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Epothilone B in Treating Patients With CNS Metastases From Breast Cancer

Primary Purpose

Breast Cancer, Metastatic Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
epothilone B
Sponsored by
David Peereboom, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring recurrent breast cancer, stage IV breast cancer, tumors metastatic to brain, leptomeningeal metastases, male breast cancer

Eligibility Criteria

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

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed carcinoma of the breast
  • CNS metastases (i.e., brain parenchymal lesions and/or leptomeningeal disease), meeting 1 of the following criteria:

    • Recurrent or progressive CNS metastases after whole brain radiotherapy

      • If only evaluable site of CNS progression has been previously treated with stereotactic radiosurgery, radiation necrosis must be excluded by radiographic (e.g., positron emission tomography scan or magnetic resonance spectroscopy) or histologic assessment
    • Newly diagnosed, untreated, asymptomatic brain or leptomeningeal metastases
  • Patient must be neurologically stable, as demonstrated by a stable dose of steroids and anticonvulsants for ≥ 1 week prior to obtaining baseline gadolinium-enhanced MRI of the brain and/or ≥ 1 week prior to beginning study treatment
  • No CNS complications requiring urgent neurosurgical intervention (e.g., resection or shunt placement)
  • Hormone receptor status not specified

PATIENT CHARACTERISTICS:

  • Male or female
  • Menopausal status not specified
  • Karnofsky performance status 60-100%
  • Life expectancy ≥ 3 months
  • Absolute neutrophil count > 1,500/mm^3
  • Hemoglobin > 9.0 g/dL
  • Platelet count > 100,000/mm^3 (red blood cell transfusion and repeat evaluation allowed)
  • Bilirubin < 1.5 times upper limit of normal (ULN)
  • AST and ALT < 2.5 times ULN
  • Alkaline phosphatase < 2.5 times ULN
  • Creatinine < 1.5 times ULN
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 months after completion of study therapy
  • No known hypersensitivity to epothilones
  • No peripheral neuropathy > grade 1
  • No unresolved diarrhea within the past 7 days

    • Grade 0 diarrhea required at study entry
  • No concurrent serious medical illness (e.g., HIV positivity or active hepatitis B or C)
  • No severe cardiac insufficiency (e.g., New York Heart Association class III-IV heart disease) with uncontrolled and/or unstable cardiac or coronary artery disease
  • No active or suspected acute or chronic uncontrolled infection, including abscess or fistulae
  • No other malignancy within the past 3 years except curatively treated nonmelanoma skin cancer, prostate cancer, or carcinoma in situ of the cervix
  • No history of noncompliance to medical regimens or inability or unwillingness to return for all scheduled visits
  • No contraindications to MRI, including any of the following:

    • Pacemaker
    • Ferromagnetic implants
    • Claustrophobia
    • Extreme obesity

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • More than 2 weeks since prior noncytotoxic drugs (e.g., small molecule-targeted drugs) and recovered
  • More than 3 weeks since prior cytotoxic chemotherapy (6 weeks for nitrosoureas or mitomycin C) and recovered
  • More than 3 weeks since prior intracranial surgery and recovered
  • More than 4 weeks since prior radiotherapy and recovered
  • More than 4 weeks since prior major surgery
  • More than 28 days since prior investigational compounds or drugs
  • No prior epothilones
  • No concurrent known diarrheagenic agents
  • No other concurrent anticancer agents, including investigational agents, biological agents, or chemotherapy
  • No other concurrent experimental therapies
  • Concurrent hormone therapy and/or trastuzumab (Herceptin®) allowed
  • No concurrent Coumadin® or other agents containing warfarin

    • Low dose Coumadin® (≤ 1 mg) for prophylactic maintenance of indwelling lines or ports allowed
  • No concurrent radiotherapy for central metastases (e.g., vertebral or mediastinal metastases)

    • Concurrent radiotherapy for local peripheral metastases not being used as marker lesions allowed
  • No concurrent prophylactic hematopoietic growth factors during course 1
  • No concurrent herbal or nontraditional medications

Sites / Locations

  • Massachusetts General Hospital
  • University of Michigan Comprehensive Cancer Center
  • Memorial Sloan-Kettering Cancer Center
  • Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center
  • Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Epothilone B

Arm Description

Outcomes

Primary Outcome Measures

Central Nervous System (CNS) Progression-free Survival(PFS)
The number of patients that are documented to have progression free survival at 3 months after treatment. Progression free is define as <25% increase in tumor area. PFS will be measured from the date of entry into the trial to the date of documented progression of brain metastases or death.

