Evidence map›Paper›PMID 21724502›Full record

ArticleIEEE transactions on medical imaging2011

A statistical modeling approach to the analysis of spatial patterns of FDG-PET uptake in human sarcoma.

F O'Sullivan, E Wolsztynski, J O'Sullivan, T Richards, E U Conrad, J F Eary

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In one paragraph

Article in IEEE transactions on medical imaging, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Assessment of different quantification metrics of [Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2022
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  6. Towards enhanced PET quantification in clinical oncology.The British journal of radiology · 2018
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  7. Article
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  9. Rhabdomyosarcoma in adults: new perspectives on therapy.Current treatment options in oncology · 2015
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Role of Textural Analysis of PretreatmentIndian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
    Article
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

6 authors at 2 institutions in 2 countries.

F O'SullivanDepartment of Statistics, University College Cork, Ireland, and with the Center for Orthopedic and Sports Medicine and Division of Nuclear Medicine, University of Washington Medical Center, Seattle, WA 98195, USA. f.osullivan@ucc.ie
E Wolsztynski
J O'Sullivan
T Richards
E U Conrad
J F Eary
University College Cork · IEUniversity of Washington Medical Center · US

Funding

PET IN SARCOMA--A CLINICAL TRIALR01CA065537 · NCI · UNIVERSITY OF WASHINGTON · PI EARY, JANET F. · 1995 to 2011
$5.0M
NCI NIH HHS CA-65537NCI NIH HHS R01 CA065537
6 · The paper itself

Abstract

Clinical experience with positron emission tomography (PET) scanning of sarcoma, using fluorodeoxyglucose (FDG), has established spatial heterogeneity in the standardized uptake values within the tumor mass as a key prognostic indicator of patient survival. But it may be that a more detailed quantitation of the tumor FDG uptake pattern could provide additional insights into risk. The present work develops a statistical model for this purpose. The approach is based on a tubular representation of the tumor mass with a simplified radial analysis of uptake, transverse to the tubular axis. The technique provides novel ways of characterizing the overall profile of the tumor, including the introduction of an approach for the measurement of its phase of development. The phase measure can distinguish between early phase tumors, in which the uptake is highest at the core, and later stage masses, in which there can often be central voids in FDG uptake. Biologically, these voids arise from necrosis and fluid, fat or cartilage accumulations. The tumor profiling technique is implemented using open-source software tools and illustrations are provided with clinically representative scans. A series of FDG-PET studies from 185 patients is used to formally evaluate the prognostic benefit. Significant improvements in the prediction of patient survival and progression are obtained from the tumor profiling analysis. After adjustment for other factors including heterogeneity, a typical one standard deviation increase in phase (as determined by the analysis) is associated with close to 20% more risk of progression or death. The work confirms that more detailed quantitative assessments of the spatial pattern of PET imaging data of tumor masses, beyond the maximum FDG uptake (SUV(max)) and previously considered measures of heterogeneity, provide improved prognostic information for potential input to treatment decisions for future patients.

Indexed as

Models, BiologicalProportional Hazards ModelsFluorodeoxyglucose F18HumansKaplan-Meier EstimatePositron-Emission TomographyPrognosisRadiopharmaceuticalsRegression AnalysisSarcomaFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID21724502
PMCPMC4753574
OpenAlexW2113381603

What OpenQuestion holds

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Registered trials

None linked

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.