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.
Original language | English |
---|---|
Pages (from-to) | 2468-2477 |
Number of pages | 10 |
Journal | Journal of Clinical Oncology |
Volume | 34 |
Issue number | 21 |
DOIs | |
Publication status | Published - 20 Jul 2016 |
Externally published | Yes |
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Therapeutic impact of cytoreductive surgery and irradiation of posterior fossa ependymoma in the molecular era : A retrospective multicohort analysis. / Ramaswamy, Vijay; Hielscher, Thomas; Mack, Stephen C.; Lassaletta, Alvaro; Lin, Tong; Pajtler, Kristian W.; Jones, David T.W.; Luu, Betty; Cavalli, Florence M.G.; Aldape, Kenneth; Remke, Marc; Mynarek, Martin; Rutkowski, Stefan; Gururangan, Sridharan; McLendon, Roger E.; Lipp, Eric S.; Dunham, Christopher; Hukin, Juliette; Eisenstat, David D.; Fulton, Dorcas; Van Landeghem, Frank K.H.; Santi, Mariarita; Van Veelen, Marie Lise C.; Van Meir, Erwin G.; Osuka, Satoru; Fan, Xing; Muraszko, Karin M.; Tirapelli, Daniela P.C.; Oba-Shinjo, Sueli M.; Marie, Suely K.N.; Carlotti, Carlos G.; Lee, Ji Yeoun; Rao, Amulya A.Nageswara; Giannini, Caterina; Faria, Claudia C.; Nunes, Sofia; Mora, Jaume; Hamilton, Ronald L; Hauser, Peter; Jabado, Nada; Petrecca, Kevin; Jung, Shin; Massimi, Luca; Zollo, Massimo; Cinalli, Giuseppe; Bognár, László; Klekner, Almos; Hortobágyi, Tibor; Leary, Sarah; Ermoian, Ralph P.; Olson, James M; Leonard, Jeffrey R.; Gardner, Corrine; Grajkowska, Wieslawa A.; Chambless, Lola B.; Cain, Jason; Eberhart, Charles G; Ahsan, Sama; Massimino, Maura; Giangaspero, Felice; Buttarelli, Francesca R.; Packer, Roger J.; Emery, Lyndsey; Yong, William H.; Soto, Horacio; Liau, Linda M.; Everson, Richard; Grossbach, Andrew; Shalaby, Tarek; Grotzer, Michael A; Karajannis, Matthias A; Zagzag, David S; Wheeler, Helen; Von Hoff, Katja; Alonso, Marta M.; Tuñon, Teresa; Schüller, Ulrich; Zitterbart, Karel; Sterba, Jaroslav; Chan, Jennifer A; Guzman, Miguel; Elbabaa, Samer K.; Colman, Howard; Dhall, Girish; Fisher, Paul G.; Fouladi, Maryam; Gajjar, Amar; Goldman, Stewart; Hwang, Eugene; Kool, Marcel; Ladha, Harshad; Vera-Bolanos, Elizabeth; Wani, Khalida; Lieberman, Frank; Mikkelsen, Tom; Omuro, Antonio M.; Pollack, Ian F.; Prados, Michael; Robins, H. Ian; Soffietti, Riccardo; Wu, Jing; Metellus, Phillipe; Tabori, Uri; Bartels, Ute; Bouffet, Eric; Hawkins, Cynthia E.; Rutka, James T.; Dirks, Peter; Pfister, Stefan M.; Merchant, Thomas E.; Gilbert, Mark R.; Armstrong, Terri S.; Korshunov, Andrey; Ellison, David W; Taylor, Michael D.
In: Journal of Clinical Oncology, Vol. 34, No. 21, 20.07.2016, p. 2468-2477.Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - Therapeutic impact of cytoreductive surgery and irradiation of posterior fossa ependymoma in the molecular era
T2 - A retrospective multicohort analysis
AU - Ramaswamy, Vijay
AU - Hielscher, Thomas
AU - Mack, Stephen C.
AU - Lassaletta, Alvaro
AU - Lin, Tong
AU - Pajtler, Kristian W.
AU - Jones, David T.W.
