EpendymomaPhase 2NCT02125786
A Trial of Surgery and Fractionated Re-Irradiation for Recurrent Ependymoma
A Phase 2 study testing Irradiation, Surgery and ^1^8F-Fluorodeoxyglucose in people with Ependymoma, run by St. Jude Children's Research Hospital at 1 site in United States.
Trial summary
The primary purpose of this study is to investigate whether surgery and re-irradiation will help treat ependymoma that has come back after initial treatment. The combined doses of the first and second courses of radiation are higher than what is usual standard of care. Read more about this study
- Who is it for?
- Ages 1 year to 21 years
- Conditions the study is for
- Ependymoma
- What is being tested?
- Irradiation, Surgery and ^1^8F-Fluorodeoxyglucose
- Type of treatment
- Injection or infusion, Medical device, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 68 participants
- Where
- 1 siteUnited States
- Study dates
- 7 May 2014to May 2028
- Phase
- Phase 2
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 1 year to 21 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Progressive intracranial ependymoma after prior focal irradiation
- Patients aged 1-21 years at the time of enrollment
- Adequate performance status (ECOG < 3) and research participant does not require mechanical ventilation
- Interval from start of initial radiation therapy to enrollment > 9 months
Who cannot join
- Prior craniospinal irradiation
- Pregnant women are excluded from enrollment on this study because radiation therapy is an agent with the potential for teratogenic or abortifacient effects
- Any patient with both metastatic ependymoma and age < 3 years at the time of enrollment
Trial locations and contacts
1 site in 1 country.
United States1 site
St. Jude Children's Research Hospital
Memphis, Tennessee, 38105
About this study
Official title: A Phase II Trial of Surgery and Fractionated Re-Irradiation for Recurrent Ependymoma
The primary purpose of this study is to investigate whether surgery and re-irradiation will help treat ependymoma that has come back after initial treatment. The combined doses of the first and second courses of radiation are higher than what is usual standard of care. The investigators will study the effects and side effects of surgery and re-irradiation. They will also evaluate and study tumor tissue and blood to learn more about the tumor and how it does or does not respond to treatments and will use magnetic resonance imaging (MRI) and positron emission tomography (PET) scans to see if they can predict tumor response and tumor recurrence.
Participants will be followed for up to 5 years following enrollment. Evaluations during radiation therapy will be done weekly while receiving therapy for up to 7 weeks. Other evaluations will be done at enrollment, every 4 months from enrollment through 3 years, and every 6 months during the 4th and 5th year.
Read the detailed description
Stratification for treatment will be determined when radiation therapy planning is initiated. Patients will be stratified for outcome according to diagnosis and prior therapy.
- Stratum 1 (initial pattern of failure is local); disease confined to primary site; age >12 months at time of enrollment to < 21 years. Treatment: focal irradiation.
- Stratum 2 (initial pattern of failure is metastatic); neuraxis metastatic disease without equivocal evidence of local failure; age > 36 months at time of enrollment to < 21 years. Treatment: craniospinal irradiation.
- Stratum 3 (Initial pattern of failure is both local and metastatic): neuraxis metastatic disease with unequivocal evidence of local failure; age > 36 months at time of enrollment to < 21 years. Treatment: craniospinal irradiation.
- Stratum 4 (initial pattern of failure is local): disease confined to primary site, age >36 months at time of enrollment to <21 years; tumor shows presence of 1g gain. Treatment: craniospinal irradiation (optional).
PRIMARY OBJECTIVE:
- To prospectively estimate the progression-free and overall survival distributions for children and young adults with recurrent ependymoma treated with a second course of irradiation while monitoring for excessive central nervous system necrosis.
SECONDARY OBJECTIVES:
- To explore potential associations of clinical and treatment factors with the incidence and severity of neurological, endocrine and cognitive deficits in children and young adults with ependymoma treated with a second course of irradiation.
- Using specific measures of sleep quality, excessive daytime sleepiness, daytime activity, fatigue, symptom distress, and quality of life, explore associations of sleep, fatigue and quality of life with other measures of CNS effects, clinical and treatment factors in children and young adults with ependymoma treated with a second course of irradiation.
- To evaluate and explore differences in physical performance and movement in children and young adults with ependymoma treated with a second course of irradiation.
