Overview

Pyroxamide in Treating Patients With Advanced Cancer

Status:
Completed
Trial end date:
2002-09-01
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 I trial to study the effectiveness of pyroxamide in treating patients who have advanced cancer.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Memorial Sloan Kettering Cancer Center
Collaborator:
National Cancer Institute (NCI)
Criteria
DISEASE CHARACTERISTICS:

- Histologically or cytologically confirmed solid tumor or hematologic malignancy

- Disease that has failed standard therapies (e.g., surgery, radiotherapy,
endocrine therapy, or chemotherapy) or for which no curative or life- prolonging
therapy is available

- Measurable or clinically evaluable disease

- Elevated tumor marker is acceptable for evaluable disease

- No known carcinomatous meningitis, primary brain tumors, or metastatic brain disease

PATIENT CHARACTERISTICS:

Age

- 18 and over

Performance status

- ECOG 0-2

Life expectancy

- Not specified

Hematopoietic

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

- Platelet count at least 125,000/mm^3

- Hemoglobin at least 9.0 g/dL

Hepatic

- Bilirubin normal

- AST no greater than 2.5 times upper limit of normal (ULN) (5 times ULN if liver
metastases present)

- PT no greater than 1.5 times ULN

Renal

- Creatinine normal

Other

- HIV-positive status allowed

- Prior malignancy allowed

- No severe physical or emotional illness that would preclude study participation

- Not pregnant or nursing

- Negative pregnancy test

- Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy

- No concurrent bone marrow growth factors

Chemotherapy

- See Disease Characteristics

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

Endocrine therapy

- See Disease Characteristics

Radiotherapy

- See Disease Characteristics

- At least 4 weeks since prior wide-field radiotherapy and recovered

- At least 2 weeks since prior limited-field radiotherapy and recovered

- Recovered from prior radiotherapy

Surgery

- See Disease Characteristics

Other

- No other concurrent antitumor treatment