Ignite Creation Date:
2024-05-05 @ 11:29 AM
Last Modification Date:
2024-10-26 @ 9:08 AM
Study NCT ID:
NCT00054457
Status:
COMPLETED
Last Update Posted:
2016-12-13
First Post:
2003-02-05
Brief Title:
Docetaxel and Capecitabine in Treating Patients With Metastatic Cancer of the Stomach or Gastroesophageal Junction
Sponsor:
Alliance for Clinical Trials in Oncology
Organization:
Alliance for Clinical Trials in Oncology
Study Overview
Official Title:
A Phase II Study Of Docetaxel And Capecitabine In Patients With Measurable Metastatic Adenocarcinoma Of The Stomach And Gastroesophageal Junction
Status:
COMPLETED
Status Verified Date:
2016-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
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 use different ways to stop tumor cells from dividing so they stop growing or die Combining more than one drug may kill more tumor cells
PURPOSE Phase II trial to study of the effectiveness of combining docetaxel with capecitabine in treating patients who have metastatic cancer of the stomach or gastroesophageal junction
PURPOSE Phase II trial to study of the effectiveness of combining docetaxel with capecitabine in treating patients who have metastatic cancer of the stomach or gastroesophageal junction
Detailed Description:
OBJECTIVES
Determine the objective tumor response rate in patients with metastatic gastric or gastroesophageal junction adenocarcinoma treated with docetaxel and capecitabine
Determine the time to progression in patients treated with this regimen
Determine the overall survival in patients treated with this regimen
Determine the toxic effects of this regimen in these patients
Determine whether interleukin-1 polymorphisms are present among patients who have weight loss vs no weight loss and their relationship to a poor prognosis
Assess the quality of life and swallowing uniscale during chemotherapy in these patients
OUTLINE Patients receive docetaxel IV over 1 hour on day 1 and oral capecitabine twice daily on days 1-14 Courses repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity
Quality of life is assessed at baseline at each tumor measurement and at the end of treatment
Patients are followed every 3 months until disease progression and then every 6 months until 3 years from registration
Determine the objective tumor response rate in patients with metastatic gastric or gastroesophageal junction adenocarcinoma treated with docetaxel and capecitabine
Determine the time to progression in patients treated with this regimen
Determine the overall survival in patients treated with this regimen
Determine the toxic effects of this regimen in these patients
Determine whether interleukin-1 polymorphisms are present among patients who have weight loss vs no weight loss and their relationship to a poor prognosis
Assess the quality of life and swallowing uniscale during chemotherapy in these patients
OUTLINE Patients receive docetaxel IV over 1 hour on day 1 and oral capecitabine twice daily on days 1-14 Courses repeat every 21 days for up to 2 years in the absence of disease progression or unacceptable toxicity
Quality of life is assessed at baseline at each tumor measurement and at the end of treatment
Patients are followed every 3 months until disease progression and then every 6 months until 3 years from registration
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 |
|---|---|---|---|
| CDR0000270681 | REGISTRY | PDQ Physician Data Query | None |
| NCI-2012-02517 | REGISTRY | None | None |