Herbal Therapy in Treating Women With Metastatic Breast Cancer
キーワード
概要
説明
OBJECTIVES:
- Determine the efficacy of Scutellaria barbata (Chinese herbal extract) in terms of tumor response in women with metastatic breast cancer.
- Determine the safety and toxicity of this therapy in these patients.
- Determine the feasibility of this therapy in these patients.
- Determine the time to progression, overall survival, and resource utilization of patients treated with this therapy.
- Determine the quality of life of patients treated with this therapy.
- Determine the bioavailability and pharmacokinetics of this therapy in these patients.
OUTLINE: Patients receive oral Scutellaria barbata (Chinese herbal extract) twice daily for 12 months in the absence of disease progression or unacceptable toxicity.
Quality of life is assessed at baseline and then every 6 months thereafter.
PROJECTED ACCRUAL: A total of 25 patients will be accrued for this study.
日付
| 最終確認済み: | 08/31/2012 |
| 最初に提出された: | 01/03/2002 |
| 提出された推定登録数: | 01/25/2003 |
| 最初の投稿: | 01/26/2003 |
| 最終更新が送信されました: | 09/12/2012 |
| 最終更新日: | 09/16/2012 |
| 実際の研究開始日: | 07/31/2001 |
| 一次完了予定日: | 03/31/2006 |
| 研究完了予定日: | 03/31/2006 |
状態または病気
介入/治療
Drug: herba scutellaria barbata
Other: herba scutellaria Barbatae (HSB)
段階
適格基準
| 研究の対象となる年齢 | 18 Years に 18 Years |
| 研究に適格な性別 | Female |
| 健康なボランティアを受け入れる | はい |
| 基準 | DISEASE CHARACTERISTICS: - Histologically confirmed breast cancer (may include original primary cancer diagnosis) - Measurable disease - Metastatic involvement with minimal or no symptoms - Solitary metastases require histological confirmation - No extensive liver involvement (more than 50% of liver parenchyma) - No lymphangitic pulmonary involvement - CNS involvement or spinal cord compression allowed if stabilized by therapy for more than 3 months - Hormone receptor status: - Not specified PATIENT CHARACTERISTICS: Age: - 18 and over Sex: - Female Menopausal status: - Not specified Performance status: - ECOG 0-1 Life expectancy: - More than 6 months Hematopoietic: - WBC at least 2,500/mm^3 - Platelet count at least 75,000/mm^3 Hepatic: - See Disease Characteristics - Bilirubin no greater than 1.7 mg/dL Renal: - Creatinine no greater than 2.0 mg/dL Other: - Not pregnant - Negative pregnancy test - Fertile patients must use effective contraception - No history of multiple or severe food or medicine allergies PRIOR CONCURRENT THERAPY: Biologic therapy: - At least 1 week since prior biologic therapy - No concurrent anticancer biologic therapy Chemotherapy: - At least 1 week since prior chemotherapy - No concurrent anticancer chemotherapy Endocrine therapy: - At least 1 week since prior hormonal therapy - No concurrent anticancer hormonal therapy Radiotherapy: - Not specified Surgery: - Not specified Other: - Recovered from prior anticancer therapy - At least 1 week since prior investigational agents - At least 1 week since prior herbal medications - No other concurrent anticancer therapy - No other concurrent investigational agents - Concurrent pamidronate allowed - Concurrent acupuncture or other nonherbal therapy allowed - Concurrent nutritional vitamin supplementation (up to 5 times recommended daily allowance) allowed |
