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Using Intensity Modulated Radiation Therapy (IMRT) for Brain Metastases

Primary Purpose

Neoplasm Metastasis

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Intensity-Modulated Radiotherapy (IMRT)
Sponsored by
Sidney Kimmel Cancer Center at Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neoplasm Metastasis focused on measuring Brain metastases, Parenchymal, Neoplasm, IMRT, Intensity Modulated Radiation Therapy

Eligibility Criteria

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

Inclusion Criteria: Histologically confirmed malignancy 2-5 parenchymal brain metastases on magnetic resonance imaging (MRI) with a maximum size of 4 cm Partial resection allowed. Complete resection allowed only in patients with more than 3 lesions. Karnofsky Performance Status (KPS) equal to or greater than 60 Neurologic function equal to or greater than 2 Exclusion Criteria: Recurrent brain tumors Major medical or psychiatric illnesses Metastases in brainstem, midbrain, pons, or medulla Patients with leukemia or lymphoma

Sites / Locations

  • Thomas Jefferson University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intensity-Modulated Radiotherapy (IMRT)

Arm Description

Patients with brain metastases will be enrolled in one of three dose levels based on tumor size. For tumor size of 3 cm or less (maximum diameter in any dimension), doses of 47.5Gy, 52.5Gy, and 54.5Gy will be tested. For tumor size of greater than 3 cm (maximum diameter in any dimension), doses of 42.5Gy, 47.5Gy, and 52.5Gy will be tested.

Outcomes

Primary Outcome Measures

Unacceptable Acute CNS Toxicity
The primary endpoint is the frequency of patients developing unacceptable acute CNS toxicity.

Secondary Outcome Measures

Dose-Limiting Toxicity (DLT)
Dose-limiting toxicity will be defined as Grade 3 or greater CNS toxicity, as per NCI criteria. The observed rate of > 30% of Grade 3 or greater acute CNS toxicities will be considered unacceptable. Late toxicities will be closely monitored as well.

Full Information

First Posted
May 19, 2006
Last Updated
October 19, 2016
Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University
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1. Study Identification

Unique Protocol Identification Number
NCT00328575
Brief Title
Using Intensity Modulated Radiation Therapy (IMRT) for Brain Metastases
Official Title
Phase I Dose Escalation Trial in Patients With Brain Metastases Using IMRT
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if using intensity modulated radiation therapy for brain metastases is safe and will improve local control more than standard whole brain radiation therapy.
Detailed Description
Traditionally, whole brain radiation therapy (WBRT) has been the primary therapy for patients with brain metastases. Despite this therapy, patients still have poor survival of four to six months. Untreated patients have a median survival of one month. Up to one half of these patients die of causes related to the presence of brain metastases. In a Phase I/II RTOG trial, the efficacy and safety of delivering accelerated fractionation was investigated in patients with good prognostic factors. No toxicity was observed with escalating dose of irradiation up 70.40Gy in 1.6Gy twice daily treatments. However, in a randomized trial, the use of hyperfractionation did not appear to improve survival when compared to 30Gy whole brain irradiation delivered in 10 fractions. Current therapeutic approach also includes stereotactic radiosurgery (SRS). Several retrospective studies have demonstrated improved local tumor control of 80% with addition of SRS to WBRT. These local control rates were comparable to surgery. In a recently published randomized trial by RTOG 95-08 (TJU accrued 42 patients to this trial), Andrews et al. demonstrated improved survival in patients with solitary brain lesion treated with SRS. Median survival was 6.5 months in patients treated with WBRT and SRS compared to 4.9 months in patients treated with WBRT alone. Also, these patients were more likely to have stable or improved performance status.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasm Metastasis
Keywords
Brain metastases, Parenchymal, Neoplasm, IMRT, Intensity Modulated Radiation Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intensity-Modulated Radiotherapy (IMRT)
Arm Type
Experimental
Arm Description
Patients with brain metastases will be enrolled in one of three dose levels based on tumor size. For tumor size of 3 cm or less (maximum diameter in any dimension), doses of 47.5Gy, 52.5Gy, and 54.5Gy will be tested. For tumor size of greater than 3 cm (maximum diameter in any dimension), doses of 42.5Gy, 47.5Gy, and 52.5Gy will be tested.
Intervention Type
Radiation
Intervention Name(s)
Intensity-Modulated Radiotherapy (IMRT)
Other Intervention Name(s)
Radiation Therapy
Intervention Description
The duration of radiation therapy will be total of 3 weeks. During the first week, all patients will be treated initially with whole brain radiation therapy (WBRT) at 2.5Gy per fraction daily 5 days a week to a dose of 12.5Gy. This will be delivered through parallel-opposed fields to cover the entire cranial contents. For the remaining 2 weeks, patients will be treated using intensity-modulated radiation therapy (IMRT) technology such that a higher dose can be delivered to the tumor. IMRT is capable of generating complex 3-D dose distribution to conform closely to the target volume by modulating the radiation beam. This process is based on the "inverse method" of treatment planning to optimize radiation dose to tumor target coverage and normal tissue sparing.
Primary Outcome Measure Information:
Title
Unacceptable Acute CNS Toxicity
Description
The primary endpoint is the frequency of patients developing unacceptable acute CNS toxicity.
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Dose-Limiting Toxicity (DLT)
Description
Dose-limiting toxicity will be defined as Grade 3 or greater CNS toxicity, as per NCI criteria. The observed rate of > 30% of Grade 3 or greater acute CNS toxicities will be considered unacceptable. Late toxicities will be closely monitored as well.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed malignancy 2-5 parenchymal brain metastases on magnetic resonance imaging (MRI) with a maximum size of 4 cm Partial resection allowed. Complete resection allowed only in patients with more than 3 lesions. Karnofsky Performance Status (KPS) equal to or greater than 60 Neurologic function equal to or greater than 2 Exclusion Criteria: Recurrent brain tumors Major medical or psychiatric illnesses Metastases in brainstem, midbrain, pons, or medulla Patients with leukemia or lymphoma
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wenyin Shi, MD, PhD
Organizational Affiliation
Thomas Jefferson University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

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Using Intensity Modulated Radiation Therapy (IMRT) for Brain Metastases

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