Fluorouracil Plus Interferon Alfa in Treating Patients With Advanced Metastatic Carcinoid Tumors

Mid-Atlantic Oncology Program

Status and phase: Completed; Phase 2

Conditions: Gastrointestinal Carcinoid Tumor; Lung Cancer

Treatments: Biological: recombinant interferon alfa; Drug: fluorouracil

Study type: Interventional

Funder types: Other

Identifiers

NCT00002470

CDR0000076667 (Registry Identifier)

MAOP-5190

NCI-V90-0197

NBSG-9010

Details and patient eligibility

About

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Interferon alfa may interfere with the growth of the cancer cells. Combining interferon alfa with chemotherapy may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of fluorouracil plus interferon alfa in treating patients who have advanced metastatic carcinoid tumors.

Full description

OBJECTIVES:

• Determine the objective response rate and duration of remission in patients with advanced metastatic carcinoid tumors treated with fluorouracil and interferon alfa-2b.
• Determine the symptomatic response in patients treated with this regimen.
• Determine the toxicity of this regimen in these patients.
• Determine the quality of life of patients treated with this regimen.
• Determine the survival characteristics of patients treated with this regimen.

OUTLINE: Patients receive fluorouracil IV continuously for 10 weeks and interferon alfa subcutaneously 3 times a week for 12 weeks. Treatment continues every 12 weeks in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline and at weeks 1, 7, and 11 of each course.

Patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically proven carcinoid tumor with radiologically confirmed metastatic disease

• Recurrence after surgery or radiotherapy allowed

• Must meet at least 1 of the following conditions:

  • Symptomatic carcinoid syndrome not controlled
  • Other systemic symptoms (e.g., weight loss, anorexia)
  • 24 hour urinary 5-hydroxyindole acetic acid (5-HIAA) 100 mg or greater
  • Bone metastases
  • Carcinoid heart disease
  • Carcinoid asthma

• Measurable disease or 24-hour urinary 5-HIAA 50 mg or greater required

• No known brain metastases

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• Zubrod 0-2

Hematopoietic:

• Granulocyte count at least 1,500/mm^3
• Platelet count at least 100,000/mm^3

Hepatic:

• Bilirubin no greater than 3.0 mg/dL

Renal:

• Creatinine no greater than 2.0 mg/dL

Cardiovascular:

• See Disease Characteristics

Pulmonary:

• See Disease Characteristics

Other:

• No concurrent infection (no fever for at least 3 days prior to treatment unless fever due to tumor)
• No significant medical or psychiatric illness that would preclude study or informed consent
• No other malignancy within the past 5 years except basal cell or squamous cell skin cancer or curatively treated stage I carcinoma of the cervix
• Not pregnant
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• No prior interferon therapy

Chemotherapy:

• No other concurrent chemotherapy

Endocrine therapy:

• Prior endocrine therapy allowed
• Concurrent octreotide allowed

Radiotherapy:

• See Disease Characteristics
• At least 4 weeks since prior radiotherapy
• No concurrent radiotherapy

Surgery:

• See Disease Characteristics
• Prior surgery allowed

Other:

• No prior fluorinated pyrimidine