CNS5:Pleomorphic xanthoastrocytoma: Difference between revisions

[unchecked revision][unchecked revision]
Wkhan (talk | contribs)
Wkhan (talk | contribs)
Line 84: Line 84:
|'''Rare (<5%) PMID: 37870438'''
|'''Rare (<5%) PMID: 37870438'''
|D
|D
|Context-dependent ( e.g. For patients with CNS tumors who harbor NTRK fusions, TRK inhibitors such as larotrectinib or repotrectinib are considered a preferred therapy, regardless of histology, if other options are limited) NCCN CNS Cancer guidelines  
|Context-dependent ( e.g. For patients with CNS tumors who harbor NTRK fusions, TRK inhibitors such as larotrectinib or repotrectinib are considered a preferred therapy, regardless of histology, if other options are limited) NCCN CNS Cancer guidelines
|Reported in individual cases; more common in glioneuronal/low-grade gliomas
|Reported in individual cases; more common in glioneuronal/low-grade gliomas
|-
|-
Line 110: Line 110:
|CDKN2A, CDKN2B
|CDKN2A, CDKN2B
|D, P
|D, P
|Yes (WHO CNS5, NCCN)  
|Yes (WHO CNS5, NCCN)
|'''Defining PXA feature; occurs in >85% of cases (PMID: 28181325)'''
|'''Defining PXA feature; occurs in >85% of cases (PMID: 28181325)'''
|-
|-
Line 118: Line 118:
|EGFR not typically amplified)
|EGFR not typically amplified)
|D
|D
|No (however, frequently mentioned in literature as a recurrent copy number change in PXA (PMID:  
|No (however, frequently mentioned in literature as a recurrent copy number change in PXA (PMID:
|Trisomy, supports diagnosis; also seen in other gliomas
|Frequent but non-specific; supports PXA diagnosis
|-
|-
|<span class="blue-text">EXAMPLE:</span>
|<span class="blue-text">EXAMPLE:</span>