Secondary Outcome Measures

Toxicity as Measured by NCI CTCAE v3.0
Percent of patients that experience the most common grade 3 and above toxicities possibly related to study drug - to be measured using the NCI Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 3.0.
CNS Response Rate, for Measurable Disease Will be Assessed by the Modified McDonald Criteria
Complete Response (CR): the circumstance when the tumor is no longer seen by neuroimaging Partial Response (PR): Decrease of >50% in the product of two diameters Stable Disease (SD): the circumstance when the scan shows no change. Progression (P): a > 25% increase in tumor area (two diameters)
Systemic Disease Response Rate for Measurable Disease Will be Assessed by the Modified McDonald Criteria
Complete Response (CR): the circumstance when the tumor is no longer seen by neuroimaging Partial Response (PR): Decrease of >50% in the product of two diameters Stable Disease (SD): the circumstance when the scan shows no change. Progression (P): a > 25% increase in tumor area (two diameters)
Overall Survival
Median time (months) that patients survived during the duration of the study.

Full Information

First Posted
March 20, 2007
Last Updated
January 28, 2014
Sponsor
David Peereboom, MD
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00450866
Brief Title
Epothilone B in Treating Patients With CNS Metastases From Breast Cancer
Official Title
Phase II Trial of Patupilone in Patients With Brain Metastases From Breast Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
David Peereboom, MD
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy, such as epothilone B, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well epothilone B works in treating patients with CNS metastases from breast cancer.
Detailed Description
OBJECTIVES: Primary Determine the 3-month CNS-progression free survival of patients with CNS metastases secondary to breast cancer treated with epothilone B. Secondary Determine the toxicity of this drug in these patients. Determine the CNS response rate and duration of CNS response in patients treated with this drug. Determine the systemic disease response rate and duration of systemic response in patients treated with this drug. Determine the overall survival of patients treated with this drug. OUTLINE: This is a multicenter, open-label study. Patients receive epothilone B IV over 20 minutes on day 1. Courses repeat every 21 days in the absence of disease progression, satisfactory response, or unacceptable toxicity. After completion of study treatment, patients are followed periodically. PROJECTED ACCRUAL: A total of 55 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Metastatic Cancer
Keywords
recurrent breast cancer, stage IV breast cancer, tumors metastatic to brain, leptomeningeal metastases, male breast cancer

