Evaluation of Accelerated Partial Breast Brachytherapy

NCT00593346 | Completed Results

• 1 other identifier: 03-1205 / 201011816
• Study Type: interventional
• Target: 151
• Locations: 1 country
• Sites: 1

Brief Summary

Over the past two decades, breast conserving therapy (BCT) has become a major treatment modality for Stage I and II breast carcinoma. The major advantages of breast conserving therapy are superior cosmetic outcome and the reduced emotional and psychological trauma afforded by this procedure compared with conventional mastectomy. The principal disadvantage of BCT is its more complex and prolonged treatment regimen requiring approximately 6 weeks of external beam radiation therapy that poses problems for some patients such as the working woman, elderly patients, and those who live at a significant distance from a treatment center. These factors, along with the patient's geographic location, result in a smaller fraction of the patients who currently meet eligibility criteria for BCT actually receiving it, despite its cosmetic and probable psychological advantages. The logistical problems of BCT are primarily related to the protracted course of external beam radiation therapy to the whole breast. While some investigators reported what they believe to be acceptable local control rates in carefully selected patients treated by wide local excision without radiation therapy, the criteria for patient selection are controversial and poorly defined and probably restrict the access of many patients to breast conserving therapy. If previous observations are valid and breast irradiation following tylectomy exerts its maximal effect in eradicating occult disease remaining in the immediate vicinity of the tylectomy site, can radiation therapy be directed only to the tissue surrounding the excision cavity of the breast, using brachytherapy alone? If so, the entire course of radiation therapy could be delivered over a 4 to 7 day period immediately following tylectomy and/or axillary dissection, thus markedly reducing treatment time. Brachytherapy also inherently provides a higher central dose to the volume most at risk for recurrence. Cosmetic outcome after the use of a brachytherapy boost after external whole breast radiotherapy is comparable or slightly inferior to electron beam boost radiation therapy

Conditions

Breast Cancer

Outcome Measures

Primary Outcomes (4)

• Local Control Using Ipsilateral Breast Tumor Recurrence Rates

  2 years after treatment completion

• Local Control as Measured by Ipsilateral Breast Tumor Recurrence Rates

  5 years after treatment completion

• Local Control Using Disease-free Survival Rates

  2 years after treatment completion

• Local Control Using Disease-free Survival Rates

  5 years after treatment completion

Secondary Outcomes (8)

• Quality of Life Completion

  2 years

• Excellent-good Cosmetic Outcomes - Patient Reported

  3 years after completion of therapy

• Excellent-good Cosmetic Outcomes - Physician Reported

  3 years after completion of therapy

• Impressions of the Cause of Cosmesis Changes Over Time - Patient Reported

  3 years

• Cosmesis Outcome as Measured by Percentage of Breast Retraction Assessment (pBRA)

  Pre-treatment and 3 years

Study Arms (1)

Accelerated partial breast brachytherapy

EXPERIMENTAL

Each patient will receive accelerated partial breast brachytherapy with multiple plane implant.

Radiation: brachytherapy

Interventions

brachytherapy RADIATION

brachytherapy (radioactive implants)

Accelerated partial breast brachytherapy

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• AJCC stage 0, I, or II (TisN0, T1N0, T2N0 = 3 cm) histologically confirmed carcinoma of the breast, treated with tylectomy. Axillary sampling is required only for cases of invasive cancers. Tumor size is determined by the pathologist. Clinical size may be used if the pathologic size is indeterminate.
• Signed study-specific informed consent for participation in the study.
• Negative, or close but negative, inked histologic margins of tylectomy or reexcision specimen to be confirmed prior to placing the brachytherapy catheters. Margins generally are positive if there is invasive or noninvasive tumor at the inked resection margin, close but negative if the tumor is within 2 mm of the inked margin and negative if the tumor is at least 2 mm away from the inked edge.
• Negative post-tylectomy or post-reexcision mammography if cancer presented with malignancy-associated microcalcifications; no remaining suspicious microcalcifications in the breast before brachytherapy.
• For patients with invasive cancer, no positive axillary lymph nodes with at least 6 axillary lymph nodes sampled or a negative sentinel node.
• Invasive ductal, lobular, medullary, papillary, colloid (mucinous),or tubular histologies. Noninvasive ductal carcinoma in situ.
• Chemotherapy or hormonal therapy planned for = 2 weeks after removal of brachytherapy catheters is permitted. Hormonal therapy is allowed during brachytherapy at treating radiation oncologist's decision.
• Negative pregnancy test for premenopausal patients with an intact uterus

You may not qualify if:

• Patients with distant metastases.
• Patients with in-situ lobular carcinoma or nonepithelial breast malignancies such as sarcoma or lymphoma.
• Patients with proven multicentric carcinoma (tumors in different quadrants of the breast, or tumors separated by at least 4 cm) with other clinically or radiographically suspicious areas in the ipsilateral breast unless confirmed to be negative for malignancy by biopsy.
• Patients who are pregnant or lactating.
• Patients with histologically confirmed positive axillary nodes in the ipsilateral axilla. Palpable or radiographically suspicious contralateral axillary, supraclavicular, infraclavicular, or internal mammary nodes, unless there is histologic confirmation that these nodes are negative for tumor.
• Prior non-hormonal therapy for the present breast cancer, including radiation therapy or chemotherapy.
• Patients with systemic lupus erythematosis, scleroderma, or dermatomyositis with a CPK level above normal or with an active skin rash.
• Patients with coexisting medical conditions in whom life expectancy is \< 2 years.
• Patients with psychiatric or addictive disorders that would preclude obtaining informed consent or completing the full series of high dose rate brachytherapy treatments on an outpatient basis.
• Patients with Paget's disease of the nipple.
• Patients with skin involvement, regardless of tumor size.
• Patients with a breast unsatisfactory for brachytherapy. For example, if there is little breast tissue remaining between the skin and pectoralis muscle after surgery, placement of catheters is technically problematic.
• Patients with tylectomies so extensive that the cosmetic result is fair or poor prior to brachytherapy.
• Surgical margins which cannot be microscopically assessed or are positive at pathological evaluation.
• Any previously treated contralateral breast carcinoma or synchronous bilateral breast carcinoma.

Sponsors & Collaborators

• Washington University School of Medicine: lead

Study Sites (1)

Washington University School of Medicine

St Louis, Missouri, 63110, United States

Location

Related Links

• Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine

MeSH Terms

Conditions

Breast Neoplasms

Interventions

Brachytherapy

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Radiotherapy; Therapeutics

Results Point of Contact

• Title: Imran Zoberi, M.D.
• Organization: Washington University School of Medicine

izoberi@radonc.wustl.edu

314-362-8525

Study Officials

• Imran Zoberi, MD

  Washington University School of Medicine

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: Yes

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 2, 2008
• First Posted: January 15, 2008
• Study Start: March 1, 2004
• Primary Completion: November 1, 2013
• Study Completion: November 1, 2013
• Last Updated: June 29, 2015
• Results First Posted: May 29, 2015

Record last verified: 2015-06

Locations

US (1)