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Understanding the Late Effects of Surviving a Pediatric Brain Tumor

Active, not recruiting
Conditions
Brain Tumor
Pediatric Cancer
Pediatric Brain Tumor
Interventions
Diagnostic Test: Diffusion tensor imaging (DTI)
Diagnostic Test: Resting state functional connectivity MRI (rs-fcMRI)
Behavioral: Wechsler Intelligence Scale for Children - 5th edition (WISC-V)
Behavioral: California Verbal Learning Test (CVLT-C)
Behavioral: Beery Test of Visual Motor Integration 6th edition
Behavioral: PedsQL Multidimensional Fatigue Scale
Behavioral: Grooved Pegboard
Diagnostic Test: MRI
Registration Number
NCT03208387
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

The goal of this study is to learn about the cognitive and behavioral functioning of children being treated for cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
42
Inclusion Criteria

Children Treated for Posterior Fossa Tumors:

  • As per medical record or clinical report, successfully completed all medical treatment for either an M0 posterior fossa medulloblastoma without dissemination or posterior fossa low-grade astrocytoma without relapse or evidence of residual disease.
  • For medulloblastoma survivors only: Previously treated with gross total resection (GTR), craniospinal irradiation with conformal posterior fossa boost radiotherapy (CSI + Boost) and chemotherapy
  • For low grade astrocytoma survivors only: Previously treated with gross total resection ONLY (no chemotherapy or radiotherapy).
  • As per medical record or clinician report, between 1-10 years post completion of their medical treatment for their posterior fossa brain tumor.
  • Subject is between the ages of 6 through 16 years at time of consent.
  • As per medical record or parent report, subject is able to tolerate an MRI without sedation.

Healthy Control Participants:

  • No major medical illness, as determined by medical interview by study physician.
  • As per parent report, subject is between the ages of 6 through 16 years at time of consent.
  • As per parent report, subject is able to tolerate an MRI without sedation.
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Exclusion Criteria

All Participants:

  • Full Scale IQ as documented to be below a standard score of <70 based upon the study IQ assessment completed after consent.
  • As per self or parent report, completed any portion of the neuropsychological battery used in this study within the last year.
  • MRI contraindications (e.g., implanted ferromagnetic devices, claustrophobia) as per radiology clinical operating procedures.
  • As per self or parent report or medical record, currently taking medications that have CNS effects (i.e., antidepressants, neuroleptics, anti-seizure medications, drugs that affect blood pressure or heart rate, alpha-agonists, adrenergic blockers, lithium, sedating antihistamines, and some medications for the treatment of asthma).
  • As per self or parent report, non-fluency in English language as demonstrated by current educational placement in a non-English-speaking classroom setting.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Children Medulloblastoma SurvivorsResting state functional connectivity MRI (rs-fcMRI)Participants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Medulloblastoma SurvivorsGrooved PegboardParticipants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Astrocytoma SurvivorsDiffusion tensor imaging (DTI)Participants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Children Astrocytoma SurvivorsCalifornia Verbal Learning Test (CVLT-C)Participants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Children Astrocytoma SurvivorsBeery Test of Visual Motor Integration 6th editionParticipants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Age-Matched Healthy Children ControlsBeery Test of Visual Motor Integration 6th edition-
Children Medulloblastoma SurvivorsWechsler Intelligence Scale for Children - 5th edition (WISC-V)Participants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Astrocytoma SurvivorsWechsler Intelligence Scale for Children - 5th edition (WISC-V)Participants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Age-Matched Healthy Children ControlsPedsQL Multidimensional Fatigue Scale-
Children Medulloblastoma SurvivorsCalifornia Verbal Learning Test (CVLT-C)Participants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Medulloblastoma SurvivorsMRIParticipants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Astrocytoma SurvivorsGrooved PegboardParticipants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Age-Matched Healthy Children ControlsWechsler Intelligence Scale for Children - 5th edition (WISC-V)-
Age-Matched Healthy Children ControlsGrooved Pegboard-
Children Medulloblastoma SurvivorsDiffusion tensor imaging (DTI)Participants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Age-Matched Healthy Children ControlsCalifornia Verbal Learning Test (CVLT-C)-
Age-Matched Healthy Children ControlsMRI-
Children Medulloblastoma SurvivorsBeery Test of Visual Motor Integration 6th editionParticipants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Medulloblastoma SurvivorsPedsQL Multidimensional Fatigue ScaleParticipants previously treated for M0 non-disseminated medulloblastoma with cranio-spinal irradiation plus a boost to the posterior fossa
Children Astrocytoma SurvivorsResting state functional connectivity MRI (rs-fcMRI)Participants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Children Astrocytoma SurvivorsPedsQL Multidimensional Fatigue ScaleParticipants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Children Astrocytoma SurvivorsMRIParticipants previously treated for a low grade cerebellar astrocytoma, with surgery only and neither chemotherapy nor cranial irradiation.
Primary Outcome Measures
NameTimeMethod
Feasibilty which is the number of eligible survivors consented per month2 years

The study is a pilot study to collect information on feasibility broadly defined. The feasibility indicators are primarily descriptive variables, including a careful monitoring of accrual rate (how many eligible survivors consented per month).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

Columbia University

🇺🇸

New York, New York, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

University of Texas Southwestern Medical Center

🇺🇸

Dallas, Texas, United States

Seattle Children's Hospital

🇺🇸

Seattle, Washington, United States

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