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Epothilone B
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
epothilone B
Other Intervention Name(s)
Patupilone
Intervention Description
Patupilone will be administered as a single intravenous infusion over 20 minutes, once every 3 weeks. Patupilone will be administered at a dose of 10 mg/m2 (q3weeks) with actual body weight.
Primary Outcome Measure Information:
Title
Central Nervous System (CNS) Progression-free Survival(PFS)
Description
The number of patients that are documented to have progression free survival at 3 months after treatment. Progression free is define as <25% increase in tumor area. PFS will be measured from the date of entry into the trial to the date of documented progression of brain metastases or death.
Time Frame
3 months after treatment
Secondary Outcome Measure Information:
Title
Toxicity as Measured by NCI CTCAE v3.0
Description
Percent of patients that experience the most common grade 3 and above toxicities possibly related to study drug - to be measured using the NCI Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 3.0.
Time Frame
3 months after treatment
Title
CNS Response Rate, for Measurable Disease Will be Assessed by the Modified McDonald Criteria
Description
Complete Response (CR): the circumstance when the tumor is no longer seen by neuroimaging Partial Response (PR): Decrease of >50% in the product of two diameters Stable Disease (SD): the circumstance when the scan shows no change. Progression (P): a > 25% increase in tumor area (two diameters)
Time Frame
3 months after treatment
Title
Systemic Disease Response Rate for Measurable Disease Will be Assessed by the Modified McDonald Criteria
Description
Complete Response (CR): the circumstance when the tumor is no longer seen by neuroimaging Partial Response (PR): Decrease of >50% in the product of two diameters Stable Disease (SD): the circumstance when the scan shows no change. Progression (P): a > 25% increase in tumor area (two diameters)
Time Frame
3 months after treatment
Title
Overall Survival
Description
Median time (months) that patients survived during the duration of the study.
Time Frame
48 months from start of study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed carcinoma of the breast CNS metastases (i.e., brain parenchymal lesions and/or leptomeningeal disease), meeting 1 of the following criteria: Recurrent or progressive CNS metastases after whole brain radiotherapy If only evaluable site of CNS progression has been previously treated with stereotactic radiosurgery, radiation necrosis must be excluded by radiographic (e.g., positron emission tomography scan or magnetic resonance spectroscopy) or histologic assessment Newly diagnosed, untreated, asymptomatic brain or leptomeningeal metastases Patient must be neurologically stable, as demonstrated by a stable dose of steroids and anticonvulsants for ≥ 1 week prior to obtaining baseline gadolinium-enhanced MRI of the brain and/or ≥ 1 week prior to beginning study treatment No CNS complications requiring urgent neurosurgical intervention (e.g., resection or shunt placement) Hormone receptor status not specified PATIENT CHARACTERISTICS: Male or female Menopausal status not specified Karnofsky performance status 60-100% Life expectancy ≥ 3 months Absolute neutrophil count > 1,500/mm^3 Hemoglobin > 9.0 g/dL Platelet count > 100,000/mm^3 (red blood cell transfusion and repeat evaluation allowed) Bilirubin < 1.5 times upper limit of normal (ULN) AST and ALT < 2.5 times ULN Alkaline phosphatase < 2.5 times ULN Creatinine < 1.5 times ULN Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception during and for 3 months after completion of study therapy No known hypersensitivity to epothilones No peripheral neuropathy > grade 1 No unresolved diarrhea within the past 7 days Grade 0 diarrhea required at study entry No concurrent serious medical illness (e.g., HIV positivity or active hepatitis B or C) No severe cardiac insufficiency (e.g., New York Heart Association class III-IV heart disease) with uncontrolled and/or unstable cardiac or coronary artery disease No active or suspected acute or chronic uncontrolled infection, including abscess or fistulae No other malignancy within the past 3 years except curatively treated nonmelanoma skin cancer, prostate cancer, or carcinoma in situ of the cervix No history of noncompliance to medical regimens or inability or unwillingness to return for all scheduled visits No contraindications to MRI, including any of the following: Pacemaker Ferromagnetic implants Claustrophobia Extreme obesity PRIOR CONCURRENT THERAPY: See Disease Characteristics More than 2 weeks since prior noncytotoxic drugs (e.g., small molecule-targeted drugs) and recovered More than 3 weeks since prior cytotoxic chemotherapy (6 weeks for nitrosoureas or mitomycin C) and recovered More than 3 weeks since prior intracranial surgery and recovered More than 4 weeks since prior radiotherapy and recovered More than 4 weeks since prior major surgery More than 28 days since prior investigational compounds or drugs No prior epothilones No concurrent known diarrheagenic agents No other concurrent anticancer agents, including investigational agents, biological agents, or chemotherapy No other concurrent experimental therapies Concurrent hormone therapy and/or trastuzumab (Herceptin®) allowed No concurrent Coumadin® or other agents containing warfarin Low dose Coumadin® (≤ 1 mg) for prophylactic maintenance of indwelling lines or ports allowed No concurrent radiotherapy for central metastases (e.g., vertebral or mediastinal metastases) Concurrent radiotherapy for local peripheral metastases not being used as marker lesions allowed No concurrent prophylactic hematopoietic growth factors during course 1 No concurrent herbal or nontraditional medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David M. Peereboom, MD
Organizational Affiliation
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joseph Baar, MD
Organizational Affiliation
Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
University of Michigan Comprehensive Cancer Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Memorial Sloan-Kettering Cancer Center
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Facility Name
Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106-5065
Country
United States
Facility Name
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Epothilone B in Treating Patients With CNS Metastases From Breast Cancer

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