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 logo

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: Docetaxel
Drug: Cisplatin

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.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems