Instituto do Cancer do Estado de Sao Paulo
São Paulo, 05409-011, Brazil
NCT Number: NCT01695122
The purpose of this study is to evaluate if the addition of valproic acid to standard platinum-based chemoradiation as definitive treatment of locally advanced Head and Neck squamous cell carcinoma can improve treatment outcomes, such as response rate.
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Notify MeUp to 65 year
All sexes
Interventional
Phase 2
São Paulo, 05409-011, Brazil
Valproic acid is a known histone deacetylase inhibitor. In addition to activating apoptosis pathways, cell differentiation and downregulating expression of growth factors, it also promotes radiosensitization.
Most patients with Head and Neck squamous cell carcinoma are diagnosed with locally advanced disease, in which long term disease control is still a challenge. The incorporation of epigenetic regulation into standard treatment could improve results of definitive platinum-based chemoradiation in such patients.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: sodium valproate
Time frame: Within 6 to 8 weeks after completion of chemoradiation
RECIST v 1.1
Time frame: Three years
Time frame: Three Years
Instituto do Cancer do Estado de São Paulo
Other
Efficacy Evaluation of the Combination of Valproic Acid and Standard Platinum-based Chemoradiation in Patients With Locally Advanced Head and Neck Squamous Cell Carcinoma
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