search
Back to results

ABCSG C08-Exercise II: Trial of Endurance Exercise Following Adjuvant Chemotherapy for Colorectal Cancer (ABCSG C08)

Primary Purpose

Colorectal Carcinoma

Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
endurance exercise
control
Sponsored by
Austrian Breast & Colorectal Cancer Study Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Carcinoma focused on measuring endurance exercise

Eligibility Criteria

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

Inclusion Criteria:

  • completely resected, histologically confirmed adenocarcinoma of the colon or rectum
  • patients, who have completed adjuvant chemotherapy 4-16 weeks prior to randomization
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Age ≥18 years
  • adequate hematologic functions <=28d prior to randomization
  • able to perform endurance exercise according to protocol
  • ability to perform ergometry in order to assess physical capability at the discretion of the investigator
  • signed informed consent prior to randomization

Exclusion Criteria:

  • significant comorbid conditions precluding participation in a physical activity program (investigators decision)
  • disabled patients unable to participate in the physical activity program
  • Regular (3-times a week) vigorous physical activity of >150 minutes (type of physical activity: bicycling, cross walking (cross trainer), jogging, walking at a brisk pace, nordic walking, cross country skiing) within the last year before diagnosis of colorectal cancer
  • patients unwilling to complete endurance exercise or complete all questionnaires related to the study
  • past or current history of other malignant neoplasms other than colorectal cancer in the last 5 years except basal cell carcinoma of the skin and/or in situ carcinoma of the cervix
  • clinically significant cardiovascular disease
  • left bundle branch block
  • current study with chemotherapy or radiation
  • current pregnancy or plans to become pregnant within the next 3 years

Sites / Locations

  • Med. Univ. GrazRecruiting
  • BKH KufsteinRecruiting
  • KH St. Josef BraunauRecruiting
  • Hospital BHS Linz, Coop. Study GroupRecruiting
  • Kepler Universitätsklinikum LinzRecruiting
  • Hospital BHS Ried
  • State Hospital SteyrRecruiting
  • Klinikum Wels-GrieskirchenRecruiting
  • LKH Salzburg-PMU, UNiv. KLinik f. Innere Med IIIRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

A - endurance exercise

B - control arm

Arm Description

All patients receive a pulse-controlled endurance exercise program based on the study results by O'Donovan. The individual pulse-controlled endurance exercise should be performed 3 times a week. On the basis of age, weight, sex and body fat the normal weight will be calculated. The kilocalories (kcal), which correspond to the metabolic equivalent task (MET) hour per week, will be calculated after age and gender adjustment of the normal weight. The endurance exercise will be increased gradually until reaching 18 MET-hours/wk during the year of endurance exercise. Patients in arm A can perform different types of endurance exercise (bicycling, cross walking, jogging, walking, nordic walking, cross country skiing)

Patients in this arm should maintain their habitual physical activity pattern as before the diagnoses of colorectal cancer.

Outcomes

Primary Outcome Measures

Primary Endpoint - disease free survival (DFS)
DFS is defined as the time from randomization to locoregional or metastatic recurrence or the appearance of secondary cancer or death, whichever occurs first. Recurrence may be either histologically proven or evidenced by imaging via MRI or CT. Isolated CEA evaluation will not be sufficient to determine a relapse.

