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Exploratory Study of Radium-223 and VEGF-Targeted Therapy in Patients With Metastatic Renal Cell Carcinoma and Bone Mets

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02406521
Recruitment Status : Completed
First Posted : April 2, 2015
Last Update Posted : March 4, 2020
Sponsor:
Collaborator:
Bayer
Information provided by (Responsible Party):
Mark Pomerantz, MD, Dana-Farber Cancer Institute

Brief Summary:

This research study is comparing different drug combinations as a possible treatment for metastatic renal cell carcinoma (mRCC) and bone metastases.

The names of the study interventions involved in this study are:

  • Combination of Radium-223 and Sorafenib
  • Combination of Radium-223 and Pazopanib

Condition or disease Intervention/treatment Phase
Metastatic Renal Cell Carcinoma Drug: Pazopanib Drug: Sorafenib Drug: Radium-223 Phase 1

Detailed Description:

The FDA (the U.S. Food and Drug Administration) has not approved the combination of sorafenib and radium-223 or the combination of pazopanib and radium-223 as a treatment for any disease. Sorafenib and pazopanib are both approved as single agents for the treatment of metastatic renal cell carcinoma. Additionally, radium-223 is FDA approved for the treatment of advanced prostate cancer and has shown to have effects on prostate cancer.

Currently, there are limited options for patients with metastatic renal cell cancer who also have bone metastases. Bone metastases are related to a higher incidence of skeletal complications, including skeletal pain, fractures, spinal cord compression, and an increase in the amount of calcium in blood. Such skeletal complications could result in radiation or surgery to the bone. Since radium-223 is shown to be effective for patients with metastatic prostate cancer who also have bone metastases, researchers want to explore radium-223 with VEGF-targeting therapies to understand how the drug combinations affect safety, quality of life, incidence of skeletal complications, and the progression of cancer.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 30 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase I Study of Radium-223 and Vascular Endothelial Growth Factor-Targeted Therapy in Patients With Metastatic Renal Cell Carcinoma and Bone Metastases
Study Start Date : April 2015
Actual Primary Completion Date : December 2017
Actual Study Completion Date : December 31, 2019


Arm Intervention/treatment
Experimental: Arm A: Pazopanib with Radium-223

No prior targeted therapy

  • Pazopanib oral, daily and at predetermined dosage per cycle
  • Radium-223 predetermined dosage via IV, per cycle
Drug: Pazopanib
Other Name: Votrient

Drug: Radium-223
Other Names:
  • Radium 223 Dichloride
  • Xofigo®

Experimental: Arm B: Sorafenib with Radium-223

At least one line of prior targeted therapy:

  • Sorafenib at predetermined dosage, mouth twice daily
  • Radium-223 predetermined dosage via IV, per cycle
Drug: Sorafenib
Other Name: Nexavar®

Drug: Radium-223
Other Names:
  • Radium 223 Dichloride
  • Xofigo®




Primary Outcome Measures :
  1. Biomarkers of osteoblast and osteoclast activity [ Time Frame: Baseline, 2 Years ]

Secondary Outcome Measures :
  1. Symptomatic skeletal events (SSEs) [ Time Frame: Baseline, 2 Years ]
  2. Time to SSE [ Time Frame: Baseline, 2 Years ]
  3. Quality of life using the FKSI-19 [ Time Frame: Baseline, 2 Years ]
  4. Pain using the Brief Pain Inventory (Short Form) [ Time Frame: Baseline, 2 Years ]
  5. Analgesic use [ Time Frame: Baseline, 2 Years ]
  6. Overall response rate by RECIST version 1.1 [ Time Frame: 2 Years ]
  7. Duration of response by RECIST version 1.1 [ Time Frame: 2 Years ]
  8. Overall survival [ Time Frame: 2 Years ]
  9. Progression-free survival [ Time Frame: 2 Years ]
  10. Response as determined by PERCIST Criteria [ Time Frame: 2 Years ]
  11. Response as determined by MDA Bone Response Criteria [ Time Frame: 2 Years ]
  12. Response within bone biomarker subgroups [ Time Frame: 2 Years ]
  13. Time to first SSE within bone biomarker subgroups [ Time Frame: 2 Years ]
  14. PFS within bone biomarker subgroups [ Time Frame: 2 Years ]
  15. OS within bone biomarker subgroups [ Time Frame: 2 Years ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age ≥ 18 years.
  • Documented pathologic diagnosis of RCC. All subtypes eligible including but not limited to clear cell, papillary, chromophobe, collecting duct carcinoma, medullary carcinoma, and unclassified categories. Sarcomatoid and rhabdoid differentiation are allowed.
  • Presence of at least one metastatic bone lesion(s). Patients with non-measurable bone-only disease are allowed.
  • ECOG performance status of 0-2 (Appendix A).
  • Must have adequate organ and bone marrow function.

