BACKGROUND: This prospective study stratified patients by surgical resection (complete = NED vs incomplete = ED) and centrally reviewed histology (World Health Organization [WHO] grade II vs III). METHODS: WHO grade II/NED patients received focal radiotherapy (RT) up to 59.4 Gy with 1.8 Gy/day. Grade III/NED received 4 courses of VEC (vincristine, etoposide, cyclophosphamide) after RT. ED patients received 1-4 VEC courses, second-look surgery, and 59.4 Gy followed by an 8-Gy boost in 2 fractions on still measurable residue. NED children aged 1-3 years with grade II tumors could receive 6 VEC courses alone. RESULTS: From January 2002 to December 2014, one hundred sixty consecutive children entered the protocol (median age, 4.9 y; males, 100). Follow-up was a median of 67 months. An infratentorial origin was identified in 110 cases. After surgery, 110 patients were NED, and 84 had grade III disease. Multiple resections were performed in 46/160 children (28.8%). A boost was given to 24/40 ED patients achieving progression-free survival (PFS) and overall survival (OS) rates of 58.1% and 68.7%, respectively, in this poor prognosis subgroup. For the whole series, 5-year PFS and OS rates were 65.4% and 81.1%, with no toxic deaths. On multivariable analysis, NED status and grade II were favorable for OS, and for PFS grade II remained favorable. CONCLUSIONS: In a multicenter collaboration, this trial accrued the highest number of patients published so far, and results are comparable to the best single-institution series. The RT boost, when feasible, seemed effective in improving prognosis. Even after multiple procedures, complete resection confirmed its prognostic strength, along with tumor grade. Biological parameters emerging in this series will be the object of future correlatives and reports.

Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma / Massimino, Maura; Miceli, Rosalba; Giangaspero, Felice; Boschetti, Luna; Modena, Piergiorgio; Antonelli, Manila; Ferroli, Paolo; Bertin, Daniele; Pecori, Emilia; Valentini, Laura; Biassoni, Veronica; Garrè, Maria Luisa; Schiavello, Elisabetta; Sardi, Iacopo; Cama, Armando; Viscardi, Elisabetta; Scarzello, Giovanni; Scoccianti, Silvia; Mascarin, Maurizio; Quaglietta, Lucia; Cinalli, Giuseppe; Diletto, Barbara; Genitori, Lorenzo; Peretta, Paola; Mussano, Anna; Buccoliero, Annamaria; Calareso, Giuseppina; Barra, Salvina; Mastronuzzi, Angela; Giussani, Carlo; Marras, Carlo Efisio; Balter, Rita; Bertolini, Patrizia; Giombelli, Ermanno; La Spina, Milena; Buttarelli, Francesca Romana; Pollo, Bianca; Gandola, Lorenza. - In: NEURO-ONCOLOGY. - ISSN 1522-8517. - 18:10(2016), pp. 1451-1460. [10.1093/neuonc/now108]

Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma

GIANGASPERO, FELICE;ANTONELLI, MANILA
Methodology
;
MASTRONUZZI, ANGELA;BUTTARELLI, Francesca Romana;
2016

Abstract

BACKGROUND: This prospective study stratified patients by surgical resection (complete = NED vs incomplete = ED) and centrally reviewed histology (World Health Organization [WHO] grade II vs III). METHODS: WHO grade II/NED patients received focal radiotherapy (RT) up to 59.4 Gy with 1.8 Gy/day. Grade III/NED received 4 courses of VEC (vincristine, etoposide, cyclophosphamide) after RT. ED patients received 1-4 VEC courses, second-look surgery, and 59.4 Gy followed by an 8-Gy boost in 2 fractions on still measurable residue. NED children aged 1-3 years with grade II tumors could receive 6 VEC courses alone. RESULTS: From January 2002 to December 2014, one hundred sixty consecutive children entered the protocol (median age, 4.9 y; males, 100). Follow-up was a median of 67 months. An infratentorial origin was identified in 110 cases. After surgery, 110 patients were NED, and 84 had grade III disease. Multiple resections were performed in 46/160 children (28.8%). A boost was given to 24/40 ED patients achieving progression-free survival (PFS) and overall survival (OS) rates of 58.1% and 68.7%, respectively, in this poor prognosis subgroup. For the whole series, 5-year PFS and OS rates were 65.4% and 81.1%, with no toxic deaths. On multivariable analysis, NED status and grade II were favorable for OS, and for PFS grade II remained favorable. CONCLUSIONS: In a multicenter collaboration, this trial accrued the highest number of patients published so far, and results are comparable to the best single-institution series. The RT boost, when feasible, seemed effective in improving prognosis. Even after multiple procedures, complete resection confirmed its prognostic strength, along with tumor grade. Biological parameters emerging in this series will be the object of future correlatives and reports.
2016
boost; ependymoma; grade; prognosis; surgery
01 Pubblicazione su rivista::01a Articolo in rivista
Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma / Massimino, Maura; Miceli, Rosalba; Giangaspero, Felice; Boschetti, Luna; Modena, Piergiorgio; Antonelli, Manila; Ferroli, Paolo; Bertin, Daniele; Pecori, Emilia; Valentini, Laura; Biassoni, Veronica; Garrè, Maria Luisa; Schiavello, Elisabetta; Sardi, Iacopo; Cama, Armando; Viscardi, Elisabetta; Scarzello, Giovanni; Scoccianti, Silvia; Mascarin, Maurizio; Quaglietta, Lucia; Cinalli, Giuseppe; Diletto, Barbara; Genitori, Lorenzo; Peretta, Paola; Mussano, Anna; Buccoliero, Annamaria; Calareso, Giuseppina; Barra, Salvina; Mastronuzzi, Angela; Giussani, Carlo; Marras, Carlo Efisio; Balter, Rita; Bertolini, Patrizia; Giombelli, Ermanno; La Spina, Milena; Buttarelli, Francesca Romana; Pollo, Bianca; Gandola, Lorenza. - In: NEURO-ONCOLOGY. - ISSN 1522-8517. - 18:10(2016), pp. 1451-1460. [10.1093/neuonc/now108]
File allegati a questo prodotto
File Dimensione Formato  
Massimino_Final-results_2016.pdf

accesso aperto

Note: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035526/
Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 776.63 kB
Formato Adobe PDF
776.63 kB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/878332
Citazioni
  • ???jsp.display-item.citation.pmc??? 35
  • Scopus 99
  • ???jsp.display-item.citation.isi??? 86
social impact