Overview

Thalidomide in Treating Patients With Recurrent or Metastatic Head and Neck Cancer

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
Phase II trial to study the effectiveness of thalidomide in treating patients with recurrent or metastatic head and neck cancer. Thalidomide may stop the growth of head and neck cancer by stopping blood flow to the tumor.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Cancer Institute (NCI)
Treatments:
Thalidomide
Criteria
DISEASE CHARACTERISTICS:

- Histologically proven squamous cell carcinoma of the head and neck

- Recurrent disease OR metastatic disease at initial diagnosis or at recurrence

- Initial therapy of surgery and/or radiotherapy, induction chemotherapy, or concurrent
chemotherapy and radiotherapy allowed

- No more than one prior regimen of chemotherapy or biologic therapy for metastatic
disease

- Recurrence after adjuvant or induction chemotherapy may have received one additional
course of chemotherapy or biologic therapy

PATIENT CHARACTERISTICS:

- Age: 18 and over

- Performance status: Zubrod 0-2

- Life expectancy: At least 3 months

- WBC at least 3000/mm3

- Platelet count at least 100,000/mm3

- Hematocrit at least 30%

- Bilirubin no greater than 1.5 times normal

- SGOT/SGPT no greater than 1.5 times normal

- Creatinine no greater than 1.5 mg/dL

- Not pregnant or nursing

- Negative pregnancy test

- Fertile women must use 2 methods of effective contraception, 1 barrier and 1 hormonal,
beginning at least 4 weeks before study and continuing during and for 1 month after
study

- Men must use effective barrier contraception during and for 1 month after study

- No grade 2 or greater peripheral neuropathy

- No serious infection or other concurrent illness requiring immediate therapy

- Must be able to take oral medications

- No medical or social factors that would interfere with compliance

PRIOR CONCURRENT THERAPY:

- Any number of courses of one regimen of chemotherapy allowed

- No concurrent cytotoxic chemotherapy

- No concurrent radiotherapy