Overview

Chemotherapy in Treating Patients With 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 DHA-paclitaxel in treating patients who have locally advanced, metastatic, or unresectable kidney cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Theradex
Treatments:
Albumin-Bound Paclitaxel
Paclitaxel
Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed renal cell cancer
Locally advanced OR Metastatic OR Unresectable Measurable disease No known or clinical
evidence of CNS metastasis

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-1 Life expectancy: Not
specified Hematopoietic: Absolute neutrophil count at least 1,500/mm3 Platelet count at
least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 times upper limit of normal (ULN)
SGOT or SGPT no greater than 2.5 times ULN Renal: Creatinine no greater than 2.5 mg/dL
Cardiovascular: No uncontrolled ventricular arrhythmia No myocardial infarction within the
past 3 months No superior vena cava syndrome Neurologic: No peripheral neuropathy greater
than grade 1 No uncontrolled major seizure disorder No spinal cord compression Other: No
other prior malignancy except: Curatively treated nonmelanoma skin cancer or carcinoma in
situ of the cervix OR Cancer curatively treated with surgery alone that has not recurred
for more than 5 years No concurrent serious infection requiring parenteral therapy No
unstable or serious concurrent medical conditions No psychiatric disorder that would
preclude study Not pregnant or nursing Negative pregnancy test Fertile patients must use
effective contraception during and for 6 months after study

PRIOR CONCURRENT THERAPY: Biologic therapy: At least 28 days since prior immunotherapy No
concurrent immunotherapy Chemotherapy: No prior chemotherapy for advanced disease No prior
taxanes At least 28 days since prior chemotherapy No other concurrent chemotherapy
Endocrine therapy: At least 28 days since prior hormonal therapy No concurrent hormonal
therapy Radiotherapy: At least 28 days since prior large-field radiotherapy No concurrent
radiotherapy Surgery: At least 14 days since prior major surgery Other: Concurrent
bisphosphonates allowed if on stable dose for at least 30 days prior to study No other
concurrent anticancer therapy