Secondary Outcome Measures

Secondary Efficacy Endpoint I - relapse free survival (RFS)
RFS is defined as the time from randomization to locoregional or metastatic recurrence of colorectal cancer or death, whichever occurs first
Secondary Efficacy Endpoint II - overall survival (OS)
OS is defined as time from randomization to death from any cause
Physical Activity Endpoint I - physical activity measured by MET-hours
Evaluation of physical activities measured by MET-hours in the domains "work", "leisure time ", "sedentary behavior" and "transporation" by Global Physical Activity Questionnaire (GPAQ) within each study arm and compared between study arms at baseline, at 3, at 6, at 12, at 24 and at 36 months
Physical Activity Endpoint II - endurance exercise measured by MET-hours
Evaluation of endurance exercise measured by MET-hours by pulse-control in arm A at 3, at 6 and at 12 months
Physical Activity Endpoint III - performance enhancement measured by MET-hours by ergometry
Evaluation of performance enhancement measured by MET-hours by ergometry within each study arm (arm A at baseline, at 3, at 6 and at 12 months; arm B at baseline and at 12 months) and compared between study arms at baseline and at 12 months
Physical Activity Endpoint IV - physical activity measures
Correlation of MET-hours in the domains "work", "leisure time ", "sedentary behavior" and "transporation" by Global Physical Activity Questionnaire (GPAQ) and results of endurance exercise as well as performance enhancement by ergometry (both measured by MET-hours) with DFS, RFS and OS
Patient Reported Outcome Endpoint I - fatigue
Evaluation of fatigue as measured by EORTC - QLQ FATIGUE CAT Theta scores compared between study arms. Score has no fixed upper and lower limit and a high score represents a high level of fatigue.
Patient Reported Outcome Endpoint II - emotional functioning score
Evaluation of the emotional functioning score (based in the functional scale EF) as measured by EORTC QLQ-C30 emotional functioning (based on items) compared between study arms, where a high score for a functional scale represents a high/healthy level of functioning.
Patient Reported Outcome Endpoint III - physical functioning score
Evaluation of the standardized physical functioning score (based on the revised functional scale PF2) as measured by EORTC QLQ-C30 physical functioning compared between study arms, where a high score for a functional scale represents a high/healthy level of functioning
Patient Reported Outcome Endpoint IV - global quality of life (QoL) score
Evaluation of the standardized global health status/QoL score (based on the revised global health status/QoL QL2) as measured by EORTC QLQ-C30 summary score compared between study arms, where a high score for the global health status/QoL represents a high QoL.
Patient Reported Outcome Endpoint V - patient reported outcomes (fatigue, emotional functioning, physical functioning, global quality of life)
Correlation of all patient reported outcomes explained above (fatigue, emotional functioning, physical functioning, global quality of life) with MET-hours
Body Composition Endpoint I - body mass index (BMI)
Evaluation of the influence of BMI on DFS, RFS and OS
Body Composition Endpoint II - body fat
Evaluation of the influence of body fat on DFS, RFS and OS
Body Composition Endpoint III - waist circumference
Evaluation of the influence of waist circumference on DFS, RFS and OS
Cardiovascular Endpoint - cardiovascular complications
Evaluation of the incidence of cardiovascular complications (myocardial infarction, stroke, newly diagnosed diabetes mellitus, newly diagnosed hypertension)
Safety Endpoint I - serious adverse events (SAEs)
Evaluation of the incidence of physical activity related SAEs and physical activity related deaths in both arms
Safety Endpoint II - time to SAEs
Evaluation of time from study start to physical activity related SAEs
Exploratory Endpoint - molecular and biochemical markers (will be defined during the course of the study)
Correlation of molecular and biochemical markers with DFS, RFS, OS and with physical activity. The analysis of molecular markers will depend on the markers which will be defined during the course of the study in addition to Insulin & ILGF.

Full Information

First Posted
November 29, 2018
Last Updated
June 14, 2023
Sponsor
Austrian Breast & Colorectal Cancer Study Group
Collaborators
Oberösterreichische Krebshilfe
search

1. Study Identification

Unique Protocol Identification Number
NCT03822572
Brief Title
ABCSG C08-Exercise II: Trial of Endurance Exercise Following Adjuvant Chemotherapy for Colorectal Cancer
Acronym
ABCSG C08
Official Title
ABCSG C08 - Exercise II: Randomized Trial of Endurance Exercise Following Adjuvant Chemotherapy for Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 14, 2019 (Actual)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Austrian Breast & Colorectal Cancer Study Group
Collaborators
Oberösterreichische Krebshilfe

