Repeat Breast Conserving Surgery Followed by Daily Partial Breast Irradiation in Ipsilateral Breast
- Conditions
- Tumor, BreastBreast Cancer
- Interventions
- Radiation: Radiation Therapy
- Registration Number
- NCT06129747
- Lead Sponsor
- Case Comprehensive Cancer Center
- Brief Summary
The standard treatment for participants whose cancer has returned after breast conserving surgery is radiation given twice daily (separated by at least 6 hours) for a total of 30 treatments. The purpose of this study is to find out if giving radiation once a day for 15 treatments after repeat breast conserving surgery works as well as giving it the standard way.
- Detailed Description
Breast cancer survival rates have greatly improved with advances in both screening and treatment. The standard of care for both early stage and selected locally advanced breast cancers is breast conserving therapy (BCT), consisting of a partial mastectomy followed by radiation treatment. Traditionally, a salvage mastectomy was the standard treatment for women who initially underwent BCT and experienced an ipsilateral breast tumor recurrence (IBTR). Many participants have become increasingly motivated to avoid mastectomy, and there has been rising interest in repeat BCS (Breast Conserving Surgery) with focal radiation for certain participants motivated to keep their breast. The current standard of care for breast re-irradiation after an in-breast tumor recurrence is partial breast irradiation consisting of a dose of 45 Gy delivered BID for 30 fractions. While this regimen demonstrated excellent local control and low AEs, the regimen itself is difficult for participants. Receiving RT twice daily at smaller doses per fraction (1.5 Gy) for 30 treatments can be burdensome, especially for those without reliable transportation or difficulty getting time away from work. Given the excellent local control rates and low rate of AEs, in this study, we hypothesize that daily hypofractionated EBRT(External Beam Radiation Therapy) for re-irradiation after repeat BCS would be at least as well tolerated with good local control and provide a more convenient option for participants than the current standard of care established by RTOG 1014. Some participants will present with high-risk features (e.g. age \<50, high grade, ER negative tumors, close margins) making dose escalation an attractive option to improve local control. Options for dose escalation include sequential and concurrent administration of a boost.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 55
- Participants' recurrences must have histologically confirmed ductal carcinoma in-situ, invasive ductal, medullary, papillary, colloid (mucinous), tubular or mixed histologies.
- Lesion size < 3 cm treated with a partial mastectomy. Participants with invasive cancer and clinically and radiographically negative axillas do not require an axillary lymph node sampling unless they did not have prior axillary lymph node sampling (e.g. previous cancer was DCIS). Patients with DCIS as their recurrence do not require surgical assessment of the axilla. Repeat sentinel lymph node biopsy is permitted.
- Negative resection margins with at least a no tumor on ink or a negative re-excision.
- Hormonal therapy is allowed. If chemotherapy is planned, it can be delivered either prior or after the radiation is delivered. There must be at least 2 weeks between radiation and chemotherapy. HER2 directed therapy can be delivered concurrently with radiation.
- Participants must be > 18 years of age. Because no dosing or adverse event data are currently available on the use of breast re-irradiation in participants ≤18 years of age, children are excluded from this study.
- Participants must have the ability to understand and the willingness to sign a written informed consent document.
- Performance status: ECOG Performance status ≤ 2.
- Life expectancy of ≥ 12months, in the opinion of and as documented by the investigator.
- Not based on gender; this trial is open to any gender, defined as self-representation of gender identity.
- Participants with nodal or distant metastatic disease
- Participants with invasive pure lobular carcinoma, extensive lobular carcinoma in-situ, extensive ductal carcinoma in-situ (spanning more than 3 cm), or uncontrolled nonepithelial breast malignancies such as lymphoma or sarcoma.
- Participants with multicentric carcinoma (tumors in different quadrants of the breast or tumors separated by at least 4 cm). Palpable or radiographically suspicious contralateral axillary, ipsilateral or contralateral supraclavicular, infraclavicular, or internal mammary lymph nodes unless these are histologically or cytologically confirmed negative.
- Participants with Paget's disease of the nipple.
- Participants with skin involvement.
- Participants with scleroderma, or dermatomyositis.
- Participants with psychiatric, neurologic, or addictive disorders that would preclude obtaining informed consent.
- Participants who are pregnant or lactating due to potential fetal exposure to radiation and unknown effects of radiation on lactating females.
- Participants with known BRCA 1/BRCA 2 mutations.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Radiation Therapy(RT) Radiation Therapy There will be one treatment cohort. Radiation therapy will be delivered daily for 15 daily fractions, 2.67Gy per fraction, delivered using a 3-D or IMRT(Intensity Modulate Radiation Therapy) plan. For participants with high-risk features deemed by the radiation oncologist who would otherwise be a candidate for a boost (age \<50, high grade, poor biology, close margins), 48 Gy delivered in fifteen fractions of 3.2 Gy is allowed.
- Primary Outcome Measures
Name Time Method Treatment-related adverse events as graded by CTCAE criteria 1 year from the completion of re-irradiation Rate of grade 3+ treatment-related skin, fibrosis, and breast pain adverse events occurring within 1 year from the completion of re-irradiation as graded by CTCAE criteria.
- Secondary Outcome Measures
Name Time Method Overall survival rate 10 years Overall survival will be estimated using Kaplan-Meier Method
Rate of freedom from mastectomy 10 years The freedom from mastectomy rate will be estimated using the cumulative incidence function.
In-breast tumor recurrence rate 10 years The overall in-breast tumor recurrence rate will be estimated using the cumulative incidence function.
Treatment-related adverse events Overall for 3 years from completion of re-irradiation All treatment-related adverse events for the defined time periods
Evaluation of Cosmesis 3 years Determined by an established Global Cosmesis Score grading from 1 through 4, with 1 being excellent and 4 being rated as poor
Mastectomy-free survival rate 10 years Mastectomy-free survival will be estimated using Kaplan-Meier Method
Trial Locations
- Locations (2)
University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center
🇺🇸Cleveland, Ohio, United States
Cleveland Clinic Taussig Cancer Center, Case Comprehensive Cancer Center
🇺🇸Cleveland, Ohio, United States