Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study
Primary Purpose
Tumors Metastatic to Brain
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
radiosurgery
therapeutic conventional surgery
quality-of-life assessment
Sponsored by
About this trial
This is an interventional treatment trial for Tumors Metastatic to Brain
Eligibility Criteria
Inclusion Criteria:
- Have a prior histologic diagnosis of cancer other than small cell lung cancer, lymphoma, and germ cell histologies
- Magnetic resonance imaging (MRI) evidence of 1-4 brain metastases, with at least one lesion > 20 mm and ≤ 50 mm in maximal diameter and determined to be appropriate for SRS and gross total resection; all other brain metastases are appropriate for SRS
- Patient can have prior SRS to lesions other than the one planned for neoadjuvant SRS and resection
- Patient must have a Karnofsky performance score of ≥ 70
Exclusion Criteria:
- Patient deemed medically unfit to undergo surgical resection of brain metastasis
- Prior whole brain radiotherapy
- Patient with contraindication for imaging with MRI
- Inability to participate in study activities due to physical or mental limitations
- Inability or unwillingness to return for all the required follow-up visits
- At the time of planning, unable to deliver 10 Gray (Gy) or less to optic nerve/chiasm
- Tumor located in the brainstem
- Imaging or cytologic evidence of leptomeningeal disease
Sites / Locations
- University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
- Cleveland Clinic, Case Comprehensive Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Treatment (radiosurgery, surgery)
Arm Description
Patients undergo radiosurgery on day 0. Within 2 weeks, patients undergo surgical resection.
Outcomes
Primary Outcome Measures
Maximum tolerated dose (MTD)
MTD of radiosurgery determined by dose-limiting toxicities graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0 (Phase I)
Proportion of participants without local failure (Phase II)
Local control of brain metastases, as measured by proportion of participants without local failure (Local failure is tumor progression of the metastasis treated on the study)
(Phase II)
The Kaplan-Meier method will be used.
Secondary Outcome Measures
Proportion of participants with distant brain failure
Rate of distant brain failure, defined as progression of brain metastases outside of the brain metastasis treated on study. The Kaplan-Meier method will be used.
Rate of radiation necrosis/steroid dependency
Rate of radiation necrosis/steroid dependency
Rate of salvage treatment
Number of patients that have any salvage treatment, including surgery, stereotactic radiosurgery (SRS), or whole brain radiation therapy (WBRT)
Full Information
NCT ID
NCT01891318
First Posted
June 26, 2013
Last Updated
August 14, 2023
Sponsor
Case Comprehensive Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT01891318
Brief Title
Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study
Official Title
Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 3, 2013 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Case Comprehensive Cancer Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This Phase I/II trial studies the ability to stop brain metastases from coming back after treatment with radiosurgery followed by surgical resection. It will also evaluate the side effects of these combined treatments and help determine the best radiosurgery dose. Radiosurgery focuses the x-rays directly to the tumor and cause less damage to the normal tissue in the brain.
Detailed Description
PRIMARY OBJECTIVES:
I. To determine the safety (risk of acute and long-term toxicities) of neoadjuvant radiosurgery at escalating doses followed by surgical resection of brain metastases. (Phase I)
II. To determine the local control of brain metastases treated with neoadjuvant radiosurgery followed by surgical resection. (Phase II)
SECONDARY OBJECTIVES:
I. To determine the rate of distant brain failure when brain metastases are managed with neoadjuvant radiosurgery followed by surgical resection.
II. To estimate the rate of salvage surgery, whole brain radiation therapy (WBRT), or stereotactic radiosurgery (SRS) for participants treated with neoadjuvant radiosurgery followed by surgical resection.
III. To determine the rate of radiation necrosis/steroid dependency. IV. To determine the radiobiologic impact of neoadjuvant radiosurgery for resected brain metastases.
OUTLINE: This is a phase I, dose-escalation study of radiosurgery followed by a phase II study.
The following outcomes were removed from the protocol in an amendment:
Changes in neurocognitive function as measured by the Hopkins Verbal Learning Test (HVLT), Controlled Oral Word Association (COWA) & Trailmaking Test B, and Trailmaking Test A
QOL measured by FACT-BR and EORTC-QLQ30
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tumors Metastatic to Brain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Treatment (radiosurgery, surgery)
Arm Type
Experimental
Arm Description
Patients undergo radiosurgery on day 0. Within 2 weeks, patients undergo surgical resection.
Intervention Type
Radiation
Intervention Name(s)
radiosurgery
Other Intervention Name(s)
radiation surgery
Intervention Description
Undergo radiosurgery
Intervention Type
Procedure
Intervention Name(s)
therapeutic conventional surgery
Intervention Description
Undergo surgical resection
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Other Intervention Name(s)
quality of life assessment
Intervention Description
Ancillary studies
Primary Outcome Measure Information:
Title
Maximum tolerated dose (MTD)
Description
MTD of radiosurgery determined by dose-limiting toxicities graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.0 (Phase I)
Time Frame
Day 0
Title
Proportion of participants without local failure (Phase II)
Description
Local control of brain metastases, as measured by proportion of participants without local failure (Local failure is tumor progression of the metastasis treated on the study)
(Phase II)
The Kaplan-Meier method will be used.
Time Frame
Up to 3 years
Secondary Outcome Measure Information:
Title
Proportion of participants with distant brain failure
Description
Rate of distant brain failure, defined as progression of brain metastases outside of the brain metastasis treated on study. The Kaplan-Meier method will be used.
Time Frame
Up to 3 years
Title
Rate of radiation necrosis/steroid dependency
Description
Rate of radiation necrosis/steroid dependency
Time Frame
Up to 3 years
Title
Rate of salvage treatment
Description
Number of patients that have any salvage treatment, including surgery, stereotactic radiosurgery (SRS), or whole brain radiation therapy (WBRT)
Time Frame
Up to 3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Have a prior histologic diagnosis of cancer other than small cell lung cancer, lymphoma, and germ cell histologies
Magnetic resonance imaging (MRI) evidence of 1-4 brain metastases, with at least one lesion > 20 mm and ≤ 50 mm in maximal diameter and determined to be appropriate for SRS and gross total resection; all other brain metastases are appropriate for SRS
Patient can have prior SRS to lesions other than the one planned for neoadjuvant SRS and resection
Patient must have a Karnofsky performance score of ≥ 70
Exclusion Criteria:
Patient deemed medically unfit to undergo surgical resection of brain metastasis
Prior whole brain radiotherapy
Patient with contraindication for imaging with MRI
Inability to participate in study activities due to physical or mental limitations
Inability or unwillingness to return for all the required follow-up visits
At the time of planning, unable to deliver 10 Gray (Gy) or less to optic nerve/chiasm
Tumor located in the brainstem
Imaging or cytologic evidence of leptomeningeal disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Erin Murphy, MD
Phone
1-866-223-8100
Email
TaussigResearch@ccf.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erin Murphy, MD
Organizational Affiliation
Case Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Individual Site Status
Withdrawn
Facility Name
Cleveland Clinic, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erin Murphy, MD
Phone
866-223-8100
Email
TaussigResearch@ccf.org
First Name & Middle Initial & Last Name & Degree
Erin Murphy, MD
12. IPD Sharing Statement
Learn more about this trial
Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study
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