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Assessment of Frequency of Surveillance After Curative Resection in Patients With Stage II and III Colorectal Cancer

Primary Purpose

Colorectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
CT-scan, CEA, X-ray of lungs
CT-scan, CEA, X-ray of lungs
Sponsored by
Bispebjerg Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring Follow-up

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Radical surgery (R0-resection) for colorectal adenocarcinoma - with or without adjuvant treatment Age < 75 years Provision of written informed consent for participation "Clean colon" verified by perioperative barium enema or colonoscopy last 3 months post-surgery Tumour stage: II-III (Tany N1-2 M0, T3-4NanyM0, Dukes´ B - C) Exclusion Criteria: A clinical diagnosis of HNPCC (non hereditary polyposis colorectal cancer) or FAP (familial polyposis coli) Local resection for colorectal cancer (e.g., TEM-procedure) Life-expectancy less than 2 years due to concurrent disease (e.g., cardiac disease, terminal multiple sclerosis, liver cirrhosis) Inability to provide informed consent or refusal to do so Inability to comply with the control or intense follow-up program Participation in other clinical trials interfering with the control-programs Previous malignancies (except for non-melanoma skin cancer)

Sites / Locations

  • Peer Wille-Jørgensen

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

1 frequent control

2 less frequent control

Arm Description

Follow-up 6, 12, 18, 24 and 36 months after surgery

Follow-up 12 and 36 months after surgery

Outcomes

Primary Outcome Measures

Overall and cancer-specific mortality

Secondary Outcome Measures

Quality of life. Cost-effectiveness of follow-up

Full Information

First Posted
September 22, 2005
Last Updated
December 21, 2015
Sponsor
Bispebjerg Hospital
Collaborators
Nordic Cancer Union, Danish Cancer Society, Danish Colorectal Cancer Group
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1. Study Identification

Unique Protocol Identification Number
NCT00225641
Brief Title
Assessment of Frequency of Surveillance After Curative Resection in Patients With Stage II and III Colorectal Cancer
Official Title
COLOFOL - A Pragmatic Study to Assess the Frequency of Surveillance Tests After Curative Resection in Patients With Stage II and III Colorectal Cancer - a Randomised Multicentre Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
March 2006 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bispebjerg Hospital
Collaborators
Nordic Cancer Union, Danish Cancer Society, Danish Colorectal Cancer Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim is to conduct a prospective multicentre randomised study comparing two different control regimens after resection for colorectal cancer stage II - III. Follow-up after surgery for colorectal cancer is a controversial issue. The reasons for follow-up are: to obtain a better overall survival, for scientific purposes and/or for psychological reasons and/or as quality assessment. Meta-analyses of randomised controlled studies have lately shown that a beneficial effect on the overall mortality could be found with intense follow-up compared to sporadic. This study compares the regimen of CT-scan or MR scan of the liver, control of the carcinoembryonic antigen (CEA), and CT-scan or X-ray of the lungs in two groups with either control after 12 and 36 months, or after 6, 12, 18, 24, and 36 months. The efficacy parameters are total and cancer-specific mortality.
Detailed Description
The aim is to investigate the efficiency of two follow-up programs after radical surgery for colorectal cancer. Colorectal cancer attacks between 3-5% of the European population during their lifetime, and about 75% of these will have potential curative surgery performed. Follow up after surgery is costly and time consuming for both patients and the Health Care Systems. The intensity of follow up as well as the methods employed vary tremendously from center to centre and from country to country. Until recently the scientific documentation for the cost-effectiveness of follow-up was very sparse, but recent compiling of data indicates that intense follow up can save lives as compared to sporadic follow-up at an acceptable cost. However, the optimal follow-up intervals and the best methods are unknown. Previous results indicate that scanning of the liver and measuring of the tumor-marker CEA may be a way forward. A prospective randomised multicenter study in centers from Denmark (approx. 15), Sweden (approx. 20), Poland (approx. 6), Hungary (approx. 2) and perhaps The Netherlands and UK is starting in 2005 after basic work with protocols, ethical committees now has been finished. This basic work was supported by the Nordic Cancer Union with a grant of 25,000 EUROS. The patients will be randomised to follow-up with CEA, multislice CT scan of the liver and X-ray of the lungs, either 12 and 36 months after surgery or 6, 12, 18, 24 and 36 months after surgery. If recurrence is detected, the patient will be offered the best available treatment either as repeated surgery with curative intent or palliative oncological treatment. Data will be collected electronically via the internet to an already constructed database. The primary efficacy parameter is 3 and 5 years overall and cancer-specific survival. It is planned that recruitment will be at least 2,500 patients, which is feasible in 2 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Follow-up

