The purpose of this study is to compare whether a 3-month treatment is at least not inferior to a 6-month treatment (FOLFOX-4 6 vs. 12 cycles or XELOX 4 cycles vs. 8 cycles) in terms of RFS in patients with high risk stage II or stage III radically resected colon cancer.
Six months of adjuvant chemotherapy with 5-FU and oxaliplatin for patients with stage III colon cancer is the world-wide standard of care, based on the MOSAIC and C-07 trials. However, it leads to significant cost, toxicity, and inconvenience. In particular, the onset of oxaliplatin induced cumulative dose-dependent neuropathies is a significant issue. The ability to maintain efficacy with a reduced duration of therapy would have clear advantage to patients, to providers, and to the health care system. Multiple large trials in the 1990s demonstrated that the previous standard of 12 months of therapy could be reduced to 6 months. A single small trial with 5-FU alone demonstrated similar outcomes for 3 versus 6 months of therapy. Thus, it is proposed to definitively evaluate the non-inferiority of 3 months of oxaliplatin-based adjuvant chemotherapy versus the current standard of 6 months. The primary endpoint will be disease-free survival (DFS). It is essential to have sufficient power to eliminate the possibility of clinically meaningful inferiority of 3 months of therapy: a huge number of patients will be necessary. Previous efforts and experience have conclusively demonstrated that in colon cancer, a single, global trial is impractical. Consequently, an international, prospective pooled analysis will be performed, gathering data of independent trials run in different countries, to answer the single primary hypothesis that 3 months of adjuvant therapy with FOLFOX/XELOX is non-inferior to the current standard of 6 months. Among six planned countries, the Greek intergroup will conduct one of these trials.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
2,000
5-FU 400mg/m2 Bolus and then 22 hours 5-FU 600mg/m2 IV, days 1 \& 2, q2w, for 12 cycles
Leucovorin 200mg/m2 IV in 2 hours, days 1 \& 2, q2w, for 12 cycles
Oxaliplatin 85mg/m2 in 2 hours IV, day 1, q2w, for 12 cycles
University Hospital of Crete, Dep of Medical Oncology
Heraklion, Greece
Relapse Free Survival
Time frame: 3-years
Overall Survival
Time frame: 3-years
Safety Profil according to NCI-CTAE v 3.0
Percentage (%) of treatments delays and interaptions in each arm Percentage (%) of dose received versus planned dose in each arm
Time frame: q2w
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Capecitabine 1000 mg/m2 X 2 ,days 1-14, q2w, for 8 cycles
Oxaliplatin 130 mg/m2 in 2 hours IV, day 1, q2w, for 8 cycles
5-FU 400mg/m2 Bolus and then 22 hours 5-FU 600mg/m2 IV, days 1 \& 2, q2w, for 6 cycles
Leucovorin 200mg/m2 IV in 2 hours, days 1 \& 2, q2w, for 6 cycles
Capecitabine 1000 mg/m2 X 2 ,days 1-14, q2w, for 4 cycles
Oxaliplatin 130 mg/m2 in 2 hours IV, day 1, q2w, for 4 cycles
Oxaliplatin 85mg/m2 in 2 hours IV, day 1, q2w, for 6 cycles