Breast Cancer
Conditions
Brief summary
The radiotherapy treatment plan (also called dosimetry) used for all treatment sessions is based on the dosimetric scanner. During the sessions, the anatomy of the breast may vary, and these variations may impact the quality of the treatment. Adaptive radiotherapy is a new technique that allows these changes to be taken into account during treatment by automatically rescheduling the treatment for each session. The proposed trial aims to clinically evaluate one of these adaptive radiotherapy tools (PreciseART) based on deformable registration in order to determine if it can be used in daily practice in the treatment of breast cancer by tomotherapy. The trial will also clarify whether factors, such as duration of treatment, impact the quality of this algorithm.
Detailed description
The dosimetric scanner needed to calculate the dose to be delivered to the tissues will be carried out according to the standard practice. The treatment plan will be carried out by the physicist in accordance with the dose constraints and validated by the radiation therapist. Each treatment session is preceded by positioning imaging to ensure high precision in the treated area. During the first session, the acquisition of the positioning scanner will take into account the entire region of the target volume in accordance with the classic treatment protocol. Usually, the positioning scans of the remaining sessions are carried out on a smaller area around the operating bed in order to reduce the acquisition time. However, in the context of this study, mid- and end-of-treatment positioning scans will be acquired over the same exploration range as on the first day. These scanners will make it possible to compare the contouring work carried out manually by the radiotherapist and that obtained by the deformable registration algorithm.
Interventions
OTHERComplete Positioning scans
Entire treatment zone imaging at mi-treatment and at end of treatment
Sponsors
Institut de cancérologie Strasbourg Europe
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Inclusion criteria
Female * With invasive breast carcinoma (or axillary lymphadenopathy whose pathological examination is compatible with the origin of breast cancer but without an identified primary breast tumor) * Breast surgery (conservative surgery or mastectomy) * Treated by (neo)adjuvant chemotherapy or hormonotherapy * eligible to normo-fractionated breast radiotherapy in 25 sessions of 2 Gray or 15 sessions of 2.67 Gray, associated or not to bed irradiation whatever the delivered dose * eligible to an irradiation of sus-clavicular, inner mammary chain or axillary lymph nodes * With helicoidal tomotherapy
Exclusion criteria
* Absence of indication for breast radiotherapy * Absence of indication for lymph nodes irradiation * partial irradiation of breast * in situ carcinoma * intranodal isolated tumor cells * radiotherapy on prosthesis or surgically reconstructed breast * antecedent of breast irradiation opr homolateral lymh node irradiation * bilateral breast cancer
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Differences between dosimetric metrics on deformed and delineated contours. | Before treatment | Description of the differences between metrics calculated on delineated contours and contours deformed by artificial intelligence |
Countries
France
Outcome results
None listed