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Gemcitabine and Oxaliplatin in Treating Patients With Metastatic Pancreatic Cancer

Primary Purpose

Pancreatic Cancer

Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
gemcitabine hydrochloride
oxaliplatin
Sponsored by
GERCOR - Multidisciplinary Oncology Cooperative Group
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Cancer focused on measuring adenocarcinoma of the pancreas, stage IV pancreatic cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the pancreas Metastatic disease Measurable disease (primary tumor or metastasis) At least 1 cm in diameter by spiral CT scan No ampulla of Vater carcinoma or biliary adenocarcinoma No known brain metastases PATIENT CHARACTERISTICS: ECOG performance status (PS) 0-2 or Karnofsky PS 60-100% Life expectancy more than 12 weeks Absolute neutrophil count > 1,500/mm^3 Platelet count > 100,000/mm^3 Alkaline phosphatase < 5 times normal Bilirubin < 1.5 times normal Creatinine < 1.5 times normal No pre-existing neuropathy No unstable or uncontrolled pain Not pregnant or nursing Fertile patients must use effective contraception No serious cardiovascular disease No serious respiratory disease No uncontrolled or persistent hypercalcemia No psychological, familial, social, or geographical condition that would preclude study treatment No other active malignancy PRIOR CONCURRENT THERAPY: No prior chemotherapy or radiotherapy No concurrent corticosteroids

Sites / Locations

  • Hopital Duffaut
  • C.H.G. Beauvais
  • Hopital Drevon
  • Centre Hospitalier de Dreux
  • Centre Hospitalier Departemental
  • Hopital Saint - Louis
  • Hopital Louis Pasteur - Le Coudray
  • Clinique Victor Hugo
  • Polyclinique des Quatre Pavillons
  • Clinique Saint Jean
  • Hopital Saint Antoine
  • Hopital Tenon
  • Centre Hospitalier Lyon Sud
  • Polyclinique De Courlancy
  • C.H. Senlis

Outcomes

Primary Outcome Measures

Objective response rate

Secondary Outcome Measures

Clinical benefits and tolerability
Progression-free and overall survival

Full Information

First Posted
December 20, 2005
Last Updated
May 23, 2008
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group
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1. Study Identification

Unique Protocol Identification Number
NCT00268411
Brief Title
Gemcitabine and Oxaliplatin in Treating Patients With Metastatic Pancreatic Cancer
Official Title
Phase II Randomisee Dans Les Adenocarcinomes Metastatiques Du Pancreas: Gemox Et Gemox Simplifie. [GEMOX]
Study Type
Interventional

2. Study Status

Record Verification Date
May 2007
Overall Recruitment Status
Unknown status
Study Start Date
September 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy, such as gemcitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. It is not yet known whether giving both of these drugs on the same day is more effective than giving them on different days. PURPOSE: This randomized phase III trial is studying two different schedules of gemcitabine and oxaliplatin to compare how well they work in treating patients with metastatic pancreatic cancer.
Detailed Description
OBJECTIVES: Primary Compare the objective response rate in patients with metastatic adenocarcinoma of the pancreas treated with two different schedules of gemcitabine hydrochloride and oxaliplatin. Secondary Compare the clinical benefits and tolerability of these regimens in these patients. Compare the progression-free and overall survival of patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to the participating center and ECOG performance status (0 or 1 vs 2). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive gemcitabine hydrochloride IV over 100 minutes on day 1 and oxaliplatin IV over 2 hours on day 2. Arm II: Patients receive gemcitabine hydrochloride IV over 100 minutes followed by oxaliplatin IV over 2 hours on day 1. In both arms, treatment repeats every 14 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed periodically. PROJECTED ACCRUAL: A total of 80 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Cancer
Keywords
adenocarcinoma of the pancreas, stage IV pancreatic cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
gemcitabine hydrochloride
Intervention Type
Drug
Intervention Name(s)
oxaliplatin
Primary Outcome Measure Information:
Title
Objective response rate
Secondary Outcome Measure Information:
Title
Clinical benefits and tolerability
Title
Progression-free and overall survival

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the pancreas Metastatic disease Measurable disease (primary tumor or metastasis) At least 1 cm in diameter by spiral CT scan No ampulla of Vater carcinoma or biliary adenocarcinoma No known brain metastases PATIENT CHARACTERISTICS: ECOG performance status (PS) 0-2 or Karnofsky PS 60-100% Life expectancy more than 12 weeks Absolute neutrophil count > 1,500/mm^3 Platelet count > 100,000/mm^3 Alkaline phosphatase < 5 times normal Bilirubin < 1.5 times normal Creatinine < 1.5 times normal No pre-existing neuropathy No unstable or uncontrolled pain Not pregnant or nursing Fertile patients must use effective contraception No serious cardiovascular disease No serious respiratory disease No uncontrolled or persistent hypercalcemia No psychological, familial, social, or geographical condition that would preclude study treatment No other active malignancy PRIOR CONCURRENT THERAPY: No prior chemotherapy or radiotherapy No concurrent corticosteroids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe Louvet, MD, PhD
Organizational Affiliation
Hopital Saint Antoine
Official's Role
Study Chair
Facility Information:
Facility Name
Hopital Duffaut
City
Avignon
ZIP/Postal Code
84902
Country
France
Facility Name
C.H.G. Beauvais
City
Beauvais
ZIP/Postal Code
60021
Country
France
Facility Name
Hopital Drevon
City
Dijon
ZIP/Postal Code
21000
Country
France
Facility Name
Centre Hospitalier de Dreux
City
Dreux
ZIP/Postal Code
28100
Country
France
Facility Name
Centre Hospitalier Departemental
City
La Roche Sur Yon
ZIP/Postal Code
F-85025
Country
France
Facility Name
Hopital Saint - Louis
City
La Rochelle
ZIP/Postal Code
17000
Country
France
Facility Name
Hopital Louis Pasteur - Le Coudray
City
Le Coudray
ZIP/Postal Code
28630
Country
France
Facility Name
Clinique Victor Hugo
City
Le Mans
ZIP/Postal Code
F-72000
Country
France
Facility Name
Polyclinique des Quatre Pavillons
City
Lormont
ZIP/Postal Code
33310
Country
France
Facility Name
Clinique Saint Jean
City
Lyon
ZIP/Postal Code
69008
Country
France
Facility Name
Hopital Saint Antoine
City
Paris
ZIP/Postal Code
75571
Country
France
Facility Name
Hopital Tenon
City
Paris
ZIP/Postal Code
75970
Country
France
Facility Name
Centre Hospitalier Lyon Sud
City
Pierre Benite
ZIP/Postal Code
69495
Country
France
Facility Name
Polyclinique De Courlancy
City
Reims
ZIP/Postal Code
F-51100
Country
France
Facility Name
C.H. Senlis
City
Senlis
ZIP/Postal Code
60309
Country
France

12. IPD Sharing Statement

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Gemcitabine and Oxaliplatin in Treating Patients With Metastatic Pancreatic Cancer

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