4. Oversight

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

5. Study Description

Brief Summary
ABCSG C08 is a randomized, two-arm, multicenter trial to investigate the efficacy of endurance exercise following adjuvant chemotherapy in patients with colorectal cancer. Indication: Locally advanced colorectal cancer after adjuvant chemotherapy. Evidence supporting the beneficial effects of exercise programs during chemotherapy are available, the results across studies are not entirely consistent. Additional studies are needed to determine the optimal content, intensity, and form of training programs.
Detailed Description
Colorectal cancer is the second leading cause of cancer mortality in Western countries after breast cancer among women and lung cancer among men. About 5.000 new cases are diagnosed each year in Austria. This represents an annual incidence of 50-60 per 100.000 inhabitants. In patients with colorectal cancer stage III and in certain situations even in stage II adjuvant chemotherapy is indicated after R0 resection. Despite recent advances in adjuvant chemotherapy 20-30% of these patients still relapse. About 80% of recurrences occur in the first three years. There is consistent evidence from several observational epidemiologic studies that physical activity reduces the risk of developing colon cancer. In recent years several observational studies even showed a reduction in relapse rate, colon cancer-specific mortality and overall mortality by physical activity in patients with colon and breast cancer. Colon cancer survivors who engaged in higher levels of physical activity experienced a 50-60% improvement in long-term outcomes compared to inactive patients. Different mechanisms for the protective effect of physical activity on colon cancer have been proposed and it is believed that the same mechanisms of physical activity are also involved in the improvement of disease outcomes in gastrointestinal cancer survivors. Physical activity leads to decrease of inflammation, decreased levels of insulin-like growth factor (IGF) and insulin, reduced transit time through the gut and increased levels of vitamin D. Factors, that are associated with a reduced risk of colon polyps, colon cancer and colon cancer mortality. A review on the impact of various exercise programs on fatigue, found good evidence that exercise not only decreased levels of fatigue, but also increased quality of life, mood and functioning. While there is evidence supporting the beneficial effects of exercise programs during chemotherapy, the results across studies are not entirely consistent. Additional studies are needed to determine the optimal content, intensity, and form of training programs. Recently ABCSG has investigated the feasibility of endurance exercise after adjuvant chemotherapy in patients with locally advanced colorectal cancer in the investigator's study group (ABCSG C07 Exercise - pilot study). Results concerning compliance of patients have been considered for sample size estimations and study planning.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Carcinoma
Keywords
endurance exercise

