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Safety and Toxicity Study of Sorafenib in Patients With Kidney Cancer

Primary Purpose

Carcinoma, Renal Cell

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sorafenib
Sponsored by
The Methodist Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carcinoma, Renal Cell focused on measuring Metastatic Renal Cell Carcinoma, Metastatic RCC, Kidney Cancer, M3thodist

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept 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.

Sites / Locations

  • Methodist Hospital - Baylor College of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

Intrapatient dose escalation study of sorafenib

Outcomes

Primary Outcome Measures

Tumor progression rate by RECIST criteria

Secondary Outcome Measures

Overall response rate
Time to progression and overall survival

Full Information

First Posted
March 7, 2007
Last Updated
March 15, 2016
Sponsor
The Methodist Hospital Research Institute
Collaborators
Bayer, Amgen
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1. Study Identification

Unique Protocol Identification Number
NCT00445042
Brief Title
Safety and Toxicity Study of Sorafenib in Patients With Kidney Cancer
Official Title
A Phase II Study of Sorafenib in Patients With Metastatic Renal Cell Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
October 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Methodist Hospital Research Institute
Collaborators
Bayer, Amgen

4. Oversight

Data Monitoring Committee
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Renal Cell
Keywords
Metastatic Renal Cell Carcinoma, Metastatic RCC, Kidney Cancer, M3thodist

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
71 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Intrapatient dose escalation study of sorafenib
Intervention Type
Drug
Intervention Name(s)
Sorafenib
Other Intervention Name(s)
Nexavar
Intervention Description
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.
Primary Outcome Measure Information:
Title
Tumor progression rate by RECIST criteria
Time Frame
restaging every 8 weeks
Secondary Outcome Measure Information:
Title
Overall response rate
Time Frame
restaging every 8 weeks
Title
Time to progression and overall survival
Time Frame
restaging every 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert J Amato, DO
Organizational Affiliation
Baylor College of Medicine - Methodist Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Methodist Hospital - Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Safety and Toxicity Study of Sorafenib in Patients With Kidney Cancer

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