Q-TWiST analysis to estimate overall benefit for patients with metastatic renal cell carcinoma treated in a phase III trial of sunitinib vs interferon-α

被引:28
作者
Patil, S. [1 ]
Figlin, R. A. [2 ]
Hutson, T. E. [3 ]
Michaelson, M. D. [4 ]
Negrier, S. [5 ]
Kim, S. T. [6 ]
Huang, X. [6 ]
Motzer, R. J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[2] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Los Angeles, CA 90048 USA
[3] Baylor Sammons Canc Ctr, Dallas, TX 75246 USA
[4] Massachusetts Gen Hosp, Boston, MA 02114 USA
[5] Ctr Leon Berard, F-69008 Lyon, France
[6] Pfizer La Jolla, San Diego, CA 92121 USA
关键词
sunitinib; metastatic renal cell carcinoma; TWiST; Q-TWiST; progression-free survival; quality-adjusted survival; QUALITY-OF-LIFE; ADJUVANT THERAPY; SURVIVAL;
D O I
10.1038/bjc.2012.149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In a randomised phase III trial of treatment-naive patients with metastatic renal cell carcinoma, sunitinib showed significant improvement in progression-free survival (PFS) compared with interferon (IFN)-alpha. We assessed between-treatment differences in overall benefit using a quality-adjusted Time Without Symptoms of disease progression or Toxicity of treatment (TWiST; Gelber and Goldhirsch, 1986) analysis. METHODS: In this analysis, in which only grade 3/4 treatment-related toxicities were included, overall survival was partitioned into three health states: toxicity (time with toxicity after randomisation and before progression), time without symptoms of disease progression or toxicity, and time from progression until death. Between-treatment differences in the mean duration of each state were calculated. A threshold utility analysis was used to assess quality-adjusted TWiST (Q-TWiST) outcomes. RESULTS: Q-TWiST scores showed that quality-adjusted survival time was greater with sunitinib than with IFN-alpha, even though certain grade 3/4 toxicities occurred more frequently with sunitinib. For both treatments, the mean number of days with toxicity was small compared with PFS. This effect was more pronounced with sunitinib in which time spent without progression or toxicity was 151 days greater than with IFN-alpha. CONCLUSION: Patients randomised to sunitinib had longer clinical benefit, defined as Q-TWiST scores, than patients randomised to IFN-alpha. British Journal of Cancer (2012) 106, 1587-1590. doi:10.1038/bjc.2012.149 www.bjcancer.com (C) 2012 Cancer Research UK
引用
收藏
页码:1587 / 1590
页数:4
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