About this trial

The study will include the prospective acquisition of optimized MR imaging data of prostate and breast patients treated with radiotherapy (RT).

Within the prospective study, biological specimens from patients undergoing in-room biopsy before RT, will be collected. Histological evaluation and cell culture (and organoid preparation) will be conducted, and samples/organoids will be irradiated with RT for biological validation.

Eligibility criteria

Qualifiers

Unifocal infiltrating ductal breast carcinoma, non-special histotype

clinical stage T1-T2,N0

No contraindications to MRI, or metal joint prostheses from knee to shoulder included, or femoral stent.

Patients aged >18 years

Disqualifiers

Nodule involvement and metastasis (cN1 and/or cM1)

Concomitant inflammation of the intestine

Significant systemic diseases or ongoing oral anticoagulant therapy

Non-compliance of dose constraints in the treatment plan

Trial design

Treatments tested in this trial

  • prostate patient
  • breast patients

Treatment groups

35 Participants
are divided into 2 treatment groups

Locations

1
European Institute of Oncology20141, MilanItaly, Italy

Sponsors and collaborators

European Institute of Oncology

Lead sponsor