AU - Luu, Betty
AU - Cavalli, Florence M.G.
AU - Aldape, Kenneth
AU - Remke, Marc
AU - Mynarek, Martin
AU - Rutkowski, Stefan
AU - Gururangan, Sridharan
AU - McLendon, Roger E.
AU - Lipp, Eric S.
AU - Dunham, Christopher
AU - Hukin, Juliette
AU - Eisenstat, David D.
AU - Fulton, Dorcas
AU - Van Landeghem, Frank K.H.
AU - Santi, Mariarita
AU - Van Veelen, Marie Lise C.
AU - Van Meir, Erwin G.
AU - Osuka, Satoru
AU - Fan, Xing
AU - Muraszko, Karin M.
AU - Tirapelli, Daniela P.C.
AU - Oba-Shinjo, Sueli M.
AU - Marie, Suely K.N.
AU - Carlotti, Carlos G.
AU - Lee, Ji Yeoun
AU - Rao, Amulya A.Nageswara
AU - Giannini, Caterina
AU - Faria, Claudia C.
AU - Nunes, Sofia
AU - Mora, Jaume
AU - Hamilton, Ronald L
AU - Hauser, Peter
AU - Jabado, Nada
AU - Petrecca, Kevin
AU - Jung, Shin
AU - Massimi, Luca
AU - Zollo, Massimo
AU - Cinalli, Giuseppe
AU - Bognár, László
AU - Klekner, Almos
AU - Hortobágyi, Tibor
AU - Leary, Sarah
AU - Ermoian, Ralph P.
AU - Olson, James M
AU - Leonard, Jeffrey R.
AU - Gardner, Corrine
AU - Grajkowska, Wieslawa A.
AU - Chambless, Lola B.
AU - Cain, Jason
AU - Eberhart, Charles G
AU - Ahsan, Sama
AU - Massimino, Maura
AU - Giangaspero, Felice
AU - Buttarelli, Francesca R.
AU - Packer, Roger J.
AU - Emery, Lyndsey
AU - Yong, William H.
AU - Soto, Horacio
AU - Liau, Linda M.
AU - Everson, Richard
AU - Grossbach, Andrew
AU - Shalaby, Tarek
AU - Grotzer, Michael A
AU - Karajannis, Matthias A
AU - Zagzag, David S
AU - Wheeler, Helen
AU - Von Hoff, Katja
AU - Alonso, Marta M.
AU - Tuñon, Teresa
AU - Schüller, Ulrich
AU - Zitterbart, Karel
AU - Sterba, Jaroslav
AU - Chan, Jennifer A
AU - Guzman, Miguel
AU - Elbabaa, Samer K.
AU - Colman, Howard
AU - Dhall, Girish
AU - Fisher, Paul G.
AU - Fouladi, Maryam
AU - Gajjar, Amar
AU - Goldman, Stewart
AU - Hwang, Eugene
AU - Kool, Marcel
AU - Ladha, Harshad
AU - Vera-Bolanos, Elizabeth
AU - Wani, Khalida
AU - Lieberman, Frank
AU - Mikkelsen, Tom
AU - Omuro, Antonio M.
AU - Pollack, Ian F.
AU - Prados, Michael
AU - Robins, H. Ian
AU - Soffietti, Riccardo
AU - Wu, Jing
AU - Metellus, Phillipe
AU - Tabori, Uri
AU - Bartels, Ute
AU - Bouffet, Eric
AU - Hawkins, Cynthia E.
AU - Rutka, James T.
AU - Dirks, Peter
AU - Pfister, Stefan M.
AU - Merchant, Thomas E.
AU - Gilbert, Mark R.
AU - Armstrong, Terri S.
AU - Korshunov, Andrey
AU - Ellison, David W
AU - Taylor, Michael D.
PY - 2016/7/20
Y1 - 2016/7/20
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84978701824&partnerID=8YFLogxK
U2 - 10.1200/JCO.2015.65.7825
DO - 10.1200/JCO.2015.65.7825
M3 - Article
AN - SCOPUS:84978701824
VL - 34
SP - 2468
EP - 2477
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
SN - 0732-183X
IS - 21
ER -