Children's Oncology Group's 2023 blueprint for research: Central nervous system tumors

Tumors of the central nervous system (CNS) are a leading cause of morbidity and mortality in the pediatric population. Molecular characterization in the last decade has redefined CNS tumor diagnoses and risk stratification; confirmed the unique biology of pediatric tumors as distinct entities from tumors that occur in adulthood; and led to the first novel targeted therapies receiving Food and Drug Administration (FDA) approval for children with CNS tumors. There remain significant challenges to overcome: children with unresectable low‐grade glioma may require multiple prolonged courses of therapy affecting quality of life; children with high‐grade glioma have a dismal long‐term prognosis; children with medulloblastoma may suffer significant short‐ and long‐term morbidity from multimodal cytotoxic therapy, and approaches to improve survival in ependymoma remain elusive. The Children's Oncology Group (COG) is uniquely positioned to conduct the next generation of practice‐changing clinical trials through rapid prospective molecular characterization and therapy evaluation in well‐defined clinical and molecular groups.

[1]  Trevor J Pugh,et al.  Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency , 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

[2]  J. Blay,et al.  Dabrafenib plus trametinib in BRAFV600E-mutated rare cancers: the phase 2 ROAR trial , 2023, Nature Medicine.

[3]  M. Souweidane,et al.  Leptomeningeal dissemination in pediatric brain tumors. , 2023, Neoplasia.

[4]  A. Panigrahy,et al.  Imaging of pediatric brain tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee/ASPNR White Paper , 2022, Pediatric blood & cancer.

[5]  G. Dhall,et al.  Primary central nervous system germ cell tumors in children and young adults: A review of controversies in diagnostic and treatment approach , 2022, Neoplasia.

[6]  J. Barnholtz-Sloan,et al.  CBTRUS Statistical Report: Pediatric Brain Tumor Foundation Childhood and Adolescent Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2014-2018. , 2022, Neuro-oncology.

[7]  J. Palmer,et al.  Medulloblastoma in the Modern Era: Review of Contemporary Trials, Molecular Advances, and Updates in Management , 2022, Neurotherapeutics.

[8]  S. Bens,et al.  ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance , 2022, Acta Neuropathologica.

[9]  S. Khatua,et al.  A Phase 2 Trial of Response-Based Radiation Therapy for Localized Central Nervous System Germ Cell Tumors: Patterns of Failure and Radiation Dosimetry for Nongerminomatous Germ Cell Tumors. , 2022, International journal of radiation oncology, biology, physics.

[10]  P. Adamson,et al.  Phase 1/2 Trial of Vorinostat and Radiation and Maintenance Vorinostat in Children with Diffuse Intrinsic Pontine Glioma: A Children's Oncology Group Report. , 2021, Neuro-oncology.

[11]  Jennifer L. Hadley,et al.  Efficacy of Carboplatin and Isotretinoin in Children With High-risk Medulloblastoma: A Randomized Clinical Trial From the Children's Oncology Group. , 2021, JAMA oncology.

[12]  P. Varlet,et al.  Clinical and molecular analysis of smoothened inhibitors in Sonic Hedgehog medulloblastoma , 2021, Neuro-oncology advances.

[13]  G. Reifenberger,et al.  The 2021 WHO Classification of Tumors of the Central Nervous System: a summary. , 2021, Neuro-oncology.

[14]  Jennifer L. Hadley,et al.  Children's Oncology Group Phase III Trial of Reduced-Dose and Reduced-Volume Radiotherapy With Chemotherapy for Newly Diagnosed Average-Risk Medulloblastoma , 2021, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[15]  M. Kool,et al.  Histopathological patterns in atypical teratoid/rhabdoid tumors are related to molecular subgroup , 2021, Brain pathology.

[16]  Sandeep Kumar Dhanda,et al.  Relevance of Molecular Groups in Children with Newly Diagnosed Atypical Teratoid Rhabdoid Tumor: Results from Prospective St. Jude Multi-institutional Trials , 2021, Clinical Cancer Research.

[17]  A. Ligon,et al.  A Phase 2 Trial of Selumetinib in Children with Recurrent Optic Pathway and Hypothalamic Low-Grade Glioma without NF1: A Pediatric Brain Tumor Consortium Study. , 2021, Neuro-oncology.

[18]  T. Merchant,et al.  Outcomes by Clinical and Molecular Features in Children With Medulloblastoma Treated With Risk-Adapted Therapy: Results of an International Phase III Trial (SJMB03). , 2021, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[19]  D. Ellison,et al.  EPEN-54. ACNS0831, PHASE III RANDOMIZED TRIAL OF POST-RADIATION CHEMOTHERAPY IN PATIENTS WITH NEWLY DIAGNOSED EPENDYMOMA AGES 1 TO 21 YEARS , 2020, Neuro-Oncology.

