Phase II Protocol of Proton Therapy for Partial Breast Irradiation in Early Stage Breast Cancer

NCT01766297 | Recruiting Phase 2 DMC

• 1 other identifier: BRE007-12
• Study Type: interventional
• Target: 132
• Locations: 1 country
• Sites: 9

Brief Summary

The purpose of this research study is to compare the effects (good and bad) on women and their cancer using proton radiation therapy. This study is being done to see if proton radiation therapy will prove to be beneficial for women with early stage breast cancer. A clinical study is necessary to compare the results (good or bad) of proton radiation therapy.

Conditions

Breast Cancer; Breast Neoplasm; Breast Tumor; Cancer of the Breast

Keywords

Breast Cancer; Proton; Radiation

Outcome Measures

Primary Outcomes (1)

• To assess events of freedom from ipsilateral breast recurrence occurrences in patients receiving partial breast proton radiation therapy limited to the region of the tumor.

  Freedom from failure (FFF): The events for FFF will be the first ipsilateral breast cancer recurrence. It is expected that less than 3% of patients will experience an ipsilateral breast cancer recurrence (FFF ≥ 97%). A recurrence rate of ≥ 10% (FFF ≤ 90%) is considered unacceptable. Therefore, the null hypothesis is the FFF of ipsilateral breast cancer recurrence is 90% or lower and the alternative hypothesis is that FFF of ipsilateral breast cancer is 97% or higher.

  At 3 years

Secondary Outcomes (5)

• Assess number and severity of acute and long-term toxicity of partial breast irradiation using proton therapy for the treatment of early stage breast cancer.

  On average every 6 months for life

• To assess relationship between breast size and partial breast dosimetry.

  Average every 6 months for 3 years

• Determine quality of life results.

  Average every 6 months for 3 years

• To determine overall survival rate of patients with breast cancer treated with proton radiation.

  At 3 years

• To determine recurrence pattern of patients with breast cancer treated with proton partial breast irradiation.

  At 3 years

Study Arms (1)

Proton Radiotherapy

EXPERIMENTAL

Proton Radiotherapy 4.0 Gy (RBE) x10 fractions to 40 Gy (RBE) Total Dose

Radiation: Proton Radiotherapy

Interventions

Proton Radiotherapy RADIATION

Proton Radiotherapy

Eligibility Criteria

• Age: 50 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Must sign study-specific, IRB approved informed consent form prior to study entry. Note consent by legally authorized representative is not allowed for this trial.
• Must be female.
• Must be \> = 50 years of age.
• Must have a life expectancy of at least 5 years based on age and co-morbidities.
• Must have pathology proven invasive ductal carcinoma (lobular is not allowed) and/or ductal carcinoma in situ (DCIS).
• One of the following criteria must be met: (a) Tumors that are microscopically multifocal must be 3.0 cm or less in total aggregate size and encompassed within a single scar (b) Patient does not have microscopically multifocal tumor.
• For tumors that are invasive, if in the presence of extensive intraductal component (EIC), the entire pathologic tumor size (including both the intraductal and invasive component) must be 3.0 cm or less.
• Must be Stage 0, I, II (Tis, T1, or T2, N0, M0 per AJCC criteria 7th and/or 8th Ed.). If stage II, the tumor size must be \< = 3.0 cm. A patient with invasive histology must have nodal stage pN0 by H\&E stains on sentinel node biopsy or axillary lymph node dissection.
• Must have ER positive disease with ER/PR report available.
• For tumors that are invasive, HER2 must be performed (positive or negative is acceptable).
• Must have a lumpectomy performed, with documented negative surgical margins by 0.2 cm or more. If re-excision results in negative surgical margins 0.2 cm or more, patient is eligible.
• If image guidance with daily cone beam CT with direct physician visual assessment is used for treatment positioning, the presence of markers or clips in the surgical bed is recommended but not required. If cone beam CT imaging will NOT be used for image guidance, then the patient must be prepared to have 2 fiducial markers minimum, 3 preferred, placed prior to treatment (if not previously done).
• If markers or clips were placed at the time of surgery, patient must be able to start treatment within 12 weeks after lumpectomy or re-excision for adequate margins.
• If markers were not placed at the time of surgery and are needed, patient must have markers placed within 6 weeks after surgery.
• If systemic chemotherapy was given, patient must have had clips or markers placed at the time of surgery (if they are needed) and patient must have simulation scans within 6 weeks of the completion of the chemotherapy.

You may not qualify if:

• Previous history of ipsilateral invasive breast cancer or DCIS.
• Any clinical or radiographically suspicious nodes, unless biopsy proven benign.
• Non-epithelial malignancies such as sarcoma or lymphoma.
• Suspicious residual microcalcifications on mammography of either breast, unless negative for malignancy on pathology.
• Multicentric or bilateral disease unless biopsy of the clinical abnormalities are performed and result is negative.
• Lymphovascular space invasion (LVSI) on pathology specimen.
• Any previously treated breast carcinoma or synchronous breast carcinoma in ipsilateral breast.
• Prior radiation therapy to the ipsilateral breast or thorax.
• Paget's disease of the nipple.
• Histologic examination showing invasive lobular histology.
• Skin involvement.
• Breasts technically unsatisfactory for radiation treatment upon the discretion of the treating physician.
• Significant infection or other co-existing medical condition that would preclude protocol therapy such as pregnancy, HIV/AIDS or collagen vascular diseases specifically systemic lupus erythematosus, scleroderma, or dermatomyositis.
• Known BRCA 1 or BRCA 2 mutation.
• Pregnant or lactating.

Sponsors & Collaborators

• Proton Collaborative Group: lead

Study Sites (9)

Mayo Clinic

Scottsdale, Arizona, 85259, United States

RECRUITING

California Protons Cancer Therapy Center

San Diego, California, 92121, United States

RECRUITING

Northwestern Medicine Chicago Proton Center

Warrenville, Illinois, 60555, United States

RECRUITING

Maryland Proton Treatment Center

Baltimore, Maryland, 21201, United States

RECRUITING

McLaren Proton Therapy Center

Flint, Michigan, 48532, United States

RECRUITING

New York Proton Center

New York, New York, 10035, United States

RECRUITING

Oklahoma Proton Center

Oklahoma City, Oklahoma, 73142, United States

RECRUITING

Inova Schar Cancer Institute

Fairfax, Virginia, 22031, United States

RECRUITING

Hampton University Proton Therapy Institute

Hampton, Virginia, 23666, United States

RECRUITING

MeSH Terms

Conditions

Breast Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Study Officials

• Andrew Chang, MD

  Proton Collaborative Group

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: NETWORK
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 28, 2012
• First Posted: January 11, 2013
• Study Start: February 1, 2013
• Primary Completion (Estimated): January 1, 2027
• Study Completion (Estimated): January 1, 2035
• Last Updated: September 9, 2025

Record last verified: 2025-09

Locations

US (9)