- Estimate and compare the response of residual tumor and the incidence and severity of structural, physiological, and vascular effects of normal brain in children and young adults with ependymoma after treatment with a second course of irradiation using specific methods of diffusion, contrast-enhancement, magnetization transfer, vascular and functional neuroimaging, and explore the association between these and other measures of CNS effects and clinical and treatment factors. Determine the time course of gray matter and white matter tract injury and recovery post irradiation and the association between imaging metrics derived from serial quantitative neural imaging and radiation dosimetry as well as neuro-cognitive outcomes.
Other Pre-Specified (Exploratory) Objectives:
- Estimate the avidity of ependymoma to 18F-fluorodeoxyglucose (FDG) and 11C-methionine positron emission tomography (IND # 104987) prior to radiation therapy and correlate change in avidity 12, 24 and 36 months after a second course of irradiation with tumor progression.
- Measure growth factor and cytokine responses in children and young adults with ependymoma after treatment with a second course of irradiation, and explore associations between these and other measures of CNS effects and clinical and treatment factors. Descriptively compare findings for patients treated with an initial course of irradiation.
- To conduct a variety of exploratory molecular analyses on tumor samples (and blood where a germline control is required), including but not limited to broad (genome-wide / array-based) or focused (gene-specific) analyses at the DNA, RNA, or protein level and next generation (whole genome, exome, transcriptome) sequencing in an effort to improve the investigators understanding of ependymoma biology, and to explore associations between molecular findings and treatment response and various side effects including vasculopathy, hearing loss, cognitive deficits, and growth hormone deficiency and other measures as appropriate.
- To explore the association of chemotherapy given prior to re-irradiation with progression-free survival and overall survival distributions
- To compare the progression-free and overall survival distributions for children (age >3 years) and young adults with recurrent ependymoma and 1g gain treated with a second course of irradiation (focal or craniospinal) while monitoring for excessive central nervous system necrosis.
- Conditions
- Ependymoma
- Being tested
- Irradiation, Surgery, ^1^8F-Fluorodeoxyglucose, ^1^1C-methionine, Photon therapy
- Medical subject headings
- Ependymoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
IrradiationRadiation
Also called Focal irradiation, Craniospinal irradiation
Radiation therapy on this protocol will be based on extent of disease, extent of resection and location. The allowed treatment modalities include conformal or intensity-modulated radiation therapy using photons or proton therapy using double-scattering or spot-scanning methods. The general goal is to initiate radiation therapy within 12 weeks of last surgery performed at the time of recurrence.
SurgeryProcedure or surgery
Also called Metastasectomy
When applicable, surgery will be used to remove metastases. The goal of surgery is to achieve gross total resection of all imaging visible residual tumor.
^1^8F-FluorodeoxyglucoseDrug
Also called 18F-FDG, Contrast Media
This is a contrast media that will be given intravenously to aid in tumor visualization.
^1^1C-methionineDrug
Also called Contrast Media
This is a contrast media that will be given intravenously to aid in tumor visualization.
Photon therapyDevice
Also called Photon linear accelerator
Participants will receive one or both: Photon or proton therapy.
Proton therapyDevice
Also called Proton synchroton
Participants will receive one or both: Photon or proton therapy.
| Study group | Role | What they receive |
|---|---|---|
| Stratum 1: Local Failure | Experimental | Participants exhibit an initial pattern of failure that is local (disease confined to primary site). Treatment is surgery and a second course of focal irradiation. The total dose for the second course of irradiation will be 54Gy.
Participants may receive one or both: Photon therapy or proton therapy.
Participants receive ^1^8F-fluorodeoxyglucose and ^1^1C-methionine to aid in tumor visualization. Receives: Radiation: Irradiation; Procedure: Surgery; Drug: ^1^8F-Fluorodeoxyglucose; Drug: ^1^1C-methionine; Device: Photon therapy; Device: Proton therapy |
| Stratum 2: Metastatic Failure | Experimental | Participants exhibit an initial pattern of failure that is metastatic (neuraxis metastatic disease without equivocal evidence of local failure). Treatment is surgery and craniospinal irradiation. Craniospinal irradiation (36-39.6Gy) will include focal boost treatment of metastatic sites (54-59.4Gy) depending on location, extent of resection and target volume.
Participants may receive one or both: Photon therapy or proton therapy.