    • Absolute neutrophil count (ANC) ≥ 1500/mm3 (without use of G-CSF 4 weeks prior to enrollment).
    • Platelet count ≥100,000/mm3.
    • Hemoglobin ≥ 9 g/dL (transfusions allowed).
    • ALT and AST ≤ 3.0 x the upper limit of normal (ULN).
    • Total bilirubin ≤ 1.5 x ULN. For participants with Gilbert's disease ≤ 3.0 mg/dL.
    • Calculated creatinine clearance ≥ 30 mL/min using the Cockroft-gault equation.
    • Urine protein-to-creatinine (UPC) ratio ≤ 2 mg/mg creatinine or 24-hour urine protein < 2 g.
  • Recovery to baseline or ≤ grade 1 CTCAE version 4.0 from toxicities related to any prior treatment, unless adverse events are clinically non-significant and/or stable on supportive therapy.
  • Capable of understanding and complying with the protocol requirements and has signed the informed consent document.
  • Sexually active participants and their partners must agree to use medically accepted methods of contraception.
  • Female participants of childbearing potential must not be pregnant at screening.
  • Sexually active participants (men and women) must agree to use highly effective contraceptive methods during the course of the study and for 6 months after completing treatment with radium-223.

Exclusion Criteria:

  • For patients in the sorafenib cohort, no prior therapy with sorafenib is allowed and at least 1 line of prior therapy is required including prior: VEGF-targeting therapy (such as sunitinib, axitinib, tivozanib, bevacizumab), mTOR-targeting therapy (such as everolimus, temsirolimus), immunotherapy (such as anti-PD-1 or anti-PD-L1), cytokine therapy (such as interleukin-2, IFN-a) or cytotoxic systemic chemotherapy allowed.
  • For patients in the pazopanib cohort, no prior systemic therapy for mRCC is allowed, with the exception of prior cytokine therapy (such as interleukin-2, IFN-a), immunotherapy (such as anti-PD-1 or anti-PD-L1), or supportive therapies (such as zoledronic acid, denosumab).
  • Receipt of any type of small molecular kinase inhibitor (including investigational kinase inhibitors) within 2 weeks of enrollment or receipt of any anti-cancer therapy (including investigational therapy, monoclonal antibodies, cytokine therapy) within 3 weeks of enrollment.
  • Radiation therapy for bone metastases within 2 weeks, other external radiation therapy within 4 weeks of enrollment.
  • Received prior hemibody external radiotherapy.
  • Prior therapy with radium-223 or systemic radiotherapy (such as samarium, strontium).
  • Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy, radiosurgery, or surgery and stable for at least 4 weeks of enrollment as documented by MRI or CT imaging. Treated brain metastases are defined as having no ongoing requirement for steroids (must be off steroids for at least 4 weeks) and no evidence of progression or hemorrhage after treatment for at least 4 weeks of enrollment as documented by MRI or CT imaging.
  • Imminent or established spinal cord compression based on clinical and/or imaging. In patients with untreated imminent or established spinal cord compression, treatment with standard of care as clinically indicated should be completed at least 4 weeks before enrollment.
  • The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:

