Radiation Therapy in Treating Patients With Recurrent Breast Cancer - Full Text View

Sponsor:	Case Comprehensive Cancer Center
Collaborator:	National Cancer Institute (NCI)
Information provided by:	National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:	NCT00945061

Purpose

RATIONALE: Radiation therapy uses high-energy x-rays and other types of radiation to kill tumor cells. It is not yet known whether a single dose of radiation therapy is more effective than implant radiation therapy for 5 days in treating patients with recurrent breast cancer.

PURPOSE: This phase I trial is studying implant radiation therapy to see how well it works compared with radiation therapy during surgery in treating patients with recurrent breast cancer.

Condition	Intervention	Phase
Breast Cancer	Radiation: intracavitary balloon brachytherapy Radiation: intraoperative radiation therapy	Phase I

Study Type:	Interventional
Study Design:	Treatment, Open Label
Official Title:	Partial Breast Re-Irradiation for Patients With Ipsilateral Breast Tumor Recurrence, After First Being Treated With Breast Conservation for Early Stage Breast Cancer: An Efficacy Trial Comparing Mammosite® and Intraoperative Radiation

Resource links provided by NLM:

Genetics Home Reference related topics: breast cancer

MedlinePlus related topics: Breast Cancer Cancer

U.S. FDA Resources

Further study details as provided by National Cancer Institute (NCI):

Primary Outcome Measures:

Ipsilateral breast tumor recurrence rates [ Designated as safety issue: No ]
Tumor bed recurrence rates [ Designated as safety issue: No ]
Cosmetic outcome as determined by an established scale [ Designated as safety issue: No ]
Patient satisfaction with the procedure as determined by a patient questionnaire [ Designated as safety issue: No ]
Wound healing and overall complication rate [ Designated as safety issue: No ]
Determination of which patients are best suited for each individual technique of performing partial breast irradiation [ Designated as safety issue: No ]

Estimated Enrollment:	30
Study Start Date:	September 2008
Estimated Primary Completion Date:	September 2011 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Group 1: Experimental Patients undergo partial breast irradiation delivered as a single intra-operative radiation dose to the tumor bed.	Radiation: intraoperative radiation therapy Patients undergo radiotherapy
Group 2: Experimental Patients undergo partial breast irradiation delivered as MammoSite® brachytherapy consisting of 10 fractions over 5 days.	Radiation: intracavitary balloon brachytherapy Patients undergo brachytherapy

Detailed Description:

OBJECTIVES:

To determine the in breast recurrence rate following repeat radiation to the breast with Mammosite® brachytherapy or intraoperative radiotherapy in patients with recurrent ipsilateral breast cancer.
To determine the cosmetic outcome resulting from partial breast re-irradiation using different techniques, including both physician- and patient-rated scales.
To determine patient satisfaction of partial breast re-irradiation as it pertains to their overall treatment experience, as measured by a questionnaire.
To determine if there are patient factors which limit a patient's suitability to receive partial breast re-irradiation delivered by a particular technique.
To evaluate tylectomy wound healing and overall complication rate after partial breast re-irradiation.
To determine ipsilateral breast tumor recurrence rates and tumor bed recurrence rates.

OUTLINE: Patients are stratified according to which modality is best suited for the patient. Patients are assigned to 1 of 2 groups.

All patients undergo excisional biopsy or needle localization removal of the tumor. Patients with margins < 2 mm undergo re-excision of the biopsy cavity.

Group 1: Patients undergo partial breast irradiation delivered as a single intra-operative radiation dose to the tumor bed.
Group 2: Patients undergo partial breast irradiation delivered by Mammosite® brachytherapy consisting of 10 fractions over 5 days.

Quality of life is assessed at baseline, 1 month after completion of radiotherapy, and then at follow-up visits.