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
788 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A - endurance exercise
Arm Type
Experimental
Arm Description
All patients receive a pulse-controlled endurance exercise program based on the study results by O'Donovan. The individual pulse-controlled endurance exercise should be performed 3 times a week. On the basis of age, weight, sex and body fat the normal weight will be calculated. The kilocalories (kcal), which correspond to the metabolic equivalent task (MET) hour per week, will be calculated after age and gender adjustment of the normal weight. The endurance exercise will be increased gradually until reaching 18 MET-hours/wk during the year of endurance exercise. Patients in arm A can perform different types of endurance exercise (bicycling, cross walking, jogging, walking, nordic walking, cross country skiing)
Arm Title
B - control arm
Arm Type
Other
Arm Description
Patients in this arm should maintain their habitual physical activity pattern as before the diagnoses of colorectal cancer.
Intervention Type
Other
Intervention Name(s)
endurance exercise
Intervention Description
defined exercise program
Intervention Type
Other
Intervention Name(s)
control
Intervention Description
habitual physical activity before the diagnosis
Primary Outcome Measure Information:
Title
Primary Endpoint - disease free survival (DFS)
Description
DFS is defined as the time from randomization to locoregional or metastatic recurrence or the appearance of secondary cancer or death, whichever occurs first. Recurrence may be either histologically proven or evidenced by imaging via MRI or CT. Isolated CEA evaluation will not be sufficient to determine a relapse.
Time Frame
8 years (after Last Patient Out (LPO))
Secondary Outcome Measure Information:
Title
Secondary Efficacy Endpoint I - relapse free survival (RFS)
Description
RFS is defined as the time from randomization to locoregional or metastatic recurrence of colorectal cancer or death, whichever occurs first
Time Frame
8 years (after Last Patient Out (LPO))
Title
Secondary Efficacy Endpoint II - overall survival (OS)
Description
OS is defined as time from randomization to death from any cause
Time Frame
8 years (after Last Patient Out (LPO))
Title
Physical Activity Endpoint I - physical activity measured by MET-hours
Description
Evaluation of physical activities measured by MET-hours in the domains "work", "leisure time ", "sedentary behavior" and "transporation" by Global Physical Activity Questionnaire (GPAQ) within each study arm and compared between study arms at baseline, at 3, at 6, at 12, at 24 and at 36 months
Time Frame
8 years (after Last Patient Out (LPO))
Title
Physical Activity Endpoint II - endurance exercise measured by MET-hours
Description
Evaluation of endurance exercise measured by MET-hours by pulse-control in arm A at 3, at 6 and at 12 months
Time Frame
8 years (after Last Patient Out (LPO))
Title
Physical Activity Endpoint III - performance enhancement measured by MET-hours by ergometry
Description
Evaluation of performance enhancement measured by MET-hours by ergometry within each study arm (arm A at baseline, at 3, at 6 and at 12 months; arm B at baseline and at 12 months) and compared between study arms at baseline and at 12 months
Time Frame
8 years (after Last Patient Out (LPO))
Title
Physical Activity Endpoint IV - physical activity measures
Description
Correlation of MET-hours in the domains "work", "leisure time ", "sedentary behavior" and "transporation" by Global Physical Activity Questionnaire (GPAQ) and results of endurance exercise as well as performance enhancement by ergometry (both measured by MET-hours) with DFS, RFS and OS
Time Frame
8 years (after Last Patient Out (LPO))
Title
Patient Reported Outcome Endpoint I - fatigue
Description
Evaluation of fatigue as measured by EORTC - QLQ FATIGUE CAT Theta scores compared between study arms. Score has no fixed upper and lower limit and a high score represents a high level of fatigue.
Time Frame
8 years (after Last Patient Out (LPO))
Title
Patient Reported Outcome Endpoint II - emotional functioning score
Description
Evaluation of the emotional functioning score (based in the functional scale EF) as measured by EORTC QLQ-C30 emotional functioning (based on items) compared between study arms, where a high score for a functional scale represents a high/healthy level of functioning.
Time Frame
8 years (after Last Patient Out (LPO))
Title
Patient Reported Outcome Endpoint III - physical functioning score
Description
Evaluation of the standardized physical functioning score (based on the revised functional scale PF2) as measured by EORTC QLQ-C30 physical functioning compared between study arms, where a high score for a functional scale represents a high/healthy level of functioning
Time Frame
8 years (after Last Patient Out (LPO))
Title
Patient Reported Outcome Endpoint IV - global quality of life (QoL) score
Description
Evaluation of the standardized global health status/QoL score (based on the revised global health status/QoL QL2) as measured by EORTC QLQ-C30 summary score compared between study arms, where a high score for the global health status/QoL represents a high QoL.
Time Frame
8 years (after Last Patient Out (LPO))
Title
Patient Reported Outcome Endpoint V - patient reported outcomes (fatigue, emotional functioning, physical functioning, global quality of life)
Description
Correlation of all patient reported outcomes explained above (fatigue, emotional functioning, physical functioning, global quality of life) with MET-hours
Time Frame
8 years (after Last Patient Out (LPO))
Title
Body Composition Endpoint I - body mass index (BMI)
Description
Evaluation of the influence of BMI on DFS, RFS and OS
Time Frame
8 years (after Last Patient Out (LPO))
Title
Body Composition Endpoint II - body fat
Description
Evaluation of the influence of body fat on DFS, RFS and OS
Time Frame
8 years (after Last Patient Out (LPO))
Title
Body Composition Endpoint III - waist circumference
Description
Evaluation of the influence of waist circumference on DFS, RFS and OS
Time Frame
8 years (after Last Patient Out (LPO))
Title
Cardiovascular Endpoint - cardiovascular complications
Description
Evaluation of the incidence of cardiovascular complications (myocardial infarction, stroke, newly diagnosed diabetes mellitus, newly diagnosed hypertension)
Time Frame
8 years (after Last Patient Out (LPO))
Title
Safety Endpoint I - serious adverse events (SAEs)
Description
Evaluation of the incidence of physical activity related SAEs and physical activity related deaths in both arms
Time Frame
8 years (after Last Patient Out (LPO))
Title
Safety Endpoint II - time to SAEs
Description
Evaluation of time from study start to physical activity related SAEs
Time Frame
8 years (after Last Patient Out (LPO))
Title
Exploratory Endpoint - molecular and biochemical markers (will be defined during the course of the study)
Description
Correlation of molecular and biochemical markers with DFS, RFS, OS and with physical activity. The analysis of molecular markers will depend on the markers which will be defined during the course of the study in addition to Insulin & ILGF.
Time Frame
8 years (after Last Patient Out (LPO))

