Aim
FOxTROT1 established a new standard of care for managing locally advanced colon cancer (CC) with neoadjuvant chemotherapy (NAC). Six weeks of neoadjuvant oxaliplatin and fluoropyrimidine (OxFp) chemotherapy was associated with greater 2-year disease-free survival (DFS) when compared to proceeding straight to surgery (STS). There is now a need to refine the use of NAC and identify those most likely to benefit. FOxTROT2 will investigate NAC in older adults and those with frailty. FOxTROT3 will assess whether intensified triplet NAC provides additional benefits over OxFp.
Methods
FOxTROT2 and FOxTROT3 are international, open-label, phase III randomised-controlled trials. Eligible patients will be identified by the multidisciplinary team. Patient age, frailty and comorbidities will be considered to guide trial entry. Participants will be randomised 2:1 to the intervention or control arm: six weeks of dose-adapted neoadjuvant OxFp vs. STS in FOxTROT2 and six weeks of neoadjuvant modified oxaliplatin, 5FU and irinotecan (mFOLFOXIRI) vs. OxFp in FOxTROT3. The primary endpoint in FOxTROT2 is 3-year DFS. In FOxTROT3, tumour regression grade and 3-year DFS are co-primary endpoints.
Discussion
FOxTROT2 and FOxTROT3 will establish the FOxTROT platform, a key part of our long-term strategy to develop neoadjuvant treatments for CC. FOxTROT2 will investigate NAC in a population under-represented in FOxTROT1 and wider research. FOxTROT3 will assess whether it is possible to induce greater early tumour responses and whether this translates to superior long-term outcomes. Looking ahead, the FOxTROT platform will facilitate further trial comparisons and extensive translational research to optimise the use of NAC in CC.
CORE (COnnecting REpositories)
CORE (COnnecting REpositories)