ATRT-40. IMPACT OF MOLECULAR SUBTYPES ON TREATMENT OUTCOMES IN RHABDOID TUMORS - A REPORT FROM THE RARE TUMOR CONSORTIUM
Abstract BACKGROUND Rhabdoid Tumors (RTs) are rare heritable cancers with bi-allelic SMARCB1/A4 alterations, arising in the brain (Atypical Teratoid/Rhabdoid Tumors/ATRTs) and in various extra-cranial locations (Malignant Rhabdoid Tumors/MRTs). Recent studies uncovered molecular sub-types of ATRTs a...
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Veröffentlicht in: | Neuro-oncology (Charlottesville, Va.) Va.), 2018-06, Vol.20 (suppl_2), p.i36-i36 |
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Sprache: | eng |
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Zusammenfassung: | Abstract
BACKGROUND
Rhabdoid Tumors (RTs) are rare heritable cancers with bi-allelic SMARCB1/A4 alterations, arising in the brain (Atypical Teratoid/Rhabdoid Tumors/ATRTs) and in various extra-cranial locations (Malignant Rhabdoid Tumors/MRTs). Recent studies uncovered molecular sub-types of ATRTs and MRTs, however, the molecular relationship and clinico-pathologic implications of MRTs and ATRTs sub-types remain unclear.
METHODS
To inform clinical understanding of ATRTs and MRTs, 450/850K methylation array profiles generated from 202 ATRTs and 57 MRTs were used to define molecular categories of ATRTs/MRTs and examine their clinical significance.
RESULTS
ATRTs segregated into 3 known molecular subgroups, group 1/SHH (n=87), group 2A/TYR (n=69), group 2B/MYC (n= 46); 13 and 44 MRTs respectively segregated with group 2A/TYR and 2B/MYC ATRTs. Median patient age was 19.1 months for group 1/SHH, 12.3 months for group 2A/TYR and 22.3 months for group 2B/MYC Rhabdoid tumors. Complete clinical information and treatment information available for 162 patients (n=125 ATRTs and n=37 MRTs), indicated only 65 patients received a combined chemo-radiation therapy. 24-month PFS was 30%,38% and 28% and the 24-month OS was 43%,48% and 43% for subgroups 1/SHH, 2A/TYR and 2B/MYC tumors respectively.
CONCLUSION
MRT and ATRT comprise a biological spectrum with overlapping molecular features. Clinicopathologic analysis suggest ATRT/MRT molecular subtypes have different therapeutic response to chemo-radiotherapeutic regimens. |
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ISSN: | 1522-8517 1523-5866 |
DOI: | 10.1093/neuonc/noy059.037 |