Breast Conservation Treatment for Breast Cancer Recurrence
Personalized Second Chance Breast Conservation (PSCBC): A Prospective Phase II Clinical Study
Recruiting
N/AInterventional Study
Breast Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
19 – 90
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
Weill Medical College of Cornell University · Other
Who this trial is looking for
This trial is looking for women who have experienced a return of breast cancer after previous treatment. Participants will receive a type of radiation therapy to help preserve their breast tissue.
Are You a Good Fit for This Trial?
You may be able to join if
I have an isolated breast cancer lesion that is unifocal
My breast cancer lesion is smaller than 2-3 cm
I have a confirmed diagnosis of invasive breast cancer or carcinoma in situ
I have negative margins from my previous surgery
I have 0 to 3 positive lymph nodes without extension outside the capsule
I do not have any distant cancer spread
I am at least 18 years old
It has been at least 12 months since my initial breast cancer treatment
You may not be able to join if
I have regional cancer recurrences in my axilla or supraclavicular area
I have positive margins from my past surgery
I have metastatic disease
I have poor cosmetic results from previous surgery or treatment
I have extensive intraductal component
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of the study is to investigate the feasibility of enabling a second chance for breast conservation in patients with in-breast recurrences after a previous lumpectomy and RT, investigators propose to test partial breast irradiation with the target volume encompassing the entire surgical bed with 1.0-1.5 cm margins.
An additional goal of the study is to investigate the feasibility of enabl…
The goal of the study is to investigate the feasibility of enabling a second chance for breast conservation in patients with in-breast recurrences after a previous lumpectomy and RT, investigators propose to test partial breast irradiation with the target volume encompassing the entire surgical bed with 1.0-1.5 cm margins.
An additional goal of the study is to investigate the feasibility of enabling a second chance for breast conservation in patients with inbreast recurrences after a previous lumpectomy and PBI, the investigators propose to test whole breast RT (WBRT) with the target as the whole breast volume.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Isolated ipsilateral unifocal breast lesions
* Limited size (\< 2-3 cm) without evidence of skin involvement
* Histologically proven invasive breast carcinoma or carcinoma in situ
* Negative histologic margins of resection
* Patients with 0 to 3 positive axillary lymph nodes w…
Inclusion Criteria:
* Isolated ipsilateral unifocal breast lesions
* Limited size (\< 2-3 cm) without evidence of skin involvement
* Histologically proven invasive breast carcinoma or carcinoma in situ
* Negative histologic margins of resection
* Patients with 0 to 3 positive axillary lymph nodes without extracapsular extension
* No synchronous distant metastases
* Age ≥ 18 years
* ≥ 12 months interval between initial breast conserving therapy (surgery and whole breast radiotherapy) and recurrence
* Previous WBI or IORT, brachytherapy or external beam partial breast treatment
* Technical feasibility
* Every kind of systemic therapy is allowed
* Informed consent for clinical and research purposes signed
Exclusion Criteria:
* Regional recurrences (axillary, supraclavicular)
* Positive histologic margins at resection
* Metastatic disease
* Poor cosmesis from previous surgery and RT
* Extensive Intraductal Component
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