High Definition Medicine for Solid Tumors Oncology

Inclusion Criteria13

• 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.