Literature DB >> 27269943

Therapeutic Impact of Cytoreductive Surgery and Irradiation of Posterior Fossa Ependymoma in the Molecular Era: A Retrospective Multicohort Analysis.

Vijay Ramaswamy1, Thomas Hielscher1, Stephen C Mack1, Alvaro Lassaletta1, Tong Lin1, Kristian W Pajtler1, David T W Jones1, Betty Luu1, Florence M G Cavalli1, Kenneth Aldape1, Marc Remke1, Martin Mynarek1, Stefan Rutkowski1, Sridharan Gururangan1, Roger E McLendon1, Eric S Lipp1, Christopher Dunham1, Juliette Hukin1, David D Eisenstat1, Dorcas Fulton1, Frank K H van Landeghem1, Mariarita Santi1, Marie-Lise C van Veelen1, Erwin G Van Meir1, Satoru Osuka1, Xing Fan1, Karin M Muraszko1, Daniela P C Tirapelli1, Sueli M Oba-Shinjo1, Suely K N Marie1, Carlos G Carlotti1, Ji Yeoun Lee1, Amulya A Nageswara Rao1, Caterina Giannini1, Claudia C Faria1, Sofia Nunes1, Jaume Mora1, Ronald L Hamilton1, Peter Hauser1, Nada Jabado1, Kevin Petrecca1, Shin Jung1, Luca Massimi1, Massimo Zollo1, Giuseppe Cinalli1, László Bognár1, Almos Klekner1, Tibor Hortobágyi1, Sarah Leary1, Ralph P Ermoian1, James M Olson1, Jeffrey R Leonard1, Corrine Gardner1, Wieslawa A Grajkowska1, Lola B Chambless1, Jason Cain1, Charles G Eberhart1, Sama Ahsan1, Maura Massimino1, Felice Giangaspero1, Francesca R Buttarelli1, Roger J Packer1, Lyndsey Emery1, William H Yong1, Horacio Soto1, Linda M Liau1, Richard Everson1, Andrew Grossbach1, Tarek Shalaby1, Michael Grotzer1, Matthias A Karajannis1, David Zagzag1, Helen Wheeler1, Katja von Hoff1, Marta M Alonso1, Teresa Tuñon1, Ulrich Schüller1, Karel Zitterbart1, Jaroslav Sterba1, Jennifer A Chan1, Miguel Guzman1, Samer K Elbabaa1, Howard Colman1, Girish Dhall1, Paul G Fisher1, Maryam Fouladi1, Amar Gajjar1, Stewart Goldman1, Eugene Hwang1, Marcel Kool1, Harshad Ladha1, Elizabeth Vera-Bolanos1, Khalida Wani1, Frank Lieberman1, Tom Mikkelsen1, Antonio M Omuro1, Ian F Pollack1, Michael Prados1, H Ian Robins1, Riccardo Soffietti1, Jing Wu1, Phillipe Metellus1, Uri Tabori1, Ute Bartels1, Eric Bouffet1, Cynthia E Hawkins1, James T Rutka1, Peter Dirks1, Stefan M Pfister1, Thomas E Merchant1, Mark R Gilbert1, Terri S Armstrong1, Andrey Korshunov1, David W Ellison1, Michael D Taylor1.   

Abstract

PURPOSE: Posterior fossa ependymoma comprises two distinct molecular variants termed EPN_PFA and EPN_PFB that have a distinct biology and natural history. The therapeutic value of cytoreductive surgery and radiation therapy for posterior fossa ependymoma after accounting for molecular subgroup is not known.
METHODS: Four independent nonoverlapping retrospective cohorts of posterior fossa ependymomas (n = 820) were profiled using genome-wide methylation arrays. Risk stratification models were designed based on known clinical and newly described molecular biomarkers identified by multivariable Cox proportional hazards analyses.
RESULTS: Molecular subgroup is a powerful independent predictor of outcome even when accounting for age or treatment regimen. Incompletely resected EPN_PFA ependymomas have a dismal prognosis, with a 5-year progression-free survival ranging from 26.1% to 56.8% across all four cohorts. Although first-line (adjuvant) radiation is clearly beneficial for completely resected EPN_PFA, a substantial proportion of patients with EPN_PFB can be cured with surgery alone, and patients with relapsed EPN_PFB can often be treated successfully with delayed external-beam irradiation.
CONCLUSION: The most impactful biomarker for posterior fossa ependymoma is molecular subgroup affiliation, independent of other demographic or treatment variables. However, both EPN_PFA and EPN_PFB still benefit from increased extent of resection, with the survival rates being particularly poor for subtotally resected EPN_PFA, even with adjuvant radiation therapy. Patients with EPN_PFB who undergo gross total resection are at lower risk for relapse and should be considered for inclusion in a randomized clinical trial of observation alone with radiation reserved for those who experience recurrence.
© 2016 by American Society of Clinical Oncology.

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Year:  2016        PMID: 27269943      PMCID: PMC4962737          DOI: 10.1200/JCO.2015.65.7825

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  31 in total

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Review 10.  Molecular genetics of ependymoma.

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4.  Survival and functional outcomes of molecularly defined childhood posterior fossa ependymoma: Cure at a cost.

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5.  Molecular grouping and outcomes of young children with newly diagnosed ependymoma treated on the multi-institutional SJYC07 trial.

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6.  Is H3K27me3 status really a strong prognostic indicator for pediatric posterior fossa ependymomas? A single surgeon, single center experience.

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7.  H3 K27M mutations are extremely rare in posterior fossa group A ependymoma.

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8.  Subgroup-specific outcomes of children with malignant childhood brain tumors treated with an irradiation-sparing protocol.

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