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Disease-free survival versus overall survival as a primary end point for adjuvant colon cancer studies: Individual patient data from 20,898 patients on 18 randomized trials

  • Daniel J. Sargent
  • , Harry S. Wieand
  • , Daniel G. Haller
  • , Richard Gray
  • , Jacqueline K. Benedetti
  • , Marc Buyse
  • , Roberto Labianca
  • , Jean Francois Seitz
  • , Christopher J. O'Callaghan
  • , Guido Francini
  • , Axel Grothey
  • , Michael O'Connell
  • , Paul J. Catalano
  • , Charles D. Blanke
  • , David Kerr
  • , Erin Green
  • , Norman Wolmark
  • , Thierry Andre
  • , Richard M. Goldberg
  • , Aimery De Gramont

Research output: Contribution to journalArticlepeer-review

Abstract

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. Median time from recurrence to death was 12 months. Eighty percent of recurrences were in the first 3 years; 91% of patients with recurrence by 3 years died before 5 years. Correlation between 3-year DFS and 5-year OS was 0.89. Comparing control versus experimental arms within each trial, the correlation between hazard ratios for DFS and OS was 0.92. Within-trial log-rank testing using both DFS and OS provided the same conclusion in 23 (92%) of 25 cases. Formal measures of surrogacy were satisfied. Conclusion: In patients treated on phase III adjuvant colon clinical trials, DFS and OS are highly correlated, both within patients and across trials. These results suggest that DFS after 3 years of median follow-up is an appropriate end point for adjuvant colon cancer clinical trials of fluorouracil-based regimens, although marginally significant DFS improvements may not translate into significant OS benefits.

Original languageEnglish (US)
Pages (from-to)8664-8670
Number of pages7
JournalJournal of Clinical Oncology
Volume23
Issue number34
DOIs
StatePublished - 2005

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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