MedPath

Gemcitabine and Radiation Therapy Compared With Gemcitabine Alone in Treating Patients Who Have Undergone Surgery for Pancreatic Cancer

Phase 2
Completed
Conditions
Pancreatic Cancer
Registration Number
NCT00064207
Lead Sponsor
European Organisation for Research and Treatment of Cancer - EORTC
Brief Summary

RATIONALE: Drugs used in chemotherapy such as gemcitabine use different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving these treatments after surgery may kill any tumor cells that remain after surgery. It is not yet known whether giving gemcitabine together with radiation therapy is more effective than gemcitabine alone following surgery in treating pancreatic cancer.

PURPOSE: This randomized phase II/III trial is studying how well giving gemcitabine together with radiation therapy works and compares it to gemcitabine alone in treating patients who have undergone surgery for pancreatic cancer.

Detailed Description

OBJECTIVES:

Phase II:

* Determine the feasibility of gemcitabine followed by chemoradiotherapy with gemcitabine vs gemcitabine alone after prior curative resection in patients with pancreatic head adenocarcinoma.

* Compare the tolerability of these regimens, in terms of acute and late toxicity, in these patients.

Phase III:

* Compare the disease-free and overall survival of patients treated with these regimens .

* Compare the quality of life of patients treated with these regimens.

* Compare the toxicity of these regimens in these patients.

* Determine the sites of recurrence in patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to ECOG/WHO performance status (0-1 vs 2), participating center, and N stage (N0 vs N1 vs NX). Patients are randomized to 1 of 2 treatment arms.

* Arm I: Within 8 weeks after prior surgical resection, patients receive gemcitabine IV over 30 minutes on days 1, 8, and 15. Treatment repeats every 4 weeks for 2 courses.

Patients then receive additional gemcitabine IV over 30 minutes on days 57, 64, 71, 78, 85, and 92. Beginning on day 57, patients also undergo radiotherapy once daily, 5 days a week, for 6 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity.

* Arm II: Patients receive gemcitabine IV over 30 minutes on days 1, 8, and 15. Treatment repeats every 4 weeks for 4 courses.

Quality of life (QOL) is assessed in both arms, according to the following schedules:

* Arm I: QOL is assessed at baseline; at 3 weeks after the beginning of chemoradiotherapy; after the completion of chemoradiotherapy; every 3 months for 2 years; and then every 6 months for 1 year.

* Arm II: QOL is assessed at baseline; at 12 weeks; at 16 weeks; every 3 months for 2 years; and then every 6 months for 1 year.

Patients are followed every 3 months for 2 years and then every 6 months thereafter.

PROJECTED ACCRUAL: A total of 538 patients (269 per treatment arm) will be accrued for this study within 3 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
97
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Feasibility of full completion of treatment as measured by the number of patients completing treatment 1 month after treatment in phase II
Tolerability in terms of acute toxicity as measured by NCI-CTC v2.0 1 month after completion of treatment in phase II
Tolerability in terms of late toxicity as measured by EORTC and RTOG 1 month after completion of treatment in phase II
Overall survival as measured by Logrank every 3 months in years 1-2, and every 6 months thereafter in phase III
Secondary Outcome Measures
NameTimeMethod
Disease-free survival as measured by Logrank every 3 months in years 1-2, and every 6 months thereafter
Acute toxicity as measured by NCI-CTC v2.0 every 3 months in years 1-2, and every 6 months thereafter
Late toxicity as measured by EORTC and RTOG every 3 months in years1-2, and every 6 months thereafter
Quality of life as measured by Quality of Life Questionnaire Core 30 (QLQ-C30) v3.0 and EORTC QLQ PAN-26 every 3 months in years 1-2 and every 6 months thereafter

Trial Locations

Locations (59)

