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Cited 84 time in webofscience Cited 85 time in scopus
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Axitinib versus sorafenib in advanced renal cell carcinoma: subanalyses by prior therapy from a randomised phase III trialopen access

Authors
Escudier, B[Escudier, B.]Michaelson, MD[Michaelson, M. D.]Motzer, RJ[Motzer, R. J.]Hutson, TE[Hutson, T. E.]Clark, JI[Clark, J. I.]Lim, HY[Lim, H. Y.]Porfiri, E[Porfiri, E.]Zalewski, P[Zalewski, P.]Kannourakis, G[Kannourakis, G.]Staehler, M[Staehler, M.]Tarazi, J[Tarazi, J.]Rosbrook, B[Rosbrook, B.]Cisar, L[Cisar, L.]Hariharan, S[Hariharan, S.]Kim, S[Kim, S.]Rini, BI[Rini, B. I.]
Issue Date
10-Jun-2014
Publisher
NATURE PUBLISHING GROUP
Keywords
Axitinib; Prior therapy; Renal cell carcinoma; Sorafenib; VEGF receptor inhibitor
Citation
BRITISH JOURNAL OF CANCER, v.110, no.12, pp.2821 - 2828
Indexed
SCIE
SCOPUS
Journal Title
BRITISH JOURNAL OF CANCER
Volume
110
Number
12
Start Page
2821
End Page
2828
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/52640
DOI
10.1038/bjc.2014.244
ISSN
0007-0920
Abstract
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.
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