Gemcitabine and Oxaliplatin in Treating Patients With Metastatic Pancreatic Cancer

NCT ID: NCT00268411

Last Updated: 2008-05-27

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-09-30

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.

Conditions

Pancreatic Cancer

Keywords

adenocarcinoma of the pancreas; stage IV pancreatic cancer

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT

Interventions

gemcitabine hydrochloride

Intervention Type: DRUG

oxaliplatin

Intervention Type: DRUG

Eligibility Criteria

Inclusion 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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GERCOR - Multidisciplinary Oncology Cooperative Group

OTHER

Sponsor Role: lead

Principal Investigators

Christophe Louvet, MD, PhD

Role: STUDY_CHAIR

Hopital Saint Antoine

Locations

Hopital Duffaut

Avignon, , France

C.H.G. Beauvais

Beauvais, , France

Hopital Drevon

Dijon, , France

Centre Hospitalier de Dreux

Dreux, , France

Centre Hospitalier Departemental

La Roche-sur-Yon, , France

Hopital Saint - Louis

La Rochelle, , France

Hopital Louis Pasteur - Le Coudray

Le Coudray, , France

Clinique Victor Hugo

Le Mans, , France

Polyclinique des Quatre Pavillons

Lormont, , France

Clinique Saint Jean

Lyon, , France

Hopital Saint Antoine

Paris, , France

Hopital Tenon

Paris, , France

Centre Hospitalier Lyon Sud

Pierre-Bénite, , France

Polyclinique De Courlancy

Reims, , France

C.H. Senlis

Senlis, , France

Countries

France

Other Identifiers

GERCOR-D04-1-GEMOX

Identifier Type: -

Identifier Source: secondary_id

EU-20569

Identifier Type: -

Identifier Source: secondary_id

SANOFI-GERCOR-D04-1-GEMOX

Identifier Type: -

Identifier Source: secondary_id

CDR0000453849

Identifier Type: -

Identifier Source: org_study_id