Evidence map›Paper›PMID 28245291›Full record

ArticlePloS one2017

Progressive disease in glioblastoma: Benefits and limitations of semi-automated volumetry.

Thomas Huber, Georgina Alber, Stefanie Bette, Johannes Kaesmacher, Tobias Boeckh-Behrens, Jens Gempt, Florian Ringel, Hanno M Specht, Bernhard Meyer, Claus Zimmer and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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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 at 1 institution in 1 country.

Thomas HuberDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.ORCID http://orcid.org/0000-0002-8167-8651
Georgina AlberDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Stefanie BetteDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Johannes KaesmacherDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Tobias Boeckh-BehrensDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Jens GemptDepartment of Neurosurgery, Klinikum rechts der Isar, Technical University of Munich, Germany.
Florian RingelDepartment of Neurosurgery, Klinikum rechts der Isar, Technical University of Munich, Germany.
Hanno M SpechtDepartment of Radiation Oncology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Bernhard MeyerDepartment of Neurosurgery, Klinikum rechts der Isar, Technical University of Munich, Germany.
Claus ZimmerDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Benedikt WiestlerDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
Jan S KirschkeDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Germany.
TUM Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeUnambiguous evaluation of glioblastoma (GB) progression is crucial, both for clinical trials as well as day by day routine management of GB patients. 3D-volumetry in the follow-up of GB provides quantitative data on tumor extent and growth, and therefore has the potential to facilitate objective disease assessment. The present study investigated the utility of absolute changes in volume (delta) or regional, segmentation-based subtractions for detecting disease progression in longitudinal MRI follow-ups.

methods165 high resolution 3-Tesla MRIs of 30 GB patients (23m, mean age 60.2y) were retrospectively included in this single center study. Contrast enhancement (CV) and tumor-related signal alterations in FLAIR images (FV) were semi-automatically segmented. Delta volume (dCV, dFV) and regional subtractions (sCV, sFV) were calculated. Disease progression was classified for every follow-up according to histopathologic results, decisions of the local multidisciplinary CNS tumor board and a consensus rating of the neuro-radiologic report.

resultsA generalized logistic mixed model for disease progression (yes / no) with dCV, dFV, sCV and sFV as input variables revealed that only dCV was significantly associated with prediction of disease progression (P = .005). Delta volume had a better accuracy than regional, segmentation-based subtractions (79% versus 72%) and a higher area under the curve by trend in ROC curves (.83 versus .75).

conclusionAbsolute volume changes of the contrast enhancing tumor part were the most accurate volumetric determinant to detect progressive disease in assessment of GB and outweighed FLAIR changes as well as regional, segmentation-based image subtractions. This parameter might be useful in upcoming objective response criteria for glioblastoma.

Indexed as

AgedBrain NeoplasmsContrast MediaFemaleGlioblastomaHumansMagnetic Resonance ImagingMaleMiddle AgedModels, TheoreticalRetrospective StudiesContrast Media

Identifiers

PMID28245291
PMCPMC5330491
OpenAlexW2593069390

What OpenQuestion holds

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Registered trials

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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.