Atezolizumab with mFOLFOX6 Boosts 3-Year DFS by 10.1% in Stage III dMMR Colon Cancer
This phase 3 randomized controlled trial evaluated the efficacy of adding atezolizumab to the standard mFOLFOX6 regimen in patients with resected stage III mismatch repair-deficient (dMMR) colon cancer. A total of 712 patients were enrolled and randomized in a 1:1 ratio to receive either atezolizumab plus mFOLFOX6 for 6 months, followed by atezolizumab monotherapy for a total of 12 months, or mFOLFOX6 alone for 6 months. The primary endpoint was disease-free survival (DFS). At a median follow-up of 40.9 months, the 3-year DFS was significantly higher in the atezolizumab-mFOLFOX6 group at 86.3% compared to 76.2% in the mFOLFOX6 group, with a hazard ratio for disease recurrence or death of 0.50 (95% CI, 0.35 to 0.73; P<0.001). Secondary endpoints included overall survival and adverse event profiles. Grade 3 or 4 adverse events were reported in 84.1% of patients receiving atezolizumab plus mFOLFOX6, compared to 71.9% in the mFOLFOX6 alone group. These findings suggest that the addition of atezolizumab to mFOLFOX6 significantly improves DFS in this patient population, although with a higher incidence of severe adverse events. Clinicians should weigh the benefits of improved DFS against the increased risk of adverse events when considering this treatment regimen.