About this trial
In a multicentric randomized controlled trial, we will compare standard surgery (consisting in removal of the primary cancer) followed by 6 months of adjuvant chemotherapy associated with 3 cycles of oxaliplatin-based PIPAC (4-6 weeks apart), to standard surgery followed by 6 months of adjuvant systemic chemotherapy (routine treatment), in patients with colorectal cancer at high risk for metachronous peritoneal carcinomatosis (pT4 pN0-2 cM0 pMMR colorectal cancer of the colon, colorectal junction or high rectum and/or with positive cytology) in terms of 1-year and 3-year peritoneal metastasis-free survival (as measured by imaging and/or surgical exploration), 1-year and 3-year disease-free survival, as well as 1-year and 3-year overall survival. In terms of outcomes measurement, patients in both groups will benefit from diagnostic laparoscopy at 6 months from the index surgery, and standard surveillance consisting in clinical examination, CEA determination and thoraco-abdominal CT at 6, 12, 24, 36, 48 and 60 months after index surgery.
Eligibility criteria
Qualifiers
Patients operated (in emergency or elective settings) for colorectal cancer (of the colon, colorectal junction or high rectum).
Definitive pathological stage pT4 pN0-2 cM0 pMMR and/or pT3-4 pN0-2 cM0 pMMR with positive cytology and/or pT3-4 pN0-2 M1c pMMR with limited peritoneal carcinomatosis which is limited to one abdominal quadrant and was resected during index surgery and no other distant lesion (small indeterminate pulmonary nodules to be followed are accepted)
Performance status 0-1.
Age > 18 years.
Disqualifiers
Infraperitoneal rectal cancer (middle or low rectum).
Age <18 year old.
Age > 80 year old.
Hereditary colorectal cancer.
Trial design
Treatments tested in this trial
- oxaliplatin-based PIPAC
- Control (Standard treatment)
Treatment groups
Locations
Sponsors and collaborators
Jeremy Meyer
Lead sponsor
University Hospital, Geneva
Sponsor institution
University Hospital, Geneva
Collaborator