Prospective international phase-III study to improve neurocognitive outcomes in young children with low-risk medulloblastoma (YCMB-LR)
Project Number5R01CA283045-02
Contact PI/Project LeaderSANDS, STEPHEN ALAN
Awardee OrganizationSLOAN-KETTERING INST CAN RESEARCH
Description
Abstract Text
PROJECT SUMMARY / ABSTRACT
Cancer is the second most frequent cause of death in children under 15 years of age, and primary central
nervous system (CNS) tumors are the most frequent cause of cancer-related childhood deaths. Medulloblastoma
(MB) is the most frequent malignant childhood brain tumor (incidence of 5.5/million/year). About 40% of cases
occur in children <5 years old, which can be sub-divided by biological markers into two groups: low-risk group,
biologically defined by either Wingless/Integrated (WNT) or Sonic Hedgehog (SHH) activation TP53-wt, while
the high-risk group is defined by non-WNT/non-SHH biology. As WNT-activated MB is extremely rare in early
childhood, only young patients (<5 years of age) with low-risk (SHH-activated) MB are eligible and have an
excellent prognosis if treated with either of the two randomized arms in this research study. Craniospinal
irradiation (CSI) is an integral component in the treatment of MB; however, because of the devastating impact
upon the central nervous system (CNS) and neurocognitive outcomes, it must be avoided whenever possible
given the significant interference with educational and vocational attainment. Consequently, maintaining or
improving neurocognitive and QoL functioning is an essential opportunity for early childhood survivors who can
now be cured with treatment that does not include CSI. The Prospective International SIOPE/CONNECT
phase-III study to improve neurocognitive outcomes in young children with low-risk medulloblastoma
(YCMB-LR) is the first ever randomized study directly comparing two highly effective irradiation-sparing
treatment regimens, Head Start 4 and HIT-SKK, which will take place at pediatric oncology centers across
Europe and North America and is the first to include neuropsychological and QoL outcome as the primary
objective. Aim 1) Compare the overall intelligence and IQ subdomains as measured by the Wechsler Preschool
and Primary Scale of Intelligence administered 2.5 years after diagnosis between patients with newly diagnosed,
non-metastatic, SHH-activated, TP53-wt MB randomized to the interventional arms A (Head Start 4) or B (HIT-
SKK). Aim 2) Compare the trajectory between the two randomized groups at baseline and again at 2.5 years
post diagnosis for: a) overall intelligence and IQ subdomains, b) behavioral development and c) QoL, along with
analyses at 2.5 years post diagnosis for: d) fine motor dexterity and processing speed, e) visual-motor
integration, f) executive functioning, and g) social-emotional functioning. Aim 3) Several quantitative imaging
metrics with regard to brain volumes and white matter injury will serve as ancillary noninvasive biomarkers for
comparison of the two interventional arms in Aim 1, and will be statistically correlated with the neurocognitive,
QoL and behavioral outcomes in Aim 2. Impact: Our work will define the new “gold standard” of treatment in
early childhood low-risk MB that is associated with better neurocognitive outcomes with less severe late-effects
and ultimately yield a better QoL in survivorship, while simultaneously improving and harmonizing international
diagnostic and therapeutic standards not only for MB, but also for other pediatric CNS tumors.
Public Health Relevance Statement
PROJECT NARRATIVE
This prospective international SIOPE/CONNECT phase-III study to improve neurocognitive outcomes in young
children with low-risk medulloblastoma (YCMB-LR) is one of the first to prospectively include new biological
information into the risk prediction of Medulloblastoma (MB) by intensive molecular profiling and pathway
analysis to compare two highly effective irradiation-sparing treatment regimens (Head Start 4 and HIT-SKK) in
young patients with low-risk early childhood MB treated at European and North American pediatric oncology
centers in terms of neurocognitive, developmental and QoL outcomes at diagnosis and again at 2.5 years post
diagnosis. The goal of this research project is to define the new “gold standard” of treatment in early childhood,
clarifying which of the two compared regimens, both highly effective for brain tumor control, is associated with
better functional outcomes within the domains of overall intelligence, working memory, processing speed,
executive functioning, visual-motor integration, and fine motor dexterity, in addition to overall quality of life and
several domains of adaptive and emotional functioning, while simultaneously improving and harmonizing
international diagnostic and therapeutic standards not only for MB, but also for other pediatric CNS tumors.
NIH Spending Category
No NIH Spending Category available.
Project Terms
15 year old2 year old5 year oldAdaptive BehaviorsAdjuvant TherapyAgeAgreementAmericanAutologousBehavioralBiologicalBiological MarkersBiologyBrainBrain NeoplasmsCancer EtiologyCause of DeathCellsCentral Nervous SystemCentral Nervous System NeoplasmsCessation of lifeChildChildhoodChildhood Brain NeoplasmChildhood Central Nervous System NeoplasmChildhood LeukemiaChildhood Malignant Brain TumorChildhood MedulloblastomasCorrelation StudiesDataDevelopmentDiagnosisDiagnosticDoseEducationEligibility DeterminationEuropeEuropeanExcisionFundingGoalsGuidelinesHead Start ProgramHematopoieticHigh Dose ChemotherapyIncidenceInfantIntelligenceInternationalIntravenousIntraventricularLanguageLate EffectsMagnetic Resonance ImagingMalignant NeoplasmsMeasuresMedical centerMedulloblastomaMethotrexateMolecular ProfilingMotorNervous System TraumaNeurocognitiveNeurocognitive DeficitNeurologic DeficitNeuropsychological TestsNeuropsychologyNewly DiagnosedNonmetastaticNorth AmericaNursery SchoolsOutcomePathogenesisPathway AnalysisPatientsPediatric OncologyPrognosisProgression-Free SurvivalsProtocols documentationQuality of lifeRandomizedRegimenResearch Project GrantsRiskSHH geneSecureShort-Term MemorySiteSocietiesStandardizationSurvival RateSurvivorsTestingTherapeuticTimeTranslatingTreatment ProtocolsVocationWorkarmbehavioral outcomebrain volumechemotherapyclinically relevantdexterityearly childhoodemotional functioningexecutive functionfunctional outcomeshigh risk populationimprovedirradiationlife spanneurocognitive testneurosurgerynovel therapeuticsphase 3 studyprocessing speedprospectivequantitative imagingresearch studyrisk predictionsocialstandard carestandard measuresurvivorshiptreatment armtumorvisual-motor integrationwhite matter injury
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