Participants receive ^1^8F-fluorodeoxyglucose and ^1^1C-methionine to aid in tumor visualization. Receives: Radiation: Irradiation; Procedure: Surgery; Drug: ^1^8F-Fluorodeoxyglucose; Drug: ^1^1C-methionine; Device: Photon therapy; Device: Proton therapy |
| Stratum 3: Local and Metastatic Failure | Experimental | Participants exhibit an initial pattern of failure that is both local and metastatic (neuraxis metastatic disease with equivocal evidence of local failure). Treatment is surgery and craniospinal irradiation.
Participants may receive one or both: Photon therapy or proton therapy.
Participants receive ^1^8F-fluorodeoxyglucose and ^1^1C-methionine to aid in tumor visualization. Receives: Radiation: Irradiation; Procedure: Surgery; Drug: ^1^8F-Fluorodeoxyglucose; Drug: ^1^1C-methionine; Device: Photon therapy; Device: Proton therapy |
| Stratum 4: Local Failure | Experimental | Local Failure Participants exhibit an initial pattern of failure that is local (disease confined to primary site). Age is >36 months at time of enrollment to <21 years. Tumor shows presence of 1q gain. Treatment is optional craniospinal irradiation.
Participants may receive one or both: Photon therapy or proton therapy.
Participants receive ^1^8F-fluorodeoxyglucose and ^1^1C-methionine to aid in tumor visualization. Receives: Radiation: Irradiation; Procedure: Surgery; Drug: ^1^8F-Fluorodeoxyglucose; Drug: ^1^1C-methionine; Device: Photon therapy; Device: Proton therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
3-year Progression-free Survival Rate
To prospectively estimate the progression-free distribution for children and young adults with recurrent ependymoma treated with a second course of irradiation.
Measured: 2 years follow-up after initiation of radiation therapy for the last patient enrolled
3-year Overall Survival Rate
OS was calculated from the date of initial radiation therapy to date of death or date of last contact for the patients who were treated with RT. The event of interest was death.
Measured: 2 years follow-up after initiation of radiation therapy for the last patient enrolled
Secondary outcomes (24)
Incidence Rate of Neurological Deficits
Evaluation will be in children and young adults with ependymoma treated with a second course of irradiation.
Outcomes will be reported by p-values.
Measured: Through 5 years after initiation of second course of irradiation
Incidence Rate of Ophthalmological Deficits
Evaluation will be in children and young adults with ependymoma treated with a second course of irradiation.
Outcome will be reported with p values.
Measured: Through 5 years after initiation of second course of irradiation
Incidence Rate of Audiological Deficits
Evaluation will be in children and young adults with ependymoma treated with a second course of irradiation.
Outcome will be reported with p-values.
Measured: Through 5 years after initiation of second course of irradiation
Incidence Rate of Endocrine Deficits
Evaluation will be in children and young adults with ependymoma treated with a second course of irradiation.
Outcome will be reported with p-values.
Measured: Through 5 years after initiation of second course of irradiation
Number of Neurocognitive Deficits
Measured: Through 5 years after initiation of second course of irradiation
Mean Change in Quality of Life by Treatment Arm
Baseline is defined as day 1 of radiation therapy.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Measured Task Sets
Baseline is defined as day 1 of radiation therapy.
Measured task sets: BOT2 (4-21 years old) and PPT (≥22 years old).
- BOT2 outcome: total motor composite, a standardized score range from 20 to 80, with a mean of 50 and a standard deviation of 10.
- PPT (7-item questionnaire) outcome: a score range from 0 to 28. The normative data is available from the human performance lab.
The above scores will be standardized into z-scores/T-scores for data analysis based on normative data.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Physical Function
Baseline is defined as day 1 of radiation therapy.
Self-reported instruments (PROMIS): Three questionnaires.
- Pediatric Physical Function - Mobility - SF1: 8-item questionnaire with the score range from 0 to 32.
- Pediatric Physical Function - Upper Extremity - SF1: same as above.
- Physical Function - SF1: 10-item questionnaire with the score range from 0 to 50.
The above scores will be standardized into z-scores/T-scores for data analysis based on normative data
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Body Mass Index (kg/m2)
Baseline is defined as day 1 of radiation therapy
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Waist/Hip Ratio (cm/cm)
Baseline is defined as day 1 of radiation therapy.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Ankle Dorsiflexion
Baseline is defined as day 1 of radiation therapy.
