Evaluation of Repeated Whole Brain Radiotherapy Versus Best Supportive Care for Multiple Brain Metastases. (ERASER)
Primary Purpose
Brain Metastasases
Status
Unknown status
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
Whole Brain Radiotherapy
Best Supportive Care
Sponsored by
About this trial
This is an interventional treatment trial for Brain Metastasases
Eligibility Criteria
Inclusion criteria:
- histologically confirmed malignancy
- previous WBRT
- MR-imaging confirmed cerebral metastases (>1)
- age ≥ 18 years of age
- Karnofsky Performance Score ³60
- For women with childbearing potential, (and men) adequate contraception.
- Ability of subject to understand character and individual consequences of the clinical trial
- Written informed consent (must be available before enrolment in the trial)
Exclusion Criteria
- refusal of the patients to take part in the study
- Patients who have not yet recovered from acute high-grade toxicities of prior therapies
- Pregnant or lactating women
- Participation in another clinical study or observation period of competing trials, respectively
Sites / Locations
- Technische Universität München (TUM), Klinikum rechts der IsarRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Arm 1 - WBRT 10 x 2 Gy
Arm 2 - WBRT 15 x 2 Gy
Arm 3 - Best Supportive Care
Arm Description
Arm 1 - WBRT 10 x 2 Gy Whole brain radiotherapy with a total dose of 20 Gy in single fractions of 2 Gy
Arm 2 - WBRT 15 x 2 Gy Whole brain radiotherapy with a total dose of 30 Gy in single fractions of 2 Gy
Symptomatic treatment includes steroids, pain medication, nutritional support etc.
Outcomes
Primary Outcome Measures
Toxicity
The primary endpoint is toxicity according to CTCAE after whole brain radiotherapy.
Secondary Outcome Measures
loco-regional progression-free survival
follow-up and local control of brain metastases as well as loco-regional control
Quality of Life (QOL)
QOL
Survival
survival after radiotherapy
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03288272
Brief Title
Evaluation of Repeated Whole Brain Radiotherapy Versus Best Supportive Care for Multiple Brain Metastases.
Acronym
ERASER
Official Title
Evaluation of Repeated Whole Brain Radiotherapy Versus Best Supportive Care for Multiple Brain Metastases - the Randomized Trial ERASER.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
May 2018 (Anticipated)
Study Completion Date
May 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Stephanie Combs
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Whole Brain Radiotherapy (WBRT) has been established as the treatment standard in patients with multiple cerebral metastases from solid tumors. However, intracerebral recurrence is possible and a repeated WBRT may be indicated to improve intracerebral tumor control. Each institutsion offers different dosing regimens, which have all been published to be safe and effective. Some favor best supportive care only.
The current study protocol is aimed at evaluating primarily the toxicity as well as secondarily the local and loco-regional tumor control, overall survival and QoL after repeated WBRT using 2 different dose concepts (20 Gy in 10 Fx vs. 30 Gy in 15 Fx) compared to BSC.
Detailed Description
According to Nussbaum et al., 24-45% of cancer patients develop cerebral metastases during the course of the disease. Brain metastases are generally associated with a poor prognosis and high morbidity. Published median survival rates after WBRT are between 2 and 7 months. Standard of care in multiple BM is WBRT delivered as 30 Gy in 10 fractions, leading to modest palliation with a median survival of 3 to 5 months. Prognostic factors include the RPA-classification, performance status, response to steroids and evidence of systemic disease.
Unfortunately, intracerebral recurrence happens. For example, in the cohort of Meyners et al.(2010) on WBRT in relatively radioresistant tumors, median time to recurrence was 4.5months and the local control rates at 6 and 12 months post radiationem were 37% and 15%, respectively. Furthermore, the treatment of intracerebral recurrence after previous WBRT is challenging. In case of </= 3 recurrent BM, surgery or radiosurgery (RS) are options. One other option, especially in case of >3 recurrent BM is repeated WBRT. In this setting, one of the first reports on repeated WBRT was published by Cooper et al. in 1990. The authors reported on repeated WBRT (n=52) consisting of 25 Gy in 10 fractions. Response to reirradiation was seen in 42% of the patients. Furthermore, the patients improved by at least one level in their neurologic function status. Survival after second therapy averaged 5 months. In the report by Wong et al. (1996) median dose of retreatment (n=86) was 20 Gy. Resolution of symptoms was achieved in 27% of patients, partial improvement in 43% and no improvement or worsening of symptoms was seen in 29% of patients. The majority of patients had no significant toxicity secondary to re-irradiation. Five patients had radiographic abnormalities of their brain consistent with radiation-related changes. One patient had symptoms of dementia that was thought to be caused by radiotherapy. Sadikov et al. (2007) reported on 72 patients who underwent repeated WBRT for recurrent or progressive BM. The median survival after re-irradiation was 4.1 months. One patient was reported as having memory impairment and pituitary insufficiency after 5 months of progression-free survival.
