%0 Journal Article %1 Hayes:2017:Neuro-Oncol:29077933 %A Hayes, J %A Yu, Y %A Jalbert, L E %A Mazor, T %A Jones, L E %A Wood, M D %A Walsh, K M %A Bengtsson, H %A Hong, C %A Oberndorfer, S %A Roetzer, T %A Smirnov, I V %A Clarke, J L %A Aghi, M K %A Chang, S M %A Nelson, S J %A Woehrer, A %A Phillips, J J %A Solomon, D A %A Costello, J F %D 2017 %J Neuro Oncol %K LGG cancer-research glioma %R 10.1093/neuonc/nox205 %T Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas %U https://www.ncbi.nlm.nih.gov/pubmed/29077933 %X Rare multicentric lower-grade gliomas (LGG) represent a unique opportunity to study the heterogeneity between distinct tumor foci in a single patient, and to infer their origins and parallel patterns of evolution.In this study, we integrate clinical features, histology and immunohistochemistry for 4 patients with multicentric LGG, arising both synchronously and metachronously. For 3 patients we analyze the phylogeny of the lesions using exome sequencing, including one case with a total of 8 samples from the two lesions.One patient was diagnosed with multicentric IDH1 mutated diffuse astrocytomas harboring distinct IDH1 mutations, R132H and R132C; the latter mutation has been associated with Li-Fraumeni syndrome, which was subsequently confirmed in the patient's germline DNA and shown in additional cases with TCGA data. In another patient, phylogenetic analysis of synchronously arising grade II and grade III diffuse astrocytomas demonstrated a single shared mutation, IDH1 R132H, and revealed convergent evolution via non-overlapping mutations in ATRX and TP53. In 2 cases, there was divergent evolution of IDH1-mutated and chromosomes 1p/19q-codeleted oligodendroglioma and IDH1 mutated and 1p/19q intact diffuse astrocytoma, occurring synchronously in one case and metachronously in a second.Each tumor in multicentric LGG cases may arise independently or may diverge very early in their development, presenting as genetically and histologically distinct tumors. Comprehensive sampling of these lesions can therefore significantly alter diagnosis and management. Additionally, somatic IDH1 R132C mutation in either multicentric or solitary LGG identifies unsuspected germline TP53 mutation, validating the limited number of published cases.

@article{Hayes:2017:Neuro-Oncol:29077933, abstract = {Rare multicentric lower-grade gliomas (LGG) represent a unique opportunity to study the heterogeneity between distinct tumor foci in a single patient, and to infer their origins and parallel patterns of evolution.In this study, we integrate clinical features, histology and immunohistochemistry for 4 patients with multicentric LGG, arising both synchronously and metachronously. For 3 patients we analyze the phylogeny of the lesions using exome sequencing, including one case with a total of 8 samples from the two lesions.One patient was diagnosed with multicentric IDH1 mutated diffuse astrocytomas harboring distinct IDH1 mutations, R132H and R132C; the latter mutation has been associated with Li-Fraumeni syndrome, which was subsequently confirmed in the patient's germline DNA and shown in additional cases with TCGA data. In another patient, phylogenetic analysis of synchronously arising grade II and grade III diffuse astrocytomas demonstrated a single shared mutation, IDH1 R132H, and revealed convergent evolution via non-overlapping mutations in ATRX and TP53. In 2 cases, there was divergent evolution of IDH1-mutated and chromosomes 1p/19q-codeleted oligodendroglioma and IDH1 mutated and 1p/19q intact diffuse astrocytoma, occurring synchronously in one case and metachronously in a second.Each tumor in multicentric LGG cases may arise independently or may diverge very early in their development, presenting as genetically and histologically distinct tumors. Comprehensive sampling of these lesions can therefore significantly alter diagnosis and management. Additionally, somatic IDH1 R132C mutation in either multicentric or solitary LGG identifies unsuspected germline TP53 mutation, validating the limited number of published cases.}, added-at = {2017-12-26T19:22:36.000+0100}, author = {Hayes, J and Yu, Y and Jalbert, L E and Mazor, T and Jones, L E and Wood, M D and Walsh, K M and Bengtsson, H and Hong, C and Oberndorfer, S and Roetzer, T and Smirnov, I V and Clarke, J L and Aghi, M K and Chang, S M and Nelson, S J and Woehrer, A and Phillips, J J and Solomon, D A and Costello, J F}, biburl = {https://www.bibsonomy.org/bibtex/2b730f502b983af3ec284acf7ae714e54/marcsaric}, description = {Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas. - PubMed - NCBI}, doi = {10.1093/neuonc/nox205}, interhash = {62adf92d2405d5b2dfc9715528af8085}, intrahash = {b730f502b983af3ec284acf7ae714e54}, journal = {Neuro Oncol}, keywords = {LGG cancer-research glioma}, month = oct, pmid = {29077933}, timestamp = {2017-12-26T19:22:36.000+0100}, title = {Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas}, url = {https://www.ncbi.nlm.nih.gov/pubmed/29077933}, year = 2017 }