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A Trial Comparing Radiosurgery With Surgery for Solitary Brain Metastases

Primary Purpose

Neoplasm Metastasis, Brain Neoplasm

Status
Completed
Phase
Phase 3
Locations
Australia
Study Type
Interventional
Intervention
Surgery + WBRT
Radiosurgery + WBRT
Sponsored by
Royal Adelaide Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neoplasm Metastasis focused on measuring Radiosurgery, Brain metastases, Whole Brain Radiotherapy, Neurosurgery, Solitary Brain Metastases, Adult Tumours Metastatic to Brain

Eligibility Criteria

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

Inclusion Criteria: Single presumed brain metastasis on contrast magnetic resonance imaging (MRI) scan within two weeks before commencement of treatment. Systemic cancer diagnosed histologically or cytologically synchronous with, or within 5 years of treatment of the presumed brain metastasis (other than non-melanoma skin cancer and cancer in-situ of the cervix, neither of which would be reasonably attributable as the primary site). Exception - melanoma diagnosed > 5 years previously is allowable in view of the extremely variable natural history of melanoma. Age >= 18 (no upper age limit). Considered suitable for both S and RS by the neurosurgeon and radiation oncologist (see exclusions). Patient must agree to adjuvant WBRT. RTOG RPA Class 1 or 2 (Karnofsky Performance Status [KPS] >= 70 after adequate trial of corticosteroids). RPA Class 3 patients (KPS < 70) eligible if it is considered that the poor performance status is due primarily to the solitary metastasis, aggressive local treatment of which may be expected to restore good performance status. This would ordinarily be associated with minimal systemic disease burden. Accessible for treatment and follow-up. Patient is infertile or is aware of the risk of becoming pregnant or fathering children and will use adequate contraception. Written informed consent Exclusion Criteria: Previous history of brain metastasis(es) Surgery indicated to relieve life-threatening raised intracranial pressure or excision required for tissue diagnosis (no extra-cranial site to biopsy ie unknown primary). However, prior diagnostic (non-excisional) biopsy is allowable - it is acknowledged that the 50% probability of a repeat surgical procedure on subsequent randomisation would not be acceptable to many patients and clinicians. Surgery contraindicated by site (e.g. thalamus, brain stem) or medical co-morbidities. Leptomeningeal disease. Primary is small cell lung cancer, germ cell tumour, lymphoma, leukaemia or myeloma. Prior cranial RT (including RS). Patient is pregnant.

Sites / Locations

  • Royal Adelaide Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Surgery + Whole Brain Radiotherapy

RadioSurgery + Whole Brain Radiotherapy

Arm Description

Outcomes

Primary Outcome Measures

Overall survival and Quality of life

Secondary Outcome Measures

Local and distant recurrence
Failure free survival
Acute and late toxicities

Full Information

First Posted
July 27, 2005
Last Updated
September 2, 2010
Sponsor
Royal Adelaide Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00124761
Brief Title
A Trial Comparing Radiosurgery With Surgery for Solitary Brain Metastases
Official Title
A Randomised Trial of Surgery Plus Whole Brain Radiotherapy (WBRT) Versus Radiosurgery Plus WBRT for Solitary Brain Metastases
Study Type
Interventional

2. Study Status

Record Verification Date
September 2010
Overall Recruitment Status
Completed
Study Start Date
December 2002 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Royal Adelaide Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study examines surgery versus radiosurgery (highly focussed radiation) for the treatment of cancer which has spread to one spot in the brain (solitary brain "metastasis"). For these two treatment options, it will compare patients' survival times, quality of life, control rate of the brain metastases and side effects. It uses the most rigorous scientific method available called "randomisation" which minimises biases that exist with other types of studies. It will involve 30 - 40 patients.
Detailed Description
Primary objectives - to evaluate for solitary brain metastases whether both overall survival and health related quality of life (HQoL) in patients treated with radiosurgery (RS) plus whole brain radiotherapy (WBRT) are non-inferior to those of patients treated with surgery (S) plus WBRT. Secondary objectives - to compare between the two treatment arms time to local and distant brain recurrence, failure free survival, acute and late toxicity. Hypothesis - Patients treated with RS + WBRT have neither worse survival nor worse quality of life than those treated with S + WBRT. Research plan: Trial design - Single-centre prospective randomised Phase III controlled two arm non-inferiority study with the "gold standard" of surgery (plus WBRT) as the control arm. Blinding to trial arm will not be feasible. Stratification is by Radiation Therapy Oncology Group Recursive Partitioning Analysis (RPA) prognostic Class 1 vs 2 vs 3. Main eligibility criteria - single presumed metastasis on MRI brain; systemic cancer diagnosed within the last 5 years; considered suitable for both S and RS; written informed consent. Main exclusion criteria - surgery indicated for life-threatening raised intra-cranial pressure or tissue diagnosis; surgery contra-indicated by site or medical co-morbidities; leptomeningeal disease; primary is small cell lung cancer, germ cell tumour, lymphoma, leukaemia or myeloma. Radiation - WBRT dose is 30 Gy in 10 fractions over 2 weeks. RS dose is based on lesion size up to 4 cm (15-20 Gy). Surgery - Aim is complete excision. Treatment sequence and patient assessments - Any sequencing of S/RS and WBRT is allowable, as long as the brain treatment is commenced within 2 weeks after, and completed within 6½ weeks after the diagnostic MRI brain. Assessments at baseline, during brain treatment, at 2 and 3 months after commencement, then 3 monthly, with MRI brain at 3 and 6 months, and/or as clinically indicated. Acute toxicity monitored by NCI Common Toxicity Criteria, late toxicity by RTOG/EORTC Late Radiation Morbidity Scheme. HQoL assessed by EORTC QLQ-C30 and QLQ-BN20. Sample size - 30-40 patients over 5 years. Outcomes and Significance: The trial will enable Level I evidence to be applied to this common clinical problem. Patients will be able to make an informed choice based upon valid survival, quality of life and toxicity comparisons.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasm Metastasis, Brain Neoplasm
Keywords
Radiosurgery, Brain metastases, Whole Brain Radiotherapy, Neurosurgery, Solitary Brain Metastases, Adult Tumours Metastatic to Brain

