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WHOle Brain Irradiation or STEreotactic Radiosurgery for Five or More Brain Metastases (WHOBI-STER) (WHOBI-STER)

Primary Purpose

Neurocognitive Deficit, Quality of Life, Activities of Daily Living

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Stereotactic RadioTherapy
Whole Brain Irradiation
Sponsored by
Mediterranean Institute of Oncology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Neurocognitive Deficit focused on measuring multiple brain metastasis, neurocognitive decay, whole brain radiotherapy, stereotactic radiosurgery, stereotactic body radiotherapy, quality of life, solid tumor, Activities of Daily Living, best supportive care, palliative radiotherapy

Eligibility Criteria

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

Inclusion Criteria:

  • Age > 18
  • Life expectancy > 3 months
  • Brain metastases number ≥ 5
  • Primary tumor histologic diagnosis
  • Complete Extracranial staging
  • Montreal Cognitive Assessment ≥ 20/30
  • Barthel Activities of Daily Living ≥ 90/100
  • KPS ≥ 70
  • Signed Informed Consent

Exclusion Criteria:

  • Brain-MRI contraindications
  • Contraindications to SRS
  • Pregnancy
  • Hemorrhagic cerebral disease
  • Miliary metastases
  • Massive perilesional edema
  • Leptomeningeal involvement
  • Previous brain irradiation
  • Dementia
  • Non-solid brain tumor
  • Ischaemic event
  • Alcohol and/or drugs abuse
  • Anxiety and depression
  • KPS ≤ 60
  • Life expectancy < 3 months

Sites / Locations

  • Fondazione Istituto Oncologico del MediterraneoRecruiting
  • REM Radiotherapy (parent company of Mediterranean Institute of Oncology)Recruiting
  • Radiation Oncology Unit - Department of Biomedical, Dental Science and Morphological and Functional Images, University of MessinaRecruiting
  • Radiation Oncology, ARNAS-Civico HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

SRS/SBRT arm

WBI arm

Arm Description

Patients with five or more brain metastasis assigned by randomization to Stereotactic RadioSurgery (SRS) or Stereotactic Body RadioTherapy (SBRT) will be treated with a highly-conformal metastasis-directed single dose between 15 and 24 Gy or fractionated dose (e.g. 27 Gy in 3 fractions), respectively, depending on lesion size, while sparing clinically negative brain. The treatment will be delivered using five non-coplanar arcs and a mono-isocentric technique.

Patients with five or more brain metastasis assigned by randomization to Whole Brain Irradiation (WBI) will be treated using a 3D-Conformal RadioTherapy technique for a uniform dose delivery of 30 Gy in 10 daily/fractions to the target, that is entire brain.

Outcomes

Primary Outcome Measures

Neurocognitive changes detected through Moca Score
To assess how neurocognitive performance changes after SRS/SBRT compared to WBI
Changes of Autonomy in daily activities detected through the Barthel Index
To assess how level of autonomy in activities of daily living changes after SRS/SBRT compared to WBI
Change in quality of life detected though the EORTC QLQ-C15-PAL questionnaire
To assess how quality of life changes after SRS/SBRT compared to WBI
Neurocognitive changes detected through Hopkins Verbal Learning Test - Revised
To assess how neurocognitive performance changes after SRS/SBRT compared to WBI
Change in quality of life detected though the BN-20 questionnaire
To assess how quality of life changes after SRS/SBRT compared to WBI

Secondary Outcome Measures

Time to local failure
Time between treatment and cerebral disease progression detected through Magnetic Resonance imaging
Overall Survival
Time from the first day of treatment to exitus
Re-treatment rate
Difference in needing further subsequent radiotherapy treatment between SRS/SBRT and WBI arms
Acute Central Nervous System (CNS) toxicities evaluated by means of Radiation Therapy Oncology Group (RTOG)/ European Organization for Research and Treatment of Cancer (EORTC) Radiation Toxicity Grading
Toxicities registered within three months from treatment
Late Central Nervous System (CNS) toxicities evaluated by means of Radiation Therapy Oncology Group (RTOG)/ European Organization for Research and Treatment of Cancer (EORTC) Radiation Toxicity Grading
Toxicities registered after three months from treatment
Karnofsky Performance Status changing
Evaluation of how patient's performance status modifies after treatment

