Overview
S0225 Capecitabine in Treating Patients Who Have Undergone Surgery for Locally Recurrent or Persistent Head and Neck Cancer
Status:
Withdrawn
Withdrawn
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
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.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Southwest Oncology GroupCollaborator:
National Cancer Institute (NCI)Treatments:
Capecitabine
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 definitive or post-operative radiotherapy at the time of initial
curative treatment
- 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
- No definitive or adjuvant radiotherapy or reirradiation for recurrent or persistent
disease allowed at the time of salvage 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 concurrent radiotherapy
Surgery
- See Disease Characteristics
- Recovered from prior surgery