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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT03126266


Additional trial details provided through ANZCTR are available at the end of this record.


Registration number
NCT03126266
Ethics application status
Date submitted
19/04/2017
Date registered
24/04/2017
Date last updated
2/08/2023

Titles & IDs
Public title
Re-Irradiation of Progressive or Recurrent DIPG
Scientific title
ReRAD: A Phase II Canadian Pediatric Brain Tumour Consortium Study of Re-Irradiation as Treatment of Progressive or Recurrent Diffuse Intrinsic Pontine Glioma
Secondary ID [1] 0 0
HREBA.CC16-0143
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Recurrent or Progressive Diffuse Intrinsic Pontine Glioma 0 0
Condition category
Condition code
Cancer 0 0 0 0
Brain
Other 0 0 0 0
Research that is not of generic health relevance and not applicable to specific health categories listed above

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Other - re-irradiation

Experimental: Patients receiving re-irradiation - Patients will receive 30.6 Gy or 36 Gy of a second course of radiation therapy for progressive or recurrent DIPG


Treatment: Other: re-irradiation
if DIPG has progressed or recurred at 180 days or later from completion of primary radiation therapy, a second course of radiation therapy will be given
Intervention code [1] 0 0
Treatment: Other
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
second progression-free survival
Timepoint [1] 0 0
up to 18 months from the start of re-irradiation
Secondary outcome [1] 0 0
overall survival
Timepoint [1] 0 0
up to three years from initial diagnosis of DIPG

Eligibility
Key inclusion criteria
All of these criteria must be met for a patient to be eligible for this study:

1. Each site may accept a patient on study of any age that they have permission to treat
and follow on study per their institutional policy.

2. The patient has no evidence of metastases on cranial or spinal MR imaging

3. The patient has received RT in the past, given to a total cumulative dose of <60 Gy;
prior radiation using opposed lateral fields, conformal 3-D fields, IMRT or using
protons is acceptable

4. At least 180 days have elapsed from the last day of primary RT for DIPG

5. The patient has recovered from all acute and subacute toxicities of prior RT and of
chemotherapy, if chemotherapy was utilized in the past

6. The patient has been off all anti-tumour therapy for at least 14 days

7. The patient has a Lansky score of 40% or higher

8. The patient has a life expectancy anticipated to be at least 8 weeks with treatment
using re-irradiation, with or without dexamethasone

9. The patient has no uncontrolled medical condition (e.g., seizures, diabetes,
infection) that would interfere with the delivery of rRT

10. The patient agrees to not enroll on any other clinical trial of an anti-tumour
intervention

11. The patient agrees to report and have recorded the use of all medications taken during
ReRAD therapy, from the time of diagnosis of progression or recurrence, then through
and after completion of, ReRAD therapy; this includes the use of complementary,
alternative and dietary therapies

12. The patient is treated at a site where the study is approved by the local ethics board

13. Males and females of child-bearing potential must agree to use effective birth control
measures during rRT

14. Consent, and, if applicable, assent, has been obtained according to institutional
standards
Minimum age
No limit
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
If the patient fulfills any of these criteria, then he or she will not be eligible for the
study:

1. Females who are pregnant, due to risks from rRT on the developing fetus.

2. Any patient with a condition that prohibits the planned delivery of rRT as prescribed
in this study.

3. Patients who are receiving any other clinical trial of an anti-tumour intervention

Study design
Purpose of the study
Treatment
Allocation to intervention
N/A
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
15/04/2017
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/12/2024
Actual
Sample size
Target
27
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC,WA
Recruitment hospital [1] 0 0
The Children's Hospital at Westmead - Westmead
Recruitment hospital [2] 0 0
Queensland Children's Hospital - Brisbane
Recruitment hospital [3] 0 0
Monash Children's Hospital - Clayton
Recruitment hospital [4] 0 0
Royal Children's Hospital - Parkville
Recruitment hospital [5] 0 0
Perth Children's Hospital - Perth
Recruitment postcode(s) [1] 0 0
- Westmead
Recruitment postcode(s) [2] 0 0
- Brisbane
Recruitment postcode(s) [3] 0 0
- Clayton
Recruitment postcode(s) [4] 0 0
- Parkville
Recruitment postcode(s) [5] 0 0
- Perth
Recruitment outside Australia
Country [1] 0 0
Canada
State/province [1] 0 0
Alberta
Country [2] 0 0
Canada
State/province [2] 0 0
British Columbia
Country [3] 0 0
Canada
State/province [3] 0 0
Newfoundland and Labrador
Country [4] 0 0
Canada
State/province [4] 0 0
Nova Scotia
Country [5] 0 0
Canada
State/province [5] 0 0
Ontario
Country [6] 0 0
Canada
State/province [6] 0 0
Quebec
Country [7] 0 0
New Zealand
State/province [7] 0 0
Auckland

Funding & Sponsors
Primary sponsor type
Other
Name
University of Calgary
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This is a single-arm, non-randomized study of re-irradiation of diffuse intrinsic pontine
glioma (DIPG)
Trial website
https://clinicaltrials.gov/ct2/show/NCT03126266
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Lucie Lafay-Cousin, MD
Address 0 0
University of Calgary
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Lucie Lafay-Cousin, MD
Address 0 0
Country 0 0
Phone 0 0
1 403 955 2554
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT03126266

Additional trial details provided through ANZCTR
Accrual to date
Recruiting in Australia
Recruitment state(s)
NSW,WA,VIC
Recruiting in New Zealand
Province(s)/district(s)
Auckland
Funding & Sponsors
Primary sponsor
Other Collaborative groups
Primary sponsor name
Australian and New Zealand Children's Haematology and Oncology Group
Primary sponsor address
27-31 Wright Street, Clayton, VIC, 3168
Primary sponsor country
Australia
Ethics approval
Ethics application status
Approved
 
Public notes
The Children's Hospital Westmead
Monash Children's Hospital
Perth Children's Hospital
Queensland Children's Hospital
The Royal Children's Hospital
Starship Children's Hospital

Contacts
Principal investigator
Title 213 0
Name 213 0
Dr Jennifer Chard
Address 213 0
Hawkesbury Rd, Westmead NSW 2145
Country 213 0
Australia
Phone 213 0
+612 8890 5200
Fax 213 0
Email 213 0
[email protected]
Contact person for public queries
Title 214 0
Mrs
Name 214 0
Robyn Strong
Address 214 0
27-31 Wright Street, Clayton, VIC, 3168
Country 214 0
Australia
Phone 214 0
+613 8572 2684
Fax 214 0
Email 214 0
Contact person for scientific queries
Title 215 0
Name 215 0
Dr Jennifer Chard
Address 215 0
Hawkesbury Rd, Westmead NSW 2145
Country 215 0
Australia
Phone 215 0
+612 8890 5200
Fax 215 0
Email 215 0
[email protected]