Proactive Management of Endoperitoneal Spread in Colonic Cancer (PROMENADE)
Colon Cancer, Intraperitoneal Rectal Cancer
About this trial
This is an interventional prevention trial for Colon Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients with colon cancer or intraperitoneal rectosigmoid cancer with clinical (by CT) high-risk(> 5mm) T3, T4 tumors, any N, M0
- Performance Status (ECOG) 0, 1 or 2
- Signed informed consent
Exclusion Criteria:
- BMI> 30
- Impossibility of an adequate follow-up
- Intra and extraabdominal metastatic disease, multiple colorectal cancer or other malignancies
- Active infections or severe associated medical conditions (ASA IV or V)
- Abnormal bone marrow or renal and liver function indices
Sites / Locations
- ASST Nord Milano P.O. Città di Sesto S. Giovanni
- ASO S. Croce e Carle
- Azienda Ospedaliera dei Colli
- Istituto Nazionale Tumori IRCCS Fondazione Pascale di Napoli
- Ospedale di Rimini
- University of Rome Sapienza
- Ospedale Sant'Eugenio
- Azienda Ospedaliera Universitaria Integrata di Verona
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard surgical treatment group
Proactive management group
Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.
Colon cancer patients (high-risk T3 and T4) without peritoneal or systemic metastases are resected for cure. Simultaneously patients will undergo infracolic omentectomy, appendectomy, exeresis of the liver round ligament and, in women, a bilateral oophorectomy. At the end of surgical procedure HIPEC will be performed with oxaliplatin 460 mg/m2 and before the beginning of HIPEC an intravenous infusion of 400 mg/m2 of 5-FU and 20 mg/m2 of leucovorin will be administered. Standard adjuvant systemic chemotherapy (FOLFOX or CAPOX regimens for 6 months) will be reserved in pT3 tumors with poor prognostic factors, pT4 tumor and if lymph-nodes metastases are present. Presence or absence of peritoneal recurrence will be evaluated by MDCT.