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Histologic Correlates of Molecular Group 4 Pediatric Medulloblastoma: A Retrospective Canadian Review.
Triscott, Joanna; Yip, Stephen; Johnston, Donna; Michaud, Jean; Rassekh, Shahrad R; Hukin, Juliette; Dunn, Sandra; Dunham, Christopher.
Affiliation
  • Triscott J; Department of Pediatrics, British Columbia Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Yip S; Department of BioMedical Research, University of Bern, Bern, Switzerland.
  • Johnston D; Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Michaud J; Division of Hematology/Oncology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
  • Rassekh SR; Department of Pathology and Laboratory Medicine, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
  • Hukin J; Department of Pediatrics, Division of Bone Marrow Therapy, Hematology and Oncology, British Columbia Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Dunn S; Department of Pediatrics, Divisions of Neurology & Bone Marrow Therapy, Hematology and Oncology, British Columbia Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Dunham C; Phoenix Molecular Designs, Vancouver, British Columbia, Canada.
Pediatr Dev Pathol ; 24(4): 309-317, 2021.
Article in En | MEDLINE | ID: mdl-33749384
ABSTRACT

INTRODUCTION:

The World Health Organization currently classifies medulloblastoma (MB) into four molecular groups (WNT, SHH, Group 3 and Group 4) and four histologic subtypes (classic, desmoplastic nodular, MB with extensive nodularity, and large cell/anaplastic). "Classic" MB is the most frequent histology, but unfortunately it does not predict molecular group or patient outcome. While MB may exhibit additional histologic features outside of the traditional WHO subtypes, the clinical significance of such features, in a molecular context, is unclear.

METHODS:

The clinicopathologic features of 120 pediatric MB were reviewed in the context of NanoString molecular grouping. Each case was evaluated for five ancillary histologic features, including nodularity without desmoplasia (i.e., "biphasic", B-MB), rhythmic palisades, and focal anaplasia. Molecular and histological features were statistically correlated to clinical outcome using Chi-square, log-rank, and multivariate Cox regression analysis.

RESULTS:

While B-MB (N = 32) and rhythmic palisades (N = 12) were enriched amongst non-WNT/SHH MB (especially Group 4), they were not statistically associated with outcome. In contrast, focal anaplasia (N = 12) was not associated with any molecular group, but did predict unfavorable outcome.

CONCLUSION:

These data nominate B-MB as a surrogate marker of Groups 3 and particularly 4 MB, which may earmark a clinically significant subset of cases.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Biomarkers, Tumor / Cerebellar Neoplasms / Wnt Proteins / Hedgehog Proteins / Medulloblastoma Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: America do norte Language: En Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Biomarkers, Tumor / Cerebellar Neoplasms / Wnt Proteins / Hedgehog Proteins / Medulloblastoma Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Country/Region as subject: America do norte Language: En Year: 2021 Type: Article