GammaPod Dose Escalation Radiation for Early Stage Breast Cancer

Breast Cancer Clinical Trial

Official title:

GCC 1926- Phase Ib Dose Escalation of Single-Fraction Preoperative Stereotactic Partial-Breast Irradiation for Early-Stage Breast Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04234386
• Other study ID #: HP-00084710
• Status: Recruiting
• Phase: N/A
• Start date: September 15, 2021
• Est. completion date: December 2028

Study information

• Verified date: September 2023
• Source: University of Maryland, Baltimore
• Contact: Elizabeth Nichols, MD
• Phone: 410-328-6080
• Email: enichols1[@]umm.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The GammaPod machine was made by Xcision Medical Systems and is already FDA cleared to deliver focused radiation within the breast. Unlike current radiation machines, the GammaPod was designed specifically for treating breast cancer. The GammaPod can pinpoint radiation to the tumor bed in the breast which lowers the amount of radiation to nearby tissues. The machine uses a breast cup system to hold the breast in place for the treatment. This breast cup system was tested at MSGCCC (Marlene Stewart Greenebaum Comprehensive Cancer Center). Patients reported this system was more comfortable than an MRI or mammogram. The cup system was able to securely position the breast for treatment in the correct location.

Receiving radiation before surgery is not a new concept in cancer management. Preoperative radiation has proven to result in improved disease free survival in certain types of cancer.

With this study treatment, the participants will receive a dose of breast radiation therapy before the lumpectomy surgery. The lumpectomy surgery is where they remove the participant's tumor.

The purpose of this research study is to determine a safe and effective dose of pre-operative radiation to treat early stage breast cancer. The pre-operative radiation is delivered using the FDA approved, GammaPod machine. The study will also determine the cosmesis of pre-operative radiation at different doses. Cosmesis is another word for looking at skin changes. The research team will use questionnaires for patient and physicians to assess adverse cosmesis changes as accurately as possible. In addition, the investigators are going to assess radiation related changes using photo software analysis tools and patients quality of life.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: December 2028
• Est. primary completion date: December 2026
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 45 Years and older

Eligibility

Inclusion Criteria:

• Patients must sign consent for study participation.

• Patients must be female with a diagnosis of invasive ductal carcinoma. Lobular histologies will not be included, because of difficulty in defining the extent of disease with imaging.

• Patients must be deemed appropriate candidates for breast-conserving therapy (i.e., not pregnant, never had RT to the treated breast, breast size would allow adequate cosmesis after volume loss from partial mastectomy).

• Tumor must not involve the overlying skin or underlying chest wall, based on imaging evaluation and/or clinical exam.

• Greatest tumor dimension is <3 cm based on US. MR imaging measurements can be included only if performed BEFORE the biopsy (postbiopsy measurements can be larger as a result of hematoma formation or increased edema).

• Tumor must be unifocal.

• Patients must be > 45 years old.

• The tumor must be visible on a CT scan.

• Patients must undergo MR imaging for work-up to aid in tumor delineation and to rule out additional foci of disease. If additional foci of disease are found to be present, then these must be biopsied with negative results to proceed with treatment.

• The tumor must be clinically and radiographically N0 (node negative). If a suspicious node is visualized, it must be biopsied with negative results.

• Patients must be estrogen-receptor positive.

• Patients must be HER2neu negative.

• Patients must weigh <150 kg (330 lb), which is the limit of the imaging loader.

• Patients must be <6'6" in height, again because of instrumentation limitations.

• Patients must be able to lie prone for treatment.

• Patients must have no lymphovascular invasion on biopsy.

• Patients may be taking hormonal therapy prior to initiation of treatment. This will be documented.

Exclusion Criteria:

• Multicentric disease.

• Prior RT to the involved breast.

• Inability to fit into the immobilization breast cup because of breast size or other anatomic reasons.

• Inability to obtain an adequate seal when using the immobilization breast cup.

• Male sex.

• Breast implants.

• Patient cannot comfortably lie in the prone position (i.e., physical disability).

• Patients who are planned to be treated surgically with a mastectomy.

• Tumor <5 mm from the skin surface or chest wall on clinical exam and/or radiographic imaging.

• Tumor size >3 cm.

• Patients with psychiatric or addictive disorders that would preclude obtaining informed consent or study completion.

• Patients who are pregnant or lactating (because of potential RT exposure to the fetus and unknown effects of RT in lactating women).

• Patient unable to undergo MR imaging (e.g., because of known contrast reaction or concerns about contrast and existing health status).

• Lymphovascular invasion on original biopsy.

• Tumor histologies other than invasive ductal carcinoma (including invasive lobular carcinoma).

• ER-negative tumors.

• HER2neu-positive tumors.

• Pure ductal carcinoma in situ (no invasive component).

• Weight >330 lb

• Prior ipsilateral breast cancer.

• Diffuse calcifications on mammogram (BIRADS 3, 4, 5).

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Radiation:
• GammaPod Radiation
The basic design is a dose-escalation phase Ib study with 4 predefined dose levels. With this study treatment, participants will receive the dose level assigned treatment of radiation therapy before the lumpectomy surgery.

Locations

Country	Name	City	State
United States	UMMC	Baltimore	Maryland
United States	Upper Chesapeake Health	Bel Air	Maryland
United States	Central Maryland Oncology Center	Columbia	Maryland
United States	Baltimore Washington Medical Center	Glen Burnie	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
University of Maryland, Baltimore

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Establish the single-fraction radiation dose (MTD)	To establish the single-fraction radiation dose (MTD) delivered with the GammaPod that causes an incidence of dose-limiting toxicities (DLTs) that is statistically significantly 10% or lower.	5 years
Primary	Incidence of Dose-Limiting Toxicities (DLTs)	The primary endpoint is DLTs defined as one or more instances of: Surgical infection: Defined as redness that resolves on antibiotics (sometimes the surgical site may look red as a result of natural healing processes and does not resolve with antibiotics) with or without fever and/or elevated white blood cell count. The risk of infection for this surgical procedure (lumpectomy ± SLN biopsy) is <5%.; Nonhealing surgical incision (>30 days). The risk is <5%.; Reoperation secondary to infection/wound healing problem. Risk is <5%.	5 years
Secondary	Establish a Comprehensive Safety Profile of single-fraction PBI delivered with the GammaPod	To establish the comprehensive safety profile of single-fraction PBI delivered with the GammaPod. The following secondary toxicity and quality-of-life endpoints will be collected and reported: Acute toxicity (NCI-CTCAE v 5), including skin toxicity and fatigue.; Late toxicity (NCI-CTCAE v 5), including rates of fat necrosis.	5 years
Secondary	Establish a Comprehensive Safety Profile of single-fraction PBI delivered with the GammaPod	To establish the comprehensive safety profile of single-fraction PBI delivered with the GammaPod. The following secondary toxicity and quality-of-life endpoints will be collected and reported: -Rates of surgical morbidity (defined below), including seroma formation. Seroma will be defined as any palpable seroma on follow-up exam. If seroma results in pain/discomfort and/or requires drainage this should be noted as a 'symptomatic' seroma. Seroma formation is normal following lumpectomy surgery but is asymptomatic in the majority of cases.	5 years
Secondary	Establish a Comprehensive Safety Profile of single-fraction PBI delivered with the GammaPod	To establish the comprehensive safety profile of single-fraction PBI delivered with the GammaPod. The following secondary toxicity and quality-of-life endpoints will be collected and reported: -Patient and physician-assessed cosmesis after radiotherapy and surgery via questionnaire.	5 years
Secondary	Establish a Comprehensive Safety Profile of single-fraction PBI delivered with the GammaPod	To establish the comprehensive safety profile of single-fraction PBI delivered with the GammaPod. The following secondary toxicity and quality-of-life endpoints will be collected and reported: - Patient Quality of Life Assessments [EORTC QLQ-C30- scale goes from 1/not at all to 4/very much. There is additionally a rate of overall health and quality of life that is a scale from 1 to 7.]	5 years
Secondary	Rate of pathologic complete response (pCR)	To establish the rate of pathologic complete response (pCR) as a function of dose. pCR will be scored by pathology review of H&E slides.	5 years
Secondary	Rate of ipsilateral local tumor recurrence	Report ipsilateral local tumor recurrence using the Kaplan-Meier method.	5 years