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Radiotherapy With Cisplatin Versus Radiotherapy With Cetuximab After Induction Chemotherapy for Larynx Preservation

This study is currently recruiting participants.
Study NCT00169247.   Last updated on September 23, 2006.   Information provided by Groupe Oncologie Radiotherapie Tete et Cou

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Descriptive Information Fields
Brief Title  Radiotherapy With Cisplatin Versus Radiotherapy With Cetuximab After Induction Chemotherapy for Larynx Preservation
Official Title  Larynx Preservation With Induction Chemotherapy (Cisplatin, 5FU, Docetaxel) Followed by Radiotherapy Combined With Either Cisplatin or Cetuximab in Laryngopharyngeal Squamous Cell Carcinoma - A Randomised Phase II Study
Brief Summary

Larynx preservation remains a very challenging approach in patients with larynx/pharynx cancer. A first attempt consisted of induction chemotherapy followed in good responders by irradiation. This approach allowed to preserve 60 % of the larynx without any significant difference in survival. The second attempt consisted of concurrent chemo-irradiation. This approach provided a higher larynx preservation rate but survival remained unchanged and mucosal toxicity was also higher. A third approach is currently under evaluation: induction chemotherapy followed by concurrent chemo-irradiation in good responders.

Detailed Description

At ASCO 2004 there were 3 major presentations issuing an increasing in survival:

  • the update of the MACH-NC meta-analysis showed that actually only concurrent chemo-irradiation trials found a significantly improved survival (in particular the addition of cisplatinum alone to radiotherapy)
  • the addition of docetaxel to the cisplatinum-5FU regimen (TPF) when compared with cisplatinum--5FU (PF)
  • the addition of cetuximab to irradiation

On this basis we decided to carry-out a randomized phase II for previously untreated patients requiring a total laryngectomy:

All patients after a complete work-up including a CTscan will receive 3 cycles of TPF(T: 75 mg/m², P: 75 mg/m² and 5FU 750 mg/m²).

Patients with response over 50 % (endoscopy and CTscan) will be randomized to receive either irradiation (70 Gy) and cisplatinum (100 mg/m² on D1, D22 and D43) or irradiation (70 Gy) with cetuximab (loading dose of 400 mg followed by weekly 250 mg for a total of 8 cycles.

Patients with less than 50% decease in tumour volume after TPF, patients with residual or recurrent disease after either RT-CDDP or RT-cetuximab will get salvage total laryngectomy.

Study Phase Phase II
Study Type  Interventional
Study Design  Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Primary Outcome Measure  rate of laryngeal preservation
Secondary Outcome Measure  quality of life
Condition  Larynx Cancer
Hypopharynx Cancer
Intervention  Drug: cetuximab
Drug: Cisplatin
Procedure: Radiotherapy 70 Gy, 35 fractions
MEDLINE PMIDs
Links Related Info This link exits the ClinicalTrials.gov site
Related Info This link exits the ClinicalTrials.gov site
Recruitment Information Fields
Recruitment Status  Recruiting
Enrollment  156
Start Date  October 2005
Completion Date
Eligibility Criteria 

Inclusion Criteria:

  • Larynx or hypopharynx squamous cell carcinoma proven by histology, locally advanced, only eligible for surgery as total or sub-total (pharyngo-)laryngectomy
  • Performance status 0-1
  • Neutrophils >=1.5 x 109/l, Platelets count >=100 x 109/l, haemoglobin >=10 g/dl
  • Total bilirubin <= 1.5 x upper reference range
  • ASAT and ALAT <= 2.5 x upper reference range, Alkaline Phosphatases <= 5 x upper reference range
  • Serum creatinine <= 120 µmol/l
  • Weight loss < 10 % within last 3 months
  • Written inform consent

Exclusion Criteria:

  • Infiltrative transglottic tumor or clinical cartilage invasion
  • Distant metastasis
  • Previous chemotherapy or radiotherapy
  • Contra-indication to chemotherapy
Gender Both
Ages 18 Years to 75 Years
Accepts Healthy Volunteers No
Contacts ††
Contact: Jean-Louis Lefebvre     33 3 20 29 59 54     jl-lefebvre@o-lambret.fr    
Location Countries  France
Administrative Information Fields
NCT ID  NCT00169247
Organization ID GORTEC-TREMPLIN
Secondary IDs ††
Study Sponsor  Groupe Oncologie Radiotherapie Tete et Cou
Collaborators †† Groupe d'Etude des Tumeurs de la Tête Et du Cou
Investigators 
Principal Investigator:     Jean-Louis Lefebvre     Centre Oscar Lambret    
Information Provided By Groupe Oncologie Radiotherapie Tete et Cou
Verification Date September 2006
First Received Date  September 12, 2005
Last Updated Date September 23, 2006

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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