NCT00352118

Combination Chemotherapy and Radiation Therapy in Treating Patients With Locally Advanced Head and Neck Cancer

Phase II Pilot Study of TPF (Docetaxel, Cisplatin, and 5-FU) Induction Chemotherapy Followed by Concurrent Cisplatin and Reduced Dose Radiation in Locally Advanced Head and Neck Cancer

• Status: Terminated
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 4 (actual)
• Sponsor: Masonic Cancer Center, University of Minnesota · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, cisplatin, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving combination chemotherapy together with radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with radiation therapy works in treating patients with locally advanced head and neck cancer. The doctor also wants to find out if patients who receive this treatment need a feeding tube 1 year after starting treatment.

Detailed description

OBJECTIVES: Primary * Determine feeding tube dependency at 12 months in patients with locally advanced head and neck cancer treated with induction chemotherapy comprising docetaxel, cisplatin, and fluorouracil followed by cisplatin and reduced-dose radiotherapy. Secondary * Determine the progression-free, disease-free, and overall survival of patients treated with this regimen. * Determine the pattern of failure in patients treated with this regimen. * Evaluate the quality of life of patients treated with this regimen. * Assess pre- and post-treatment swallowing ability of patients and the impact on their quality of life. Tertiary * Quantify salivary flow rates of patients receiving chemotherapy with radiotherapy for head and neck malignancy. * Evaluate the quality of saliva by examining total protein concentrations. * Quantify proangiogenic cytokines (interleukin \[IL\]-1, IL-6, IL-8, and vascular endothelial growth factor) in the saliva of these patients. * Determine the degree of mucositis and xerostomia of patients receiving chemotherapy with radiotherapy for head and neck malignancy. * Compare salivary flow rates with the grade of mucositis and xerostomia of patients receiving chemotherapy with radiotherapy for head and neck malignancy. OUTLINE: This is a pilot study. * Induction therapy: Patients receive docetaxel IV over 1 hour and cisplatin IV over 1 hour on day 1 followed by fluorouracil IV continuously on days 1- 4. Patients also receive filgrastim (G-CSF) subcutaneously (SC) on days 5-14 or pegfilgrastim SC on day 5. Treatment repeats every 3 weeks for 2 courses in the absence of disease progression or unacceptable toxicity. Patients achieving a partial or clinical complete response proceed to chemoradiotherapy 3 weeks later. * Chemoradiotherapy: Patients receive cisplatin IV over 1 hour on day 1. Treatment repeats every 3 weeks for 3 courses in the absence of disease progression or unacceptable toxicity. Patients also undergo concurrent reduced-dose radiotherapy 5 days a week for 6 weeks. * Surgery: Approximately 6 to 8 weeks after completing chemoradiotherapy, patients with residual neck disease or disease initially staged at N2 or greater undergo neck dissection. Saliva is collected periodically to measure flow rates and quality; quantify proangiogenic cytokines (interleukin \[IL\]-1, IL-6, IL-8 and vascular endothelial growth factor); and examine the grade of mucositis and xerostomia. Quality of life is assessed at baseline, before chemoradiotherapy, 1 month after the last radiation treatment, every 3 months for 1 year, and then every 6 months for 1 year. After completion of study treatment, patients are followed periodically for 5 years and then annually thereafter. PROJECTED ACCRUAL: A total of 36 patients will be accrued for this study.

Conditions

• Head and Neck Cancer

Interventions

Type	Name	Description
BIOLOGICAL	filgrastim	subcutaneously on Days 5-14, repeating every 3 weeks for 2 courses.
BIOLOGICAL	pegfilgrastim	If applicable on day 5, repeating every 3 weeks for 2 courses.
DRUG	cisplatin	Intravenous over 1 hour on day 1, every 3 weeks for 3 courses.
DRUG	docetaxel	Intravenous over 1 hour on day 1.
DRUG	fluorouracil	Intravenous continuously on days 1-4.
PROCEDURE	conventional surgery	As appropriate, neck dissection.
RADIATION	radiation therapy	60 Gy 5 days/week x 6 weeks with cisplatin

Timeline

• Start date: 2006-03-01
• Primary completion: 2008-04-01
• Completion: 2008-04-01
• First posted: 2006-07-14
• Last updated: 2017-12-28
• Results posted: 2009-07-21

Locations

1 site across 1 country: United States