ExCell: Exercise in Testicular Germ Cell Cancer Survivors

Sponsor
Slovak Academy of Sciences (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05063760
Collaborator
Comenius University (Other)
60
2
2
53.5
30
0.6

Study Details

Study Description

Brief Summary

Regular exercise is effective in prevention & treatment of chronic diseases. Exercise can reduce late toxicity of chemotherapy, commonly found in cancer survivors, which is yet to be translated into clinical practice.

Mechanisms of exercise benefits in oncologic patients are far from being elucidated, and include increase in muscle mass, reduction of fat mass, systemic inflammation and cardiometabolic risk. Synchronization of exercise adaptive response is, to an extent, mediated by bioactive molecules released from muscle, with anti-inflammatory & tumor-suppressing properties. Muscle satellite cells are a source of regeneration, muscle structural integrity & functional capacity. Phenotypes of muscle cells, such as secretory profile, lipid & glucose metabolism, mirror clinical phenotypes of the donor. Importantly, muscle cells' metabolism in vitro can be modulated by 8-12 week training in vivo. Epigenetic mechanisms regulating muscle & systemic metabolism in cancer survivors are not yet understood.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: aerobic-strength exercise intervention (6-months)
N/A

Detailed Description

Aims:
  • To assess the impact of 6-month supervised, individualized aerobic-strength exercise training intervention in cancer survivors with chemotherapy-induced late toxicity . (i) on the whole-body energy and glucose metabolism, anthropometric parameters, physical fitness & activity profile, motor functions and quality of life in testicular germ cell cancer (TGCC) survivors, more than 3 years after cisplatin-based chemotherapy; with the 2-year follow up; . (ii) on skeletal muscle mass, morphology as well as functional and metabolic state detected in vivo (31P-MR spectroscopy).

(iii) on metabolic characteristics of primary skeletal muscle cells;

  • To determine the impact of exercise intervention on circulating bioactive molecules (exerkines), putative mediators of exercise health benefits as well as on levels of circulating inflammatory cytokines, which likely contribute to the pathogenesis of chemotherapy-induced late toxicity;

  • To evaluate the role of (a) selected exercise-regulated bioactive molecules, (b) exercise-mimicking treatment (by electric pulse stimulation) and (c) cisplatin treatment on metabolism and mitochondrial function of differentiated human muscle cells in culture;

  • To investigate the associations between intervention-induced shifts in circulating bioactive molecules and selected metabolic, anthropometric and motor parameters.

The generated results will enable us (i) to gain a better insight into pathomechanisms of muscle-associated chemotherapy-induced late toxicity and the role of skeletal muscle & systemic mediators in the exercise-induced health benefits in TGCC survivors; and (ii) to validate the effectiveness of the individually-tailored exercise intervention in reducing chemotherapy-related toxicity in patients with TGCC, with the aim to transfer this knowledge into clinical practice.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
controled trial with exercise interventioncontroled trial with exercise intervention
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
lab technicians and statistician are blinded.
Primary Purpose:
Supportive Care
Official Title:
Exercise in Prevention & Treatment of Chemotherapy-related Late Toxicity in Testicular Germ Cell Cancer Survivors: the Role of Skeletal Muscle
Actual Study Start Date :
Jan 15, 2020
Anticipated Primary Completion Date :
Dec 15, 2023
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: TGCT patients - exercise

TGCT survivors, men, 25-55 yrs old, 3 and more years after successful treatment of TGCT, with the capacity to undergo aerobic-strength intervention assessed by cardiologist

Behavioral: aerobic-strength exercise intervention (6-months)
6 month supervised exercise intervention in TGCT survivors (1 hour sessions 3 x per week),

No Intervention: TGCT patients - nonexercising controls

TGCT survivors, men, 25-55 yrs old, 3 and more years after successful treatment of TGCT, with the capacity to undergo aerobic-strength intervention assessed by cardiologist

Outcome Measures

Primary Outcome Measures

  1. change in the glucose tolerance [parameter will be measured before and after 6 month intervention]

    change in glucose tolerance (as measured by oral glucose tolerance test)

  2. change in resting energy expenditiure and metabolic substrate preference [parameters will be measured twice before and after 6 month intervention]

    change in resting energy expenditure calculated by Weir equation from VO2 and metabolic substrate preference RQ VCO2/VO2 (as measured by indirect calorimetry)

  3. change anthropometric parameters of obesity [parameters will be measured twice before and after 6 month intervention]

    BMI (kg.m-2) , fat mass (% electric bioimpedance), lean body mass (% electric bioimpedance), visceral adiposity (%, elecgtric bioimpedance)

  4. change physical fitness [parameter will be measured twice before and after 6 month intervention]

    VO2max (mlO2 per kg BW min) as measured by bicycle spiroergometry

Secondary Outcome Measures

  1. change in quality of life for cancer patients [measured twice before and after 6 month intervention]

    validated questionnaire

  2. change in muscle strength [measured twice before and after 6 month intervention]

    dynamometry

  3. change in cognitive functions [measured twice before and after 6 month intervention]

    standardised cognitive test Cogstate

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 55 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • TGCT survivors, with chemotherapy-induced metabolic toxicity, men, 25-55 years old, with the capacity to undergo training, signed written informed consent
Exclusion Criteria:
  • serious / uncontrolled chronic diseases, non-compliance, other health issues as assessed by oncologists / investigators

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Cancer Institute Bratislava Please Select Slovakia 800 00
2 Biomedical Research Center Slovak Academy of Sciences Bratislava Please Select Slovakia 84505

Sponsors and Collaborators

  • Slovak Academy of Sciences
  • Comenius University

Investigators

  • Principal Investigator: Barbara Ukropcova, MD, PhD, Prof, Biomedical Research Center, Slovak Acad Sci

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jozef Ukropec, PhD, DSc, Slovak Academy of Sciences
ClinicalTrials.gov Identifier:
NCT05063760
Other Study ID Numbers:
  • 2/0164/20
  • SRDA19-0411
First Posted:
Oct 1, 2021
Last Update Posted:
Oct 1, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jozef Ukropec, PhD, DSc, Slovak Academy of Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 1, 2021