Association of supratotal resection with progression-free survival, malignant transformation, and overall survival in lower-grade gliomas.

lower-grade gliomas malignant progression-free survival overall survival progression-free survival supratotal resection

Journal

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

Informations de publication

Date de publication:
05 05 2021
Historique:
pubmed: 14 10 2020
medline: 21 5 2021
entrez: 13 10 2020
Statut: ppublish

Résumé

Supratotal resection is advocated in lower-grade gliomas (LGGs) based on theoretical advantages but with limited verification of functional risk and data on oncological outcomes. We assessed the association of supratotal resection in molecularly defined LGGs with oncological outcomes. Included were 460 presumptive LGGs; 404 resected; 347 were LGGs, 319 isocitrate dehydrogenase (IDH)-mutated, 28 wildtype. All patients had clinical, imaging, and molecular data. Resection aimed at supratotal resection without any patient or tumor a priori selection. The association of extent of resection (EOR), categorized on volumetric fluid attenuated inversion recovery images as residual tumor volume, along with postsurgical management with progression-free survival (PFS), malignant (M)PFS, and overall survival (OS) assessed by univariate, multivariate, and propensity score analysis. The study mainly focused on IDH-mutated LGGs, the "typical LGGs." Median follow-up was 6.8 years (interquartile range, 5-8). Out of 319 IDH-mutated LGGs, 190 (59.6%) progressed, median PFS: 4.7 years (95% CI: 4-5.3). Total and supratotal resection obtained in 39% and 35% of patients with IDH1-mutated tumors. In IDH-mutated tumors, most patients in the partial/subtotal group progressed, 82.4% in total, only 6 (5.4%) in supratotal. Median PFS was 29 months (95% CI: 25-36) in subtotal, 46 months (95% CI: 38-48) in total, while at 92 months, PFS in supratotal was 94.0%. There was no association with molecular subtypes and grade. At random forest analysis, PFS strongly associated with EOR, radiotherapy, and previous treatment. In the propensity score analysis, EOR associated with PFS (hazard ratio, 0.03; 95% CI: 0.01-0.13). MPFS occurred in 32.1% of subtotal total groups; 1 event in supratotal. EOR, grade III, previous treatment correlated to MPFS. At random forest analysis, OS associated with EOR as well. Supratotal resection strongly associated with PFS, MPFS, and OS in LGGs, regardless of molecular subtypes and grade, right from the beginning of clinical presentation.

Sections du résumé

BACKGROUND
Supratotal resection is advocated in lower-grade gliomas (LGGs) based on theoretical advantages but with limited verification of functional risk and data on oncological outcomes. We assessed the association of supratotal resection in molecularly defined LGGs with oncological outcomes.
METHODS
Included were 460 presumptive LGGs; 404 resected; 347 were LGGs, 319 isocitrate dehydrogenase (IDH)-mutated, 28 wildtype. All patients had clinical, imaging, and molecular data. Resection aimed at supratotal resection without any patient or tumor a priori selection. The association of extent of resection (EOR), categorized on volumetric fluid attenuated inversion recovery images as residual tumor volume, along with postsurgical management with progression-free survival (PFS), malignant (M)PFS, and overall survival (OS) assessed by univariate, multivariate, and propensity score analysis. The study mainly focused on IDH-mutated LGGs, the "typical LGGs."
RESULTS
Median follow-up was 6.8 years (interquartile range, 5-8). Out of 319 IDH-mutated LGGs, 190 (59.6%) progressed, median PFS: 4.7 years (95% CI: 4-5.3). Total and supratotal resection obtained in 39% and 35% of patients with IDH1-mutated tumors. In IDH-mutated tumors, most patients in the partial/subtotal group progressed, 82.4% in total, only 6 (5.4%) in supratotal. Median PFS was 29 months (95% CI: 25-36) in subtotal, 46 months (95% CI: 38-48) in total, while at 92 months, PFS in supratotal was 94.0%. There was no association with molecular subtypes and grade. At random forest analysis, PFS strongly associated with EOR, radiotherapy, and previous treatment. In the propensity score analysis, EOR associated with PFS (hazard ratio, 0.03; 95% CI: 0.01-0.13). MPFS occurred in 32.1% of subtotal total groups; 1 event in supratotal. EOR, grade III, previous treatment correlated to MPFS. At random forest analysis, OS associated with EOR as well.
CONCLUSIONS
Supratotal resection strongly associated with PFS, MPFS, and OS in LGGs, regardless of molecular subtypes and grade, right from the beginning of clinical presentation.

Identifiants

pubmed: 33049063
pii: 5922564
doi: 10.1093/neuonc/noaa225
pmc: PMC8099476
doi:

Substances chimiques

Isocitrate Dehydrogenase EC 1.1.1.41

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

812-826

Informations de copyright

© The Author(s) 2020. 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

Marco Rossi (M)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Lorenzo Gay (L)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Federico Ambrogi (F)

Laboratory of Medical Statistics, Biometry and Epidemiology "G.A.Maccararo," Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Marco Conti Nibali (M)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Tommaso Sciortino (T)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Guglielmo Puglisi (G)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Antonella Leonetti (A)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Cristina Mocellini (C)

Neuro-oncologia, Divisione di Neurologia, Ospedale Santa Croce e Carle, Cuneo, Italy.

Manuela Caroli (M)

Neurochirurgia, Fondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milano, Italy.

Susanna Cordera (S)

Neuro-oncologia, Divisione di Neurologia, Ospedale Regionale Parini, Aosta, Italy.

Matteo Simonelli (M)

Humanitas Cancer Center, Humanitas Research Hospital, IRCCS, Rozzano, Italy.

Federico Pessina (F)

Humanitas Cancer Center, Humanitas Research Hospital, IRCCS, Rozzano, Italy.

Piera Navarria (P)

Humanitas Cancer Center, Humanitas Research Hospital, IRCCS, Rozzano, Italy.

Andrea Pace (A)

Neuro-Oncologia, Istituto Nazionale Tumori Regina Elena, Roma, Italy.

Riccardo Soffietti (R)

Neuro-Oncologia, Città della Salute e della Scienza, Università di Torino, Torino, Italy.

Roberta Rudà (R)

Neuro-Oncologia, Città della Salute e della Scienza, Università di Torino, Torino, Italy.

Marco Riva (M)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

Lorenzo Bello (L)

Neurosurgical Oncology Unit, Dept of Oncology and Hemato-Oncology, Università degli Studi di Milano, Milano, Italy.
IRCCS Istituto Ortopedico Galeazzi, Neurosurgical Oncology Unit, Milano, Italy.

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