Overview

UCN-01 in Treating Patients With Advanced or Metastatic Kidney Cancer

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of UCN-01 in treating patients who have unresectable stage III or stage IV kidney cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of California, San Francisco
Collaborator:
National Cancer Institute (NCI)
Treatments:
7-hydroxystaurosporine
Staurosporine
Criteria
DISEASE CHARACTERISTICS:

- Histologically or cytologically confirmed stage IV or unresectable stage III renal
cell carcinoma

- Metastatic disease must be amenable to biopsy or appropriate for nephrectomy
before study therapy

- At least 1 unidimensionally measurable lesion

- At least 20 mm by conventional techniques OR at least 10 mm by spiral CT scan

- No known prior or concurrent CNS metastases

PATIENT CHARACTERISTICS:

Age:

- 18 and over

Performance status:

- ECOG 0-2 OR

- Karnofsky 60-100%

Life expectancy:

- More than 3 months

Hematopoietic:

- WBC at least 3,000/mm^3

- Absolute neutrophil count at least 1,500/mm^3

- Platelet count at least 100,000/mm^3

Hepatic:

- Bilirubin normal

- AST/ALT no greater than 2.5 times upper limit of normal

Renal:

- Creatinine normal OR

- Creatinine clearance at least 60 mL/min

Cardiovascular:

- No history of clinically significant coronary artery disease

- No symptomatic cardiac dysfunction

- No symptomatic congestive heart failure

- No unstable angina pectoris

- No cardiac arrhythmia

Pulmonary:

- No symptomatic pulmonary dysfunction

Other:

- No prior allergic reactions to compounds of similar chemical or biological composition
to UCN-01

- No other uncontrolled concurrent illness

- No active or ongoing infection

- No known immune deficiency

- No psychiatric illness or social situation that would preclude study compliance

- No insulin-dependent diabetes mellitus

- Not pregnant or nursing

- Negative pregnancy test

- Fertile patients must use effective contraception during and for 6 months after study
participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

- Not specified

Chemotherapy:

- At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin) and
recovered

Endocrine therapy:

- Not specified

Radiotherapy:

- At least 4 weeks since prior radiotherapy and recovered

- No prior mediastinal radiation

Surgery:

- See Disease Characteristics

- At least 4 weeks since prior nephrectomy

Other:

- No more than 2 prior systemic therapies for metastatic renal cell carcinoma

- No other concurrent investigational agents