Breast Neoplasm
Conditions
Keywords
Feasibility study, Early breast cancer, Stereotactic body radiotherapy, Cyberknife, Pre-operative radiotherapy
Brief summary
Most women with early breast cancer are treated with breast conserving therapy (BCT), consisting of breast conserving surgery (surgery to remove the cancer itself) followed by radiation to the breast. This treatment can take time and is associated with its own side effect profile. An innovative radiation technique called stereotactic body radiotherapy (SBRT) can deliver large doses of radiation precisely to the tumour while avoiding critical organs, therefore destroying the cancer and avoiding surgery altogether. SBRT has been successfully used for a number of cancers and it is proposed that it could be used to eradicate breast cancer. This feasibility study will investigate the feasibility and safety of treatment using SBRT in women with early stage breast cancer. Thirty-two women age 70 years or older with early breast cancer will be treated with SBRT (5 treatments) followed by breast conserving surgery and hormonal therapy. An MRI and breast conserving surgery will be performed at 8-12 weeks after radiation to assess response to treatment. The primary outcome of the study will be feasibility, meaning the ability to deliver radiation treatment as planned. Secondary outcomes will include treatment related toxicity and pathological response. If this study shows that SBRT can be used to treat patients primarily, it will lead to further evaluation of SBRT for early breast cancer.
Interventions
RADIATIONStereotactic body radiotherapy (SBRT)
Sponsors
Juravinski Cancer Centre Foundation
Canadian Breast Cancer Foundation
Juravinski Cancer Center
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
70 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Women age ≥ 70 years; * New histological diagnosis of invasive carcinoma of the breast, grade I or II, estrogen and progesterone receptor (ER and PR) positive, HER2 negative on needle biopsy and limited to Stage I (T1 N0 M0) on clinical and radiological assessment with MRI of the breasts and axillary ultrasound; * Candidate for breast conserving surgery; * Signed study consent form completed prior to study entry.
Exclusion criteria
* Breast cancer with disease within 5 mm from skin or chest wall; * Previous or concomitant invasive malignancies treated within 5 years of study entry; * Serious non-malignant disease (cardiovascular, pulmonary, systemic lupus or scleroderma), which would preclude to definitive radiation therapy; * Psychiatric disorders, which would preclude from obtaining informed consent * Geographic inaccessibility for follow-up
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility | At time of radiation treatment delivery | The primary outcome for this study will be successful delivery of SBRT as per protocol without a major deviation. |
Secondary
| Measure | Time frame |
|---|---|
| Acute Radiation Toxicity | Within 3 months from radiation |
| Late Radiation Toxicity | 3 months or more after radiation |
| Pathological Response | At time of surgery (10-12 weeks post-radiation) |
| Ipsilateral Breast Tumour Recurrence | At 5 years post-registration |
| Disease Free Survival | At 5 years post-registration |
Countries
Canada
Contacts
Primary ContactShelley Chambers, MA
Backup ContactJulie Arsenault, MD, FRCPC
Outcome results
None listed