Trials / Terminated
TerminatedNCT00683787
Docetaxel With or Without Vandetanib in Treating Patients With Metastatic Stomach Cancer or Gastroesophageal Junction Cancer
Multicenter Randomized Phase II Trial of Docetaxel With/Without VANDETANIB for Advanced Gastroesophageal Cancer
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- Roswell Park Cancer Institute · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Vandetanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. It is not yet known whether docetaxel is more effective when given together with or without vandetanib. PURPOSE: This randomized phase II trial is studying docetaxel to see how well it works compared with docetaxel given together with vandetanib in treating patients with metastatic stomach cancer or gastroesophageal junction cancer.
Detailed description
OBJECTIVES: Primary * To test the hypothesis that the addition of a targeted agent, such as vandetanib, to standard chemotherapy with docetaxel will result in incremental responses in patients with metastatic gastric or gastroesophageal junction cancer. Secondary * To assess progression-free survival and overall survival of patients treated with this regimen. * To study the toxicity profile of this regimen in these patients. OUTLINE: This is a multicenter study. Patients are stratified according to clinical site. Patients are randomized to 1 of 3 treatment arms. * Arm I: Patients receive docetaxel IV once every 3 weeks. * Arm II: Patients receive docetaxel IV as in arm I and oral vandetanib (100 mg) once daily. * Arm III: Patients receive docetaxel IV as in arm I and oral vandetanib (300 mg) once daily. In all arms, courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 2 months for 5 years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | docetaxel | Given IV once every 3 weeks |
| DRUG | vandetanib | Oral vandetanib once daily |
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2009-04-01
- Completion
- 2011-03-01
- First posted
- 2008-05-23
- Last updated
- 2015-01-08
- Results posted
- 2015-01-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00683787. Inclusion in this directory is not an endorsement.