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The "SPARCOL" Study

Primary Purpose

Colon Cancer, Frailty

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Combined Endoscopic Laparoscopic Surgery (CELS)
Standard resection
Sponsored by
Zealand University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

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

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Active Comparator

Arm Label

CELS

Standard Surgery

Arm Description

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.

Outcomes

Primary Outcome Measures

Change in patient-reported postoperative recovery - Quality of Recovery 15
Validated to measure recovery after surgery and general anesthesia, and additionally validated for use in Danish language and culture. The scale is arbitrary and ranges from 0 to 150. Higher scores means better recovery. The established minimum clinically important difference in QoR-15 is 8.0, and the SD of QoR- 15 scores after major surgery is in the order of 16.

Secondary Outcome Measures

Change in exercise capacity and physical condition
The 30 Second Sit to Stand Test. A measurement that assesses functional lower extremity strength in older adults. Test result is the number of times the participant comes to a full standing position in 30 seconds. Higher number of stands within 30 seconds means better result.
Change in exercise capacity and physical condition
Six minutes' walk test is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.
Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire - EORTC C30.
EORTC C30, questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).
Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire- EORTC CRC.
EORTC CRC questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).
Frailty questionnaire Geriatric 8 (G8)
The G-8 Score is a screening tool containing 8 questions. The total G-8 score lies between 0 and 17. A higher score indicates a better health status.
Duration of surgery
Duration of surgery in minutes
Blood loss
Blood loss in ml
Intraoperative complications
Descriptive registration of intraoperative complications;
Conversion rate
Conversion rate (%) from laparoscopic surgery to open surgery
Rate of complete resection margin
R0 (tumor-free margin >1 mm) corresponds to resection for cure or complete remission. R1 to microscopic residual tumor, R2 to macroscopic residual tumor.
Assessment of histopathological risk factors
Assessment of histopathological risk factor defined as presence of at least one of the risk factors: Kikuchi level ≥sm2, vascular invasion, lymphatic invasion, poorly differentiated adenocarcinoma, and tumour budding BD2-3.
Long-term oncological outcomes: Disease-free survival
Time from surgery until the recurrence of disease or death
Long-term oncological outcomes: Overall survival
Overall survival was defined as the time elapsed from the date of surgery to the last day of follow-up or the date of death
Long-term oncological outcomes: Recurrence
Locoregional and/or distant recurrence after surgery defined as any histological, morphological, and clinical evidence of tumour growth during follow-up periode
Clavien-Dindo classification
Grading system used in surgery for grading adverse events (i.e. complications) which occur as a result of surgical procedures. Grade I to V, where V is death of the patient
The Comprehensive Complication Index
e Comprehensive Complication Index (CCI®) reflects the gravity of this overall complication burden on the patient on a scale from 0 (no complication) to 100 (death)
Length of hospital stay
Clinical metric that measures the length of time in days elapsed between a patient's hospital admittance and discharge.
90-day mortality
Death within 90 days after surgery, as either an inpatient or outpatient
Hospital readmissions
Unplanned readmissions that happen within 3 days of discharge from the index (i.e., initial) admission
Rate of secondary standard resection
Rate in percent of performed secondary surgery after primary CELS resection

Full Information

First Posted
January 16, 2023
Last Updated
July 24, 2023
Sponsor
Zealand University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05734300
Brief Title
The "SPARCOL" Study
Official Title
Organ SPARring Surgery vs. Standard Resection for Early Stage COLon Cancer in Elderly Frail Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2023 (Actual)
Primary Completion Date
May 1, 2025 (Anticipated)
Study Completion Date
September 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zealand University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Mortality following elective colorectal cancer surgery range between 2.5-6% and increase for the elderly and frail patient regardless of T-stage. Around 80% of the patients who present with a colon cancer and is in a condition where surgery is possible will be offered resection of the tumor. A part of the colon is always removed together with the lymph nodes in order to ensure that cancer cells are not left behind. The risk of lymph node metastasis is dependent on several histopathological characteristics of the tumor. The overall risk of lymph node metastases is less than 20 % in patients with early colon cancer. This indicates that the majority of patients with early colon cancer have no benefit of additional resection besides local tumor excision. The alternative to resecting a larger part of the bowel is to make more focused surgery only resecting a small part of the bowel part through a combination of laparoscopic and endoscopic techniques. This new organ sparing approach is called Combined Endoscopic Laparoscopic Surgery (CELS). The investigators aimed to examinate the hypothesis that organ preserving approach (CELS) provides superior quality of recovery in elderly frail patients with small colon cancers when compared with standard surgery in RCT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer, Frailty
Keywords
Colon Cancer, Elderly population, Early colo-rectal cancer, Organ Preserving Approach, Combined Endoscopic Laparoscopic Surgery (CELS)

