Trial Testing Ftorafur (UFT) Associated With Neoadjuvant Radiotherapy Versus Radiotherapy Alone in Rectal Adenocarcinoma

Last updated: March 23, 2020
Sponsor: Institut Cancerologie de l'Ouest
Overall Status: Terminated

Phase

3

Condition

Digestive System Neoplasms

Colon Cancer

Adenocarcinoma

Treatment

N/A

Clinical Study ID

NCT00207831
CPP276
  • Ages 18-80
  • All Genders

Study Summary

RATIONALE: Drugs used in chemotherapy, such as 5-fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing and also as a radiosensibilisant. Radiation therapy uses high-energy x-rays to kill tumor cells. 5-fluorouracil may make tumor cells more sensitive to radiation therapy. Oral 5-fluorouracil is more convenient for ambulatory patients. Giving UFT (Tegafur and Uracil) with radiation therapy before surgery may shrink the tumor so it can be removed.

PURPOSE: This phase III trial is studying how well giving UFT with radiation therapy works in treating patients who are undergoing surgery for operable rectal cancer.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS:

  • Histologically confirmed invasive adenocarcinoma of the rectum , M0, lower side < 10 cm from anal verge

  • T3 or T4 disease (T4 exclusive anal extension )

PATIENT CHARACTERISTICS:

Performance status

  • ECOG 0-2 OR

  • Zubrod 0-2

Life expectancy

  • Not specified

Hematopoietic

  • Absolute neutrophil count > 1,500/mm^3

  • Platelet count ≥ 100,000/mm^3

Hepatic

  • Bilirubin < x2 UNL

Renal

  • Creatinine < 150 µMol/L

Gastrointestinal

  • No history of inflammatory bowel disease

  • No history of difficulty or inability to take or absorb oral medications

Neurologic

  • Not specified

Other

  • Not pregnant or nursing

  • Negative pregnancy test

  • Fertile patients must use effective contraception

  • No other malignancy within the past 5 years except curatively treated basal cell skin cancer or carcinoma in situ of the cervix

  • No history of psychiatric conditions or diminished mental capacity that would preclude study compliance or giving informed consent

PRIOR CONCURRENT THERAPY:

Chemotherapy

  • No prior chemotherapy

Radiotherapy

  • No prior radiotherapy to the pelvis

Other

  • No other concurrent investigational drugs

  • No other concurrent anticancer treatment

Study Design

Total Participants: 219
Study Start date:
July 01, 2004
Estimated Completion Date:
February 29, 2008

Study Description

Adenocarcinoma of the rectum

Stage II/stage III rectal cancer (if T4 only anal extension eligible)

Drug: UFT

Procedure: chemotherapy

Procedure: conventional surgery

Procedure: neoadjuvant therapy

Procedure: radiation therapy

Procedure: radiosensitization

Procedure: surgery

Connect with a study center

  • Clinique Sainte Catherine

    Avignon, 84000
    France

    Site Not Available

  • Hopital Avicenne

    Bobigny, 93
    France

    Site Not Available

  • Institut de Cancérologie et d'Hématologie

    Brest, 29609
    France

    Site Not Available

  • Centre Hospitalier

    Brive La Gaillarde, 19312
    France

    Site Not Available

  • Centre d'Oncologie-radiothérapie d'Eure et Loir

    Chartres, 28006
    France

    Site Not Available

  • Centre Jean Perrin

    Clermont Ferrand, 63011
    France

    Site Not Available

  • Centre Médical République

    Clermont-ferrand, 63023
    France

    Site Not Available

  • Clinique du Mail

    Grenoble, 38100
    France

    Site Not Available

  • Centre léon Bérard

    LYON Cedex 08, 69373
    France

    Site Not Available

  • Centre Hospitalier Départemental

    La Roche Sur Yon, 85025
    France

    Site Not Available

  • Centre Guillaume le Conquérant

    Le Havre, 76600
    France

    Site Not Available

  • Centre Oscar Lambret

    Lille, 59020
    France

    Site Not Available

  • Centre Hospitalier

    Lorient, 56322
    France

    Site Not Available

  • Centre Gray

    Maubeuge, 59600
    France

    Site Not Available

  • Clinique du Pont de Chaume

    Montauban, 82017
    France

    Site Not Available

  • Polyclinique St Roch

    Montpellier, 34967
    France

    Site Not Available

  • Clinique Valdegour

    Nimes, 30900
    France

    Site Not Available

  • Centre Hospitalier

    Niort, 79021
    France

    Site Not Available

  • Centre Hospitalier Universitaire

    Poitiers, 86021
    France

    Site Not Available

  • Centre Hospitalier de Cornouaille

    Quimper, 29000
    France

    Site Not Available

  • Centre Eugène Marquis

    Rennes, 35042
    France

    Site Not Available

  • Centre Hospitalier

    Rodez, 12027
    France

    Site Not Available

  • Centre Frédéric Joliot

    Rouen, 76000
    France

    Site Not Available

  • Clinique Armoricaine de Radiologie

    Saint Brieuc, 22015
    France

    Site Not Available

  • Centre de Radiothérapie

    Strasbourg, 67000
    France

    Site Not Available

  • Centre des Hautes Energies

    Toulouse, 31400
    France

    Site Not Available

  • Clinique Fleming

    Tours, 37000
    France

    Site Not Available

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