The "SPARCOL" Study
Colon Cancer, Frailty
About this trial
This is an interventional other trial for Colon Cancer focused on measuring Colon Cancer, Elderly population, Early colo-rectal cancer, Organ Preserving Approach, Combined Endoscopic Laparoscopic Surgery (CELS)
Eligibility Criteria
Inclusion Criteria: Male and Female participants providing written informed consent aged 75 years and older PS score ≥1 and /or ASA score ≥3 Macroscopically or pathological colonic adenocarcinoma Clinical TNM classification T1/T2 N0 M0 Eligible and suitable for CELS resection according to MDT Tumor must be located in colon, and not involving the ileac valve or taking up more than 50% of the lumen in an air-distended bowel wall Exclusion Criteria: Unable to give informed consent Histological high-risk features in biopsy material from tumor (mucin, signet cells, de- differentiation) Suspected other malignancy than adenocarcinoma (e.g. neuroendocrine tumors) Preoperative chemo/radiotherapy Creation of stoma perioperative Non-Danish speakers
Sites / Locations
- Copenhagen University Hospital - HerlevRecruiting
- Hospital Soenderjylland
- Zealand University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
CELS
Standard Surgery
The Combined Endoscopic Laparoscopic Surgery (CELS) is a hybrid procedure that enables large local excisions of the colon without segmental resection while under general anaesthesia. In our study, CELS refers only to endoscopic assisted laparoscopic resection.
Standard surgical resection of colonic cancer following standard oncologic principles while under general anaesthesia.