The purpose of this study is to determine if the dose of radiation therapy that is effective in producing a treatment response, delivered over a shorter treatment period, is a safe approach that causes few or mild side effects in women with newly diagnosed breast cancer or DCIS who have had a lumpectomy procedure.
Full Title of Study: “Ultra-Short External Beam-Based Accelerated Partial Breast Irradiation (APBI): A Phase II Toxicity Study Nested With a Non-inferiority Assessment of APBI in New Patient Cohorts”
- Study Type: Interventional
- Study Design
- Intervention Model: Single Group Assignment
- Primary Purpose: Treatment
- Masking: None (Open Label)
- Study Primary Completion Date: August 30, 2022
- Radiation: Accelerated Partial Breast Irradiation
- Treatment will consist of APBI delivered using external beam RT techniques to a dose of 24 Gy in 3 fractions of 8.0 Gy delivered on consecutive weekdays
Arms, Groups and Cohorts
- Experimental: Participants with Breast Cancer
- Participants will have unicentric pathological stage I invasive ductal breast cancer or Grade 1 or 2 DCIS measuring <3cm in longest diameter on pathology and/or mammogram that is histologically confirmed at MSKCC.
Clinical Trial Outcome Measures
- Toxicity with novel APBI schedule as determined by CTCAE version 5
- Time Frame: 24 months
- The study is deemed too toxic if the rate of serious toxicity is >/= 10%.
Participating in This Clinical Trial
- Age >/= 45 years
- Unicentric pathological stage I (pT1 or T2 pN0_M0) invasive ductal breast cancer or Grade 1 or 2 (low or intermediate grade) DCIS measuring <3 cm in longest diameter on pathology and/or mammogram that is histologically confirmed at MSKCC. If T2, the tumor must be less than 3cm in longest diameter. Note: Women > 70 years or older with T1 invasive ductal carcinoma who are estrogen- receptor positive (ER+) with clinically negative axillary nodes, and do not undergo surgical lymph node mapping or dissection (i.e., if tumor deposit is 0.2 mm or less, regardless of whether the deposit is detected by immunohistochemistry or hematoxylin and eosin staining) will also be eligible
- Histologically negative tumor margin or no tumor in a re-excision specimen on final shaved specimen.
- ECOG Performance Status of 0 or 1.
- Clips must be placed in the lumpectomy cavity at the time of final excision in order to aid in the delineation of the tumor cavity at the time of simulation and radiation delivery.
- Negative serum pregnancy test within 14 days prior to study treatment if a woman has child-bearing potential. Subjects of child bearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year
- Written informed consent obtained from subject and ability for subject or comply with the requirements of the study
- Female subjects of childbearing potential should be willing to use 2 methods or birth control or be surgically sterile or abstain from heterosexual activity for the duration of study participation. Should a woman become pregnant while participating on study, she should inform the treating physician immediately.
Inclusion Criteria for intermediate risk substudy:
- Post-NAC cohort patients: clinical T1 or T2 (less than or equal to 5cm in longest diameter on available imaging) and clinical N0 (on exam and imaging) with pathological pT0 or pTis and pN0 (any regimen of neoadjuvant chemotherapy agents is allowed)
- Oncotype RS score of 26 or higher
- PAM50 ROR scored as "HIGH"
- Presence or LVI (focal, limited or "not otherwise specified") in the lumpectomy specimen
- Patients with distant metastasis
- Patients who are pregnant or breastfeeding
- Patients with diffuse (>1 quadrant or >5cm) suspicious microcalcifications or patients with known multicentric OR multifocal disease.
- Prior radiation therapy to the ipsilateral or contralateral breast or thorax.
- Histological evidence of extensive lymphovascular invasion (LVI)
- Histological evidence of extensive intraductal component (EIC), defined as the presence of intraductal carcinoma both within the primary infiltrating ductal tumor (comprising at least 25% of the tumo area) and intraductal carcinoma present clearly beyond the edges of the invasive tumor, or as a predominantly intraductal tumor with one or more areas of focal invasion
- Patients are not required to undergo BRCA1 and BRCA2 or other genetic mutation tests in order to enroll on the study. Note: in the event a patient is tested and is found to be a mutation carrier, she would be excluded from the study. It would be an extremely rare/unlikely scenario for patients to be discovered BRCA positive after the completion of PBI, as all patients with risk factors for BRCA mutations (positive family history, Ashkenazi Jewish descent, ER-/PR-/her2-neu-negative receptor status) are usually tested prior to radiation. Should such a situation exist, these patients will be given the option of remaining on the breast conservation paradigm or opting for mastectomy (as is done in this rare scenario is standard of care practice). The patient will be replaced on the trial.
- History of cosmetic or reconstructive breast surgery.
- Medical condition such as uncontrolled infection (including HIV), uncontrolled diabetes mellitus, or connective tissue diseases (lupus, systemic sclerosis, or other collagen vascular diseases) that, in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient.
- Patients with a "currently active" second malignancy other than non-melanoma skin cancers. Patients are not considered to have "currently active" malignancies if they have completed therapy and are considered by their physicians to be at <5% risk of relapse within 3 years.
- Patients who are already enrolled in or planning to enroll in other adjuvant systemic therapy protocols for both non-invasive or invasive breast cancer
- Expecting to conceive within the projected duration of the trials, starting with screening visit through 180 days after the last dose of trial treatment
- Concomitant anti-neoplastic treatment is not allowed during protocol treatment and should be completed at least 2 weeks prior to commencement of protocol treatment, with resolution of associated acute toxicities. Bisphosponates are permitted without restriction even during protocol treatment.
- Ongoing therapy with other investigational agents. Patients may not be receiving any other investigational agents.
Gender Eligibility: Female
Minimum Age: 45 Years
Maximum Age: N/A
Are Healthy Volunteers Accepted: No
- Lead Sponsor
- Memorial Sloan Kettering Cancer Center
- Provider of Information About this Clinical Study
- Overall Official(s)
- Atif J Khan, MD, Principal Investigator, Memorial Sloan Kettering Cancer Center
- Overall Contact(s)
- Atif J Khan, MD, 848-225-6334, firstname.lastname@example.org
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