- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02514915
Pre-operative Stereotactic Radiosurgery Followed by Resection for Brain Metastases
June 6, 2025 updated by: Christopher Wilke
Phase II Study Determining the Efficacy of Pre-operative Stereotactic Radiosurgery Followed by Resection for Brain Metastases
The primary goal of this research study is to determine the efficacy of giving pre-operative radiosurgery to patients pending resection of a brain metastasis.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients who have a brain metastasis surgically resected have very high local rates of disease relapse, and so the standard of care is to give either whole brain irradiation or stereotactic radiosurgery to the resection cavity in order to prevent disease recurrence.
Stereotactic radiosurgery generally offers a more favorable side effect profile than whole brain irradiation, but targeting a surgical resection bed can be a challenge, as post surgical changes make it more difficult to distinguish residual tumor from scar, and much of the dose ends up being focused on the center of the resection cavity, where there are no substantial tumor cells.
Study Type
Interventional
Enrollment (Actual)
24
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15232
- UPMC Shadyside Radiation Oncology Department
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Life expectancy of at least 12 weeks
- Karnofsky performance status of at least 50
- No contraindications to MRI scanning with intravenous contrast.
- MRI scan consistent with brain metastasis as per radiology report.
- Target lesion must measure at least 15 mm in at least one dimension, and no more than 4 cm in any dimension.
- Patients must have an extra-cranial primary tumor diagnosis.
- Patients will have no more than 4 distinct lesions within the brain. At least 1 lesion has been recommended for surgical removal based on size, symptomology, or regional mass effect on the brain.
- Additional lesions will each be treated with stereotactic radiosurgery.
- Patients with a documented symptomatic lesion size smaller than 3cm requiring clinical surgical resection
- Must be aware of the neoplastic nature of his/her disease and willingly provide written, informed consent after being informed of the procedure to be followed, the experimental nature of the therapy, alternatives, potential benefits, side-effects, risks and discomforts
Exclusion Criteria:
- Primary tumor histology of lymphoma, leukemia, multiple myeloma or germ cell tumor. Moribund status or status epilepticus.
- Supratentorial mass effect with greater than 5 mm of midline shift or hydrocephalus. Infratentorial mass effect with fourth ventricle effacement or hydrocephalus.
- More than four additional diagnosed brain metastases.
- Contraindication to general anesthesia.
- Adjacent tumor location to optic apparatus or brainstem, precluding achievement of meaningful dose with SRS.
- Primary brain tumor.
- Contraindication to MRI scans or intravenous contrast.
- Pregnant and breast-feeding females.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Stereotactic Radiosurgery
Subjects will receive stereotactic radiosurgery prior to resection
|
Radiation therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Local Control Rate (LCR) at 6 Months
Time Frame: At 6 months
|
The probability that patients experience a change in size of a tumor (measured by the amount of space taken up by the tumor).
Tumor volume was measured at 6 months compared to the tumor volume at the start of radiotherapy.
|
At 6 months
|
|
Local Control Rate (LCR) at 12 Months
Time Frame: At 12 months
|
The probability that patients experience a change in size of a tumor (measured by the amount of space taken up by the tumor).
Tumor volume was measured at 12 months compared to the tumor volume at the start of radiotherapy.
|
At 12 months
|
|
Local Control Rate (LCR) at 24 Months
Time Frame: At 24 months
|
The probability that patients experience a change in size of a tumor (measured by the amount of space taken up by the tumor).
Tumor volume was measured at 24 months compared to the tumor volume at the start of radiotherapy.
|
At 24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
6-month Overall Survival (OS)
Time Frame: At 6 months
|
The probability of patients being alive at 6 months after the beginning of treatment.
|
At 6 months
|
|
12-month Overall Survival (OS)
Time Frame: At 12 months
|
The probability of patients being alive at 12 months after the beginning of treatment.
|
At 12 months
|
|
24-month Overall Survival (OS)
Time Frame: At 24 months
|
The probability of patients being alive at 24 months after the beginning of treatment.
|
At 24 months
|
|
Distant Intracranial Failure
Time Frame: At 6 months
|
The probability of new brain metastases at 6 months identified via magnetic resonance imaging.
|
At 6 months
|
|
Distant Intracranial Failure
Time Frame: At 12 months
|
The probability of new brain metastases at 12 months identified via magnetic resonance imaging.
|
At 12 months
|
|
Distant Intracranial Failure
Time Frame: At 24 months
|
The probability of new brain metastases at 24 months identified via magnetic resonance imaging.
|
At 24 months
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 6 months (1.5-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life.
|
At 6 months (1.5-month window)
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 6 months (3-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life.
|
At 6 months (3-month window)
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 12 months (1.5-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life.
|
At 12 months (1.5-month window)
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 12 months (3-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life.
|
At 12 months (3-month window)
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 24 months (1.5-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life..
|
At 24 months (1.5-month window)
|
|
Health Related Quality of Life (HRQL) - FACT - BR (FACT - BRAIN)
Time Frame: At 24 months (3-month window)
|
The Functional Assessment of Cancer Therapy - Brain (FACT-Br) (23 questions that assess brain-tumor related issues) including the FACT-General (FACT-G), a core questionnaire used to determine the more general domains of QOL among all cancer patients was administered.
This assessment is a 50 item, self-administered questionnaire used to assess Quality of Life, including, Physical Well-Being, Social/Family Well-Being, Emotional Well-Being, and Functional Well-Being.
Subscale scores range from 0-4.
FACT-G = (PWB - 7 items, score range 0-28) + (SWB - 7 items, score range 0-28) + (EWB - 6 items, score 0-24) + (FWB - 7 items, 0-28).
The assessment takes 10-15 minutes to completed and is scored using a 5-point Likert-type scale.
FACT Gen Scores range from 0-108.
Brain (FACT-Br) Scores range from 0-92 (23 questions with 0-4 score).
Thus, total assessments combine scores range from 0-200.
Higher total scores indicating better quality of life.
|
At 24 months (3-month window)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Christopher A Wilke, MD, PhD, University of Pittsburgh
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
July 22, 2021
Study Completion (Actual)
July 22, 2021
Study Registration Dates
First Submitted
July 30, 2015
First Submitted That Met QC Criteria
July 31, 2015
First Posted (Estimated)
August 4, 2015
Study Record Updates
Last Update Posted (Actual)
June 26, 2025
Last Update Submitted That Met QC Criteria
June 6, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HCC 14-150
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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