Safety and Toxicity Study of Sorafenib in Patients With Kidney Cancer

Sponsor

The Methodist Hospital Research Institute (Other)

Overall Status

Completed

CT.gov ID

NCT00445042

Collaborator

Bayer (Industry), Amgen (Industry)

Enrollment

Location

Arm

Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the safety and toxicity levels of Dose Escalated Sorafenib in the treatment of patients with renal cancer.

Condition or Disease	Intervention/Treatment	Phase
Carcinoma, Renal Cell	Drug: Sorafenib	Phase 2

Detailed Description

Because tumors may have multiple mechanisms to induce angiogenesis, blockade with sorafenib may demonstrate efficacy. Doses of sorafenib (400 mg b.i.d.) as a single agent is with minimal toxicity, presents an opportunity to explore a more intensive drug administration. This study will allow individual patient titration (e,g,, intrapatient dose escalation) as per protocol.

This provides the basis for the dose escalation development of sorafenib. The study is designed to evaluate the ability for patients to dose escalate. Secondary endpoints include; response, time to progression, and overall survival in patients with MRCC. Tissue correlation to evaluate the impact of expression of receptor on clinical outcome will be retrospectively performed. Laboratory correlation of plasma VEGF levels will be correlated and evaluated to clinical outcome.

Study Design

Study Type:

Interventional

Actual Enrollment :

71 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase II Study of Sorafenib in Patients With Metastatic Renal Cell Carcinoma

Study Start Date :

Nov 1, 2005

Actual Primary Completion Date :

Sep 1, 2008

Actual Study Completion Date :

Oct 1, 2008

Arms and Interventions

Arm	Intervention/Treatment
Experimental: A Intrapatient dose escalation study of sorafenib	Drug: Sorafenib The initial dose of Sorafenib will be administered orally with a dose of 400 mg twice a day, daily. Intrapatient dose escalation will occur as defined in the protocol, providing no dose limiting toxicity (Grade 3 or 4) is observed. Other Names: Nexavar

Arm

Intervention/Treatment

Experimental: A

Intrapatient dose escalation study of sorafenib

Drug: Sorafenib

The initial dose of Sorafenib will be administered orally with a dose of 400 mg twice a day, daily. Intrapatient dose escalation will occur as defined in the protocol, providing no dose limiting toxicity (Grade 3 or 4) is observed.

Other Names:

Nexavar

Outcome Measures

Primary Outcome Measures

Tumor progression rate by RECIST criteria [restaging every 8 weeks]

Secondary Outcome Measures

Overall response rate [restaging every 8 weeks]
Time to progression and overall survival [restaging every 8 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytological confirmed metastatic or unresectable clear cell renal cell carcinoma.
No more than one prior systemic therapy. No prior vascular endothelial growth factor receptor agents.
Patients with primary tumor in place are strongly encouraged to undergo nephrectomy prior to initiation of study agent.
Prior palliative radiotherapy to metastatic lesion(s) is permitted.
All major surgery of any type and/or radiotherapy must be completed at least 4 weeks prior to registration.
Patients must have metastatic or unresectable disease.
Paraffin RCC tissue blocks or unstained slides must be available.
Karnofsky performance status > 70 % .
Not pregnant
Age > 18
Must meet required initial laboratory values

Exclusion Criteria:

No ongoing hemoptysis, or cerebrovascular accident within 12 months, or peripheral vascular disease with claudication on less than 1 block, or history of clinically significant bleeding.
No deep vein thrombosis or pulmonary embolus within one year of study enrollment and no ongoing need for full-dose oral or parenteral anticoagulation. Low dose coumadin (1 mg) for maintenance of catheter patency or daily prophylactic aspirin is allowed.
No evidence of current central nervous system (CNS) metastasis. All patients must undergo an MRI or CT scan of the brain (with contrast, if possible) within 42 days prior to registration. Any imaging abnormality indicative of CNS metastases will exclude the patient from the study.
No significant cardiovascular disease defined as congestive heart failure (New York Heart Association Class II, II or IV) angina pectoris requiring nitrate therapy, or recent myocardial infarction (within the last 6 months).
No patients with uncontrolled hypertension (defined as blood pressure of >160 mmHg systolic and/or > 90 mmHg diastolic on medication).
Any ongoing requirement for systemic corticosteroid therapy is not permitted. Topical and/or inhaled steroids are allowed.
No pre-existing thyroid abnormality whose thyroid function cannot be maintained in the normal range by medication are ineligible.
No uncontrolled psychiatric disorder.
Patients with delayed healing of wounds, ulcers and/or bone fractures are not eligible
Patients with a 'currently active' second malignancy other than non-melanoma skin cancers are not eligible. Patients are not considered to have a 'currently active' malignancy if they have completed anti-cancer therapy and are considered by their physician to be a less than 30% risk of relapse.