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Safety and Efficacy Study of Concomitant Radiotherapy and Zoledronic Acid for Bone Metastases Palliation

Primary Purpose

Bone Metastases, Breast Cancer, Lung Cancer

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
zoledronic acid
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Metastases focused on measuring bone metastases, breast cancer, lung cancer, prostate cancer, zoledronic acid, radiation therapy

Eligibility Criteria

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

Inclusion Criteria: >18 years of age biopsy proven breast, lung, and/or prostate cancer boney metastases with an indication for radiation, either diagnosed radiologically or biopsy proven Karnofsky Performance Status >60 Life expectancy of at least 6 months Serum creatinine level ≤ 2.0 mg/dL and calculated creatinine clearance of > 60 mL/min Leukocyte count ≥ 3500/mm3 Hemoglobulin > 11 g/dl Platelets > 100,000 / mm3 Total bilirubin < 2.5 mg/dl Exclusion Criteria: pregnant and lactating women (breast and lung cancer) hormonotherapy started less than 3 months prior to randomization (prostate cancer) history of allergic reactions to bisphosphonates receiving concomitant nephrotoxic chemotherapy participation in another clinical trial with an investigational drug or completed an investigational drug trial within the past 30 days liver function tests > 1.5 times normal values IV calcitonin administration less than 30 days prior to randomization laboratory evidence of renal disease previous RT to the region of bone metastasis which will be treated in this study currently receiving oral or IV bisphosphonate therapy presence of ascites clinically significant electrocardiographic changes hypercalcemia, pathologic fracture, or epidural spinal cord compression other organ metastasis known hypersensitivity to Zometa® (zoledronic acid) or other bisphosphonates current active dental problems including infection of the teeth or jawbone (maxilla or mandibular); dental or fixture trauma, or a current or prior diagnosis of osteonecrosis of the jaw (ONJ), of exposed bone in the mouth, or of slow healing after dental procedures. recent (within 6 weeks) or planned dental or jaw surgery (e.g.. extraction, implants)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    1

    Arm Description

    zoledronic acid plus radiation therapy

    Outcomes

    Primary Outcome Measures

    PET-CT

    Secondary Outcome Measures

    X-ray, baseline
    physical exam
    physical exam

    Full Information

    First Posted
    December 6, 2005
    Last Updated
    December 20, 2010
    Sponsor
    The Cleveland Clinic
    Collaborators
    Novartis
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00264420
    Brief Title
    Safety and Efficacy Study of Concomitant Radiotherapy and Zoledronic Acid for Bone Metastases Palliation
    Official Title
    A Phase I Pilot Trial to Study the Safety and Efficacy of Concomitant Radiotherapy and Zoledronic Acid for the Palliation of Bone Metastases From Breast Cancer, Prostate Cancer and Lung Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2010
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2005 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    March 2007 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    The Cleveland Clinic
    Collaborators
    Novartis

