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Impact of Aerobic Exercise on Immune Response and Side Effects of Cancer Treatments (CANEX-2)

Primary Purpose

Colorectal Cancer Stage IV

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Resting state (Control)
Moderate Intensity Continuous Exercise (MICE)
High Intensity Interval Exercise (HIIE)
Sponsored by
Université de Sherbrooke
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Colorectal Cancer Stage IV

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of metastatic colorectal cancer
  • At the beginning of their chemotherapy treatment
  • Eastern Cooperative Oncology Group (ECOG) performance status between grades 0 to 1
  • Physically capable to realise HIIT and continous moderate aerobic exercise on ergocycle

Exclusion Criteria:

  • Orthopedic, cardiac or metabolic limitations preventing aerobic effort
  • Betablockers
  • Surgery planned for the next two months following recruitment

Sites / Locations

  • Research Centre on Aging

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Cancer patients with MRI

Cancer patients without MRI

Healthy patients

Arm Description

9 cancer patients will be recruited and received the 3 experimental conditions : first the rest condition (with MRI), then randomly MICE condition and HIIT condition (with MRI).

9 cancer patients will be recruited and received the 3 experimental conditions : first the rest condition, then randomly MICE condition and HIIT condition, all without MRI.

9 healthy patients will be recruited and received 2 experimental conditions : first the rest condition (with a MRI), then HIIT condition (with MRI).

Outcomes

Primary Outcome Measures

Change in the concentration of different peripheral blood mononuclear cells (Natural Killer Cells, T cells and monocytes)
Flow cytometry

Secondary Outcome Measures

Change in the concentration of inflammatory mediators in peripheral blood (chemokines, pro- and anti-inflammatory cytokines)
Luminex immunoassay
Change of hormonal profile (cortisol, corticotropin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), adrenaline and noradrenaline)
ELISA Kits and Salivary Cortisol Enzyme ImmunoAssay Kit
Change of Indoleamine-2,3-Dioxygenase activation
Liquid chromatography-mass spectrometry (LCMS)
Cancer-Related Fatigue
Visual Analogue Scale, graduated from 0 (no fatigue) to 10 (extreme fatigue)
Cerebral integrity - Cerebral blood flow
Functional MRI (pcASL technique)
Heart rate variability
Heart rate monitor

Full Information

First Posted
December 11, 2020
Last Updated
November 4, 2022
Sponsor
Université de Sherbrooke
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1. Study Identification

Unique Protocol Identification Number
NCT04715061
Brief Title
Impact of Aerobic Exercise on Immune Response and Side Effects of Cancer Treatments
Acronym
CANEX-2
Official Title
Modulation of Immune Response and Side Effects of Cancer Treatments by Aerobic Exercise: Role of Exercise Intensity
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
November 4, 2020 (Actual)
Primary Completion Date
September 29, 2022 (Actual)
Study Completion Date
October 4, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Université de Sherbrooke

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
Aerobic exercise is associated with many benefits in patients with cancer treatments. Among these, the reduction of cancer-related fatigue (CRF) is one of the best demonstrated. Besides, several animal models have shown a marked reduction in tumor growth with aerobic exercise, sometimes by more than 60%. As the level of physical activity is convincingly associated with a reduction in the risk of cancer or recurrences, this suggests that aerobic exercise may represent a central therapeutic approach during treatment, both against CRF and for its potential anti-tumor effect. Both benefits have been suggested to be based on the immunostimulatory and anti-inflammatory effects of exercise. Indeed, systemic inflammatory activity seems to play a central role in the etiology of CRF during cancer treatments, among other things by stimulating the neuro-inflammatory activity of the central nervous system. Also, regarding the anti-tumor effect of exercise, animal models show that this benefit is partly explained by an increase in the activity of immune cells called natural killers (Natural Killer; NK) in tumor tissue and a reduction in the activity of regulatory T cells, the latter having an immunosuppressive effect. However, in humans, the results vary. While some improvement in NK cell activity has been reported in response to aerobic training in breast cancer survivors, others have seen no effect on the immune profile of patients and survivors. On the other hand, some authors report an improvement in the inflammatory profile with training, while others report little or no effect, as well as weak associations with the perception of fatigue. Although these results seem to discredit the hypothesis of immune and inflammatory regulation of exercise in humans, these studies have all looked at the effect of several weeks of training on the inflammatory and immune profile on an empty stomach and rest. However, several results from the field of exercise immunology convincingly show that the anti-inflammatory effect, as well as the immunostimulating effect of aerobic exercise (including the anti-tumor activity of NK cells) are mainly acute and transient, ie. in the hours following the end of the effort. Furthermore, certain results suggest that in the context of chemotherapy treatments, cyclical treatment by nature, the peaks of fatigue are also acute (i.e. in the days following the treatment) and parallel to peaks of inflammatory activity. Considering these results, it is therefore plausible to assume that the effect of aerobic exercise on suppressing tumor growth and reducing CRF results rather than the repetition of this acute response at each exercise session. In this case, the prescription of aerobic exercise preceding a session of chemotherapy could potentially represent an interesting therapeutic modality, allowing both the reduction of the CRF associated with this treatment, as well as a better response to the treatment. Besides, as this acute response seems to be highly dependent on the intensity of the effort, high-intensity interval training (HIIT) could be a particularly interesting approach in this context, because it does not require that the high intensity or long-lasting exercise. However, considering the immunosuppressive and pro-inflammatory effects of chemotherapy, the extent of the acute response to exercise may not allow this type of therapeutic use to be considered in this population. To date, no study has attempted to characterize the acute immune and inflammatory response following aerobic exercise in patients currently undergoing chemotherapy treatments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer Stage IV

