Predictive Toxicity Test Linked to Radiotherapy After Mastectomy and Immediate Implant Reconstruction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorInstitut du Cancer de Montpellier - Val d'Aurelle

About this trial

This study evaluates the capacity of the NovaGray RILA Breast® test to predict the toxicity linked to radiotherapy and the impact of implant breast reconstruction.

Eligibility criteria

Qualifiers

Age ≥18 years

Patients with histologically confirmed breast cancer with indication of mastectomy or surgery with mastectomy performed

Indication of wall chest radiation after mastectomy

Patient's agreement to receive or having had an immediate breast reconstruction by implant in one or two steps, with or without a dermal or synthetic matrix (depending on the habits of the center)

Disqualifiers

Breast reconstruction with flap

Inflammatory breast cancer (cT4d)

Skin or parietal breast cancer (cT4 a, b or c)

Metastatic patients

Trial design

Treatments tested in this trial

  • NovaGray RILA Breast® test

Treatment groups

250 Participants
are divided into 1 treatment group