Ignite Creation Date:
2024-05-05 @ 4:41 PM
Last Modification Date:
2024-10-26 @ 9:23 AM
Study NCT ID:
NCT00293332
Status:
TERMINATED
Last Update Posted:
2011-02-09
First Post:
2006-02-16
Brief Title:
Docetaxel Carboplatin and Bevacizumab in Treating Patients With Stage I Stage II or Stage III Non-Small Cell Lung Cancer That Can Be Removed By Surgery
Sponsor:
University of California San Francisco
Organization:
University of California San Francisco
Study Overview
Official Title:
A Phase II Study of Neoadjuvant Therapy With Docetaxel Carboplatin and Bevacizumab in Patients With Resectable Early Stage Non-Small Cell Lung Cancer
Status:
TERMINATED
Status Verified Date:
2007-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Terminated due to low subject accrual
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
RATIONALE Drugs used in chemotherapy such as docetaxel and carboplatin work in different ways to stop the growth of tumor cells either by killing the cells or by stopping them from dividing Monoclonal antibodies such as bevacizumab can block tumor growth in different ways Some block the ability of tumor cells to grow and spread Others find tumor cells and help kill them or carry tumor-killing substances to them Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor Giving docetaxel and carboplatin together with bevacizumab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed
PURPOSE This phase II trial is studying how well giving docetaxel and carboplatin together with bevacizumab works in treating patients with stage I stage II or stage III non-small cell lung cancer that can be removed by surgery
PURPOSE This phase II trial is studying how well giving docetaxel and carboplatin together with bevacizumab works in treating patients with stage I stage II or stage III non-small cell lung cancer that can be removed by surgery
Detailed Description:
OBJECTIVES
Primary
Determine the clinical response rate in patients with stage IB-IIIA non-small cell lung cancer treated with neoadjuvant docetaxel carboplatin and bevacizumab
Secondary
Determine the median and overall survival of patients treated with this regimen
Determine the safety profile of this regimen
Determine the time to treatment failure of patients treated with this regimen
Determine the pathologic response rate and the resectability rate in patients treated with this regimen
Correlate vascular endothelial growth factor VEGF levels or expression with response and survival of patients treated with this regimen
OUTLINE Patients receive docetaxel IV over 15-60 minutes carboplatin IV over 30-60 minutes and bevacizumab IV over 30-90 minutes on day 1 Treatment repeats every 21 days for up to 3 courses in the absence of disease progression or unacceptable toxicity Approximately 4-6 weeks after completion of chemotherapy eligible patients with no distant or mediastinal disease progression undergo lobectomy pneumonectomy or segmentectomy with standard radical mediastinal lymph node dissection
NOTE Bevacizumab is only administered during courses 1 and 2
After completion of study treatment patients are followed periodically for 8 years
PROJECTED ACCRUAL A total of 50 patients will be accrued for this study
Primary
Determine the clinical response rate in patients with stage IB-IIIA non-small cell lung cancer treated with neoadjuvant docetaxel carboplatin and bevacizumab
Secondary
Determine the median and overall survival of patients treated with this regimen
Determine the safety profile of this regimen
Determine the time to treatment failure of patients treated with this regimen
Determine the pathologic response rate and the resectability rate in patients treated with this regimen
Correlate vascular endothelial growth factor VEGF levels or expression with response and survival of patients treated with this regimen
OUTLINE Patients receive docetaxel IV over 15-60 minutes carboplatin IV over 30-60 minutes and bevacizumab IV over 30-90 minutes on day 1 Treatment repeats every 21 days for up to 3 courses in the absence of disease progression or unacceptable toxicity Approximately 4-6 weeks after completion of chemotherapy eligible patients with no distant or mediastinal disease progression undergo lobectomy pneumonectomy or segmentectomy with standard radical mediastinal lymph node dissection
NOTE Bevacizumab is only administered during courses 1 and 2
After completion of study treatment patients are followed periodically for 8 years
PROJECTED ACCRUAL A total of 50 patients will be accrued for this study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| UCSF-H5535-25047-01A | None | None | None |
| UCSF-04652 | None | None | None |
| UCSF-IIT-12198 | None | None | None |