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Summary
Aminoglutethimide plus cortisone acetate showed a 43% objective remission rate in postmenopausal women with advanced breast cancer. This combination therapy is a safe and effective second-line endocrine treatment option.
Area of Science:
- Oncology
- Endocrinology
- Pharmacology
Background:
- Metastatic breast cancer in postmenopausal women requires effective endocrine therapies.
- Aminoglutethimide is an aromatase inhibitor used in breast cancer treatment.
- Cortisone acetate is often used as supportive therapy with aminoglutethimide.
Purpose of the Study:
- To evaluate the efficacy and safety of aminoglutethimide plus cortisone acetate in postmenopausal women with progressive metastatic breast cancer.
- To determine response rates, duration of response, and impact of disease site on treatment outcomes.
- To identify common side effects and biochemical changes associated with this combination therapy.
Main Methods:
- A prospective study involving 61 postmenopausal women with progressive metastatic breast cancer.
- Treatment regimen: aminoglutethimide (250 mg 4 times daily) plus cortisone acetate (25 mg twice daily).
- Evaluation of objective remission (complete and partial), stable disease, and progressive disease in 51 evaluable patients.
Main Results:
- An objective remission rate of 43% (19 partial, 3 complete) was observed in 51 evaluable patients.
- Median duration of response was 60 weeks (range 12+ to 94+ weeks).
- Higher response rates were noted for soft tissue (50%) and bone (56%) metastases compared to visceral disease (29%).
- Common side effects included somnolence (69%), dizziness (41%), nausea (35%), and skin rash (27%).
- Biochemical changes included increased gamma-GT, alkaline phosphatase, and total cholesterol; decreased uric acid and indirect bilirubin.
Conclusions:
- Aminoglutethimide plus cortisone acetate is an active and relatively safe treatment for advanced breast cancer.
- This combination therapy can be recommended as a second-line endocrine treatment option.
- Treatment efficacy may vary based on the dominant site of metastatic disease.