Full Information

First Posted
April 20, 2021
Last Updated
January 16, 2023
Sponsor
Mediterranean Institute of Oncology
Collaborators
University of Messina, University of Palermo
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1. Study Identification

Unique Protocol Identification Number
NCT04891471
Brief Title
WHOle Brain Irradiation or STEreotactic Radiosurgery for Five or More Brain Metastases (WHOBI-STER)
Acronym
WHOBI-STER
Official Title
WHOle Brain Irradiation and STEreotactic Radiosurgery for Five or More Brain Metastases (WHOBI-STER): a Prospective Comparative Study of Neurocognitive Outcomes, Level of Autonomy in Daily Activities and Quality of Life
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 15, 2020 (Actual)
Primary Completion Date
September 15, 2025 (Anticipated)
Study Completion Date
September 15, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mediterranean Institute of Oncology
Collaborators
University of Messina, University of Palermo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This work aims to evaluate neurocognitive performance, daily activity and quality of life and local control among patients with brain metastasis (MBM) ≥ 5 due to solid tumors treated with Stereotactic RadioSurgery (SRS) or Whole Brain RadioTherapy (WBRT). This multicentric randomised controlled trial will be conducted at the Fondazione IOM (Viagrande) in collaboration with REM (Viagrande), Hospital G. Martino (Messina) and Hospital Civico ARNAS (Palermo). It will involve, within 5 years starting from 15 September 2020, the enrollment of 100 patients (50 for each arm) with MBM ≥ 5, age ≥ 18 years, Karnofsky Performance Status (KPS) ≥ 70, life expectancy > 3 months, histological confirmation of primary tumor, with controlled or controllable extracranial disease, baseline Montreal Cognitive Assessment (MoCA) of 20/30, Barthel Activities of Daily Living score 90/100, to be subjected to SRS on each brain lesion by LINAC with monoisocentric technique and non-coplanar arcs (experimental arm) or to WBRT (control arm). The primary endpoints are neurocognitive performance, quality of life and autonomy in daily-life activities variations, the first one assessed by Moca Score and Hopkins Verbal Learning Test - Revised, the second one through the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 15 Palliative Care (EORTC QLQ-C15-PAL) and Brain Neoplasm (BN-20) questionnaires, the third one through the Barthel Index, respectively. The secondary endpoints are time to intracranial failure, overall survival, retreatments frequency, acute and late toxicities, KPS decrease. It will be considered significant a statistical difference of at least 29% between the two arms (statistical power of 80% with a significance level of 95%). This trial has been approved by the local ethics committee on July 7th 2020 (record 70). Several studies debate what is the predominant factor accountable for the development of neurocognitive decay among patients undergoing brain irradiation for MBM: radiotherapy, especially if extended to the entire brain, or intracranial disease progression? Answer to this question may come from current opportunity, thanks to recent technological advancement, to treat, with significant time savings, improved patient comfort and at the same time minimizing the dose to healthy brain tissue, Multiple Brain Metastasis simultaneously, otherwise attackable only by panencephalic irradiation. The pursuit of a local control rate comparable to that obtainable with WBRT remains the fundamental prerequisite for the aforementioned related assessments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurocognitive Deficit, Quality of Life, Activities of Daily Living
Keywords
multiple brain metastasis, neurocognitive decay, whole brain radiotherapy, stereotactic radiosurgery, stereotactic body radiotherapy, quality of life, solid tumor, Activities of Daily Living, best supportive care, palliative radiotherapy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
SRS/SBRT arm
Arm Type
Experimental
Arm Description
