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The CyberChallenge Trial How Much is Too Much - What is the Role of Cyberknife Radiosurgery in Patients With Multiple Brain Metastases? (CyberChallenge)

Primary Purpose

Brain Metastases, Nsclc

Status
Recruiting
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
SRS
Whole Brain Radiotherapy
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Metastases focused on measuring Metastases, Cyberknife, Lung Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • histologically confirmed malignant illness
  • 4-15 suspect intracranial lesions, taking into consideration all available MRI series
  • age ≥ 18 years of age
  • 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
  • Inability to tolerate irradiation consistent with the protocol
  • Small-cell lung cancer (SCLC) or lymphoma as primary malignant illness
  • >15 suspect intracranial lesions, taking into consideration all available MRI series
  • leptomeningeal disease
  • Previous radiotherapy of the brain
  • Patients who have not yet recovered from acute high-grade toxicities of prior therapies
  • Pregnant or lactating women
  • Participation in another competing clinical study or observation period of competing trials, respectively
  • MRI contraindication (i.e. cardiac pacemaker, implanted defibrillator, certain cardiac valve replacements, certain metal implants)

Sites / Locations

  • University Hospital of Heidelberg, Radiation OncologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Experimental Treatment Arm

Standard Treatment Arm

Arm Description

Best Supportive Care + Stereotactic Radiotherapy of all Brain Metastases

Best Supportive Care ± Whole Brain Radiotherapy

Outcomes

Primary Outcome Measures

overall survival
number of alive patients
quality of life according to QLQ-C15 (questionaire for patients with advanced cancer referred for palliative radiotherapy
changes in QLQ-C15 scores, scale is 1-100 points, 100 points representing maximum score
quality of life according to BN-20 (questionaire for patients with brain neoplasm)
changes in BN-20 scores, scale is 1-100 points, 100 points representing maximum score

Secondary Outcome Measures

functional independence assessed by the Barthel ADL index
Changes in Barthel ADL index scores, scale 0-100 points
long-term cognitive Status (Hopkins Verbal Learning Test HVLT)
Changes in HVLT scores (minimum 0, maximum 12)
development of radiation-induced brain lesions
changes in amounts of Radiation-induced brain lesions
Radiation induced sideeffects
changes in toxicity rates according to CTCAE 5.0
Overall survival
amount of alive randomized patients enrolled in the trial
local progression of treated metastases
detectable progressive disease of treated metastases
intracranial progression of leptomeningeal disease
occurrence of leptomeningeal disease
intracranial progression of treated BM disease
recurrence of treated BM disease
intracranial progression of new BM disease
occurrence of new BM disease
Brain salvage during follow-up
medical idication for whole brain Radiation after inital stereotactic radiotherapy

Full Information

First Posted
January 24, 2022
Last Updated
May 13, 2022
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT05378633
Brief Title
The CyberChallenge Trial How Much is Too Much - What is the Role of Cyberknife Radiosurgery in Patients With Multiple Brain Metastases?
Acronym
CyberChallenge
Official Title
The CyberChallenge Trial How Much is Too Much - What is the Role of Cyberknife Radiosurgery in Patients With Multiple Brain Metastases?
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 24, 2022 (Actual)
Primary Completion Date
February 24, 2024 (Anticipated)
Study Completion Date
February 24, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