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CELS
Arm Type
Experimental
Arm Description
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.
Arm Title
Standard Surgery
Arm Type
Active Comparator
Arm Description
Standard surgical resection of colonic cancer following standard oncologic principles while under general anaesthesia.
Intervention Type
Procedure
Intervention Name(s)
Combined Endoscopic Laparoscopic Surgery (CELS)
Intervention Description
The main surgical advantage in this procedure is the ability to view the colon intra- and extraluminal simultaneously. The laparoscopic approach enables manipulation and mobilization of the colon, while the endoscopic view secures that the resection is complete and not overlapping the ileac valve or creating stenosis. Compared to the traditional oncological colon resection, the CELS resection is a minimally invasive procedure - organ sparing procedure leading to a reduced surgical stress response.
Intervention Type
Procedure
Intervention Name(s)
Standard resection
Intervention Description
In this study standard resection of the colon will be performed according to complete mesocolic excision (CME) principles.
Primary Outcome Measure Information:
Title
Change in patient-reported postoperative recovery - Quality of Recovery 15
Description
Validated to measure recovery after surgery and general anesthesia, and additionally validated for use in Danish language and culture. The scale is arbitrary and ranges from 0 to 150. Higher scores means better recovery. The established minimum clinically important difference in QoR-15 is 8.0, and the SD of QoR- 15 scores after major surgery is in the order of 16.
Time Frame
Change in QoR-15 will be assessed repeatedly at baseline, 4-8 hours postoperatively (4-8H), postoperative day (POD) 1, POD 2, POD 3, POD 7, POD 10-14 and POD 30
Secondary Outcome Measure Information:
Title
Change in exercise capacity and physical condition
Description
The 30 Second Sit to Stand Test. A measurement that assesses functional lower extremity strength in older adults. Test result is the number of times the participant comes to a full standing position in 30 seconds. Higher number of stands within 30 seconds means better result.
Time Frame
Changes will be assessed repeatedly at baseline, Postoperative day 1, Postoperative day 2, Postoperative day 3 or at the time of hospital discharge, whatever comes first. Postoperative day 10-14 and 30 days postoperatively.
Title
Change in exercise capacity and physical condition
Description
Six minutes' walk test is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.
Time Frame
Changes will be assessed repeatedly at baseline, Postoperative day 1, Postoperative day 2, Postoperative day 3 or at the time of hospital discharge, whatever comes first. Postoperative day 10-14 and 30 days postoperatively.
Title
Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire - EORTC C30.
Description
EORTC C30, questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).
Time Frame
Changes will be assessed repeatedly at basline, 3 months, 6 months, 1 year follow-up
Title
Changes in The European Organization for Research and Treatment of Cancer quality of life questionnaire- EORTC CRC.
Description
EORTC CRC questionnaire, developed to assess the quality of life of cancer patients. All of the scales and single-item measures range in score from 0 to 100. Higher score for the functioning scales and global health status denote a better level of functioning (i.e. a better state of the patient), while higher scores on the symptom and single-item scales indicate a higher level of symptoms (i.e. a worse state of the patient).
Time Frame
Changes will be assessed repeatedly at basline, 3 months, 6 months, 1 year follow-up
Title
Frailty questionnaire Geriatric 8 (G8)
Description
The G-8 Score is a screening tool containing 8 questions. The total G-8 score lies between 0 and 17. A higher score indicates a better health status.
Time Frame
Basline
Title
Duration of surgery
