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Trial Title:
Physical Activity and Sarcoma, Role and Impact on Outcome
NCT ID:
NCT06565858
Condition:
Sarcoma
Conditions: Official terms:
Sarcoma
Conditions: Keywords:
Sarcoma
Physical activity
Study type:
Observational
Overall status:
Not yet recruiting
Study design:
Time perspective:
Prospective
Summary:
The aim of this study is to evaluate the role/impact of physical activity (PA) in
sarcomas, in their distribution and potentially also on their prognosis, as already
demonstrated for other neoplasms. Type, intensity, frequency, duration and circumstance
of both occupational and leisure physical activity will be collected through validated
questionnaires and self-reported measurement methods.
Detailed description:
The protective role of physical activity (PA) has been demonstrated in numerous diseases,
especially cardiovascular and metabolic ones, but also in various neoplastic pathologies.
It has been estimated that approximately 25% of cancer cases globally are due to excess
weight and a sedentary lifestyle. Regular moderate-intensity or greater physical activity
is associated with a reduced risk of several types of cancer. Most studies have shown
this association especially for breast, colon, and endometrial cancer.
The mechanisms through which PA may decrease cancer risk are numerous: physical activity
might work through reducing the amount of adipose tissue, thereby lowering circulating
levels of estrogens and other sex hormones, PA improves insulin resistance, reduces
hyperinsulinaemia, might reduce inflammatory markers, thereby decreasing the exposure to
these potentially carcinogenic hormones and peptides, reduces oxidative stress, reduces
gastrointestinal transit time and improves immune system by increasing the phagocytic
activity of macrophages and neutrophils, and increasing the proliferation of natural
killer cells and lymphocytes. Other mechanisms under investigation pertain angiogenesis,
DNA repair, and growth factors.
In addition to hormone-sensitive tumors and colon cancer, new evidence suggests that
similar associations with PA might exist for other cancers for which less is known about
the potential mechanisms underlying the physical activity association, suggesting that
further mechanistic research is warranted.
Furthermore, in people who have already been diagnosed with cancer and are undergoing
oncological therapy, regular exercise helps to counteract some typical and common side
effects of anti-cancer therapies, thus improving treatment compliance and the overall
quality of life. In particular, physical activity seems to reduce fatigue, arthralgia,
nausea, improves cardiovascular and respiratory capacity, reduces the risk of
osteoporosis, and anxiety.
Even more, several studies have shown that in patients already affected by cancer,
physical activity could be associated with a better prognosis, reducing risk of
recurrence and increasing survival. The most important and largest studies are mainly
aimed at breast, colorectal, prostate and ovarian cancer [5-8].
Due to their rarity and extreme histological-molecular heterogeneity, little is known
about sarcomas, particularly regarding potential risk factors and possible factors that
may influence their clinical course.
Furthermore, starting from the evidence that cardiac tumors, both primary and secondary,
are extremely rare, the possible mechanisms responsible for this favorable
"refractoriness" of myocardial cells to neoplastic transformation and/or to the
engraftment of other neoplastic cells will be studied.
The property of cardiomyocytes most likely related to this phenomenon is their
contractility and continuous exposure to mechanical load that halt cardiomyocyte
proliferation in the human heart. This project aims at improving knowledge about the
molecular landscape and genetic aberrations involved in pathogenesis of cardiac tumors
and assessing whether the mechanical forces generated by cardiomyocyte contraction in a
beating heart inhibit the proliferation of cancer cells, thus protecting the heart from
cancer.
Engineered heart tissue will be used to silence candidate mechanosensing genes. This
should make the cell unresponsive to mechanical stimulation and thus allow it to
proliferate even with increased afterload.
The expression levels of the mechanosensing genes eventually identified, will be tested
in tumor tissue from sarcoma as located in the extremities of physically active
individuals to assess whether they are downregulated, thus making the cells able to
proliferate although located in actively contracting skeletal muscles.
Confirmation of the role of physical activity on cancer is awaited with interest.
Understanding the mechanisms that link physical activity with cancer will be useful for
several reasons. First, the identification of this mechanisms can give new clues to
cancer biology, which might help in designing other cancer prevention and innovative
treatment modalities. Second, if further data accumulate showing that increased physical
activity can prevent some cancers or improve outcomes, this would constitute an excellent
public health intervention to reduce the impact of cancer risks and costs.
Criteria for eligibility:
Study pop:
This is a prospective observational study recruiting patients diagnosed with sarcomas any
site. Since sarcoma develop in bone, soft tissue and viscera, sarcoma appear suitable to
investigate the role of physical activity on sarcoma in different locations.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- age >18;
- diagnose of sarcoma;
- Written informed consent must be signed and dated by the patient and the
investigator.
Exclusion Criteria:
- Kaposi sarcoma.
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Istituto Europeo di Oncologia
Address:
City:
Milano
Zip:
20141
Country:
Italy
Start date:
September 30, 2024
Completion date:
August 30, 2026
Lead sponsor:
Agency:
European Institute of Oncology
Agency class:
Other
Source:
European Institute of Oncology
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06565858