Phase 2
N=4
Bortezomib in Treating Patients With Metastatic Kidney Cancer
Kidney Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00276614 ↗Enrolled (actual)
4
Serious AEs
0.0%
Results posted
Apr 2012
Primary outcome: Primary: Objective Response Rate as Measured by RECIST Criteria After Every 2 Courses of Treatment for up to 6 Courses — 2 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- bortezomib (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Jonsson Comprehensive Cancer Center
- Primary completion
- Jul 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Objective Response Rate as Measured by RECIST Criteria After Every 2 Courses of Treatment for up to 6 Courses |
2 | — |
Summary
RATIONALE: Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.
PURPOSE: This phase II trial is studying how well bortezomib works in treating patients with metastatic kidney cancer.
Eligibility Criteria
Inclusion Criteria
- Histologically confirmed pure non-clear cell renal cell carcinoma (RCC)
- Distant metastatic disease (Tx, Nx, M1)
- Tumor expresses wild-type von Hippel-Lindau tumor suppressor gene/protein
- Measurable disease on imaging scan (≥ 1 cm)
- Brain metastases allowed provided they have been treated with surgery and/or radiation therapy and show no evidence of progression on cerebral CT or MRI scan 2 months following surgery and/or radiation therapy.
- Life expectancy ≥ 3 months
- Karnofsky performance status ≥ 60%
- Negative pregnancy test
- Fertile patients must use an acceptable method of contraception
- No other major illnesses likely to limit survival
- Platelet count ≥ 100,000/mm^3
- Absolute neutrophil count ≥ 1, 000/mm^3
- Hemoglobin ≥ 10 g/dL (transfusion allowed)
- Creatinine clearance ≥ 30 mL/min OR creatinine ≤ 2 mg/dL
- ALT or AST ≤ 2.5 times upper limit of normal
- At least 4 weeks since prior radiotherapy and recovered
- More than 30 days since any other prior investigational drugs
Exclusion Criteria
- active CNS metastases
- pregnant or nursing
- myocardial infarction within the past 6 months
- New York Heart Association class III or IV heart failure
- uncontrolled angina
- severe uncontrolled ventricular arrhythmias
- electrocardiographic evidence of acute ischemia or active conduction system abnormalities
- Peripheral neuropathy ≤ grade 1
- hypersensitivity to bortezomib, boron, or mannitol
- history of a non-RCC malignancy within the past 5 years except basal cell carcinoma of the skin
- serious medical or psychiatric illness that would preclude study participation
- prior cytotoxic chemotherapy for this cancer
- other concurrent investigational therapy
- concurrent chemotherapy, immunotherapy, or hormonal therapy
Data sourced from ClinicalTrials.gov (NCT00276614). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.