[20]  P. Burger,et al.  MBCL-34. EFFICACY OF METHOTREXATE (MTX) ACCORDING TO MOLECULAR SUB-TYPE IN YOUNG CHILDREN WITH MEDULLOBLASTOMA (MB): A REPORT FROM CHILDREN’S ONCOLOGY GROUP PHASE III TRIAL ACNS0334 , 2020, Neuro-Oncology.

[21]  A. Raghunathan,et al.  Atypical teratoid rhabdoid tumor: molecular insights and translation to novel therapeutics , 2020, Journal of Neuro-Oncology.

[22]  Raymond Y Huang,et al.  Evaluation of RAPNO criteria in medulloblastoma and other leptomeningeal seeding tumors using MRI and clinical data. , 2020, Neuro-oncology.

[23]  T. Zhou,et al.  Efficacy of High-Dose Chemotherapy and Three-Dimensional Conformal Radiation for Atypical Teratoid/Rhabdoid Tumor: A Report From the Children's Oncology Group Trial ACNS0333. , 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[24]  T. Yock,et al.  The role of proton therapy in pediatric malignancies: Recent advances and future directions. , 2020, Seminars in oncology.

[25]  FDA approves tazemetostat for advanced epithelioid sarcoma , 2020, Case Medical Research.

[26]  S. Bens,et al.  Age and DNA-methylation subgroup as potential independent risk factors for treatment stratification in children with Atypical Teratoid/Rhabdoid Tumors (ATRT). , 2019, Neuro-oncology.

[27]  M. Souweidane,et al.  Phase II Study of Nonmetastatic Desmoplastic Medulloblastoma in Children Younger Than 4 Years of Age: A Report of the Children's Oncology Group (ACNS1221). , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[28]  Arun K. Ramani,et al.  Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas , 2019, Nature Communications.

[29]  S. Khatua,et al.  Phase II Trial of Response-Based Radiation Therapy for Patients With Localized CNS Nongerminomatous Germ Cell Tumors: A Children's Oncology Group Study. , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[30]  N. Tarbell,et al.  Revisiting the Role of Radiation Therapy for Pediatric Low-Grade Glioma. , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  O. Oberlin,et al.  Medulloblastoma in childhood: What effects on neurocognitive functions? , 2019, Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique.

[32]  David T. W. Jones,et al.  MYCN amplification drives an aggressive form of spinal ependymoma , 2019, Acta Neuropathologica.

[33]  C. Karlson,et al.  Impact of Race and Socioeconomic Status on Psychologic Outcomes in Childhood Cancer Patients and Caregivers , 2019, Journal of pediatric hematology/oncology.

[34]  David T. W. Jones,et al.  Selumetinib in paediatric patients with BRAF-aberrant or neurofibromatosis type 1-associated recurrent, refractory, or progressive low-grade glioma: a multicentre, phase 2 trial. , 2019, The Lancet. Oncology.

[35]  M. Kool,et al.  Subgroup-specific prognostic signaling and metabolic pathways in pediatric medulloblastoma , 2019, BMC Cancer.

[36]  T. Zhou,et al.  Conformal Radiation Therapy for Pediatric Ependymoma, Chemotherapy for Incompletely Resected Ependymoma, and Observation for Completely Resected, Supratentorial Ependymoma. , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[37]  P. de Blank,et al.  Management of pediatric low-grade glioma , 2019, Current opinion in pediatrics.

[38]  D. Figarella-Branger,et al.  Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial , 2018, The Lancet. Oncology.

[39]  David T. W. Jones,et al.  Extensive Molecular and Clinical Heterogeneity in Patients With Histologically Diagnosed CNS-PNET Treated as a Single Entity: A Report From the Children's Oncology Group Randomized ACNS0332 Trial. , 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[40]  Martin Sill,et al.  Heterogeneity within the PF-EPN-B ependymoma subgroup , 2018, Acta Neuropathologica.

[41]  Jessica L. Davis,et al.  Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study. , 2018, The Lancet. Oncology.

[42]  S. Pfister,et al.  Pediatric low-grade gliomas: next biologically driven steps , 2018, Neuro-oncology.

[43]  Susan M. Chang,et al.  Response assessment in medulloblastoma and leptomeningeal seeding tumors: recommendations from the Response Assessment in Pediatric Neuro-Oncology committee , 2018, Neuro-oncology.

[44]  O. Hjemdal,et al.  Health-related quality of life and psychological distress in young adult survivors of childhood cancer and their association with treatment, education, and demographic factors , 2017, Quality of Life Research.

[45]  P. Keegan,et al.  First FDA Approval Agnostic of Cancer Site - When a Biomarker Defines the Indication. , 2017, The New England journal of medicine.

[46]  Joanna Y. Y. Chung,et al.  Determinants of quality of life outcomes for survivors of pediatric brain tumors , 2017, Pediatric blood & cancer.

[47]  D. Johnston,et al.  Immunohistochemical analysis of H3K27me3 demonstrates global reduction in group-A childhood posterior fossa ependymoma and is a powerful predictor of outcome , 2017, Acta Neuropathologica.

[48]  K. Aldape,et al.  The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variants , 2016, Acta Neuropathologica.

