Evaluation of Cryoprotection Induced Nail Toxicity Docetaxel Low Cumulative Dose
- Conditions
- Breast Neoplasms
- Interventions
- Other: cooling helmetOther: mittens and booties
- Registration Number
- NCT02283983
- Lead Sponsor
- Centre Hospitalier Departemental Vendee
- Brief Summary
For the specific patient population studied receiving 5-Fluorouracil, epirubicin and cyclophosphamide - Docetaxel sequence (cumulative dose \<300 mg / m2), using a cryoprotection has never been assessed.
The effectiveness of cryoprotection of onycholysis secondary to Docetaxel is not well established in this population (breast cancer in the adjuvant setting) and is based solely on a publication (Scotté) that does not contain the same therapeutic modalities (dose significantly higher). The few studies available have heterogeneous populations, nonrandomized, retrospective or with a small sample.
By extension to what has been observed with higher cumulative doses of docetaxel, some teams offer mittens and booties chilled to their patients, a practice that is not the subject of a national consensus.
The investigators wish to accurately assess the effectiveness of mittens and slippers chilled, their tolerance and their observance because of weak data on this specific population in the literature.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 319
- upper age to 18 years
- mammary adenocarcinoma nonmetastatic and histologically proven
- wait under an adjuvant or neoadjuvant chemotherapy according to the following conventional scheme: 3 cycles of F5-Fluorouracil, epirubicin and cyclophosphamide 100 (500 or 5-Fluorouracil 600 mg / m² J1, Epirubicin 100 mg / m² J1, Cyclophosphamide 500 or 600 mg / m² J1 or 3 cycles of Epiribucin and Cyclophosphamide 100) followed by 3 cycles of docetaxel, 100 mg / m², +/- trastuzumab if Her2+++
- Patient with the capacity/faculties to understand a newsletter and sign an informed consent
- Patient receiving social coverage
- Patient who can be treated and followed in the center for a period of at least one year
- WHO scale 0 or 1
-
Age below 18 years
-
Diseases of the scalp or whatever hair-showing against helmet or alopecia
-
Using pre nail resin before and per chemotherapy
-
mammary adenocarcinoma stage IV
-
Indication of docetaxel for cancer of another organ than breast
-
Treatment processing or programmed during chemotherapy with an innovative molecule being evaluated
-
Raynaud's syndrome, cold agglutinin disease, cryoglobulinemia and cryofibrinogenemia.
-
Uncontrolled severe arterial disease.
-
Presence of a device> grade 1 neuropathy before the start of chemotherapy
-
Patient unable to submit the protocol followed for psychological, social, family or geographical
-
Patient with an incompatible underlying disease or concomitant with the inclusion in the trial, whether psychiatric or somatic
-
Patient trust, guardianship, under legal protection measure, deprived of freedom
-
Male
-
Criteria for non randomization (before the first course of docetaxel) :
- Presence of peripheral neuropathy> grade 1 after the first 3 cycles of 5-Fluorouracil, epirubicin and cyclophosphamide 100.
- Presence of a nail or skin toxicity> grade 1 after 3 cycles of 5-Fluorouracil, epirubicin and cyclophosphamide 100.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Standard cryoprotection cooling helmet Proposal helmet without mittens and booties Cryoprotection with mittens and booties mittens and booties Standard cryoprotection with mittens and booties Cryoprotection with mittens and booties cooling helmet Standard cryoprotection with mittens and booties
- Primary Outcome Measures
Name Time Method Evaluation of the Occurrence of Nail Toxicity of Grade 2 of Common Toxicity Criteria for Adverse Effects V4.0 Evaluated at 8 Weeks Post Infusion of Docetaxel. 8 weeks post infusion of docetaxel
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (10)
CH du Mans
🇫🇷Le Mans, France
CHBA Vannes
🇫🇷Vannes, France
Centre Hospitalier de Cholet
🇫🇷Cholet, France
Institut de cancérologie de l'Ouest - Nantes
🇫🇷Saint-Herblain, France
Centre d'Oncologie Saint-Yves
🇫🇷Vannes, France
Institut de cancérologie de l'Ouest - Angers
🇫🇷Angers, France
Centre hospitalier Bretagne Sud
🇫🇷Lorient, France
Clinique Mutualiste de l'Estuaire
🇫🇷Saint-Nazaire, France
CHD Vendee
🇫🇷La Roche sur Yon, France
Centre Catherine de Sienne
🇫🇷Nantes, France