O I
10.1517/14656566.2015.1020298
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Comparing prognostic factors for overall survival (OS) in community-practice metastatic renal cell carcinoma (mRCC) patients receiving second-line everolimus with those previously reported in clinical trials. Research design and methods: Two separate chart sets (2009 - 2012) were used to develop and validate a prognostic model for patients initiating second-line everolimus after first-line tyrosine kinase inhibitor (TKI). Main outcome measures: Prognostic factors for OS have been identified and validated in separate samples. Results: One-year OS probabilities in the study (n = 220) and validation (n = 97) samples were 68 and 67%; median OS was 19 and 23 months - higher than the 1-year OS of 60% and median OS of 14.8 months of RECORD-1. Karnofsky performance score < 80%, duration of mRCC < 1 year, progression on firstline TKI, liver metastasis and clear cell histology were significant prognostic factors for shorter survival. One-year OS estimates were 84% for validation sample patients with 0 - 2 risk factors, 63% for 3 risk factors and 22% for 4 - 5 risk factors (log-rank p < 0.001). Conclusion: Real-world prognostic factors for OS following second-line everolimus for mRCC were largely consistent with those previously identified in trial data; however, OS was longer in the practice setting than in clinical trials and was not associated with type of first-line TKI.
引用
收藏
页码:805 / 819
页数:15
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