[49]  D. Johnston,et al.  Phase II Weekly Vinblastine for Chemotherapy-Naïve Children With Progressive Low-Grade Glioma: A Canadian Pediatric Brain Tumor Consortium Study. , 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[50]  K. Ligon,et al.  Pediatric low-grade gliomas: implications of the biologic era , 2016, Neuro-oncology.

[51]  I. Pollack,et al.  Nonrandomized comparison of neurofibromatosis type 1 and non–neurofibromatosis type 1 children who received carboplatin and vincristine for progressive low‐grade glioma: A report from the Children's Oncology Group , 2016, Cancer.

[52]  Mei Lu,et al.  Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors. , 2016, Cancer cell.

[53]  G. Reifenberger,et al.  The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary , 2016, Acta Neuropathologica.

[54]  M. Kool,et al.  Risk stratification of childhood medulloblastoma in the molecular era: the current consensus , 2016, Acta Neuropathologica.

[55]  D. Brat,et al.  Phase 2 study of concurrent radiotherapy and temozolomide followed by temozolomide and lomustine in the treatment of children with high-grade glioma: a report of the Children's Oncology Group ACNS0423 study. , 2016, Neuro-oncology.

[56]  Roland Eils,et al.  Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes. , 2016, Cancer cell.

[57]  T. Zhou,et al.  Phase II Trial Assessing the Ability of Neoadjuvant Chemotherapy With or Without Second-Look Surgery to Eliminate Measurable Disease for Nongerminomatous Germ Cell Tumors: A Children's Oncology Group Study. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[58]  Michael C. Rusch,et al.  Vismodegib Exerts Targeted Efficacy Against Recurrent Sonic Hedgehog-Subgroup Medulloblastoma: Results From Phase II Pediatric Brain Tumor Consortium Studies PBTC-025B and PBTC-032. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[59]  I. Pollack,et al.  TR-14A FEASIBILITY AND RANDOMIZED PHASE II STUDY OF VORINOSTAT, BEVACIZUMAB, OR TEMOZOLOMIDE DURING RADIATION FOLLOWED BY MAINTENANCE CHEMOTHERAPY IN NEWLY-DIAGNOSED PEDIATRIC HIGH-GRADE GLIOMA: CHILDREN'S ONCOLOGY GROUP STUDY ACNS0822 , 2015 .

[60]  Gary D Bader,et al.  Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis. , 2015, The Lancet. Oncology.

[61]  Gary D Bader,et al.  Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups. , 2015, Cancer cell.

[62]  H. Adami,et al.  Socioeconomic disparities in survival from childhood leukemia in the United States and globally: a meta-analysis. , 2015, Annals of oncology : official journal of the European Society for Medical Oncology.

[63]  Volker Hovestadt,et al.  Prognostic significance of clinical, histopathological, and molecular characteristics of medulloblastomas in the prospective HIT2000 multicenter clinical trial cohort , 2014, Acta Neuropathologica.

[64]  Toshihiro Kumabe,et al.  Cytogenetic prognostication within medulloblastoma subgroups. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[65]  Li Ding,et al.  C11orf95-RELA fusions drive oncogenic NF-κB signaling in ependymoma , 2014, Nature.

[66]  T. Merchant,et al.  Children's Oncology Group's 2013 blueprint for research: Central nervous system tumors , 2013, Pediatric blood & cancer.

[67]  E. Miyaoka,et al.  Primary CNS germ cell tumors in Japan and the United States: an analysis of 4 tumor registries. , 2012, Neuro-oncology.

[68]  M. Mehta,et al.  Outcome of children with metastatic medulloblastoma treated with carboplatin during craniospinal radiotherapy: a Children's Oncology Group Phase I/II study. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[69]  Gilbert Vezina,et al.  Randomized study of two chemotherapy regimens for treatment of low-grade glioma in young children: a report from the Children's Oncology Group. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[70]  B. Hinkes,et al.  Frequency, Risk‐Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Database , 2011, Pediatric blood & cancer.

[71]  T. Zhou,et al.  Temozolomide in the treatment of children with newly diagnosed diffuse intrinsic pontine gliomas: a report from the Children's Oncology Group. , 2011, Neuro-oncology.

[72]  Daniel J Brat,et al.  Temozolomide in the treatment of high-grade gliomas in children: a report from the Children's Oncology Group. , 2011, Neuro-oncology.

[73]  T. Merchant Three-dimensional conformal radiation therapy for ependymoma , 2009, Child's Nervous System.

[74]  J. Fangusaro,et al.  Pediatric central nervous system germ cell tumors: a review. , 2008, The oncologist.

[75]  P. Burger,et al.  Phase III study of craniospinal radiation therapy followed by adjuvant chemotherapy for newly diagnosed average-risk medulloblastoma. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[76]  OUP accepted manuscript , 2021, Neuro-Oncology.

[77]  T. Lightfoot,et al.  Survival from childhood acute lymphoblastic leukaemia: the impact of social inequality in the United Kingdom. , 2012, European journal of cancer.