Feasibility of Intraperitoneal Chemotherapy in the Surgical Treatment of Colon Cancer cT4
- Conditions
- Colon Cancer
- Registration Number
- NCT03561948
- Lead Sponsor
- State Scientific Centre of Coloproctology, Russian Federation
- Brief Summary
This is a randomised controlled study aims to determine the oncological effectiveness of adjuvant HIPEC, using intraperitoneal Mytomicin C following a curative resection of a cT4 Colon cancer in preventing the development of peritoneal carcinomatosis in addition to the standard adjuvant systemic treatment.
- Detailed Description
In the experimental group (50 patients) after laparotomy and revision of the abdominal cavity organs, peritoneal lavage will be performed followed by immunological examination. After performing the surgical intervention, the patient will undergo intraoperative intra-abdominal chemotherapy with mitomycin C. Further, lavage of the abdominal cavity will be repeated, followed by immunological examination.
In the control group (40 patients), after laparotomy and revision, peritoneal lavage will also be performed, followed by immunological examination. Patients of this group will not receive intraoperative intra-abdominal chemotherapy. After performing the surgical intervention, the patient will perform irrigation of the abdominal cavity with physiological saline. Further, lavage of the abdominal cavity will be repeated, followed by immunological examination.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 90
- Colon cancer which represent cT4N0-2 M0 on the basis of preoperative examination data (CT of the chest, abdominal and pelvic organs) in line with The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual:
- Histologically verified adenocarcinoma of the colon.
- Signed informed consent.
- Pregnancy or lactation.
- The presence of synchronous or metachronous malignant tumors.
- Distant metastases to the liver, lungs, peritoneal carcinomatosis and other organs.
- Neoadjuvant chemotherapy.
- Suspected Lynch syndrome.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Positive peritoneal lavage through study completion, an average of 1 year Cancer cell vitality
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
State Scientific Centre of Coloproctology
🇷🇺Moscow, Russian Federation
State Scientific Centre of Coloproctology🇷🇺Moscow, Russian Federation