Characterization of Biophysical and Mechanical Parameters on the Skin of Subjects With a Diagnosis of Breast Cancer After Surgery and Undergoing Adjuvant Treatment.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Breast Cancer
- Sponsor
- European Institute of Oncology
- Enrollment
- 150
- Locations
- 1
- Primary Endpoint
- Forearm hydration degree assessmnent
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
Aim of this study is to characterize the chemical/physical and structural parameters of the skin in patients with breast cancer undergoing oncological adjuvant treatment in order to understand how to prevent and manage adverse skin events during hormone therapy, also through the formulation of new functional dermocosmetics.
Detailed Description
Breast cancer is the most frequent neoplasm in women in industrialized countries. After surgery, an adjuvant systemic treatment is generally proposed (hormone therapy, chemotherapy, molecular targeted therapy). Side effects of endocrine treatments, including skin toxicities, are frequent and often underestimated, leading to poor treatment adherence that can compromise therapeutic outcomes. Among adjuvant chemotherapy treatments, one of the most used drug is Paclitaxel: at skin level it can induce rash, dry skin and itching. The combination of radiotherapy with these oncological treatments could aggravate cutaneous side effects. Aim of this study is to characterize the chemical/physical and structural parameters of the skin in patints with breast cancer undergoing adjuvant treatment, performing specific skin tests with professional instruments and adequate personnel. The evaluation will be carried out in Estrogen Receptor (ER) positive breast cancer patients undergoing adjuvant therapy with Tamoxifen or Aromatase Inhibitor or Paclitaxel +/- adjuvant radiotherapy.
Investigators
Eligibility Criteria
Inclusion Criteria
- •age between 40 and 70 years
- •subjects who are receiving treatment with tamoxifen, aromatase inhibitor or paclitaxel in adjuvant therapy +/- adjuvant radiotherapy
- •subjects who are receiving hormonal therapy must have suspended any chemotherapy for at least 30 days
Exclusion Criteria
- •presence of known chronic skin pathologies before adjuvant treatment start (psoriasis, lupus, atopic dermatitis)
- •inability to understand and will
- •unavailability to carry out all the tests required by the protocol
Outcomes
Primary Outcomes
Forearm hydration degree assessmnent
Time Frame: 1 day
Forearm hydration degree evaluated using instrumental skin tests
Evaluation of Effects of Skin Disease on Quality of Life
Time Frame: 1 day
Collection of Skindex29 questionnaire (minimum value: 1, maximum value: 5 - higher scores mean a greater agreement with the statement)