Cetuximab & Concomitant-Boost Accelerated RT in Patients With Locally Advanced Oropharynx Squamous Cell Carcinoma.

  • STATUS
    Recruiting
  • participants needed
    90
  • sponsor
    Trial Form Support S.L.
Updated on 7 November 2020

Summary

The purpose of this study is to determine the 1-year rate of locoregional disease control in the experimental arm, using a control arm to avoid selection bias.

Description

- To determine the 1-year rate of locoregional disease control in the experimental arm, using a control arm to avoid selection bias. - To determine the 2 and 3 year rate of locoregional disease control. - To evaluate the safety and toxicity of the combination of cetuximab and concomitant-boost accelerated radiotherapy followed by 12 weeks of complementary treatment with cetuximab. Both acute and chronic toxicity will be assessed. - To determine specific disease-free survival, event-free survival, disease-specific survival and overall survival - To determine acute and late toxicity - To determine EGFR, p53, Ki67, and evaluate its value as a prognostic factor.

Details
Condition Oropharyngeal Cancer
Treatment Cetuximab
Clinical Study IdentifierNCT00251381
SponsorTrial Form Support S.L.
Last Modified on7 November 2020

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