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
Patients suffering from malignancies in advanced stages often develop brain metastases, which limit both the life span and the quality of life. Therapy options for multiple brain metastases may vary and range from stereotactic radiosurgery (SRS), whole-brain radiotherapy (WBRT), chemotherapy, immunotherapy to palliative best supportive care. Especially the efficacy and toxicity of SRS compared to WBRT in patients with extensive brain metastases (>4) is not yet clear but of incremental relevance in this seriously ill cohort with a limited life span. These health-impaired patients might especially profit from a less toxic treatment that is also time sparing with 1 or few sessions in SRS versus 10 sessions in WBRT. On the other hand, no compromises in efficacy want to be done.
Detailed Description
In the present multicenter study, the benefit of SRS compared to conventional whole brain radiotherapy, each combined with best supportive care or best supportive care only, in patients with 4-15 brain metastases is to be prospectively investigated. The effect will be measured using quality-adjusted life-years (QUALY). Quality of life and overall survival are therefore primary endpoints. Secondary endpoints are the ability to perform basic activities of daily life (Barthel (ADL) index), progression-free survival, local and locoregional progression-free survival, extracranial progression, toxicity and its treatment, the recording of postherapeutic radiation-induced brain lesions (RIBL), long-term cognitive function, a possible salvage therapy as well as death from brain metastases. Furthermore, die CyberChallenge trial is linked to a translational program via BUB2 study. The BUB2 study conducts biobanking of blood, urine and resection or biopsy material, if available, as well as collects imaging material. This is to find diagnostic and prognostic biomarkers in our cancer patients via analyzing genetic, epigenetic and protein expression patterns as well as radiomics and correlating them to clinical data and therefore further push individualized patient care in brain metastases forward.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases, Nsclc
Keywords
Metastases, Cyberknife, Lung Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
190 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental Treatment Arm
Arm Type
Experimental
Arm Description
Best Supportive Care + Stereotactic Radiotherapy of all Brain Metastases
Arm Title
Standard Treatment Arm
Arm Type
Other
Arm Description
Best Supportive Care ± Whole Brain Radiotherapy
Intervention Type
Radiation
Intervention Name(s)
SRS
Intervention Description
Stereotactic Radiotherapy (SRS)
Intervention Type
Radiation
Intervention Name(s)
Whole Brain Radiotherapy
Intervention Description
Whole Brain Radiotherapy (WBRT)
Primary Outcome Measure Information:
Title
overall survival
Description
number of alive patients
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
quality of life according to QLQ-C15 (questionaire for patients with advanced cancer referred for palliative radiotherapy
Description
changes in QLQ-C15 scores, scale is 1-100 points, 100 points representing maximum score
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
quality of life according to BN-20 (questionaire for patients with brain neoplasm)
Description
changes in BN-20 scores, scale is 1-100 points, 100 points representing maximum score
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Secondary Outcome Measure Information:
Title
functional independence assessed by the Barthel ADL index
Description
Changes in Barthel ADL index scores, scale 0-100 points
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
long-term cognitive Status (Hopkins Verbal Learning Test HVLT)
Description
Changes in HVLT scores (minimum 0, maximum 12)
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
development of radiation-induced brain lesions
Description
changes in amounts of Radiation-induced brain lesions
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
Radiation induced sideeffects
Description
changes in toxicity rates according to CTCAE 5.0
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
Overall survival
Description
amount of alive randomized patients enrolled in the trial
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
local progression of treated metastases
Description
detectable progressive disease of treated metastases
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
intracranial progression of leptomeningeal disease
Description
occurrence of leptomeningeal disease
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
intracranial progression of treated BM disease
Description
recurrence of treated BM disease
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
intracranial progression of new BM disease
Description
occurrence of new BM disease
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month
Title
Brain salvage during follow-up
Description
medical idication for whole brain Radiation after inital stereotactic radiotherapy
Time Frame
time from randomisation until the date of death from any cause, assesd up to 24 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: histologically confirmed malignant illness 4-15 suspect intracranial lesions, taking into consideration all available MRI series age ≥ 18 years of age 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 Inability to tolerate irradiation consistent with the protocol Small-cell lung cancer (SCLC) or lymphoma as primary malignant illness >15 suspect intracranial lesions, taking into consideration all available MRI series leptomeningeal disease Previous radiotherapy of the brain Patients who have not yet recovered from acute high-grade toxicities of prior therapies Pregnant or lactating women Participation in another competing clinical study or observation period of competing trials, respectively MRI contraindication (i.e. cardiac pacemaker, implanted defibrillator, certain cardiac valve replacements, certain metal implants)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tanja Eichkorn, MD
Phone
06221 56
Ext
8201
Email
tanja.eichkorn@med.uni-heidelbeg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Adriane Hommertgen, Phd
Phone
06221 56
Ext
34091
Email
adriane.hommertgen@med.uni-heidelberg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juergen Debus, Prof.
Organizational Affiliation
Head of Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Heidelberg, Radiation Oncology
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jürgen Debus, Prof. Dr.
Phone
+49-6221-56
Ext
8202
Email
juergen.debus@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Adriane Hommertgen
Phone
+49-6221-56
Ext
34091
Email
adriane.hommertgen@med.uni-heidelberg.de

12. IPD Sharing Statement

Plan to Share IPD
No

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The CyberChallenge Trial How Much is Too Much - What is the Role of Cyberknife Radiosurgery in Patients With Multiple Brain Metastases?

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