    4. Oversight

    5. Study Description

    Brief Summary
    Zoledronic acid (Zometa) belongs to a class of drugs called bisphosphonates. Bisphosphonates are used in bone metastases to keep the cancerous lesion under control in the bone and to help prevent calcium level elevations in the blood. Cancer cell-culture studies at the Cleveland Clinic showed that zoledronic acid and radiation together have more cell killing effect than either one used alone. The purpose of this study is to monitor the healing of bone lesions when using zoledronic acid together with radiation treatment.
    Detailed Description
    Bone metastases are frequently one of the first signs of disseminated disease in cancer patients. Skeletal complications due to metastatic disease include (severe) bone pain, impaired mobility, spinal cord compression, pathological fractures, and hypercalcemia. Radiotherapy and surgery are the options for the specific local treatment of bone metastases. Chemotherapy, hormonotherapy and bisphosphonates are systemic weapons used in the treatment of bone metastases with or without hypercalcemia. Cancers with propensity to metastasize to bones such as breast, prostate, lung and myeloma may possess the capacity to interact with osteoclasts. Osteoclasts are specialized bone cells, which erode mineralized bone by secreting acids and lysosomal enzymes. In normal bone remodeling, osteoclastic bone resorption is coupled to and is in equilibrium with osteoblastic bone formation. The lytic bone destruction associated with malignant bone metastases develops because tumor cells synthesize and release soluble factors that stimulate osteoclasts to resorb bone. The malignant activation of osteoclasts results in a disruption of normal bone remodeling wherein the equilibrium between bone resorption and bone formation is shifted toward increased bone resorption. This relative increase in osteoclastic bone resorption results in a net loss of bone. Zoledronic acid (Zometa®, CGP42446) is a member of a class of compounds known as bisphosphonates. Bisphosphonates are effective inhibitors of osteoclastic bone resorption. They have therapeutic efficacy in the treatments of hypercalcemia of malignancy, lytic bone disease associated with multiple myeloma, and mixed lytic and blastic bone metastases associated with breast cancer, prostate cancer and lung cancer. In the clinical setting, zoledronic acid is the most potent bisphosphonate. Conventionally, external beam radiotherapy (RT) is a primary treatment method for the palliation of bone metastases. The aim of RT in bone metastases treatment is to eradicate malignant cells without damaging surrounding normal cells. RT is typically given to the lesion area, in order to spare as much bone marrow as possible. RT is indicated in solitary, lytic and painful bone lesions of multiple myeloma as well as bone metastases from solid tumors such as breast, prostate and lung cancer to prevent the fracture risk or to relieve the pain. The goal of this study will be to evaluate the safety and efficacy of concomitant standard RT and standard zoledronic acid on the bone metastases of breast, prostate or lung cancer patients. We chose zoledronic acid to use in this study, as it is the most effective FDA approved aminobisphosphonate.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bone Metastases, Breast Cancer, Lung Cancer, Prostate Cancer
    Keywords
    bone metastases, breast cancer, lung cancer, prostate cancer, zoledronic acid, radiation therapy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    4 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Description
    zoledronic acid plus radiation therapy
    Intervention Type
    Drug
    Intervention Name(s)
    zoledronic acid
    Intervention Description
    At baseline 4 mg IV zoledronic acid over 15 min. every 4 weeks for 6 months plus radiation therapy 30 Gy in 10 fractions (5 times per week for first two weeks)
    Primary Outcome Measure Information:
    Title
    PET-CT
    Time Frame
    baseline and 6 months
    Secondary Outcome Measure Information:
    Title
    X-ray, baseline
    Time Frame
    3 months, 6 months
    Title
    physical exam
    Time Frame
    Radiaton Oncology - visits 1, 14, 17
    Title
    physical exam
    Time Frame
    Medical Oncology - visits 1, 13, 17

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: >18 years of age biopsy proven breast, lung, and/or prostate cancer boney metastases with an indication for radiation, either diagnosed radiologically or biopsy proven Karnofsky Performance Status >60 Life expectancy of at least 6 months Serum creatinine level ≤ 2.0 mg/dL and calculated creatinine clearance of > 60 mL/min Leukocyte count ≥ 3500/mm3 Hemoglobulin > 11 g/dl Platelets > 100,000 / mm3 Total bilirubin < 2.5 mg/dl Exclusion Criteria: pregnant and lactating women (breast and lung cancer) hormonotherapy started less than 3 months prior to randomization (prostate cancer) history of allergic reactions to bisphosphonates receiving concomitant nephrotoxic chemotherapy participation in another clinical trial with an investigational drug or completed an investigational drug trial within the past 30 days liver function tests > 1.5 times normal values IV calcitonin administration less than 30 days prior to randomization laboratory evidence of renal disease previous RT to the region of bone metastasis which will be treated in this study currently receiving oral or IV bisphosphonate therapy presence of ascites clinically significant electrocardiographic changes hypercalcemia, pathologic fracture, or epidural spinal cord compression other organ metastasis known hypersensitivity to Zometa® (zoledronic acid) or other bisphosphonates current active dental problems including infection of the teeth or jawbone (maxilla or mandibular); dental or fixture trauma, or a current or prior diagnosis of osteonecrosis of the jaw (ONJ), of exposed bone in the mouth, or of slow healing after dental procedures. recent (within 6 weeks) or planned dental or jaw surgery (e.g.. extraction, implants)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Roger Macklis, MD
    Organizational Affiliation
    The Cleveland Clinic
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Safety and Efficacy Study of Concomitant Radiotherapy and Zoledronic Acid for Bone Metastases Palliation

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