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surgery + Whole Brain Radiotherapy
Arm Type
Other
Arm Title
RadioSurgery + Whole Brain Radiotherapy
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Surgery + WBRT
Other Intervention Name(s)
S + WBRT
Intervention Description
Surgery - complete excision of Solitary Brain Metastasis with 30 Gy in 10 fractions over 2 2 1/2 weeks
Intervention Type
Radiation
Intervention Name(s)
Radiosurgery + WBRT
Other Intervention Name(s)
RS + WBRT
Intervention Description
Radiosurgery - Marginal dose based on maximum tumour diameter
Primary Outcome Measure Information:
Title
Overall survival and Quality of life
Time Frame
Until death or study completion
Secondary Outcome Measure Information:
Title
Local and distant recurrence
Time Frame
Until death or study completion
Title
Failure free survival
Time Frame
Until death or study completion
Title
Acute and late toxicities
Time Frame
Acute toxicities 6 weeks post RT and late toxicities until death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Single presumed brain metastasis on contrast magnetic resonance imaging (MRI) scan within two weeks before commencement of treatment. Systemic cancer diagnosed histologically or cytologically synchronous with, or within 5 years of treatment of the presumed brain metastasis (other than non-melanoma skin cancer and cancer in-situ of the cervix, neither of which would be reasonably attributable as the primary site). Exception - melanoma diagnosed > 5 years previously is allowable in view of the extremely variable natural history of melanoma. Age >= 18 (no upper age limit). Considered suitable for both S and RS by the neurosurgeon and radiation oncologist (see exclusions). Patient must agree to adjuvant WBRT. RTOG RPA Class 1 or 2 (Karnofsky Performance Status [KPS] >= 70 after adequate trial of corticosteroids). RPA Class 3 patients (KPS < 70) eligible if it is considered that the poor performance status is due primarily to the solitary metastasis, aggressive local treatment of which may be expected to restore good performance status. This would ordinarily be associated with minimal systemic disease burden. Accessible for treatment and follow-up. Patient is infertile or is aware of the risk of becoming pregnant or fathering children and will use adequate contraception. Written informed consent Exclusion Criteria: Previous history of brain metastasis(es) Surgery indicated to relieve life-threatening raised intracranial pressure or excision required for tissue diagnosis (no extra-cranial site to biopsy ie unknown primary). However, prior diagnostic (non-excisional) biopsy is allowable - it is acknowledged that the 50% probability of a repeat surgical procedure on subsequent randomisation would not be acceptable to many patients and clinicians. Surgery contraindicated by site (e.g. thalamus, brain stem) or medical co-morbidities. Leptomeningeal disease. Primary is small cell lung cancer, germ cell tumour, lymphoma, leukaemia or myeloma. Prior cranial RT (including RS). Patient is pregnant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Roos, MD, FRANZCR
Organizational Affiliation
Royal Adelaide Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Royal Adelaide Hospital
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5000
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
12452912
Citation
Roos DE, Brophy BP, Zavgorodni SF, Katsilis ES. Radiosurgery for brain metastases at the Royal Adelaide Hospital: are we treating the right patients? Australas Radiol. 2002 Dec;46(4):402-8. doi: 10.1046/j.1440-1673.2002.t01-1-01094.x.
Results Reference
background
PubMed Identifier
21592754
Citation
Roos DE, Smith JG, Stephens SW. Radiosurgery versus surgery, both with adjuvant whole brain radiotherapy, for solitary brain metastases: a randomised controlled trial. Clin Oncol (R Coll Radiol). 2011 Nov;23(9):646-51. doi: 10.1016/j.clon.2011.04.009. Epub 2011 May 17.
Results Reference
derived

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A Trial Comparing Radiosurgery With Surgery for Solitary Brain Metastases

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