- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00006381
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.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Phase
- Phase 2
Kontakte und Standorte
Studienorte
-
-
New York
-
New York, New York, Vereinigte Staaten, 10021
- Memorial Sloan-Kettering Cancer Center
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
Mitarbeiter und Ermittler
Mitarbeiter
Ermittler
- Studienstuhl: Chau T. Dang, MD, Memorial Sloan Kettering Cancer Center
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Hautkrankheiten
- Neubildungen
- Neubildungen nach Standort
- Brusterkrankungen
- Neoplasien der Brust
- Physiologische Wirkungen von Arzneimitteln
- Molekulare Mechanismen der pharmakologischen Wirkung
- Agenten des peripheren Nervensystems
- Enzym-Inhibitoren
- Analgetika
- Agenten des sensorischen Systems
- Entzündungshemmende Mittel, nichtsteroidal
- Analgetika, nicht narkotisch
- Entzündungshemmende Mittel
- Antirheumatika
- Cyclooxygenase-Inhibitoren
- Antineoplastische Mittel
- Antineoplastische Mittel, immunologische
- Cyclooxygenase-2-Inhibitoren
- Trastuzumab
- Celecoxib
Andere Studien-ID-Nummern
- CDR0000068255
- MSKCC-00078
- NCI-G00-1869
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