Heterogeneity within the PF-EPN-B ependymoma subgroup
Florence M G Cavalli, Jens-Martin Hübner, Tanvi Sharma, Betty Luu, Martin Sill, Michal Zapotocky, Stephen C Mack, Hendrik Witt, Tong Lin, David J H Shih, Ben Ho, Mariarita Santi, Lyndsey Emery, Juliette Hukin, Christopher Dunham, Roger E McLendon, Eric S Lipp, Sridharan Gururangan, Andrew Grossbach, Pim French, Johan M Kros, Marie-Lise C van Veelen, Amulya A Nageswara Rao, Caterina Giannini, Sarah Leary, Shin Jung, Claudia C Faria, Jaume Mora, Ulrich Schüller, Marta M Alonso, Jennifer A Chan, Almos Klekner, Lola B Chambless, Eugene I Hwang, Maura Massimino, Charles G Eberhart, Matthias A Karajannis, Benjamin Lu, Linda M Liau, Massimo Zollo, Veronica Ferrucci, Carlos Carlotti, Daniela P C Tirapelli, Uri Tabori, Eric Bouffet, Marina Ryzhova, David W Ellison, Thomas E Merchant, Mark R Gilbert, Terri S Armstrong, Andrey Korshunov, Stefan M Pfister, Michael D Taylor, Kenneth Aldape, Kristian W Pajtler, Marcel Kool, Vijay Ramaswamy
Posterior fossa ependymoma comprise three distinct molecular variants, termed PF-EPN-A (PFA), PF-EPN-B (PFB), and PF-EPN-SE (subependymoma). Clinically, they are very disparate and PFB tumors are currently being considered for a trial of radiation avoidance. However, to move forward, unraveling the heterogeneity within PFB would be highly desirable. To discern the molecular heterogeneity within PFB, we performed an integrated analysis consisting of DNA methylation profiling, copy-number profiling, gene expression profiling, and clinical correlation across a cohort of 212 primary posterior fossa PFB tumors.
Unsupervised spectral clustering and t-SNE analysis of genome-wide methylation data revealed five distinct subtypes of PFB tumors, termed PFB1-5, with distinct demographics, copy-number alterations, and gene expression profiles. All PFB subtypes were distinct from PFA and posterior fossa subependymomas. Of the five subtypes, PFB4 and PFB5 are more discrete, consisting of younger and older patients, respectively, with a strong female-gender enrichment in PFB5 (age: p = 0.011, gender: p = 0.04).
Broad copy-number aberrations were common; however, many events such as chromosome 2 loss, 5 gain, and 17 loss were enriched in specific subtypes and 1q gain was enriched in PFB1. Late relapses were common across all five subtypes, but deaths were uncommon and present in only two subtypes (PFB1 and PFB3). Unlike the case in PFA ependymoma, 1q gain was not a robust marker of poor progression-free survival; however, chromosome 13q loss may represent a novel marker for risk stratification across the spectrum of PFB subtypes.
Similar to PFA ependymoma, there exists a significant intertumoral heterogeneity within PFB, with distinct molecular subtypes identified. Even when accounting for this heterogeneity, extent of resection remains the strongest predictor of poor outcome. However, this biological heterogeneity must be accounted for in future preclinical modeling and personalized therapies.
CITATION Acta Neuropathol. 2018 Aug;136(2):227-237. doi: 10.1007/s00401-018-1888-x. Epub 2018 Jul 17.