Molecular subtyping of paediatric medulloblastoma by immunohistochemistry
Four core molecular subgroups of medulloblastomas have recently been introduced disparate by their transcriptional profile, all of which have different prognostic value. We aimed to determine the histological variants and molecular subtypes of medulloblastomas by immunohistochemistry in our po...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Pusat Perubatan Universiti Kebangsaan Malaysia
2020
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| Online Access: | http://journalarticle.ukm.my/16275/ http://journalarticle.ukm.my/16275/1/13_ms0428_pdf_38169.pdf |
| Summary: | Four core molecular subgroups of medulloblastomas have recently been
introduced disparate by their transcriptional profile, all of which have different
prognostic value. We aimed to determine the histological variants and molecular
subtypes of medulloblastomas by immunohistochemistry in our population,
and to correlate that with clinicopathological parameters. Seventeen patients
aged four-month to 14.3 years diagnosed with medulloblastoma were recruited
from year 2002 to 2017. All medulloblastomas were assigned to various histological
variants and molecular subgroups by immunohistochemistry surrogate markers
(YAP-1 and beta catenin). They were then correlated with clinicopathological
parameters and outcomes. Classic histology (76.5%) was the commonest, followed
by large cell/anaplastic (LCA) (17.6%) and desmoplastic/nodular (DN) variants
(59%). The most frequent molecular subgroup was non-SHH/WNT tumours
(64.7%), seconded by SHH tumours (35.3%). Among the SHH tumours, 66.7%
was classic histology and the remaining 33.3% was LCA variant. Interestingly, one
DN histology demonstrated YAP-1 and beta catenin immunonegativity, denoting
non-SHH/WNT molecular subgroup. Majority (88.2%) medulloblastomas were at
midline 4th ventricle location, including DN variant. Estimated three-year disease�free-survival (DFS) and overall-survival (OS) was 60% and 86.7%, respectively. Age
<3 years at diagnosis, tumour size >5 cm, LCA histology and high risk group were
inversely correlated with DFS, with early relapse. Infant <3-year-old had worse OS.
Other factors had no significant impact on DFS and OS. We had demonstrated
the feasibility of simple immunohistochemistry-based surrogate markers (YAP-1
and beta catenin) to stratify medulloblastomas into distinct molecular subtypes.
Prognostic and predictive values of YAP-1 immunomarker in medulloblastomas
however await further investigations. |
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