Patients with five or more brain metastasis assigned by randomization to Stereotactic RadioSurgery (SRS) or Stereotactic Body RadioTherapy (SBRT) will be treated with a highly-conformal metastasis-directed single dose between 15 and 24 Gy or fractionated dose (e.g. 27 Gy in 3 fractions), respectively, depending on lesion size, while sparing clinically negative brain. The treatment will be delivered using five non-coplanar arcs and a mono-isocentric technique.
Arm Title
WBI arm
Arm Type
Active Comparator
Arm Description
Patients with five or more brain metastasis assigned by randomization to Whole Brain Irradiation (WBI) will be treated using a 3D-Conformal RadioTherapy technique for a uniform dose delivery of 30 Gy in 10 daily/fractions to the target, that is entire brain.
Intervention Type
Radiation
Intervention Name(s)
Stereotactic RadioTherapy
Other Intervention Name(s)
Stereotactic RadioSurgery, Stereotactic Body RadioTherapy
Intervention Description
To treat only brain metastasis identified through Magnetic Resonance imaging by means of stereotactic radiotherapy (experimental intervention) to determine if sparing of clinically uninvolved brain implies a better neurocognitive performance, quality of life and level of autonomy in activities of daily living respect to Whole Brain Irradiation (active comparator).
Intervention Type
Radiation
Intervention Name(s)
Whole Brain Irradiation
Other Intervention Name(s)
Whole Brain Radiotherapy, Panencephalic Radiotherapy
Intervention Description
To irradiate the entire brain, site of at least 5 parenchymal metastasis.
Primary Outcome Measure Information:
Title
Neurocognitive changes detected through Moca Score
Description
To assess how neurocognitive performance changes after SRS/SBRT compared to WBI
Time Frame
Change from Baseline pre-Radiotherapy Neurocognitive Functional Status every three months after treatment through study completion, an average of 1 year
Title
Changes of Autonomy in daily activities detected through the Barthel Index
Description
To assess how level of autonomy in activities of daily living changes after SRS/SBRT compared to WBI
Time Frame
Change from Baseline pre-Radiotherapy Barthel Index every three months after treatment through study completion, an average of 1 year
Title
Change in quality of life detected though the EORTC QLQ-C15-PAL questionnaire
Description
To assess how quality of life changes after SRS/SBRT compared to WBI
Time Frame
Change from Baseline pre-Radiotherapy EORTC QLQ-C15-PAL questionnaire every three months after treatment through study completion, an average of 1 year
Title
Neurocognitive changes detected through Hopkins Verbal Learning Test - Revised
Description
To assess how neurocognitive performance changes after SRS/SBRT compared to WBI
Time Frame
Change from Baseline pre-Radiotherapy Neurocognitive Functional Status every three months after treatment through study completion, an average of 1 year
Title
Change in quality of life detected though the BN-20 questionnaire
Description
To assess how quality of life changes after SRS/SBRT compared to WBI
Time Frame
Change from Baseline pre-Radiotherapy BN-20 questionnaire every three months after treatment through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
Time to local failure
Description
Time between treatment and cerebral disease progression detected through Magnetic Resonance imaging
Time Frame
every three months after treatment through study completion, an average of 1 year
Title
Overall Survival
Description
Time from the first day of treatment to exitus
Time Frame
after treatment completion through study completion, an average of 1 year
Title
Re-treatment rate
Description
Difference in needing further subsequent radiotherapy treatment between SRS/SBRT and WBI arms
Time Frame
after first treatment completion through study completion, an average of 1 year
Title
Acute Central Nervous System (CNS) toxicities evaluated by means of Radiation Therapy Oncology Group (RTOG)/ European Organization for Research and Treatment of Cancer (EORTC) Radiation Toxicity Grading
Description
Toxicities registered within three months from treatment
Time Frame
from treatment completion until three months later
Title
Late Central Nervous System (CNS) toxicities evaluated by means of Radiation Therapy Oncology Group (RTOG)/ European Organization for Research and Treatment of Cancer (EORTC) Radiation Toxicity Grading
