AI Article Synopsis

  • The study compares the effects of 3 months versus 6 months of oxaliplatin combined with fluoropyrimidine as adjuvant therapy for high-risk stage II and III colorectal cancers (CRCs) to determine the optimal treatment duration while managing neurotoxicity.* -
  • A total of 1,788 patients participated, showing that while the longer 6-month treatment resulted in higher rates of neuropathy, the 3-month treatment had comparable 3-year disease-free survival (DFS) rates, particularly for stage III patients treated with capecitabine.* -
  • The findings suggest that the shorter 3-month treatment could be an effective alternative for patients with stage III CRC, providing a balance between efficacy and reduced side

Article Abstract

Purpose: The combination of oxaliplatin and fluoropyrimidine for 6 months is one of the standard options for adjuvant therapy for high-risk stage II and III colorectal cancers (CRCs). The optimal duration of oxaliplatin to diminish neurotoxicity without compromising efficacy needs to be clarified.

Patients And Methods: This open-label, randomized, phase III, noninferiority trial randomly assigned patients with high-risk stage II and III CRC to 3 and 6 months of oxaliplatin with 6 months of fluoropyrimidine groups (3- and 6-month arms, respectively). The primary end point was disease-free survival (DFS), and the noninferiority margin was a hazard ratio (HR) of 1.25.

Results: In total, 1,788 patients were randomly assigned to the 6-month (n = 895) and 3-month (n = 893) arms, and 83.6% in the 6-month arm and 85.7% in the 3-month arm completed the treatment. The neuropathy rates with any grade were higher in the 6-month arm than in the 3-month arm (69.5% 58.3%; < .0001). The 3-year DFS rates were 83.7% and 84.7% in the 6-month and 3-month arms, respectively, with an HR of 0.953 (95% CI, 0.769 to 1.180; test for noninferiority, = .0065) within the noninferiority margin. Among patients with stage III CRC treated by capecitabine plus oxaliplatin, the 3-year DFS of the 3-month arm was noninferior as compared with that of the 6-month arm with an HR of 0.713 (95% CI, 0.530 to 0.959; = .0009). However, among patients with high-risk stage II and stage III CRC treated by infusional fluorouracil, leucovorin, and oxaliplatin, the noninferiority of the 3-month arm compared with the 6-month arm was not proven.

Conclusion: This study suggests that adding 3 months of oxaliplatin to 6 months of capecitabine could be considered an alternative adjuvant treatment for stage III CRC (ClinicalTrials.gov identifier: NCT01092481).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671755PMC
http://dx.doi.org/10.1200/JCO.21.02962DOI Listing

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