Everolimus and Imatinib Mesylate in Treating Patients With Metastatic or Unresectable Kidney Cancer

NCT ID: NCT00331409

Last Updated: 2017-10-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-01-31
• Study Completion Date: 2010-01-31

Brief Summary

RATIONALE: Everolimus and imatinib mesylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Everolimus may also block blood flow to the tumor. Giving everolimus together with imatinib mesylate may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving everolimus together with imatinib mesylate works in treating patients with metastatic or unresectable kidney cancer.

Detailed Description

OBJECTIVES:

Primary

• Estimate the proportion of patients with previously treated metastatic or unresectable clear cell carcinoma of the kidney who are progression free (complete response [CR], partial response [PR], or stable disease [SD]) at 3 months after treatment with everolimus and imatinib mesylate.

Secondary

• Estimate median time to progression in patients treated with this regimen.
• Determine the proportion of patients whose best overall response are CR, PR, SD, or progressive disease.
• Evaluate the mean and range of the maximum percent reduction in tumor size.
• Describe the toxicities of this regimen in these patients.

OUTLINE: This is an open-label, multicenter study.

Patients receive oral imatinib mesylate and oral everolimus once daily beginning on day 1 and continuing in the absence of disease progression.

PROJECTED ACCRUAL: A total of 43 patients will be accrued for this study.

Conditions

Kidney Cancer

Keywords

stage III renal cell cancer; stage IV renal cell cancer; clear cell renal cell carcinoma; recurrent renal cell cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Everolimus and Imatinib Mesylate

Everolimus: 2.5 mg daily by mouth Imatinib Mesylate: 600 mg daily by mouth

Group Type: EXPERIMENTAL

Everolimus

Intervention Type: DRUG

2.5 mg by mouth daily

imatinib mesylate

Intervention Type: DRUG

600 mg by mouth daily

Interventions

Everolimus

2.5 mg by mouth daily

Intervention Type: DRUG

imatinib mesylate

600 mg by mouth daily

Intervention Type: DRUG

Other Intervention Names

Afinitor; RAD001; Certican; Gleevec; STI-571

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed clear cell kidney cancer, meeting 1 of the following criteria:

• Measurable metastatic disease
• Locally unresectable disease
• No history of known brain metastases that have not been adequately treated with radiotherapy and/or surgery
• Must have received ≥ 1 prior systemic therapy for metastatic or unresectable renal cell carcinoma

PATIENT CHARACTERISTICS:

• Eastern Cooperative Oncology Group (ECOG) performance status 0-2
• Absolute neutrophil count > 1,500/mm³
• Platelet count > 100,000/mm³
• Hemoglobin > 8 g/dL
• Bilirubin < 1.5 times upper limit of normal (ULN)
• Serum glutamic oxaloacetic transaminase(SGOT) and Serum glutamic pyruvic transaminase(SGPT) < 2.5 times ULN
• Creatinine < 1.5 times ULN
• No New York Heat Association grade III-IV cardiac disease
• No other malignancy within the past 5 years except basal cell skin cancer, cervical carcinoma in situ, or insignificant or inactive disease
• No chronic liver disease (i.e., chronic active hepatitis or cirrhosis)
• No severe or uncontrolled medical disease
• No gastrointestinal disease or impairment that would hinder the absorption of everolimus
• No uncontrolled diabetes
• No chronic renal disease
• No active uncontrolled infection
• No congestive heart failure
• No myocardial infarction within the past 6 months

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• More than 2 weeks since prior major surgery
• More than 4 weeks since prior chemotherapy (6 weeks for nitrosourea or mitomycin C)
• More than 4 weeks since prior immunotherapy
• More than 4 weeks since other prior investigational agents
• No prior radiotherapy to > 25% of bone marrow
• No prior treatment with an mammalian target of rapamycin(mTOR) inhibitor
• No concurrent therapeutic warfarin

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

OHSU Knight Cancer Institute

OTHER

Sponsor Role: lead

Responsible Party

Christopher Ryan

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christopher W. Ryan, MD

Role: STUDY_CHAIR

OHSU Knight Cancer Institute

Locations

OHSU Knight Cancer Institute

Portland, Oregon, United States

Countries

United States

Other Identifiers

OHSU-SOL-05108-LM

Identifier Type: OTHER

Identifier Source: secondary_id

FWA00000161

Identifier Type: OTHER

Identifier Source: secondary_id

OHSU-1754

Identifier Type: OTHER

Identifier Source: secondary_id

CDR0000479150

Identifier Type: OTHER

Identifier Source: secondary_id

IRB00001754

Identifier Type: -

Identifier Source: org_study_id