RATIONALE: Drugs used in chemotherapy, such as capecitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Giving capecitabine after surgery may kill any remaining tumor cells.

PURPOSE: This phase II trial is studying how well capecitabine works in treating patients who have undergone surgery for locally recurrent or persistenthead and neck cancer.

Condition	Treatment or Intervention	Phase
recurrent squamous cell carcinoma of the lip and oral cavity recurrent squamous cell carcinoma of the paranasal sinus and nasal cavity recurrent squamous cell carcinoma of the hypopharynx recurrent squamous cell carcinoma of the larynx recurrent squamous cell carcinoma of the oropharynx	Drug: capecitabine  Procedure: adjuvant therapy  Procedure: chemotherapy	Phase II

Further Study Details: 

OBJECTIVES:

• Determine 2-year disease-free survival of patients treated with surgical salvage followed by adjuvant low-dose capecitabine for locally recurrent or persistent squamous cell carcinoma of the head and neck .
• Determine the toxic effects of this drug in these patients.
• Determine 2-year overall survival of patients treated with this drug.
• Determine patterns of disease relapse in patients treated with this drug.

OUTLINE: This is a multicenter study.

Patients receive oral capecitabine once daily for 12 months in the absence of disease progression or unacceptable toxicity.

Patients are followed every 4 months for 2 years and then annually for 1 year.

PROJECTED ACCRUAL: A total of 70 patients will be accrued for this study within 2 years.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed squamous cell carcinoma of the head and neck
• Locoregionally recurrent or persistent disease
• No thyroid gland, salivary gland, or nasopharynx disease sites
• Must have undergone salvage surgical resection within the past 56 days
• All current disease must be completely resected, including resection of recurrent primary disease and/or neck dissection, if regional nodal disease is present
• Surgical margins must be free of disease on final pathological evaluation of specimens
• Must have undergone definitive or post-operative radiotherapy at the time of initial curative treatment
• No evidence of distant disease by clinical examination and CT scan of the chest and upper abdomen (including the liver) within the past 90 days

PATIENT CHARACTERISTICS: Age

• 18 and over

Performance status

• Zubrod 0-1

Life expectancy

• Not specified

Hematopoietic

• Absolute neutrophil count ≥ 1,500/mm^3
• Platelet count ≥ 100,000/mm^3

Hepatic

• Not specified

Renal

• Creatinine clearance ≥ 30 mL/min

Other

• Not pregnant or nursing
• Fertile patients must use effective contraception
• Able to take oral tablets OR able to take crushed tablets through a gastrostomy tube
• No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY: Biologic therapy

• No concurrent biologic therapy
• No concurrent filgrastim (G-CSF)

Chemotherapy

• Prior systemic chemotherapy as definitive therapy for head and neck cancer allowed (prior treatment with fluorouracil allowed, but must be catalogued)
• More than 5 years since prior systemic chemotherapy for any other cancer diagnosis
• No other concurrent chemotherapy

Endocrine therapy

• No concurrent anticancer hormonal therapy
• Concurrent hormonal therapy for non-cancer diagnosis allowed

Radiotherapy

• See Disease Characteristics
• No prior or concurrent salvage radiotherapy for recurrent disease
• No concurrent radiotherapy

Surgery

• See Disease Characteristics
• Recovered from prior surgery

Study chairs or principal investigators

Susan G. Urba, MD,  University of Michigan Comprehensive Cancer Center   
David Schwartz, MD,  Study Chair,  M.D. Anderson Cancer Center   

Study ID Numbers:  CDR0000394169; SWOG-S0225; NCT00095641
Record last reviewed:  December 2004
Last Updated:  March 21, 2005
Record first received:  November 5, 2004
ClinicalTrials.gov Identifier:  NCT00095641
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08