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J Biopharm Stat ; 22(6): 1258-71, 2012.
Article in English | MEDLINE | ID: mdl-23075021

ABSTRACT

Clinical trials in oncology often allow patients randomized to placebo to cross over to the active treatment arm after disease progression, leading to underestimation of the treatment effect on overall survival as per the intention-to-treat analysis. We illustrate the statistical aspects and practical use of the rank-preserving structural failure time (RPSFT) model with the Fleming-Harrington family of tests to estimate the crossover-corrected treatment effect, and to assess its sensitivity to various weighting schemes in the RECORD-1 trial. The results suggest that the benefit demonstrated in progression-free survival is likely to translate into a robust overall survival benefit.


Subject(s)
Antineoplastic Agents/therapeutic use , Carcinoma, Renal Cell/mortality , Cross-Over Studies , Data Interpretation, Statistical , Kidney Neoplasms/mortality , Sirolimus/analogs & derivatives , Algorithms , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/adverse effects , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/pathology , Double-Blind Method , Everolimus , Humans , Kaplan-Meier Estimate , Kidney Neoplasms/drug therapy , Kidney Neoplasms/pathology , Models, Statistical , Models, Structural , Neoplasm Metastasis , Sirolimus/administration & dosage , Sirolimus/adverse effects , Sirolimus/therapeutic use , Treatment Failure
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