- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00088998
Docetaxel, Capecitabine, and Bevacizumab in Treating Patients With Metastatic Breast Cancer
Phase II Trial Of Docetaxel With Capecitabine And Bevacizumab As First-Line Chemotherapy For Patients With Metastatic Breast Cancer
RATIONALE: Drugs used in chemotherapy, such as docetaxel and capecitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as bevacizumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Bevacizumab may also stop the growth of tumor cells by stopping blood flow to the tumor. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells.
PURPOSE: This phase II trial is studying how well giving docetaxel and capecitabine together with bevacizumab works in treating patients with metastatic breast cancer.
연구 개요
상세 설명
OBJECTIVES:
Primary
- Determine the response rate in patients with metastatic breast cancer treated with docetaxel, capecitabine, and bevacizumab as first-line chemotherapy.
Secondary
- Determine time to disease progression in patients treated with this regimen.
- Determine survival of patients treated with this regimen.
- Determine the toxicity profile of this regimen in these patients.
- Determine the duration of response in patients treated with this regimen.
OUTLINE: This is a multicenter study.
Patients receive docetaxel IV over 1 hour and bevacizumab IV over 30-90 minutes on day 1. Patients also receive oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response (CR) receive at least 2 additional courses beyond CR.
Patients are followed every 3 months for 1 year, every 6 months for 1 year, and then annually for 3 years.
연구 유형
등록 (실제)
단계
- 2 단계
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed invasive breast cancer
Clinical evidence of metastatic disease
- No bone metastases as the only evidence of metastasis
Measurable disease
At least 1 lesion ≥ 2.0 cm by CT scan or MRI OR ≥ 1.0 cm by spiral CT scan
- Lesions on chest x-ray allowed provided they are clearly defined and surrounded by aerated lung
- Clincal lesions only considered measurable when they are superficial (e.g., skin nodules or palpable lymph nodes)
- Target lesion must not have been exposed to prior radiotherapy unless disease has progressed since completion of radiotherapy
The following are not considered measurable disease:
- Bone lesions
- Leptomeningeal disease
- Ascites
- Pleural or pericardial effusion
- Inflammatory breast disease
- Lymphangitis cutis or pulmonis
- Abdominal masses that are not confirmed and followed by imaging techniques
- Cystic lesions
- No HER2/neu-positive tumors by immunohistochemistry or amplified fluorescence in situ hybridization unless disease has progressed after trastuzumab (Herceptin®)-containing therapy alone or with antiestrogen hormonal therapy for metastatic disease OR trastuzumab is contraindicated
- Prior breast cancer allowed
- No prior or active brain metastases
Hormone receptor status:
- Not specified
PATIENT CHARACTERISTICS:
Age
- 18 and over
Sex
- Male or female
Menopausal status
- Not specified
Performance status
- ECOG 0-1
Life expectancy
- At least 3 months
Hematopoietic
- Absolute neutrophil count ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
- Hemoglobin ≥ 8.0 g/dL
- No bleeding diathesis or uncontrolled coagulopathy
Hepatic
- Bilirubin normal
Meets 1 of the following criteria:
- AST and ALT normal AND alkaline phosphatase ≤ 5 times upper limit of normal (ULN)
- AST and ALT ≤ 1.5 times ULN AND alkaline phosphatase ≤ 2.5 times ULN
- AST and ALT ≤ 5 times ULN AND alkaline phosphatase normal
Renal
- Creatinine clearance ≥ 30 mL/min
- No proteinuria OR
- Protein < 1 g by 24-hour urine collection
- No nephrotic syndrome
Cardiovascular
No uncontrolled hypertension (i.e., blood pressure > 160/90 mm Hg on ≥ 2 different observations ≥ 5 minutes apart)
- Blood pressure < 140/90 mm Hg on ≥ 3 different observations over ≥ 14 days, for patients who recently began or adjusted anti-hypertensive medication
- No atrial or venous thrombosis within the past month
No clinically significant heart disease, including any of the following:
- Congestive heart failure
- Symptomatic coronary artery disease
- Uncontrolled cardiac arrhythmias
- Unstable angina
- No myocardial infarction within the past 12 months
- No history of cerebrovascular accident
Pulmonary
- No hemoptysis within the past 6 months
Gastrointestinal
- No lack of physical integrity of the upper gastrointestinal tract
- No malabsorption syndrome
- Able to receive oral medication
Other
- No other stage III or IV invasive malignancy requiring treatment within the past 5 years
- No pre-existing peripheral neuropathy > grade 1
- No history of allergy or hypersensitivity to study drugs, agents that are chemically similar to study drugs, or drugs that contain polysorbate 80
- No prior severe reaction to fluoropyrimidines
- No known hypersensitivity to fluorouracil
- No known dihydropyrimidine dehydrogenase deficiency
- No active infection
- No significant medical condition that would preclude study participation
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 30 days after study participation
PRIOR CONCURRENT THERAPY:
Biologic therapy
- See Disease Characteristics
- No other concurrent biologic therapy
Chemotherapy
- Prior adjuvant or neoadjuvant chemotherapy allowed for primary disease
- No prior chemotherapy for metastatic disease
- More than 4 weeks since prior cytotoxic chemotherapy
- More than 6 months since prior taxanes (e.g., docetaxel or paclitaxel)
- No other concurrent chemotherapy
Endocrine therapy
- See Disease Characteristics
- Prior antiestrogen hormonal therapy allowed in the adjuvant or metastatic setting
Radiotherapy
- See Disease Characteristics
More than 4 weeks since prior radiotherapy to a target lesion
- Prior single-dose palliative radiotherapy allowed within the past 4 weeks
- No concurrent radiotherapy
Surgery
- More than 4 weeks since prior major surgery
Other
More than 2 weeks since prior aspirin, anticoagulants, or thrombolytic agents
- Concurrent low-dose warfarin (1 mg/day) to maintain patency of vascular access device allowed
- More than 4 weeks since prior investigational agents
- No concurrent aspirin, anticoagulants, or thrombolytic agents
- No concurrent participation in another clinical trial involving investigational agents or procedures
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: docetaxel + bevacizumab + capecitabine
Patients receive docetaxel IV over 1 hour and bevacizumab IV over 30-90 minutes on day 1. Patients also receive oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response (CR) receive at least 2 additional courses beyond CR. Patients are followed every 3 months for 1 year, every 6 months for 1 year, and then annually for 3 years. |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
|
Confirmed tumor response (complete or partial) rate as measured by RECIST
기간: Up to 5 years
|
Up to 5 years
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
|
무진행 생존
기간: 최대 5년
|
최대 5년
|
|
전반적인 생존
기간: 최대 5년
|
최대 5년
|
공동 작업자 및 조사자
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- NCCTG-N0432
- NCI-2012-02617 (레지스트리 식별자: CTRP (Clinical Trials Reporting System))
- CDR0000377886 (레지스트리 식별자: PDQ (Physician Data Query))
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