Description
Toxicities registered after three months from treatment
Time Frame
from three months after treatment completion through study completion, an average of 1 year
Title
Karnofsky Performance Status changing
Description
Evaluation of how patient's performance status modifies after treatment
Time Frame
after treatment completion through study completion, an average of 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 Life expectancy > 3 months Brain metastases number ≥ 5 Primary tumor histologic diagnosis Complete Extracranial staging Montreal Cognitive Assessment ≥ 20/30 Barthel Activities of Daily Living ≥ 90/100 KPS ≥ 70 Signed Informed Consent Exclusion Criteria: Brain-MRI contraindications Contraindications to SRS Pregnancy Hemorrhagic cerebral disease Miliary metastases Massive perilesional edema Leptomeningeal involvement Previous brain irradiation Dementia Non-solid brain tumor Ischaemic event Alcohol and/or drugs abuse Anxiety and depression KPS ≤ 60 Life expectancy < 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gianluca Ferini
Phone
+393311341117
Email
gianluca.ferini@grupposamed.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gianluca Ferini
Organizational Affiliation
REM Radiotherapy (parent company of Mediterranean Institute of Oncology)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fondazione Istituto Oncologico del Mediterraneo
City
Viagrande
State/Province
Catania
ZIP/Postal Code
95029
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irene R. Cravagno, Chief Radiation Oncology Unit
Email
irene_rita.cravagno@fondazioneiom.it
First Name & Middle Initial & Last Name & Degree
Anna Viola, Radiation Oncologist
Email
anna.viola@fondazioneiom.it
First Name & Middle Initial & Last Name & Degree
Anna Viola, Radiation Oncologist
Facility Name
REM Radiotherapy (parent company of Mediterranean Institute of Oncology)
City
Viagrande
State/Province
Catania
ZIP/Postal Code
95029
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gianluca Ferini, Chief Radiation Oncology Unit
Phone
+393311341117
Email
gianluca.ferini@grupposamed.com
First Name & Middle Initial & Last Name & Degree
Gianluca Ferini
First Name & Middle Initial & Last Name & Degree
Vito Valenti
First Name & Middle Initial & Last Name & Degree
Antonella Tripoli
Facility Name
Radiation Oncology Unit - Department of Biomedical, Dental Science and Morphological and Functional Images, University of Messina
City
Messina
ZIP/Postal Code
98125
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Silvana Parisi
Phone
+393406284095
Email
silvana.parisi@unime.it
First Name & Middle Initial & Last Name & Degree
Silvana Parisi
Email
silvana.parisi@unime.it
First Name & Middle Initial & Last Name & Degree
Silvana Parisi
First Name & Middle Initial & Last Name & Degree
Stefano Pergolizzi
First Name & Middle Initial & Last Name & Degree
Antonio Pontoriero
First Name & Middle Initial & Last Name & Degree
Alberto Cacciola
First Name & Middle Initial & Last Name & Degree
Sara Lillo
Facility Name
Radiation Oncology, ARNAS-Civico Hospital
City
Palermo
ZIP/Postal Code
90127
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gianluca Mortellaro
Phone
3298811698
Email
gianlucamortellaro@virgilio.it
First Name & Middle Initial & Last Name & Degree
Giuseppe Ferrera

12. IPD Sharing Statement

Plan to Share IPD
Yes
Citations:
PubMed Identifier
34926839
Citation
Ferini G, Viola A, Valenti V, Tripoli A, Molino L, Marchese VA, Illari SI, Rita Borzi G, Prestifilippo A, Umana GE, Martorana E, Mortellaro G, Ferrera G, Cacciola A, Lillo S, Pontoriero A, Pergolizzi S, Parisi S. Whole Brain Irradiation or Stereotactic RadioSurgery for five or more brain metastases (WHOBI-STER): A prospective comparative study of neurocognitive outcomes, level of autonomy in daily activities and quality of life. Clin Transl Radiat Oncol. 2021 Dec 2;32:52-58. doi: 10.1016/j.ctro.2021.11.008. eCollection 2022 Jan.
Results Reference
derived

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WHOle Brain Irradiation or STEreotactic Radiosurgery for Five or More Brain Metastases (WHOBI-STER)

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