Study of Docetaxel in Combination With Cisplatin and 5-Fluorouracil in Locally Advanced Squamous Cell Carcinoma of the Head and Neck

Dana-Farber Cancer Institute

Status and phase

Completed

Phase 2

Phase 1

Conditions

SSCHN

Squamous Cell Carcinoma of Head and Neck

Advanced Squamous Cell Carcinoma

Treatments

Drug: 5-Fluorouracil

Drug: Cisplatin

Drug: Docetaxel

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00139269

97-199

Details and patient eligibility

About

The purpose of this study is to determine the appropriate dose, that dose which is found to give maximum effect with limited toxicity, of cisplatin in combination with docetaxel and 5-fluorouracil and then to further define the safety and effectiveness of this combination of medications.

Full description

Treatment begins with a one hour infusion of docetaxel followed by a 1/2 hour infusion of cisplatin. 5-fluorouracil will be administered through continuous IV infusion through a portable pump for four days at home. A cycle is twenty-one days long ( 4 days of chemotherapy and 17 days of recovery).
During each cycle blood tests will be performed weekly. A physical exam will be performed and the impact of the chemotherapy will be assessed at the end of each cycle.
If after 2 cycles the patients cancer has not responded sufficiently they will be removed from the study.
If significant reduction in the size of the tumor is observed after cycle 2, a third and final cycle will be performed. Followed by radiation therapy twice daily for approximately 6-7 weeks.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Histologically or cytologically confirmed diagnosis of squamous cell carcinoma of head and neck (SSCHN).
At least one bi- or uni-dimensionally measurable lesion.
Stage II or IV disease without evidence of distant metastasis.
No previous chemotherapy, radiotherapy or surgery (other than biopsy) for SSCHN.
Age greater than 18 years.
ECOG performance status of 0 or 1.
Life expectancy of greater than 12 weeks.
Adequate bone marrow, hepatic and renal function.
Normal serum calcium

Exclusion criteria

Primary tumor location in nasopharynx, nasal cavity, sinuses, or salivary glands.
Patients with any non-SSCHN malignancy within 5 years of study entry, except curatively treated basal cell carcinoma or squamous cell carcinoma of the skin or carcinoma in situ of the uterine cervix.
Any prior treatment with chemotherapy.
Prior radiotherapy to major bone marrow area (> 10% bone marrow) or to head and neck.
Current peripheral neuropathy of greater than NCI grade 2.
Other serious illness or medical condition
Concurrent treatment with corticosteroids unless chronic treatment at low doses.
Pregnant or lactating females or females of childbearing potential not employing adequate contraception.