After completion of study treatment, patients are followed up at 1 month, every 3 months for 1 year, and then every 6 months for 5 years.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

DISEASE CHARACTERISTICS:

Histologically confirmed ductal carcinoma in situ (DCIS) or invasive carcinoma of the breast (ductal, medullary, papillary, colloid [mucinous], or tubular) meeting the following criteria:
- Lesion size ≤ 3 cm treated with a tylectomy and whole breast irradiation (with or without tumor bed boost)
- Unifocal breast cancer recurrence
- Negative resection margins with ≥ a 2 mm margin from invasive and in situ cancer or a negative re-excision
Patients with clinically and radiographically negative axillas should not undergo an axillary lymph node dissection unless they did not have prior axillary lymph node sampling (i.e., previous cancer was DCIS)
No invasive lobular carcinoma, extensive lobular carcinoma in situ, extensive DCIS (≥ 3 cm), or nonepithelial breast malignancies such as lymphoma or sarcoma
No multicentric carcinoma (tumors in different quadrants of the breast or tumors separated by ≥ 4 cm)
No palpable or radiographically suspicious contralateral axillary, ipsilateral, or contralateral supraclavicular, infraclavicular, or internal mammary lymph nodes unless these are histologically or cytologically confirmed negative
No extensive intraductal component by the Harvard definition, i.e., more than 25% of the invasive tumor is DCIS and DCIS present in adjacent breast tissue
No distant metastatic disease
No Paget's disease of the nipple
No skin involvement
No known BRCA1/BRCA2 mutations
Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Menopausal status not specified
No collagen vascular disorders, i.e., systemic lupus erythematosus, scleroderma, or dermatomyositis
No psychiatric, neurologic, or addictive disorders that would preclude study participation
No other malignancy within the past 5 years except nonmelanoma skin cancer
Not pregnant or nursing
Negative pregnancy test

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
At least 5 years since prior radiotherapy
No chemotherapy within 2 weeks after completion of radiotherapy
Concurrent hormonal therapy allowed

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00945061

Locations

United States, Ohio
Case Comprehensive Cancer Center	Recruiting
Cleveland, Ohio, United States, 44106-5065
Contact: Clinical Trials Office - Case Comprehensive Cancer Center 800-641-2422
Geauga Regional Hospital	Recruiting
Cleveland, Ohio, United States, 44024
Contact: Janice A Lyons 216-844-2536
Lake/University Ireland Cancer Center	Recruiting
Cleveland, Ohio, United States, 44060
Contact: Janice A Lyons 216-844-2536
Mercy Cancer Center at Mercy Medical Center	Recruiting
Cleveland, Ohio, United States, 44708
Contact: Janice A Lyons 216-844-2536
University Suburban Health Center	Recruiting
Cleveland, Ohio, United States, 44121
Contact: Janice A Lyons 216-844-2536
UHHS Chagrin Highlands Medical Center	Recruiting
Cleveland, Ohio, United States, 44122
Contact: Janice A Lyons 216-844-2536
UHHS Westlake Medical Center	Recruiting
Cleveland, Ohio, United States, 44145
Contact: Janice A Lyons 216-844-2536
Southwest General Health Center	Recruiting
Cleveland, Ohio, United States, 44130
Contact: Janice A Lyons 216-844-2536

Sponsors and Collaborators

Case Comprehensive Cancer Center

National Cancer Institute (NCI)

Investigators

Principal Investigator:	Janice Lyons	Ireland Cancer Center
Investigator:	Leda Dumadag	Ireland Cancer Center
Principal Investigator:	Timothy Zagar, MD	Ireland Cancer Center

More Information

Additional Information:

Clinical trial summary from the National Cancer Institute's PDQ® database This link exits the ClinicalTrials.gov site

No publications provided

Responsible Party:	Ireland Cancer Center at University Hospitals/Case Medical Center ( Janice Lyons )
Study ID Numbers:	CDR0000617461, CASE-11107, CASE-11107-CC479
Study First Received:	July 22, 2009
Last Updated:	July 23, 2009
ClinicalTrials.gov Identifier:	NCT00945061 History of Changes
Health Authority:	Unspecified

Keywords provided by National Cancer Institute (NCI):

ductal breast carcinoma in situ
recurrent breast cancer
invasive ductal breast carcinoma
medullary ductal breast carcinoma with lymphocytic infiltrate

mucinous ductal breast carcinoma
papillary ductal breast carcinoma
tubular ductal breast carcinoma
male breast cancer

Additional relevant MeSH terms:

Neoplasms
Neoplasms by Site
Skin Diseases
Breast Neoplasms
Breast Diseases

ClinicalTrials.gov processed this record on February 08, 2010