Treatment and outcome of intracranial ependymoma after first relapse in the 2nd AIEOP protocol.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
12 03 2022
Historique:
pubmed: 5 10 2021
medline: 23 3 2022
entrez: 4 10 2021
Statut: ppublish

Résumé

More than 40% of patients with intracranial ependymoma need a salvage treatment within 5 years after diagnosis, and no standard treatment is available as yet. We report the outcome after first relapse of 64 patients treated within the 2nd AIEOP protocol. We considered relapse sites and treatments, that is, various combinations of complete/incomplete surgery, if followed by standard or hypofractionated radiotherapy (RT) ± chemotherapy (CT). Molecular analyses were available for 38/64 samples obtained at first diagnosis. Of the 64 cases, 55 were suitable for subsequent analyses. The median follow-up was 147 months after diagnosis, 84 months after first relapse, 5-year EFS/OS were 26.2%/30.8% (median EFS/OS 13/32 months) after relapse. For patients with a local relapse (LR), the 5-year cumulative incidence of second LRs was 51.6%, with a 5-year event-specific probability of being LR-free of 40.0%. Tumor site/grade, need for shunting, age above/below 3 years, molecular subgroup at diagnosis, had no influence on outcomes. Due to variation in the RT dose/fractionation used and the subgroup sizes, it was not possible to assess the impact of the different RT modalities. Multivariable analyses identified completion of surgery, the absence of symptoms at relapse, and female sex as prognostically favorable. Tumors with a 1q gain carried a higher cumulative incidence of dissemination after first relapse. Survival after recurrence was significantly influenced by symptoms and completeness of surgery. Only a homogeneous protocol with well-posed, randomized questions could clarify the numerous issues, orient salvage treatment, and ameliorate prognosis for this group of patients.

Sections du résumé

BACKGROUND
More than 40% of patients with intracranial ependymoma need a salvage treatment within 5 years after diagnosis, and no standard treatment is available as yet. We report the outcome after first relapse of 64 patients treated within the 2nd AIEOP protocol.
METHODS
We considered relapse sites and treatments, that is, various combinations of complete/incomplete surgery, if followed by standard or hypofractionated radiotherapy (RT) ± chemotherapy (CT). Molecular analyses were available for 38/64 samples obtained at first diagnosis. Of the 64 cases, 55 were suitable for subsequent analyses.
RESULTS
The median follow-up was 147 months after diagnosis, 84 months after first relapse, 5-year EFS/OS were 26.2%/30.8% (median EFS/OS 13/32 months) after relapse. For patients with a local relapse (LR), the 5-year cumulative incidence of second LRs was 51.6%, with a 5-year event-specific probability of being LR-free of 40.0%. Tumor site/grade, need for shunting, age above/below 3 years, molecular subgroup at diagnosis, had no influence on outcomes. Due to variation in the RT dose/fractionation used and the subgroup sizes, it was not possible to assess the impact of the different RT modalities. Multivariable analyses identified completion of surgery, the absence of symptoms at relapse, and female sex as prognostically favorable. Tumors with a 1q gain carried a higher cumulative incidence of dissemination after first relapse.
CONCLUSIONS
Survival after recurrence was significantly influenced by symptoms and completeness of surgery. Only a homogeneous protocol with well-posed, randomized questions could clarify the numerous issues, orient salvage treatment, and ameliorate prognosis for this group of patients.

Identifiants

pubmed: 34605902
pii: 6380924
doi: 10.1093/neuonc/noab230
pmc: PMC8917409
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

467-479

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Maura Massimino (M)

Pediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Francesco Barretta (F)

Medical Statistics, Biometry and Bioinformatics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Piergiorgio Modena (P)

Laboratory of Genetics, S. Anna General Hospital, Como, Italy.

Pascal Johann (P)

Hopp-Children's Cancer Center Heidelberg KiTZ, German Cancer Research Center DKFZ, German Cancer Consortium DKTK, Heidelberg, Germany.

Paolo Ferroli (P)

Neurosurgery Unit, IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Manila Antonelli (M)

Department of Radiological, Oncological, and Anatomo-Pathological Sciences, La Sapienza University, Rome, Italy.

Lorenza Gandola (L)

Pediatric Radiotherapy Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Maria Luisa Garrè (ML)

Neuroncology and Neurosurgery Unit, Istituto Giannina Gaslini, Genova, Italy.

Daniele Bertin (D)

Pediatric Onco-Hematology Unit, Azienda Ospedaliera Città della Salute e della Scienza di Torino, Torino, Italy.

Angela Mastronuzzi (A)

Department of Pediatric Hematology and Oncology, Ospedale Pediatrico Bambino Gesù, Rome, Italy.

Maurizio Mascarin (M)

Department of Pediatric Radiotherapy, CRO, Aviano, Italy.

Lucia Quaglietta (L)

Pediatric Oncology Unit, Ospedale Santobono-Pausilipon, Napoli, Italy.

Elisabetta Viscardi (E)

Pediatric Oncology Unit, Padova University, Padova, Italy.

Iacopo Sardi (I)

Department of Neuroncology, Ospedale Pediatrico Meyer, Firenze, Italy.

Antonio Ruggiero (A)

Pediatric Oncology Unit, Policlinico A. Gemelli, Roma, Italy.

Luna Boschetti (L)

Pediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Marzia Giagnacovo (M)

Laboratory of Genetics, S. Anna General Hospital, Como, Italy.

Veronica Biassoni (V)

Pediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Elisabetta Schiavello (E)

Pediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Luisa Chiapparini (L)

Radiology Unit, IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Alessandra Erbetta (A)

Radiology Unit, IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Anna Mussano (A)

Radiotherapy Unit, Department of Oncology, Azienda Ospedaliera Città della Salute e della Scienza di Torino, Torino, Italy.

Carlo Giussani (C)

Neurosurgery Unit, Università Bicocca, Monza, Italy.

Rosa Maria Mura (RM)

Pediatric Oncology Unit, AO Brotzu, Cagliari, Italy.

Salvina Barra (S)

Pediatric Radiotherapy and Special Techniques Unit, Ospedale Policlinico San Martino, Genova, Italy.

Giovanni Scarzello (G)

Radiotherapy Unit, Istituto Oncologico del Veneto-IOV IRCCS, Padova, Italy.

Giuseppe Scimone (G)

Radiotherapy Unit, Azienda Ospedaliera Universitaria S. Giovanni di Dio e Ruggi D'Aragona, Salerno, Italy.
Neuropathology Laboratory IRCCS Neuromed, Pozzilli, Italy.

Andrea Carai (A)

Department of Neurosciences, Neurosurgery Unit, Ospedale Pediatrico Bambino Gesù, Rome, Italy.

Felice Giangaspero (F)

Department of Radiological, Oncological, and Anatomo-Pathological Sciences, La Sapienza University, Rome, Italy.

Francesca Romana Buttarelli (FR)

Department of Neurology and Psychiatry, La Sapienza University, Rome, Italy.

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