Pazopanib in Previously Treated Patients With Metastatic Renal Cell Carcinoma

Phase 2

Completed

• Conditions: Renal Cell Carcinoma
• Interventions: Drug: Pazopanib

• Registration Number: NCT00731211
• Lead Sponsor: SCRI Development Innovations, LLC

Brief Summary

This is a Phase II, non-randomized, open-label, single-arm study in patients with metastatic renal cell carcinoma who have received one prior targeted therapy with either sunitinib or bevacizumab. The planned enrollment for this study is 60 patients.

Detailed Description

All eligible patients will receive 800 mg of pazopanib orally each day continuously. Patients will be re-evaluated for treatment response after 8 weeks of daily oral pazopanib therapy. Response to therapy will be assigned using RECIST criteria (Section 6.0) Patients who have objective response or stable disease will continue treatment with evaluations every 8 weeks, until the time of tumor progression or intolerable treatment-related side effects.

Study Timeline

• Study First Submitted: 2008-08-05
• Study First Submitted QC: 2008-08-07
• Study First Posted: 2008-08-08
• Study Start: 2008-09
• Primary Completion: 2011-05
• Study Completion: 2012-09
• Results First Submitted: 2014-12-16
• Status Verified: 2015-05
• Results First Submitted QC: 2015-05-18
• Last Update Submitted: 2015-05-18
• Results First Posted: 2015-05-20
• Last Update Posted: 2015-05-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 57

Inclusion Criteria

1. All patients must have histologically documented metastatic or unresectable locally recurrent clear cell renal carcinoma. In patients with mixed histologies, any percentage of clear cell histology is acceptable.
2. Patients must have had only one previous targeted agent therapy with either sunitinib or bevacizumab. Patients must have progressed either during or within 3 months of discontinuing treatment with one of these agents. Patients who stopped either sunitinib or bevacizumab because of unacceptable toxicity are also eligible.
3. Patients may have received one previous regimen containing traditional immunotherapy (interferon, interleukin-2), chemotherapy, or combination chemoimmunotherapy for metastatic disease.
4. Previous nephrectomy is required unless clinically contraindicated (e.g. extensive liver or bone metastases; primary tumor <5cm).
5. An ECOG performance status of 0 or 1.
6. At least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as >20 mm with conventional techniques, or as >10 mm with spiral computerized tomography (CT) scan according to the Response Evaluation Criteria in Solid Tumors (RECIST).
7. Absolute neutrophil count (ANC) >1500; platelets >75,000 (within 7 days prior to study treatment).
8. Adequate liver function as measured by serum bilirubin <1.5 mg/dL and AST/ALT <2.5 times upper limit of normal (ULN) (or <5 x ULN in patients with documented liver metastases).
9. Serum creatinine <2.0 mg/dL.
10. Patients must be able to understand the nature of this study and give written informed consent.

Read More

Exclusion Criteria

1. Previous treatment with more than one targeted agent, or more than one previous traditional regimen (e.g., chemotherapy, immunotherapy, chemoimmunotherapy).

2. Previous treatment with sorafenib, temsirolimus, everolimus or other investigational targeted agents.

3. Inability to swallow and retain oral medication.

4. History of other malignancy. Patients who have been disease-free for 5 years, or patients with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible.

5. Concurrent disease or condition that would make the patient inappropriate for study participation including: (1) any unresolved or unstable serious toxicity from prior administration of another drug, or (2) any serious medical disorder that would interfere with the patient's safety, obtaining informed consent, or compliance with the study.

6. History or clinical evidence of central nervous system (CNS) metastases or leptomeningeal carcinomatosis, except for individuals who have previously treated parenchymal CNS metastases, are asymptomatic, and have had no requirement for steroids or anticonvulsants for >2 months prior to study enrollment. Routine screening with CNS imaging studies (computed tomography [CT] or magnetic resonance imaging [MRI]) is required only if clinically indicated, or if the patient has a history of CNS metastases.

7. Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel.

8. Active peptic ulcer disease, inflammatory bowel disease, or other gastrointestinal condition increasing the risk of perforation.