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Each participant performed 3 experimental conditions (rest, moderate continuous training and interval training).
Masking
None (Open Label)
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cancer patients with MRI
Arm Type
Experimental
Arm Description
9 cancer patients will be recruited and received the 3 experimental conditions : first the rest condition (with MRI), then randomly MICE condition and HIIT condition (with MRI).
Arm Title
Cancer patients without MRI
Arm Type
Experimental
Arm Description
9 cancer patients will be recruited and received the 3 experimental conditions : first the rest condition, then randomly MICE condition and HIIT condition, all without MRI.
Arm Title
Healthy patients
Arm Type
Active Comparator
Arm Description
9 healthy patients will be recruited and received 2 experimental conditions : first the rest condition (with a MRI), then HIIT condition (with MRI).
Intervention Type
Other
Intervention Name(s)
Resting state (Control)
Intervention Description
Participants were asking to sit on a sofa for 50 minutes.
Intervention Type
Other
Intervention Name(s)
Moderate Intensity Continuous Exercise (MICE)
Intervention Description
MICE condition consisted of 50 minutes of moderate and continuous aerobic exercise on ergocycle. This includes a warm-up and cool-down period at low intensity, and a 40-minute period at moderate intensity (power output is equivalent to an effort perception from 4 to 6/10 and lactate levels from 2 to 4 mmol/L, obtained by submaximal test)
Intervention Type
Other
Intervention Name(s)
High Intensity Interval Exercise (HIIE)
Intervention Description
HIIT condition consisted of a 30 minutes of aerobic exercise training perform on ergocycle. This includes a warm-up at low intensity, followed by 10 blocks of 1 minute at high intensity (power output corresponding to the highest power reached at the submaximal test and lactate levels > 4 mmol/L) and 1 minute of active cooldown (effort perception around 1-2/10).
Primary Outcome Measure Information:
Title
Change in the concentration of different peripheral blood mononuclear cells (Natural Killer Cells, T cells and monocytes)
Description
Flow cytometry
Time Frame
Before the start of the condition (t = 0 minute), at the end of the condition (t = 50 minutes), 1 hour post-condition (t = 110 minutes)
Secondary Outcome Measure Information:
Title
Change in the concentration of inflammatory mediators in peripheral blood (chemokines, pro- and anti-inflammatory cytokines)
Description
Luminex immunoassay
Time Frame
Before the start of the condition (t = 0 minute), At the end of the condition (t = 50 minutes), 1 hour post-condition (t = 110 minutes), 2 hour post-condition (t = 170 minutes)
Title
Change of hormonal profile (cortisol, corticotropin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), adrenaline and noradrenaline)
Description
ELISA Kits and Salivary Cortisol Enzyme ImmunoAssay Kit
Time Frame
Before the start of the condition (t = 0 minute), At the end of the condition (t = 50 minutes), 1 hour post-condition (t = 110 minutes), 2 hour post-condition (t = 170 minutes)
Title
Change of Indoleamine-2,3-Dioxygenase activation
Description
Liquid chromatography-mass spectrometry (LCMS)
Time Frame
Before the start of the condition (t = 0 minute), At the end of the condition (t = 50 minutes), 1 hour post-condition (t = 110 minutes), 2 hour post-condition (t = 170 minutes)
Title
Cancer-Related Fatigue
Description
Visual Analogue Scale, graduated from 0 (no fatigue) to 10 (extreme fatigue)
Time Frame
During 5 days after the day of the condition, 3 times per day
Title
Cerebral integrity - Cerebral blood flow
Description
Functional MRI (pcASL technique)
Time Frame
At the end of the condition (t = 50 minutes) within a 30-minute time window
Title
Heart rate variability
Description
Heart rate monitor
Time Frame
At the end of the condition, during 10 minutes (t = 50 minutes to t = 60 minutes)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of metastatic colorectal cancer At the beginning of their chemotherapy treatment Eastern Cooperative Oncology Group (ECOG) performance status between grades 0 to 1 Physically capable to realise HIIT and continous moderate aerobic exercise on ergocycle Exclusion Criteria: Orthopedic, cardiac or metabolic limitations preventing aerobic effort Betablockers Surgery planned for the next two months following recruitment
Facility Information:
Facility Name
Research Centre on Aging
City
Sherbrooke
State/Province
Quebec
ZIP/Postal Code
J1H 4C4
Country
Canada

12. IPD Sharing Statement

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Impact of Aerobic Exercise on Immune Response and Side Effects of Cancer Treatments

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