Breast Cancer
Conditions
Keywords
stage I breast cancer, stage II breast cancer
Brief summary
RATIONALE: Microwave thermotherapy kills tumor cells by heating them to several degrees above body temperature. PURPOSE: Randomized phase II trial to compare the effectiveness of microwave thermotherapy before surgery to that of surgery alone in treating women who have stage I or stage II breast cancer.
Detailed description
OBJECTIVES: * Compare the safety and efficacy of preoperative focused microwave thermotherapy followed by surgery vs surgery alone in women with early-stage primary breast cancer. * Compare the reduction of tumor cells at surgical margins and second incision rates in women treated with these regimens. * Compare the percentage of pathological cell death in women treated with these regimens. * Compare the amount of surgically removed breast and tumor tissue in women treated with these regimens. * Compare the measurement of the extent tumor margins of the surgically removed breast and tumor tissue in women treated with these regimens. OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to tumor classification (T1 vs T2) and participating center. Patients are randomized to 1 of 2 treatment arms. * Arm I:Patients undergo ultrasound-guided placement of a microwave sensor and a temperature probe (before or after compression of the breast) and external placement of 2 large opposing microwave emitters and up to 7 skin temperature sensors on the compressed breast. Patients then receive focused microwave thermotherapy that slowly heats the primary breast tumor and deep proximal breast tissue. In the absence of undue heating of the skin, a tumor temperature of 48-52° C is targeted and maintained for an equivalent thermal dose of 140-180 minutes. Within 60 days of thermotherapy, patients undergo lumpectomy. * Arm II: Patients undergo lumpectomy only. Patients are followed at 30 and 90 days after surgery, and then at the discretion of the physician. PROJECTED ACCRUAL: A total of 200-222 patients (100-111 per treatment arm) will be accrued for this study.
Interventions
Sponsors
Imunon
Study design
Allocation
RANDOMIZED
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed primary breast cancer by core needle biopsy * T1a, b, c, or T2 * Diagnosis not made with a lumpectomy or incisional biopsy * Candidate for breast conservation surgery (lumpectomy/radiotherapy) * Tumor measurable by breast ultrasound * No metastatic disease, including skin metastases * No bilateral breast cancer * No high-probability of extensive intraductal disease in situ * No clinical fixation to the pectoralis major muscle or skin * No involvement of the nipple * No inflammatory breast cancer * No multicentric disease * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * 18 and over Sex: * Female Menopausal status: * Not specified Performance status: * Karnofsky 70-100% Life expectancy: * At least 6 months Hematopoietic: * Platelet count at least 100,000/mm\^3 (no thrombocytopenia) * No bleeding disorders Hepatic: * PT, INR, and PTT less than 1.5 times normal * Bilirubin no greater than 2.0 mg/dL * Transaminases no greater than 2 times normal * No coagulopathy * No liver disease Renal: * BUN less than 30 mg/dL * Creatinine less than 1.9 mg/dL * No renal insufficiency Cardiovascular: * No pacemakers or defibrillators * No clinically significant heart disease Other: * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use 2 forms of effective contraception, including 1 barrier method * Able to tolerate prone position and breast compression * No breast implants * No prior collagen vascular disease * No other factor or condition (other than tumor size) that would preclude lumpectomy * No mental condition that would preclude study PRIOR CONCURRENT THERAPY: Biologic therapy: * Not specified Chemotherapy: * Not specified Endocrine therapy: * Not specified Radiotherapy: * See Disease Characteristics Surgery: * See Disease Characteristics Other: * No prior participation in this study * More than 30 days since prior participation in another clinical study * No concurrent anticoagulants
Countries
United Kingdom, United States
Outcome results
None listed