Evaluation of the change of outcomes over a 10-year period in patients with stage III colon cancer: pooled analysis of 6501 patients treated with fluorouracil, leucovorin, and oxaliplatin in the ACCENT database.

内科学 氟尿嘧啶 肿瘤科 胃肠病学 化疗
作者
Mohamed E. Salem,Jun Yin,Richard M. Goldberg,Levi Pederson,Norman Wolmark,Steven R. Alberts,Julien Taieb,John L. Marshall,Sara Lonardi,Takayuki Yoshino,Rachel Kerr,Greg Yothers,A. Grothey,Thierry André,A. de Gramont,Q. Shi
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:31 (4): 480-486 被引量:15
标识
DOI:10.1016/j.annonc.2019.12.007
摘要

Background Since 2004, adjuvant 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX or FLOX) have been the standard of care for patients with resected colon cancer. Herein we examine the change of outcomes over a 10-year period in patients with stage III colon cancer who received this regimen. Patients and methods Individual patient data from the ACCENT database was used to compare the outcomes in older (1998–2003) and newer (2004–2009) treatment eras for patients with stage III colon cancer who received adjuvant FOLFOX or FLOX. The outcomes were compared between the two groups by the multivariate Cox proportional-hazards model adjusting for age, sex, performance score, T stage, N stage, tumor sidedness, and histological grade. Results A total of 6501 patients with stage III colon cancer who received adjuvant FOLFOX or FLOX in six randomized trials were included in the analysis. Patients enrolled in the new era group experienced statistically significant improvement in time to recurrence [3-year rate, 76.1% versus 73.0%; adjusted hazard ratio (HRadj) = 0.83 (95% CI, 0.74–0.92), P = 0.0008], disease-free survival (DFS) [3-year rate, 74.7% versus 72.3%; HRadj = 0.88 (0.79–0.98), P = 0.024], survival after recurrence (SAR) [median time, 27.0 versus 17.7 months; HRadj = 0.65 (0.57–0.74), P  Conclusion Improved outcomes were observed in patients with stage III colon cancer enrolled in clinical trials who received adjuvant FOLFOX/FLOX therapy in 2004 or later compared with patients in the older era. Prolonged SAR calls for revalidation of 3-year DFS as the surrogate endpoint of OS in adjuvant clinical trials and reevaluation of optimal follow-up of OS to confirm the trial findings based on the DFS endpoints. Clinical Trials Numbers NCT00079274; NCT00096278; NC4931; NCT00275210; NCT00265811; NCT00112918.
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