Ankle dorsiflexion active and passive range of motion: measured by goniometer, and recorded as an angle (degree).
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Overall Flexibility in cm
Baseline is defined as day 1 of radiation therapy.
Overall flexibility: measured by sit and reach test, and recorded as a length (cm).
Measured: Baseline through 5 years after initiation of radiation therapy
Proportion Change in Balance
Baseline is defined as day 1 of radiation therapy.
Balance measured by Measured by sensory organization test (SOT), and the result from the test is the equilibrium score, a percentage range from 0% to 100%, with the higher percentage, the better balance. The outcome is a binary variable with a cutoff score of < 70% indicates future risk for a fall.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Fine Motor Coordination
Baseline is defined as day 1 of radiation therapy.
Fine motor coordination (finger and hand coordination). Measured by Composite Cerebellar Functional Severity Score (CCFS), and the outcome is an age-adjusted z-score and log transformed.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Overall Coordination
Baseline is defined as day 1 of radiation therapy.
Overall coordination measured by brief ataxia rating scale (five-item questionnaire). The outcome is a total scale range from 0 to 22.
Measured: Fine motor coordination (finger and hand coordination).
Mean Change of Lower Extremity Strength and Power
Baseline is defined as day 1 of radiation therapy.
Lower extremity strength measured by BiodexIII. The outcomes are peak torque value/body weight ratios at different speeds of motion.
The scores will be standardized into z-scores for data analysis based on normative data.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Hand Grip Strength
Baseline is defined as day 1 of radiation therapy.
Hand grip strength is measured by a Jamar hand held dynamometer and recorded in kilograms (kg).
The scores will be standardized into z-scores for data analysis based on normative data.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Resting Energy Expenditure
Baseline is defined as day 1 of radiation therapy.
Resting energy expenditure is measured with indirect calorimetry after an overnight fast and recorded as REE (kcal/day).
The scores will be standardized into z-scores for data analysis based on normative data.
Measured: Baseline through 5 years after initiation of radiation therapy
Mean Change in Cardiopulmonary Exercise Test (CPET)
Baseline is defined as day 1 of radiation therapy.
Cardiopulmonary exercise test (CPET) will be completed on a treadmill using the Balke protocol or cycle ergometer using an incremental ramping protocol. The outcome is recorded as VO2max (ml/kg/min).
The scores will be standardized into z-scores for data analysis based on normative data.
Measured: Baseline through 5 years after initiation of radiation therapy
Longitudinal Change of Size (or Extent if Leptomeningeal Dissemination) of Residual Tumor
Baseline is defined as the last MRI prior to initiation of radiation therapy.
Measured: Baseline through 5 years after initiation of radiation therapy
Longitudinal Change of Incidence and Severity of Structural Effects of Normal Brain
Baseline is defined as the last MRI prior to initiation of radiation therapy.
Measured: Baseline through 5 years after initiation of radiation therapy
Longitudinal Change in Gray and White Matter Tissues
This outcome will be evaluated by neuroimaging. Baseline is defined as day 1 of radiation therapy.
Measured: Baseline to recovery of gray and white matter tract injury, up to a maximum of 5 years
Longitudinal Change of Individual Variation and Risk Factors in Gray and White Matter Tissues
Baseline is defined as day 1 of radiation therapy.
Measured: Baseline to recovery of gray and white matter tract injury, up to a maximum of 5 years
Change Over Time in Imaging Metrics
Baseline is defined as day 1 of radiation therapy.
Measured: Baseline to recovery of gray and white matter tract injury, up to a maximum of 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Apr 2014 (estimated)
- Study start7 May 2014
- Primary completionMay 2023
- Study completionMay 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for EpendymomaStudies of the same condition, open and under way.
- More trials run by St. Jude Children's Research HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 68 participants (actual)
Sponsor and investigators
- Lead sponsor
- St. Jude Children's Research Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Thomas E. Merchant, DO, PhD, Principal investigator, St. Jude Children's Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02125786
- Sponsor's protocol ID
- RERTEP
- Other IDs
- NCI-2014-00906
- Status last verified
- Feb 2026
- First submitted
- 25 Apr 2014
- Last updated
- 24 Feb 2026
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No