Evidence map›Paper›PMID 25994353›Full record

ArticleInternational journal of cancer2015

A quantitative microscopic approach to predict local recurrence based on in vivo intraoperative imaging of sarcoma tumor margins.

Jenna L Mueller, Henry L Fu, Jeffrey K Mito, Melodi J Whitley, Rhea Chitalia, Alaattin Erkanli, Leslie Dodd, Diana M Cardona, Joseph Geradts, Rebecca M Willett and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Jenna L MuellerDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.
Henry L FuDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.
Jeffrey K MitoDepartment of Pharmacology & Cancer Biology, Duke University School of Medicine, Durham, North Carolina.
Melodi J WhitleyDepartment of Pharmacology & Cancer Biology, Duke University School of Medicine, Durham, North Carolina.
Rhea ChitaliaDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.
Alaattin ErkanliDepartment of Biostatistics & Bioinformatics, Duke University, Durham, North Carolina.
Leslie DoddDepartment of Pathology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
Diana M CardonaDepartment of Pathology, Duke University Medical Center, Durham, North Carolina.
Joseph GeradtsDepartment of Pathology, Duke University Medical Center, Durham, North Carolina.
Rebecca M WillettDepartment of Electrical and Computer Engineering, University of Wisconsin-Madison, Madison, Wisconsin.
David G KirschDepartment of Pharmacology & Cancer Biology, Duke University School of Medicine, Durham, North Carolina.
Nimmi RamanujamDepartment of Biomedical Engineering, Duke University, Durham, North Carolina.
Duke University · USDuke Medical Center · USUniversity of North Carolina at Chapel Hill · USUniversity of Wisconsin–Madison · US

Funding

A Novel Optical Spectral Imaging System for Rapid Imaging of Breast Tumor MarginsR01EB011574 · NIBIB · DUKE UNIVERSITY · PI RAMANUJAM, NIRMALA · 2011 to 2015
$4.9M
NIBIB NIH HHS 1R01 EB011574NIBIB NIH HHS R01 EB011574
6 · The paper itself

Abstract

The goal of resection of soft tissue sarcomas located in the extremity is to preserve limb function while completely excising the tumor with a margin of normal tissue. With surgery alone, one-third of patients with soft tissue sarcoma of the extremity will have local recurrence due to microscopic residual disease in the tumor bed. Currently, a limited number of intraoperative pathology-based techniques are used to assess margin status; however, few have been widely adopted due to sampling error and time constraints. To aid in intraoperative diagnosis, we developed a quantitative optical microscopy toolbox, which includes acriflavine staining, fluorescence microscopy, and analytic techniques called sparse component analysis and circle transform to yield quantitative diagnosis of tumor margins. A series of variables were quantified from images of resected primary sarcomas and used to optimize a multivariate model. The sensitivity and specificity for differentiating positive from negative ex vivo resected tumor margins was 82 and 75%. The utility of this approach was tested by imaging the in vivo tumor cavities from 34 mice after resection of a sarcoma with local recurrence as a bench mark. When applied prospectively to images from the tumor cavity, the sensitivity and specificity for differentiating local recurrence was 78 and 82%. For comparison, if pathology was used to predict local recurrence in this data set, it would achieve a sensitivity of 29% and a specificity of 71%. These results indicate a robust approach for detecting microscopic residual disease, which is an effective predictor of local recurrence.

Indexed as

AnimalsBone NeoplasmsDiagnostic ImagingHumansImage Processing, Computer-AssistedIntraoperative CareMiceNeoplasm, ResidualProspective StudiesSarcomaSensitivity and Specificityimage analysisintraoperative imaginglogistic modelsoptical fluorescence imagingsoft tissue sarcoma

Identifiers

PMID25994353
PMCPMC4575838
OpenAlexW1827503259

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.