Evidence map›Paper›PMID 33134652›Full record

ArticleIEEE transactions on radiation and plasma medical sciences2019

Combining structural and textural assessments of volumetric FDG-PET uptake in NSCLC.

Eric Wolsztynski, Janet O'Sullivan, Nicola M Hughes, Tian Mou, Peter Murphy, Finbarr O'Sullivan, Kevin O'Regan

Abstract read
In one paragraph

Article in IEEE transactions on radiation and plasma medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
  3. Article
  4. Article
  5. Review
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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

7 authors.

Eric WolsztynskiDepartment of Statistics, School of Mathematical Sciences, University College Cork, T12 XY86, Ireland.
Janet O'SullivanDepartment of Statistics, School of Mathematical Sciences, University College Cork, T12 XY86, Ireland.
Nicola M HughesRoyal College of Surgeons in Ireland, Dublin, Ireland.
Tian MouDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.
Peter MurphyPET/CT Unit (Alliance Medical), Cork University Hospital, Cork, Ireland.
Finbarr O'SullivanDepartment of Statistics, School of Mathematical Sciences, University College Cork, T12 XY86, Ireland.
Kevin O'ReganDepartment of Radiology, Cork University Hospital, Cork, Ireland.

Funding

RadiochemistryP01CA042045 · NCI · UNIVERSITY OF WASHINGTON · PI LINK, JEANNE MEYERS · 1986 to 2015
$23.2M
Area B: Multi-Tracer Volumetric PET (MTV-PET) to Measure Tumor Glutamine and Glucose Metabolic Rates in a Single Imaging SessionR33CA225310 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KARP, JOEL S, MANKOFF, DAVID A. · 2017 to 2017
$1.4M
NCI NIH HHS P01 CA042045NCI NIH HHS R33 CA225310
6 · The paper itself

Abstract

Numerous studies have reported the prognostic utility of texture analyses and the effectiveness of radiomics in PET and PET/CT assessment of non-small cell lung cancer (NSCLC). Here we explore the potential, relative to this methodology, of an alternative model-based approach to tumour characterization, which was successfully applied to sarcoma in previous works. The spatial distribution of 3D FDG-PET uptake is evaluated in the spatial referential determined by the best-fitting ellipsoidal pattern, which provides a univariate uptake profile function of the radial position of intratumoral voxels. A group of structural features is extracted from this fit that include two heterogeneity variables and statistical summaries of local metabolic gradients. We demonstrate that these variables capture aspects of tumour metabolism that are separate to those described by conventional texture features. Prognostic model selection is performed in terms of a number of classifiers, including stepwise selection of logistic models, LASSO, random forests and neural networks with respect to two-year survival status. Our results for a cohort of 93 NSCLC patients show that structural variables have significant prognostic potential, and that they may be used in conjunction with texture features in a traditional radiomics sense, towards improved baseline multivariate models of patient overall survival. The statistical significance of these models also demonstrates the relevance of these machine learning classifiers for prognostic variable selection.

Indexed as

FDG-PETheterogeneitymachine learningmetabolic gradientnon-small cell lung cancerprognosisradiomicsspatial modelingtexture

Identifiers

PMID33134652
PMCPMC7597463

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.