TY - JOUR
T1 - “Decision for adjuvant treatment in stage II colon cancer based on circulating tumor DNA:The CIRCULATE-PRODIGE 70 trial”
AU - Taïeb, Julien
AU - Benhaim, Léonor
AU - Laurent Puig, Pierre
AU - Le Malicot, Karine
AU - Emile, Jean François
AU - Geillon, Flore
AU - Tougeron, David
AU - Manfredi, Sylvain
AU - Chauvenet, Marion
AU - Taly, Valerie
AU - Lepage, Côme
AU - André, Thierry
N1 - Publisher Copyright:
© 2020 Editrice Gastroenterologica Italiana S.r.l.
PY - 2020/7/1
Y1 - 2020/7/1
N2 - Background: Adjuvant treatment for stage II colon cancer remains debated. Finding a tool to select patients at risk for disease recurrence may help the clinical decision. Circulating tumor DNA (ctDNA) has been reported recently as a potential predictive marker for disease recurrence. We thus aim to test its ability to better select stage II colon cancer patients for adjuvant therapy. Methods: This national, phase III trial (NCT 2019-000935-15) conducted in more than 100 centers in France, plans to screen around 2640 patients in order to randomize (2:1; minimization method) 198 ctDNA positive patients. Patients aged 18 to 75 years with ECOG performance status ≤1 with R0 surgical resection of a pT3-T4aN0 colon or high rectum adenocarcinoma will be randomized within 63 days after curative-intent surgery, to adjuvant mFOLFOX6 (oxaliplatin 85 mg/m², leucovorin 400 mg/m², and 5-FU bolus 400 mg/m2 then 5FU Continuous infusion 2.4 g/m²) every two weeks for 12 cycles or observation. Patients will be followed for maximum 7 years. A gain of 17.5% in 3-yr disease free survival (DFS) is expected (42.5% in the experimental arm vs. 25% in the control arm; HR:0.62; α, 5% [two-sided log-rank test]; 1-β, 80%). Secondary endpoints include 2-yr DFS, overall survival, and toxicity. Recruitement began End of January 2020.
AB - Background: Adjuvant treatment for stage II colon cancer remains debated. Finding a tool to select patients at risk for disease recurrence may help the clinical decision. Circulating tumor DNA (ctDNA) has been reported recently as a potential predictive marker for disease recurrence. We thus aim to test its ability to better select stage II colon cancer patients for adjuvant therapy. Methods: This national, phase III trial (NCT 2019-000935-15) conducted in more than 100 centers in France, plans to screen around 2640 patients in order to randomize (2:1; minimization method) 198 ctDNA positive patients. Patients aged 18 to 75 years with ECOG performance status ≤1 with R0 surgical resection of a pT3-T4aN0 colon or high rectum adenocarcinoma will be randomized within 63 days after curative-intent surgery, to adjuvant mFOLFOX6 (oxaliplatin 85 mg/m², leucovorin 400 mg/m², and 5-FU bolus 400 mg/m2 then 5FU Continuous infusion 2.4 g/m²) every two weeks for 12 cycles or observation. Patients will be followed for maximum 7 years. A gain of 17.5% in 3-yr disease free survival (DFS) is expected (42.5% in the experimental arm vs. 25% in the control arm; HR:0.62; α, 5% [two-sided log-rank test]; 1-β, 80%). Secondary endpoints include 2-yr DFS, overall survival, and toxicity. Recruitement began End of January 2020.
KW - Adjuvant
KW - Circulating tumor DNA
KW - Colon cancer
KW - Methylated biomarker
UR - http://www.scopus.com/inward/record.url?scp=85085562076&partnerID=8YFLogxK
U2 - 10.1016/j.dld.2020.04.010
DO - 10.1016/j.dld.2020.04.010
M3 - Article
C2 - 32482534
AN - SCOPUS:85085562076
SN - 1590-8658
VL - 52
SP - 730
EP - 733
JO - Digestive and Liver Disease
JF - Digestive and Liver Disease
IS - 7
ER -