Axitinib versus sorafenib in advanced renal cell carcinoma: subanalyses by prior therapy from a randomised phase III trial

被引:82
作者
Escudier, B. [1 ]
Michaelson, M. D. [2 ]
Motzer, R. J. [3 ]
Hutson, T. E. [4 ]
Clark, J. I. [5 ]
Lim, H. Y. [6 ]
Porfiri, E. [7 ]
Zalewski, P. [8 ]
Kannourakis, G. [9 ,10 ]
Staehler, M. [11 ]
Tarazi, J. [12 ]
Rosbrook, B. [12 ]
Cisar, L. [13 ]
Hariharan, S. [13 ]
Kim, S. [12 ]
Rini, B. I. [14 ]
机构
[1] Inst Gustave Roussy, Dept Med Oncol, F-94805 Villejuif, France
[2] Massachusetts Gen Hosp, Dept Med, Ctr Canc, Boston, MA 02114 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[4] Baylor Sammons Texas Oncol Phys Assoc, Sammons Canc Ctr, Dallas, TX 75246 USA
[5] Loyola Univ, Chicago Cardinal Bemardin Canc Ctr, Dept Med, Maywood, IL 60153 USA
[6] Sungkyunkwan Univ, Samsung Med Ctr, Dept Internal Med, Seoul 135710, South Korea
[7] Queen Elizabeth Hosp, Birmingham B15 2WB, W Midlands, England
[8] Durham Reg Canc Ctr, Oshawa, ON L1G 2B9, Canada
[9] Fiona Elsey Canc Res Inst, Ballarat, Vic 3355, Australia
[10] Ballarat Oncol & Haematol Serv, Ballarat, Vic 3355, Australia
[11] Univ Munich, D-80539 Munich, Germany
[12] Pfizer Oncol, San Diego, CA 92121 USA
[13] Pfizer Oncol, New York, NY 10017 USA
[14] Cleveland Clin, Taussig Canc Inst, Dept Solid Tumor Oncol, Cleveland, OH 44195 USA
关键词
TARGETED THERAPY; TUMOR BURDEN; GUIDELINES; SURVIVAL; AXIS;
D O I
10.1038/bjc.2014.244
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: In the AXIS trial, axitinib prolonged progression-free survival (PFS) vs sorafenib in patients with advanced renal cell carcinoma (RCC) previously treated with sunitinib or cytokines. Methods: In post hoc analyses, patients were grouped by objective response to prior therapy (yes vs no), prior therapy duration (< vs >= median), and tumour burden (baseline sum of the longest diameter < vs >= median). PFS and overall survival (OS), and safety by type and duration of prior therapy were evaluated. Results: Response to prior therapy did not influence outcome with second-line axitinib or sorafenib. PFS was significantly longer in axitinib-treated patients who received longer prior cytokine treatment and sorafenib-treated patients with smaller tumour burden following sunitinib. Overall survival with the second-line therapy was longer in patients who received longer duration of prior therapy, although not significant in the sunitinib-to-axitinib sequence subgroup; OS was also longer in patients with smaller tumour burden, but not significant in the cytokine-to-axitinib sequence subgroup. Safety profiles differed modestly by type and duration of prior therapy. Conclusions: AXIS data suggest that longer duration of the first-line therapy generally yields better outcome with the second-line therapy and that lack of response to first-line therapy does not preclude positive clinical outcomes with a second-line vascular endothelial growth factor-targeted agent in patients with advanced RCC.
引用
收藏
页码:2821 / 2828
页数:8
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