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: completely resected, histologically confirmed adenocarcinoma of the colon or rectum patients, who have completed adjuvant chemotherapy 4-16 weeks prior to randomization Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 Age ≥18 years adequate hematologic functions <=28d prior to randomization able to perform endurance exercise according to protocol ability to perform ergometry in order to assess physical capability at the discretion of the investigator signed informed consent prior to randomization Exclusion Criteria: significant comorbid conditions precluding participation in a physical activity program (investigators decision) disabled patients unable to participate in the physical activity program Regular (3-times a week) vigorous physical activity of >150 minutes (type of physical activity: bicycling, cross walking (cross trainer), jogging, walking at a brisk pace, nordic walking, cross country skiing) within the last year before diagnosis of colorectal cancer patients unwilling to complete endurance exercise or complete all questionnaires related to the study past or current history of other malignant neoplasms other than colorectal cancer in the last 5 years except basal cell carcinoma of the skin and/or in situ carcinoma of the cervix clinically significant cardiovascular disease left bundle branch block current study with chemotherapy or radiation current pregnancy or plans to become pregnant within the next 3 years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Martina Putz, PhD
Phone
+43 1 4089230
Email
martina.putz@abcsg.at
First Name & Middle Initial & Last Name or Official Title & Degree
Aleksandra Mystek, BBSc
Phone
+43 1 4089230
Email
aleksandra.mystek@abcsg.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Josef Thaler, MD
Organizational Affiliation
Austrian Breast & Colorectal Cancer Study Group
Official's Role
Study Chair
Facility Information:
Facility Name
Med. Univ. Graz
City
Graz
State/Province
Styria
ZIP/Postal Code
8036
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Bauernhofer, MD
First Name & Middle Initial & Last Name & Degree
Thomas Bauernhofer, MD
Facility Name
BKH Kufstein
City
Kufstein
State/Province
Tyrol
ZIP/Postal Code
6330
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
August Zabernigg, MD, Head
First Name & Middle Initial & Last Name & Degree
August Zabernigg, MD, Head
Facility Name
KH St. Josef Braunau
City
Braunau Am Inn
State/Province
Upper Austria
ZIP/Postal Code
5280
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sigrid Kastl, MD, Head
First Name & Middle Initial & Last Name & Degree
Sigrid Kastl, MD, Head
Facility Name
Hospital BHS Linz, Coop. Study Group
City
Linz
State/Province
Upper Austria
ZIP/Postal Code
4010
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andreas Petzer, MD, Head
First Name & Middle Initial & Last Name & Degree
Andreas Petzer, MD
Facility Name
Kepler Universitätsklinikum Linz
City
Linz
State/Province
Upper Austria
ZIP/Postal Code
4020
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerhard Hochreiner, MD
First Name & Middle Initial & Last Name & Degree
Hochreiner, MD
Facility Name
Hospital BHS Ried
City
Ried
State/Province
Upper Austria
ZIP/Postal Code
4910
Country
Austria
Individual Site Status
Withdrawn
Facility Name
State Hospital Steyr
City
Steyr
State/Province
Upper Austria
ZIP/Postal Code
4400
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Johannes Andel, MD, Head
First Name & Middle Initial & Last Name & Degree
Johannes Andel, MD, Head
Facility Name
Klinikum Wels-Grieskirchen
City
Wels
State/Province
Upper Austria
ZIP/Postal Code
4600
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Josef Thaler, MD, Head
First Name & Middle Initial & Last Name & Degree
Josef Thaler, MD
Facility Name
LKH Salzburg-PMU, UNiv. KLinik f. Innere Med III
City
Salzburg
ZIP/Postal Code
5020
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Richard Greil, MD, Head
First Name & Middle Initial & Last Name & Degree
Richard Greil, MD, Head

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
currently sharing of IPDs (Individual Participant Data) is not planned in this trial

Learn more about this trial

ABCSG C08-Exercise II: Trial of Endurance Exercise Following Adjuvant Chemotherapy for Colorectal Cancer

We'll reach out to this number within 24 hrs