Status:
RECRUITING
High Definition Medicine for Solid Tumors Oncology
Lead Sponsor:
Centro Nacional de Investigaciones Oncologicas CARLOS III
Conditions:
Metastatic Solid Tumor
Advanced Cancer
Eligibility:
FEMALE
18+ years
Brief Summary
The present study aims to analyze different genetic, phenotypic, environmental, social and lifestyle characteristics of cancer patients who are going to start a first line of cancer treatment with pal...
Detailed Description
The objective of this study is to obtain a cohort of patients with advanced cancer that is robust and large enough to study the nature and possible interrelation between these variables and their infl...
Eligibility Criteria
Inclusion
- Confirmed diagnosis of oncological disease of solid origin, candidate for first-line treatment (TREATMENT VIRGIN FOR METASTIC DISEASE).
- Advanced tumor stage (III or IV) not a candidate for treatment with curative intent.
- Preference will be given to the following pathologies and sub-types:
- Women with hormone-positive, HER2-negative breast cancer who will receive a CDK4/6 inhibitor plus a hormone inhibitor. o Women with lung cancer of any subtype, candidates to receive first-line treatment.
- Women with colon cancer of any subtype, candidates to receive first-line treatment.
- Patients who are going to start treatment in a clinical trial are allowed, as long as the treatment is known (in other words, patients who participate in double-blind studies would not be candidates). There are no inclusion problems for patients who have different types of therapies within the trial as long as they are known (examples such as the following, but not limited to these: women starting treatment for breast cancer with a SERD and an approved CDK4/6 inhibitor , women who start an AI and an experimental CDK4/6/2, women who start a triplet for breast cancer but include AI+CDK4/6i, women who start a triplet for lung cancer with chemotherapy, pembrolizumab, and an experimental immunotherapy , etc).
- ECOG performance status \<2.
- Sufficient capacity and knowledge to carry and use the wearable.
- Have a mobile device with internet access and an email account.
- Ability to complete quality of life, nutrition and mental health questionnaires.
- Written informed consent to participate in the trial obtained prior to any study-specific screening procedures.
- Patients with co-morbidities are not excluded - they are part of the "real world" clinic and it is necessary to know their evolution.
- For the same reason, pregnant women are not excluded.
Exclusion
- Having previously received oncological treatment for metastatic disease or with palliative intent.
- Planned participation in treatment in a double-blind trial regime.
- Previous or concomitant malignant disease of any other type that could affect compliance with the protocol or interpretation of results. Patients with curatively treated basal cell carcinoma of the skin or cervical cancer in situ are eligible for the study.
- Concurrent illnesses that may significantly interfere with participation in the study at the discretion of the investigator. No specific diseases are specified, since patients with multiple pathologies are part of the daily clinic and it is very interesting to collect data from patients with other comorbidities, as long as they have the necessary digital familiarization to wear the wearable and use the APP.
- Carriers of therapeutic electronic devices: pacemakers, defibrillators or cardiac resynchronizers (due to potential interference caused by the device).
Key Trial Info
Start Date :
March 2 2023
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2028
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT06590506
Start Date
March 2 2023
End Date
January 1 2028
Last Update
September 19 2024
Active Locations (9)
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1
Hospital Universitario A Coruña
A Coruña, A Coruña/ Galicia, Spain, 15006
2
Hospital Universitario de Fuenlabrada
Fuenlabrada, Madrid, Spain, 28942
3
Hospital Son Espases
Palma de Mallorca, Mallorca / Baleares, Spain, 07120
4
Complejo Hospitalario de Navarra
Pamplona, Navarre, Spain, 31008