Description
Duration of surgery in minutes
Time Frame
Intraoperative
Title
Blood loss
Description
Blood loss in ml
Time Frame
Intraoperative
Title
Intraoperative complications
Description
Descriptive registration of intraoperative complications;
Time Frame
Intraoperative
Title
Conversion rate
Description
Conversion rate (%) from laparoscopic surgery to open surgery
Time Frame
Intraoperative
Title
Rate of complete resection margin
Description
R0 (tumor-free margin >1 mm) corresponds to resection for cure or complete remission. R1 to microscopic residual tumor, R2 to macroscopic residual tumor.
Time Frame
Postoperative day 14
Title
Assessment of histopathological risk factors
Description
Assessment of histopathological risk factor defined as presence of at least one of the risk factors: Kikuchi level ≥sm2, vascular invasion, lymphatic invasion, poorly differentiated adenocarcinoma, and tumour budding BD2-3.
Time Frame
Postoperative day 14
Title
Long-term oncological outcomes: Disease-free survival
Description
Time from surgery until the recurrence of disease or death
Time Frame
During 3-year follow-up periode
Title
Long-term oncological outcomes: Overall survival
Description
Overall survival was defined as the time elapsed from the date of surgery to the last day of follow-up or the date of death
Time Frame
During 3-year follow-up periode
Title
Long-term oncological outcomes: Recurrence
Description
Locoregional and/or distant recurrence after surgery defined as any histological, morphological, and clinical evidence of tumour growth during follow-up periode
Time Frame
During 3-year follow-up periode
Title
Clavien-Dindo classification
Description
Grading system used in surgery for grading adverse events (i.e. complications) which occur as a result of surgical procedures. Grade I to V, where V is death of the patient
Time Frame
Within 90 days postoperative.
Title
The Comprehensive Complication Index
Description
e Comprehensive Complication Index (CCI®) reflects the gravity of this overall complication burden on the patient on a scale from 0 (no complication) to 100 (death)
Time Frame
Within 90 days postoperative.
Title
Length of hospital stay
Description
Clinical metric that measures the length of time in days elapsed between a patient's hospital admittance and discharge.
Time Frame
Within 90 days postoperative.
Title
90-day mortality
Description
Death within 90 days after surgery, as either an inpatient or outpatient
Time Frame
Within 90 days postoperative.
Title
Hospital readmissions
Description
Unplanned readmissions that happen within 3 days of discharge from the index (i.e., initial) admission
Time Frame
Within 90 days postoperative.
Title
Rate of secondary standard resection
Description
Rate in percent of performed secondary surgery after primary CELS resection
Time Frame
Within 90 days postoperative.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ilze Ose, MD
Phone
27293399
Ext
0045
Email
ilos@regionsjaelland.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Ismail Gögenur, Prof.
Phone
26336426
Ext
0045
Email
igo@regionsjaelland.dk
Facility Information:
Facility Name
Copenhagen University Hospital - Herlev
City
Copenhagen
State/Province
Herlev
ZIP/Postal Code
2730
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mads Falk Klein
Phone
38681543
Ext
0045
Email
mads.falk.klein@regionh.dk
First Name & Middle Initial & Last Name & Degree
Henrik Loft Jacobsen
Facility Name
Hospital Soenderjylland
City
Aabenraa
ZIP/Postal Code
6200
Country
Denmark
Individual Site Status
Active, not recruiting
Facility Name
Zealand University Hospital
City
Køge
ZIP/Postal Code
4600
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ilze Ose, Prof.
Phone
27293399
Ext
0045
Email
ilos@regionsjaelland.dk
First Name & Middle Initial & Last Name & Degree
Ismail Gögenur
Phone
26336426
Ext
0045
Email
igo@regionsjaelland.dk

12. IPD Sharing Statement

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The "SPARCOL" Study

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