9. History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 4 weeks prior to beginning therapy.

10. Presence of uncontrolled infection.

11. Concurrent cancer therapy (e.g., chemotherapy, radiation therapy, surgery, immunotherapy, biologic therapy, hormonal therapy, or tumor embolization).

12. Concurrent treatment with an investigational agent or participation in another clinical trial.

13. Use of an investigational anti-cancer drug within 30 days or 5 half-lives, whichever is longer, preceding the first dose of pazopanib.

14. Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to pazopanib.

15. Has taken or is taking prohibited medications.

16. Corrected QT interval (QTc) prolongation defined as QTc interval >470 msec.

17. History of any one of the following cardiac conditions within the past 6 months:

    • Cardiac angioplasty or stenting
    • Myocardial infarction
    • Unstable angina
    • History of cerebrovascular accident within the past 6 months
    • Poorly controlled hypertension (systolic blood pressure [SBP] of >140 mmHg, or diastolic blood pressure [DBP] of >90 mmHg).

    Note: Initiation or adjustment of antihypertensive medication(s) is permitted prior to study entry. The blood pressure (BP) must be re- assessed on two occasions that are separated by a minimum of 24 hours. The mean SBP-DBP values from both BP assessments must be <140/90 mmHg in order for a patient to be eligible for the study.

18. Presence of any non-healing wound, fracture, or ulcer, or the presence of symptomatic peripheral vascular disease.

19. Evidence of bleeding diathesis or coagulopathy.

20. Major surgical procedure, open biopsy, or significant traumatic injury within 4 weeks prior to beginning therapy, or anticipation of the need for a major surgical procedure during the course of the study. Minor surgical procedures such as fine needle aspiration or core biopsy within 1 week prior to beginning therapy are also excluded.

21. Pregnant or lactating female. All patients of childbearing potential must agree to use adequate contraception for 2 weeks prior to beginning pazopanib, during the entire study, and for 60 days after pazopanib is discontinued.

22. Class III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.

23. History of untreated deep venous thrombosis (DVT) within the past 6 months.

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Pazopanib	Pazopanib	800 mg of pazopanib orally each day continuously

Primary Outcome Measures

Name	Time	Method
Overall Response Rate	18 months	Proportion of patients with complete and partial response (CR and PR). CR defined as disappearance of target lesions; PR defined as at least a 30% decrease in the sum of the longest diamater of target lesions.

Secondary Outcome Measures

Name	Time	Method
Progression-free Survival	every 8 weeks until progressive disease, expected average of 18 months	Progression-free survival is measured from Day 1 of study drug administration to disease progression as defined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1, or death on study. Progression is defined in RECIST v1.1 as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions

Trial Locations

Locations (17)

Watson Clinic Center for Cancer Care and Research; 🇺🇸 Lakeland, Florida, United States

Northeast Georgia Medical Center; 🇺🇸 Gainesville, Georgia, United States

Baptist Hospital East; 🇺🇸 Louisville, Kentucky, United States

Grand Rapids Clinical Oncology Program; 🇺🇸 Grand Rapids, Michigan, United States

St. Louis Cancer Care; 🇺🇸 Chesterfield, Missouri, United States

San Francisco Oncology Associates; 🇺🇸 San Francisco, California, United States

Medical Oncology Associates of Augusta; 🇺🇸 Augusta, Georgia, United States

Gulfcoast Oncology Associates; 🇺🇸 St. Petersburg, Florida, United States

Florida Cancer Specialists; 🇺🇸 Fort Myers, Florida, United States

Virginia Cancer Institute; 🇺🇸 Richmond, Virginia, United States

Florida Hospital Cancer Institute; 🇺🇸 Orlando, Florida, United States

Oncology Hematology Care; 🇺🇸 Cincinnati, Ohio, United States

University of Nebraska Medical Center; 🇺🇸 Omaha, Nebraska, United States

South Carolina Oncology Associates, PA; 🇺🇸 Columbia, South Carolina, United States

Chattanooga Oncology Hematology Associates; 🇺🇸 Chattanooga, Tennessee, United States

Tennessee Oncology, PLLC; 🇺🇸 Nashville, Tennessee, United States

Central Maine Medical Center; 🇺🇸 Lewiston, Maine, United States