Clinique Tivoli

🇫🇷

Bordeaux, France

C.H.G. Beauvais

🇫🇷

Beauvais, France

Centre Hospitalier d'Abbeville

🇫🇷

Abbeville, France

Centre Hospitalier de Blois

🇫🇷

Blois, France

Hopital Duffaut

🇫🇷

Avignon, France

Institut Sainte Catherine

🇫🇷

Avignon, France

Centre Hospitalier Universitaire Ambroise Pare - Boulogne

🇫🇷

Boulogne Billancourt, France

Hopital Beaujon

🇫🇷

Clichy, France

Charite - Campus Charite Mitte

🇩🇪

Berlin, Germany

Centre Hospitalier Docteur Duchenne

🇫🇷

Boulogne Sur Mer, France

Hopital Robert Boulin

🇫🇷

Libourne, France

C.H.G. De Pau

🇫🇷

Pau, France

Hopital Charles Nicolle

🇫🇷

Rouen, France

Louis Mourier Hospital

🇫🇷

Colombes Cedex, France

Hopital Saint Antoine

🇫🇷

Paris, France

Munich Oncologic Practice at Elisenhof

🇩🇪

Munich, Germany

CHU Poitiers

🇫🇷

Poitiers, France

Universitaetsklinikum Duesseldorf

🇩🇪

Duesseldorf, Germany

Johannes Gutenberg University

🇩🇪

Mainz, Germany

Centre Hospitalier d'Annecy

🇫🇷

Annecy, France

Polyclinique Bordeaux Nord Aquitaine

🇫🇷

Boucher, France

CHR Clermont Ferrand, Hotel dieu

🇫🇷

Clermont-Ferrand, France

Centre Hospitalier Universitaire Henri Mondor

🇫🇷

Creteil, France

Centre Hospitalier de Dax

🇫🇷

Dax, France

Hopital Du Bocage

🇫🇷

Dijon, France

Centre Hospitalier Intercommunal St. Aubin les Elbeuf

🇫🇷

Elbeuf, France

CHU de Grenoble - Hopital de la Tronche

🇫🇷

Grenoble, France

Centre Hospitalier Departemental

🇫🇷

La Roche Sur Yon, France

Clinique Victor Hugo

🇫🇷

Le Mans, France

Clinique Saint Jean

🇫🇷

Lyon, France

CHU de la Timone

🇫🇷

Marseille, France

Centre Hospitalier General de Mont de Marsan

🇫🇷

Mont-de-Marsan, France

Centre Leon Berard

🇫🇷

Lyon, France

Centre Hospitalier de Mulhouse

🇫🇷

Mulhouse, France

C.H.U. de Nimes - Groupe Hospitals-Universitaire Caremeau

🇫🇷

Nimes, France

Centre Hospitalier Lyon Sud

🇫🇷

Pierre Benite, France

CHU Pitie-Salpetriere

🇫🇷

Paris, France

Hopital Cochin

🇫🇷

Paris, France

Hopital Tenon

🇫🇷

Paris, France

Centre Paul Strauss

🇫🇷

Strasbourg, France

Hopital Universitaire Hautepierre

🇫🇷

Strasbourg, France

Centre Hospitalier Universitaire Bretonneau de Tours

🇫🇷

Tours, France

Hopital Bichat - Claude Bernard

🇫🇷

Paris, France

Centre Hospitalier Pierre Oudot

🇫🇷

Bourgoin-Jallieu, France

CHU de Caen

🇫🇷

Caen, France

Centre Hospital Regional Universitaire de Limoges

🇫🇷

Limoges, France

Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle

🇫🇷

Montpellier, France

Hopital Europeen Georges Pompidou

🇫🇷

Paris, France

Centre Alexis Vautrin

🇫🇷

Vandoeuvre-les-Nancy, France

Robert Roessle Comprehensive Cancer Center at University of Berlin - Charite Campus Buch

🇩🇪

Berlin, Germany

Hopital Universitaire Erasme

🇧🇪

Brussels, Belgium

Universitair Ziekenhuis Gent

🇧🇪

Ghent, Belgium

Algemeen Ziekenhuis Sint-Augustinus

🇧🇪

Wilrijk, Belgium

Hopital de Jolimont

🇧🇪

Haine Saint Paul, Belgium

Academisch Medisch Centrum at University of Amsterdam

🇳🇱

Amsterdam, Netherlands

Cazk Groeninghe - Campus St-Niklaas

🇧🇪

Kortrijk, Belgium

CHU Liege - Domaine Universitaire du Sart Tilman

🇧🇪

Liege, Belgium

Rambam Medical Center

🇮🇱

Haifa, Israel

Hopital Cantonal Universitaire de Geneve

🇨🇭

Geneva, Switzerland

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