    • Cardiovascular disorders:

      • Symptomatic congestive heart failure, unstable angina pectoris, serious cardiac arrhythmias.
      • uncontrolled hypertension defined as sustained BP > 150 mm Hg systolic or > 100 mm Hg diastolic despite optimal antihypertensive treatment.
      • Stroke (including transient ischemic attack), myocardial infarction, or other ischemic event within 12 weeks of enrollment.
      • Thromboembolic event (such as deep venous thrombosis, pulmonary embolism) within 4 weeks of enrollment.
    • GI disorders including those associated with a high risk of perforation or fistula formation:

      • Tumors invading the GI-tract, active peptic ulcer disease, inflammatory bowel disease, diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis, acute pancreatitis or acute obstruction of the pancreatic or biliary duct, or gastric outlet obstruction.
      • Abdominal fistula, gastrointestinal perforation, bowel obstruction, or intraabdominal abscess within 12 weeks before enrollment. Note: Complete healing of an intra-abdominal abscess must be confirmed before enrollment.
    • Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (such as pulmonary hemorrhage) within 4 weeks of enrollment.
    • Other clinically significant disorders such as:

      • Active infection requiring systemic treatment, infection with human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness, or chronic hepatitis B or C infection.
      • Serious non-healing wound or ulcer.
      • Malabsorption syndrome.
      • Symptomatic hypothyroidism.
      • Moderate to severe hepatic impairment (Child-Pugh B or C).
      • Requirement for hemodialysis or peritoneal dialysis.
      • History of solid organ transplantation.
    • Major surgery (such as GI surgery) within 6 weeks of enrollment. However, subjects who have had a nephrectomy may be enrolled 4 weeks after surgery, providing there are no wound-healing complications. Subjects with clinically relevant ongoing complications from prior surgery are not eligible. The following are not considered to be major procedures: Thoracentesis, paracentesis, port placement, laparoscopy, thoracoscopy, bronchoscopy, endoscopic ultrasonographic procedures, mediastinoscopy, skin biopsies, incisional biopsies, imaging-guided biopsy for diagnostic purposes, and routine dental procedures.
    • QTcF > 470 msec within 4 weeks of enrollment. If the initial QTcF is found to be > 470 ms, two additional EKGs separated by at least 3 minutes should be performed. If the average of these three consecutive results for QTcF is ≤ 470 ms, the subject meets eligibility in this regard.
    • Pregnant or lactating females.
    • Inability to swallow tablets or capsules.
    • Previously identified allergy or hypersensitivity to components of the study treatment formulations.
    • Diagnosis of another malignancy within 2 years of enrollment, except for superficial skin cancers, or localized, low grade tumors deemed cured and not treated with systemic therapy by the principal investigator

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02406521


Locations
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United States, Massachusetts
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Dana Farber Cancer Institute
Boston, Massachusetts, United States, 02115
Sponsors and Collaborators
Dana-Farber Cancer Institute
Bayer
Investigators
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Principal Investigator: Mark Pomerantz, MD Dana-Farber Cancer Institute
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Responsible Party: Mark Pomerantz, MD, Assistant Professor of Medicine, Harvard Medical School, Dana-Farber Cancer Institute
ClinicalTrials.gov Identifier: NCT02406521    
Other Study ID Numbers: 14-523
First Posted: April 2, 2015    Key Record Dates
Last Update Posted: March 4, 2020
Last Verified: March 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by Mark Pomerantz, MD, Dana-Farber Cancer Institute:
Metastatic renal cell carcinoma
mRCC
Additional relevant MeSH terms:
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Carcinoma
Carcinoma, Renal Cell
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Adenocarcinoma
Kidney Neoplasms
Urologic Neoplasms
Urogenital Neoplasms
Neoplasms by Site
Kidney Diseases
Urologic Diseases
Sorafenib
Radium Ra 223 dichloride
Antineoplastic Agents
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action