Recurrent Genomic Alterations in Pediatric and Adult Central Nervous System Tumors Detected by Chromosomal Microarray: Difference between revisions
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''' Chromothripsis:''' observed | ''' Chromothripsis:''' observed | ||
|'''Loss:''' PTEN, RB1, TP53, CDKN2A/B/C | |'''Loss:''' PTEN, RB1, TP53, CDKN2A/B/C | ||
'''Fusions:''' FGFR-TACC; NTRK fusions | '''Fusions:''' FGFR-TACC; NTRK fusions <br> | ||
'''Amplification:''' PDGFRA, MYCN, MET, CDK4, CDK6 (EGFR, MDM2 amp rare)<br> | '''Amplification:''' PDGFRA, MYCN, MET, CDK4, CDK6 (EGFR, MDM2 amp rare)<br> | ||
'''Mutations:''' IDH1/2 (rare in pediatric GBM), KRAS, RAS pathway, RB1 pathway, TP53 pathway, FGFR1, H3.3/H3.1-K27M (exclusively in diffuse midline tumors), PDGFRA, NF1, SETD2, ATRX, DAXX | '''Mutations:''' IDH1/2 (rare in pediatric GBM), KRAS, RAS pathway, RB1 pathway, TP53 pathway, FGFR1, H3.3/H3.1-K27M (exclusively in diffuse midline tumors), PDGFRA, NF1, SETD2, ATRX, DAXX | ||
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|Infiltrating Gliomas | |Infiltrating Gliomas | ||
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|Diffuse astrocytoma/anaplastic Astrocytoma, WHO grade II/III, IDH mutant | |||
|'''Gain:''' 4q, 7q, 8q24, 12q<br> | |||
'''Loss:''' 9p, 19q (without 1p) | |||
|'''Gain:''' MYC <br> | |||
'''Loss:''' CDKN2A/B, PML15q22 | |||
|Better prognosis than IDH wildtype astrocytoma; Progression to grade IV will often involves loss of 10q, gain of CDK4, CDK6, and cyclin E2, and an increase in copy number alterations. | |||
|PMID:26824661; PMID:26061753; PMID:25263767 PMID:26061754; PMID:28535583; PMID:26091668 PMID: 25701198; PMID:26865861; PMID:29687258 | |||
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| | |||
|Diffuse astrocytoma/anaplastic astrocytoma, WHO grade II/III, IDH wild-type | |||
|'''Gain:''' 7, 19<br> | |||
'''Loss:''' 4, 9p 10<br> | |||
'''Amplification:''' EGFR, MDM4, CDK4 | |||
|'''Loss:''' homozygous CDKN2A/B<br> | |||
'''Mutation:''' EGFR, NF1, PTEN<br> | |||
'''Amplification:''' EGFR, MDM4, CDK4 | |||
|Poor prognosis with similar abnormalities to glioblastoma | |||
|PMID:26061754; PMID:26824661;PMID:28535583 PMID:26091668; PMID:26810070 | |||
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|Oligodendroglioma/anaplastic oligodendroglioma, WHO grade II/III, IDH mutant | |||
|'''Rearrangement:''' der(1;19)(q10;p10) leads to 1p/19q co-deletion<br> | |||
'''Loss:''' 1p/19q, 9p, 14q, less frequent 4, 18q | |||
|'''Gain:''' MYC<br> | |||
'''Loss:''' MAX (14q), FBXW7, CDN2KA/B<br> | |||
'''Mutation:''' FUBP1, CIC, IDH, TERT, NOTCH1, PIK3CA or PIK3R1 | |||
|Activation of MYC pathway is often seen with loss of 9p (CDKN2A/B), and 14q (MAX gene) and is reported to have a worse prognosis | |||
|PMID:27090007; PMID:26061753; PMID:25263767 PMID:26061754; PMID:24335697; PMID:25664944;PMID:26061753; PMID:26941959; PMID:26824661 PMID:26061751 | |||
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