PURPOSE: A traditional end point for colon adjuvant clinical trials is overall survival (OS), with 5 years demonstrating adequate follow-up. A shorter-term end point providing convincing evidence to allow treatment comparisons could significantly speed the translation of advances into practice. METHODS: Individual patient data were pooled from 18 randomized phase III colon cancer adjuvant clinical trials. Trials included 43 arms, with a pooled sample size of 20,898 patients. The primary hypothesis was that disease-free survival (DFS), with 3 years of follow-up, is an appropriate primary end point to replace OS with 5 years of follow-up. RESULTS: The recurrence rates for years 1 through 5 were 12%, 14%, 8%, 5%, and 3%, respectively. Me...
Background: The ACCENT group previously established disease-free survival (DFS) with 2 or 3 years me...
Background: A prospective, pooled analysis of six randomised phase 3 trials was done to investiga...
IF 26.303 (2017)International audiencePurpose : Reduction of adjuvant treatment duration may decrea...
PURPOSE: A traditional end point for colon adjuvant clinical trials is overall survival (OS), with 5...
PURPOSE: The traditional end point for colon adjuvant clinical trials is overall survival (OS). We p...
Background: The traditional endpoint for colon adjuvant clinical trials (CT) is OS, with 5 years (yr...
PURPOSE: Limited data are available on the time course of treatment failures (recurrence and/or deat...
Disease-free survival is increasingly being used as the primary endpoint of most trials testing adju...
Disease-free survival is increasingly being used as the primary endpoint of most trials testing adju...
PURPOSE: Progression-free survival (PFS) has previously been established as a surrogate for over...
PURPOSE: Although it is well-established that fluorouracil- (FU-) based adjuvant therapy improves su...
We previously validated disease-free survival (DFS) as a surrogate for overall survival (OS) in fluo...
Limited data are available on the time course of treatment failures (recurrence and/or death), the n...
Background: The ACCENT group previously established disease-free survival (DFS) with 2 or 3 years me...
Background: A prospective, pooled analysis of six randomised phase 3 trials was done to investiga...
IF 26.303 (2017)International audiencePurpose : Reduction of adjuvant treatment duration may decrea...
PURPOSE: A traditional end point for colon adjuvant clinical trials is overall survival (OS), with 5...
PURPOSE: The traditional end point for colon adjuvant clinical trials is overall survival (OS). We p...
Background: The traditional endpoint for colon adjuvant clinical trials (CT) is OS, with 5 years (yr...
PURPOSE: Limited data are available on the time course of treatment failures (recurrence and/or deat...
Disease-free survival is increasingly being used as the primary endpoint of most trials testing adju...
Disease-free survival is increasingly being used as the primary endpoint of most trials testing adju...
PURPOSE: Progression-free survival (PFS) has previously been established as a surrogate for over...
PURPOSE: Although it is well-established that fluorouracil- (FU-) based adjuvant therapy improves su...
We previously validated disease-free survival (DFS) as a surrogate for overall survival (OS) in fluo...
Limited data are available on the time course of treatment failures (recurrence and/or death), the n...
Background: The ACCENT group previously established disease-free survival (DFS) with 2 or 3 years me...
Background: A prospective, pooled analysis of six randomised phase 3 trials was done to investiga...
IF 26.303 (2017)International audiencePurpose : Reduction of adjuvant treatment duration may decrea...