Celecoxib and Trastuzumab in Treating Women With Metastatic Breast Cancer
Phase II Study of Celecoxib in HER-2/Neu Overexpressing Metastatic Breast Cancer Patients Who Have Failed Recombinant Humanized Anti-p 185HER Monoclonal Antibody Trastuzumab (HERCEPTIN)
RATIONALE: Celecoxib may be effective in preventing the further development of cancer. Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining trastuzumab with celecoxib may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of combining celecoxib and trastuzumab in treating women who have metastatic breast cancer that has not responded to previous trastuzumab.
調査の概要
詳細な説明
OBJECTIVES:
- Determine the efficacy of celecoxib and trastuzumab (Herceptin) in women with HER2/neu-overexpressing metastatic breast cancer that is refractory to prior trastuzumab.
- Determine the safety of celecoxib in these patients.
OUTLINE: At least 3 weeks after the last dose of prior chemotherapy, patients receive oral celecoxib twice daily. Patients continue or restart trastuzumab (Herceptin) IV over 30-90 minutes weekly or every 3 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity.
PROJECTED ACCRUAL: A total of 12-37 patients will be accrued for this study within approximately 9 months.
研究の種類
段階
- フェーズ2
連絡先と場所
研究場所
-
-
New York
-
New York、New York、アメリカ、10021
- Memorial Sloan-Kettering Cancer Center
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
DISEASE CHARACTERISTICS:
Histologically proven metastatic breast cancer
- HER2/neu-positive (overexpressing) tumor tissue
- Failed prior trastuzumab (Herceptin) therapy with or without chemotherapy
- Resected stage IV disease allowed if evidence of disease
Bidimensionally measurable or evaluable disease
- No lesions in previously irradiated field except nonbone lesions progressive after radiotherapy
- No pleural effusions
- No blastic or mixed bony metastases
- No palpable abdominal masses
- No leptomeningeal disease
Brain metastases allowed if:
- No concurrent use of steroids
- At least 3 months since prior brain irradiation
- No evidence of progression of metastases
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 3 months
Hematopoietic:
- Granulocyte count at least 1,500/mm^3
- Hemoglobin at least 8.0 g/dL
- Platelet count at least 100,000/mm^3
Hepatic:
- AST/ALT no greater than 2 times upper limit of normal (ULN)
- Bilirubin no greater than 1.5 times ULN
Renal:
- Creatinine no greater than 1.5 mg/dL
Cardiovascular:
- LVEF at least 50%
Other:
- Not pregnant
- Negative pregnancy test
- Fertile patients must use effective barrier contraception
- No other prior malignancy within the past 5 years except adequately treated carcinoma in situ of the cervix or nonmelanoma skin cancer
- No other serious medical illness
- No severe infection
- No severe malnutrition
- No prior allergic reactions to sulfonamides or celecoxib
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- See Disease Characteristics
- Prior trastuzumab (Herceptin) for breast cancer allowed, either as adjuvant/neoadjuvant or for metastatic disease
Chemotherapy:
- See Disease Characteristics
- At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and recovered
- Prior cytotoxic therapy for breast cancer allowed, either as adjuvant/neoadjuvant or for metastatic disease
Endocrine therapy:
- See Disease Characteristics
- At least 3 weeks since prior hormonal therapy
- Prior exogenous hormonal therapy for stage IV disease and/or as adjuvant therapy allowed
Radiotherapy:
- See Disease Characteristics
- At least 4 weeks since prior radiotherapy and recovered
- Prior localized radiotherapy allowed if no influence on the signal measurable lesion
- Concurrent localized radiotherapy allowed if no influence on the signal measurable lesion
Surgery:
- See Disease Characteristics
- At least 3 weeks since prior major surgery and recovered
- At least 2 weeks since prior minor surgery and recovered
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
協力者と研究者
捜査官
- スタディチェア:Chau T. Dang, MD、Memorial Sloan Kettering Cancer Center
研究記録日
主要日程の研究
研究開始
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- CDR0000068255
- MSKCC-00078
- NCI-G00-1869
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。