In the report by Mayer et al. on re-irradiation tolerance of the human brain -in this analysis focused on recurrent glioma-, the authors concluded that radiation-induced brain tissue necrosis is found to occur at normalized tolerance doses of cumulative > 100 Gy.
The current study protocol is aimed at evaluating primarily the toxicity as well as secondarily the local and loco-regional tumor control, overall survival and QoL after repeated WBRT using 2 different dose concepts (20 Gy in 10 Fx vs. 30 Gy in 15 Fx) compared to BSC.
In the present trial, the primary endpoint toxicity as well as the secondary endpoints QoL, loco-regional progression-free survival, overall survival and imaging response in patients previously treated with WBRT requiring repeated WBRT for intracerebral tumor progression will be evaluated.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastasases
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Randomization Best Supportive Care, Two Radiotherapy Dosing Regimens
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm 1 - WBRT 10 x 2 Gy
Arm Type
Active Comparator
Arm Description
Arm 1 - WBRT 10 x 2 Gy Whole brain radiotherapy with a total dose of 20 Gy in single fractions of 2 Gy
Arm Title
Arm 2 - WBRT 15 x 2 Gy
Arm Type
Active Comparator
Arm Description
Arm 2 - WBRT 15 x 2 Gy Whole brain radiotherapy with a total dose of 30 Gy in single fractions of 2 Gy
Arm Title
Arm 3 - Best Supportive Care
Arm Type
Active Comparator
Arm Description
Symptomatic treatment includes steroids, pain medication, nutritional support etc.
Intervention Type
Radiation
Intervention Name(s)
Whole Brain Radiotherapy
Intervention Description
Radiotherapy of the whole brain
Intervention Type
Other
Intervention Name(s)
Best Supportive Care
Intervention Description
Best Supportive Care including nutrition, pain medication, steroids as needed
Primary Outcome Measure Information:
Title
Toxicity
Description
The primary endpoint is toxicity according to CTCAE after whole brain radiotherapy.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
loco-regional progression-free survival
Description
follow-up and local control of brain metastases as well as loco-regional control
Time Frame
6 months
Title
Quality of Life (QOL)
Description
QOL
Time Frame
6 months
Title
Survival
Description
survival after radiotherapy
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
histologically confirmed malignancy
previous WBRT
MR-imaging confirmed cerebral metastases (>1)
age ≥ 18 years of age
Karnofsky Performance Score ³60
For women with childbearing potential, (and men) adequate contraception.
Ability of subject to understand character and individual consequences of the clinical trial
Written informed consent (must be available before enrolment in the trial)
Exclusion Criteria
refusal of the patients to take part in the study
Patients who have not yet recovered from acute high-grade toxicities of prior therapies
Pregnant or lactating women
Participation in another clinical study or observation period of competing trials, respectively
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephanie E Combs, Prof. Dr.
Phone
+49-89-4140-
Ext
4501
Email
stephanie.combs@tum.de
First Name & Middle Initial & Last Name or Official Title & Degree
Carmen Kessel, MA
Phone
+49-89-4140-
Ext
4501
Email
carmen.kessel@tum.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephanie E Combs, Prof. Dr.
Organizational Affiliation
Professor and Department Chair
Official's Role
Principal Investigator
Facility Information:
Facility Name
Technische Universität München (TUM), Klinikum rechts der Isar
City
Munich
ZIP/Postal Code
81675
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephanie E Combs, Prof. Dr.
Phone
+49-89-4140-
Ext
4501
Email
stephanie.combs@tum.de
First Name & Middle Initial & Last Name & Degree
Carmen Kessel, MA
Phone
+49-89-4140-
Ext
4501
Email
carmen.kessel@tum.de
12. IPD Sharing Statement
Plan to Share IPD
Yes
Citations:
PubMed Identifier
24387239
Citation
Scharp M, Hauswald H, Bischof M, Debus J, Combs SE. Re-irradiation in the treatment of patients with cerebral metastases of solid tumors: retrospective analysis. Radiat Oncol. 2014 Jan 3;9:4. doi: 10.1186/1748-717X-9-4.
Results Reference
result
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Evaluation of Repeated Whole Brain Radiotherapy Versus Best Supportive Care for Multiple Brain Metastases.
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