Reirradiation and Erbitux in the HNSCC

NCT01237483 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-10-26

No results posted yet for this study

Summary

The purpose of this study is to investigate in patients with cancer of the throat and recurrent inoperable a different modality treatment consisting of radiation continuously for 5 weeks and half associated with a drug directed against a receptor on cell surfaces cancer, called Erbitux ®.

The investigators hope with this shorter treatment (1.5 weeks less than the usual treatment) to improve the antitumor efficacy without additional toxic side effects.

Conditions

  • Head and Neck Cancer Squamous Cell

Interventions

DRUG

Erbitux

To begin 7 days before radiotherapy, loading dose 400 mg / m² in the first week then 250 mg / m² weekly for the duration of radiotherapy (for a total of 7 doses including the loading dose)

Sponsors & Collaborators

  • Groupe Oncologie Radiotherapie Tete et Cou

    lead OTHER

Principal Investigators

  • Laurent MARTIN, oncologist · Centre Guillaume Le Conquérant, 76600 Le Havre, France

  • Claude TUCHAIS, oncologist · Centre Paul Papin, 49933 Angers, France

  • Sauveur Marc ALFONSI, oncologist · Institut Sainte Catherine, 84082 Avignon, France

  • Xu Sh SUN, oncologist · Hôpital Jean Minoz, 25030 Besançon, France

  • Dominique DE RAUCOURT, oncologist · Centre François Baclesse, 14076 Caen, France

  • Michel LAPEYRE, oncologist · Centre Jean Perrin, 63011 Clermond-Ferrand, France

  • Philippe MAINGON, oncologist · Centre G-F Leclerc, 21079 Dijon, France

  • Muriel GARCIA-RAMIREZ, oncologist · Hôpital Robert Boulin, 33505 Libourne, France

  • Christian SIRE, oncologist · Hôpital du Scorff, 56322 Lorient, France

  • Séverine RACADOT, oncologist · Centre Léon Bérard, 69373 Lyon, France

  • Véronique FAVREL, oncologist · Centre Hospitalier Lyon Sud, 69495 Pierre-Benite, France

  • Etienne BARDET, oncologist · Centre René Gauducheau, 44805 Nantes-St Herblain, France

  • Philippe LANG, oncologist · Hôpital de La Pitié Salpitrière, 75013 Paris, France

  • Isabelle TENNEVET, oncologist · Centre Henri Becquerel, 76038 Rouen, France

  • Patricia BURBAN, oncologist · Clinique Armoricaine de Radiologie, 22015 St Brieuc, France

  • Olivier GALLOCHER, oncologist · Clinique Pasteur, 31300 Toulouse, France

  • Olivier GALLOCHER, oncologist · Polyclinique du Parc, 31078 Toulouse, France

  • Yungan TAO, oncologist · Institut Gustave Roussy, 94805 Villejuif, France

  • Pierre BOISSELIER, oncologist · Val d'Aurelle 34298 Montpellier cedex

  • Frédéric PEYRADE, oncologist · Centre Antoine Lacassagne 06189 NICE cedex 2

  • Marie SALIOU, oncologist · Clinique de l' Estuaire 44600 Pornichet

  • Cédrik LAFOND, oncologist · Centre Jean Bernard 72000 Le Mans

  • René-Jean BENSADOUN, oncologist · CHU 86021 Poitiers cedex

  • Alexandre COUTTE, oncologist · CHU Amiens sud 80004 Amiens

  • Hao QIU, oncologist · CHU 86000 Limoges

  • Florence HUGUET, oncologist · Hôpital Tenon 75020 Paris

  • Sébastien GUIHARD · Centre Paul Strauss 67065 Strasbourg

  • Xu Shan SUN, oncologist · Centre Hospitalier de Belfort Montbéliard Bd du Maréchal Juin 25200 Montbéliard

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2016-07-31
Completion
2016-07-05

Countries

  • France

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01237483 on ClinicalTrials.gov