Evidence map›Paper›PMID 34698304›Full record

ReviewTomography (Ann Arbor, Mich.)2021

Is It Worth Considering Multicentric High-Grade Glioma a Surgical Disease? Analysis of Our Clinical Experience and Literature Review.

Francesco Guerrini, Lucio Aniello Mazzeo, Giorgio Rossi, Mariarosaria Verlotta, Mattia Del Maestro, Angela Dele Rampini, Alessandro Pesce, Marco Viganò, Sabino Luzzi, Renato Juan Galzio and 2 more

Abstract readReview
In one paragraph

Review in Tomography (Ann Arbor, Mich.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Francesco GuerriniUnit of Neurosurgery, Department of Neurosciences, Hospital A. Manzoni, 23900 Lecco, Italy.
Lucio Aniello MazzeoUnit of Neurosurgery, Department of Neurosciences, Hospital A. Manzoni, 23900 Lecco, Italy.
Giorgio RossiUnit of Pathology, Department of Oncology, Hospital A. Manzoni, 23900 Lecco, Italy.
Mariarosaria VerlottaUnit of Neurosurgery, Department of Neurosciences, Hospital A. Manzoni, 23900 Lecco, Italy.
Mattia Del MaestroUnit of Neurosurgery, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100 Pavia, Italy.
Angela Dele RampiniUnit of Neurosurgery, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100 Pavia, Italy.
Alessandro PesceUnit of Neurosurgery, Hospital S. M. Goretti, 04100 Latina, Italy.
Marco ViganòOrthopedic Biotechnology Lab, IRCCS Orthopedic Institute Galeazzi, 20161 Milan, Italy.
Sabino LuzziUnit of Neurosurgery, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100 Pavia, Italy.
Renato Juan GalzioUnit of Neurosurgery, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, 27100 Pavia, Italy.
Andrea SalmaggiUnit of Neurology, Department of Neurosciences, Hospital A. Manzoni, 23900 Lecco, Italy.
Giannantonio SpenaUnit of Neurosurgery, Department of Neurosciences, Hospital A. Manzoni, 23900 Lecco, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe simultaneous presence of multiple foci of high-grade glioma is a rare condition with a poor prognosis. By definition, if an anatomical connection through white matter bundles cannot be hypothesized, multiple lesions are defined as multicentric glioma (MC); on the other hand, when this connection exists, it is better defined as multifocal glioma (MF). Whether surgery can be advantageous for these patients has not been established yet. The aim of our study was to critically review our experience and to compare it to the existing literature. MATERIALS AND

methodsRetrospective analysis of patients operated on for MC HGG in two Italian institutions was performed. Distinction between MC and MF was achieved through revision of MR FLAIR images. Clinical and radiological preoperative and postoperative data were analyzed through chart revision and phone interviews. The same data were extracted from literature review. Univariate and multivariate analyses were conducted for the literature review only, and the null hypothesis was rejected for a

resultsSixteen patients met the inclusion criteria; male predominance and an average age of 66.5 years were detected. Sensory/motor deficit was the main onset symptom both in clinical study and literature review. A tendency to operate on the largest symptomatic lesion was reported and GTR was reached in the majority of cases. GBM was the histological diagnosis in most part of the patients. OS was 8.7 months in our series compared to 7.5 months from the literature review. Age ≤ 70 years, a postoperative KPS ≥ 70, a GTR/STR, a second surgery and adjuvant treatment were shown to be significantly associated with a better prognosis. Pathological examination revealed that MC HGG did not originate by LGG.

conclusionsMC gliomas are rare conditions with high malignancy and a poor prognosis. A maximal safe resection should be attempted whenever possible, especially in younger patients with life-threatening large mass.

Indexed as

Brain NeoplasmsGliomaAgedHumansMagnetic Resonance ImagingMalePrognosisRetrospective StudiesbrainglioblastomaMRImultifocaltumor

Identifiers

PMID34698304
PMCPMC8544720

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.