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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. |
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| Detailed Description | At ASCO 2004 there were 3 major presentations issuing an increasing in survival:
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. |
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| 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 |
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| Intervention † | Drug: cetuximab Drug: Cisplatin Procedure: Radiotherapy 70 Gy, 35 fractions |
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| MEDLINE PMIDs | |||||
| Links | Related Info ![]() Related Info  ![]() |
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| Recruitment Information Fields | |||||
| Recruitment Status † | Recruiting | ||||
| Enrollment † | 156 | ||||
| Start Date † | October 2005 | ||||
| Completion Date | |||||
| Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 18 Years to 75 Years | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts †† |
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| 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 † |
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| 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 | ||||