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1 frequent control
Arm Type
Active Comparator
Arm Description
Follow-up 6, 12, 18, 24 and 36 months after surgery
Arm Title
2 less frequent control
Arm Type
Other
Arm Description
Follow-up 12 and 36 months after surgery
Intervention Type
Procedure
Intervention Name(s)
CT-scan, CEA, X-ray of lungs
Intervention Description
Arm 1: 6, 12, 18, 24 and 36 months after surgery
Intervention Type
Procedure
Intervention Name(s)
CT-scan, CEA, X-ray of lungs
Intervention Description
Arm 2: 12 and 36 months after surgery
Primary Outcome Measure Information:
Title
Overall and cancer-specific mortality
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Quality of life. Cost-effectiveness of follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Radical surgery (R0-resection) for colorectal adenocarcinoma - with or without adjuvant treatment Age < 75 years Provision of written informed consent for participation "Clean colon" verified by perioperative barium enema or colonoscopy last 3 months post-surgery Tumour stage: II-III (Tany N1-2 M0, T3-4NanyM0, Dukes´ B - C) Exclusion Criteria: A clinical diagnosis of HNPCC (non hereditary polyposis colorectal cancer) or FAP (familial polyposis coli) Local resection for colorectal cancer (e.g., TEM-procedure) Life-expectancy less than 2 years due to concurrent disease (e.g., cardiac disease, terminal multiple sclerosis, liver cirrhosis) Inability to provide informed consent or refusal to do so Inability to comply with the control or intense follow-up program Participation in other clinical trials interfering with the control-programs Previous malignancies (except for non-melanoma skin cancer)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peer Wille-Jørgensen, Ass Prof.
Organizational Affiliation
Bispebjerg Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Adam Dziki
Organizational Affiliation
Medical University of Lodz, Poland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nils Lundqvist
Organizational Affiliation
Norrtälje Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Goldinger
Organizational Affiliation
St.Görans Hospital, Stockholm, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mats Bragmark
Organizational Affiliation
Danderyd Hospital, Stockholm, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ulrik Lindforss, MD Phd
Organizational Affiliation
Södertälje Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kennet Smedh
Organizational Affiliation
Central Hospital, Västerås, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Monika Svanfeldt
Organizational Affiliation
Karolinska University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Johan Ottoson
Organizational Affiliation
Central Hospital, Kristianstad, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anna Martling
Organizational Affiliation
Karolinska University Hospital, Solna, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jonas Bengtson
Organizational Affiliation
Sahlgrenska University Hospital, Gothenburg, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Birger Sandzén
Organizational Affiliation
University Hospital of Umeå, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ingvar Syk
Organizational Affiliation
Malmö Academic Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lars Påhlman
Organizational Affiliation
Uppsala University Academic Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pamela Buchwald
Organizational Affiliation
Helsingborg Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Erling Østergaard
Organizational Affiliation
Viborg Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Per Andersen
Organizational Affiliation
Fyn Hospital, Svendborg, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mogens Madsen
Organizational Affiliation
Herning Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karl Erik Jensen
Organizational Affiliation
Esbjerg Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Per Gandrup
Organizational Affiliation
Aalborg Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Per Jess
Organizational Affiliation
Hillerød hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Henrik Christensen
Organizational Affiliation
Aarhus Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Luis Carriquiry
Organizational Affiliation
Maciel Hospital, Montevideo, Uruguay
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jósef Kladny
Organizational Affiliation
Pomeranian Medical University, Poland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christoffer Odensten
Organizational Affiliation
Sunderby Hospital, Luleå, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yngve Raab
Organizational Affiliation
Södersjukhuset, Stockholm, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Allan G Pedersen
Organizational Affiliation
Randers Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Helena Laurell
Organizational Affiliation
Mora Hospital, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ronan O'Connel
Organizational Affiliation
St. Vincents Hospital, Dublin, Ireland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peer Wille-Jørgensen
City
Copenhagen
ZIP/Postal Code
DK-2400
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
29800179
Citation
Wille-Jorgensen P, Syk I, Smedh K, Laurberg S, Nielsen DT, Petersen SH, Renehan AG, Horvath-Puho E, Pahlman L, Sorensen HT; COLOFOL Study Group. Effect of More vs Less Frequent Follow-up Testing on Overall and Colorectal Cancer-Specific Mortality in Patients With Stage II or III Colorectal Cancer: The COLOFOL Randomized Clinical Trial. JAMA. 2018 May 22;319(20):2095-2103. doi: 10.1001/jama.2018.5623.
Results Reference
derived
Links:
URL
http://www.colofol.com
Description
Related Info

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Assessment of Frequency of Surveillance After Curative Resection in Patients With Stage II and III Colorectal Cancer

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