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Radiomic signatures of posterior fossa ependymoma: Molecular subgroups and risk profiles.
Zhang, Michael; Wang, Edward; Yecies, Derek; Tam, Lydia T; Han, Michelle; Toescu, Sebastian; Wright, Jason N; Altinmakas, Emre; Chen, Eric; Radmanesh, Alireza; Nemelka, Jordan; Oztekin, Ozgur; Wagner, Matthias W; Lober, Robert M; Ertl-Wagner, Birgit; Ho, Chang Y; Mankad, Kshitij; Vitanza, Nicholas A; Cheshier, Samuel H; Jacques, Tom S; Fisher, Paul G; Aquilina, Kristian; Said, Mourad; Jaju, Alok; Pfister, Stefan; Taylor, Michael D; Grant, Gerald A; Mattonen, Sarah; Ramaswamy, Vijay; Yeom, Kristen W.
Afiliación
  • Zhang M; Department of Neurosurgery, Stanford Hospital and Clinics, Stanford, California, USA.
  • Wang E; Department of Radiology, Lucile Packard Children's Hospital, Stanford, California, USA.
  • Yecies D; Department of Medical Biophysics, Western University, London, Ontario, Canada.
  • Tam LT; Department of Neurosurgery, Stanford Hospital and Clinics, Stanford, California, USA.
  • Han M; Department of Radiology, Lucile Packard Children's Hospital, Stanford, California, USA.
  • Toescu S; Stanford School of Medicine, Stanford University, Stanford, California, USA.
  • Wright JN; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Altinmakas E; Department of Neurosurgery, Great Ormond Street Institute of Child Health, London, UK.
  • Chen E; Department of Radiology, Seattle Children's Hospital, and Harborview Medical Center, Seattle, Washington, USA.
  • Radmanesh A; Department of Radiology, Koç University School of Medicine, Istanbul, Turkey.
  • Nemelka J; Department of Clinical Radiology & Imaging Sciences, Riley Children's Hospital, Indianapolis, Indiana, USA.
  • Oztekin O; Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA.
  • Wagner MW; Division of Pediatric Neurosurgery, Department of Neurosurgery, Huntsman Cancer Institute, University of Utah School of Medicine, Intermountain Healthcare Primary Children's Hospital, Salt Lake City, Utah, USA.
  • Lober RM; Department of Neuroradiology, Cigli Education and Research Hospital, and Tepecik Education and Research Hospital, Izmir, Turkey.
  • Ertl-Wagner B; Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Ho CY; Division of Neurosurgery, Dayton Children's Hospital, Dayton, Ohio, USA.
  • Mankad K; Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Vitanza NA; Department of Clinical Radiology & Imaging Sciences, Riley Children's Hospital, Indianapolis, Indiana, USA.
  • Cheshier SH; Department of Radiology, Great Ormond Street Institute of Child Health, London, UK.
  • Jacques TS; Division of Pediatric Hematology/Oncology, Department of Pediatrics, Seattle Children's Hospital, Seattle, Washington, USA.
  • Fisher PG; Division of Pediatric Neurosurgery, Department of Neurosurgery, Huntsman Cancer Institute, University of Utah School of Medicine, Intermountain Healthcare Primary Children's Hospital, Salt Lake City, Utah, USA.
  • Aquilina K; Department of Developmental Biology & Cancer, University College London Great Ormond Street Institute of Child Health, and Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Said M; Department of Neurology, Lucile Packard Children's Hospital, Stanford University, Palo Alto, California, USA.
  • Jaju A; Department of Neurosurgery, Great Ormond Street Institute of Child Health, London, UK.
  • Pfister S; Radiology Department Centre International Carthage Médicale, Monastir, Tunisia.
  • Taylor MD; Department of Medical Imaging, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Grant GA; Department of Pediatrics, Hopp Children' Cancer Center, Heidelberg, Germany.
  • Mattonen S; Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Ramaswamy V; Department of Neurosurgery, Lucile Packard Children's Hospital, Stanford, California, USA.
  • Yeom KW; Department of Medical Biophysics, Western University, London, Ontario, Canada.
Neuro Oncol ; 24(6): 986-994, 2022 06 01.
Article en En | MEDLINE | ID: mdl-34850171
ABSTRACT

BACKGROUND:

The risk profile for posterior fossa ependymoma (EP) depends on surgical and molecular status [Group A (PFA) versus Group B (PFB)]. While subtotal tumor resection is known to confer worse prognosis, MRI-based EP risk-profiling is unexplored. We aimed to apply machine learning strategies to link MRI-based biomarkers of high-risk EP and also to distinguish PFA from PFB.

METHODS:

We extracted 1800 quantitative features from presurgical T2-weighted (T2-MRI) and gadolinium-enhanced T1-weighted (T1-MRI) imaging of 157 EP patients. We implemented nested cross-validation to identify features for risk score calculations and apply a Cox model for survival analysis. We conducted additional feature selection for PFA versus PFB and examined performance across three candidate classifiers.

RESULTS:

For all EP patients with GTR, we identified four T2-MRI-based features and stratified patients into high- and low-risk groups, with 5-year overall survival rates of 62% and 100%, respectively (P < .0001). Among presumed PFA patients with GTR, four T1-MRI and five T2-MRI features predicted divergence of high- and low-risk groups, with 5-year overall survival rates of 62.7% and 96.7%, respectively (P = .002). T1-MRI-based features showed the best performance distinguishing PFA from PFB with an AUC of 0.86.

CONCLUSIONS:

We present machine learning strategies to identify MRI phenotypes that distinguish PFA from PFB, as well as high- and low-risk PFA. We also describe quantitative image predictors of aggressive EP tumors that might assist risk-profiling after surgery. Future studies could examine translating radiomics as an adjunct to EP risk assessment when considering therapy strategies or trial candidacy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ependimoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neuro Oncol Asunto de la revista: NEOPLASIAS / NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Ependimoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neuro Oncol Asunto de la revista: NEOPLASIAS / NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos