IDH wild-type grade 2 diffuse astrocytomas: prognostic factors and impact of treatments within molecular subgroups.


Journal

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

Informations de publication

Date de publication:
04 05 2022
Historique:
pubmed: 16 10 2021
medline: 10 5 2022
entrez: 15 10 2021
Statut: ppublish

Résumé

Prognostic factors and role of treatments are not well known in isocitrate dehydrogenase (IDH) wild-type (wt) grade 2 astrocytomas. The aim of this study was to define in these tumors clinical features, molecular characteristics, and prognostic factors, with particular focus on molecular subgroups defined by cIMPACT-NOW update 3. We analyzed 120 patients with confirmed diagnosis of grade 2 IDHwt astrocytoma according to WHO 2016, collected from seven Italian centers between 1999 and 2017. Median PFS and OS of the whole cohort were 18.9 and 32.6 months. Patients older than 40 years and patients with modest contrast enhancement on MRI had a shorter PFS and OS. Gross total resection yielded superior PFS and OS over non-gross total resection. PFS and OS of patients with either pTERT mutation or EGRF amplification were significantly shorter. The prognostic value of age, contrast enhancement on MRI, and extent of surgery was different within the molecular subgroups. Gross total resection was associated with increased PFS (not reached versus 14 months, p = 0.023) and OS (117.9 versus 20 months, p = 0.023) in patients without EGFR amplification, and with increased OS in those without pTERT mutation (NR vs 53.7 months, p = 0.05). Conversely, for patients with EGFR amplification or pTERT mutation, gross total resection did not yield a significant survival benefit. Patients without EGFR amplification and pTERT mutation could be observed after gross total resection.

Sections du résumé

BACKGROUND
Prognostic factors and role of treatments are not well known in isocitrate dehydrogenase (IDH) wild-type (wt) grade 2 astrocytomas. The aim of this study was to define in these tumors clinical features, molecular characteristics, and prognostic factors, with particular focus on molecular subgroups defined by cIMPACT-NOW update 3.
METHODS
We analyzed 120 patients with confirmed diagnosis of grade 2 IDHwt astrocytoma according to WHO 2016, collected from seven Italian centers between 1999 and 2017.
RESULTS
Median PFS and OS of the whole cohort were 18.9 and 32.6 months. Patients older than 40 years and patients with modest contrast enhancement on MRI had a shorter PFS and OS. Gross total resection yielded superior PFS and OS over non-gross total resection. PFS and OS of patients with either pTERT mutation or EGRF amplification were significantly shorter. The prognostic value of age, contrast enhancement on MRI, and extent of surgery was different within the molecular subgroups. Gross total resection was associated with increased PFS (not reached versus 14 months, p = 0.023) and OS (117.9 versus 20 months, p = 0.023) in patients without EGFR amplification, and with increased OS in those without pTERT mutation (NR vs 53.7 months, p = 0.05). Conversely, for patients with EGFR amplification or pTERT mutation, gross total resection did not yield a significant survival benefit.
CONCLUSION
Patients without EGFR amplification and pTERT mutation could be observed after gross total resection.

Identifiants

pubmed: 34651653
pii: 6397643
doi: 10.1093/neuonc/noab239
pmc: PMC9071340
doi:

Substances chimiques

Isocitrate Dehydrogenase EC 1.1.1.41
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

809-820

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

Roberta Rudà (R)

Department of Neuro-Oncology, University and City of Health and Science Hospital, Turin, Italy.
Department of Neurology, Castelfranco Veneto and Brain Tumor Board Treviso Hospital, Italy.

Francesco Bruno (F)

Department of Neuro-Oncology, University and City of Health and Science Hospital, Turin, Italy.

Tamara Ius (T)

Neurosurgery Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.

Antonio Silvani (A)

Department of Neuro-Oncology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Giuseppe Minniti (G)

Radiation Oncology Unit, Department of Medicine, Surgery and Neurosciences, University Hospital, Siena, Italy.

Andrea Pace (A)

Department of Neuro-Oncology, University and City of Health and Science Hospital, Turin, Italy.

Giuseppe Lombardi (G)

Department of Oncology, Veneto Institute of Oncology, Padua, Italy.

Luca Bertero (L)

Pathology Unit, Department of Medical Sciences, University of Turin, Italy.

Stefano Pizzolitto (S)

Department of Pathology, Santa Maria della Misericordia University Hospital, Udine, Italy.

Bianca Pollo (B)

Neuropathology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Marco Conti Nibali (M)

Neurosurgical Oncology Division, Department of Oncology and Hemato-Oncology, University of Milan, Italy.

Alessia Pellerino (A)

Neuro-Oncology Unit, Regina Elena National Cancer Institute, Rome, Italy.

Enrica Migliore (E)

Unit of Cancer Epidemiology (CPO Piemonte), University of Turin, Turin, Italy.

Miran Skrap (M)

Neurosurgery Unit, Department of Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.

Lorenzo Bello (L)

Department of Pathology, Santa Maria della Misericordia University Hospital, Udine, Italy.
Neurosurgical Oncology Division, Department of Oncology and Hemato-Oncology, University of Milan, Italy.

Riccardo Soffietti (R)

Department of Neuro-Oncology, University and City of Health and Science Hospital, Turin, Italy.

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Classifications MeSH