Evidence map›Paper›PMID 28609512›Full record

ArticleJournal of biomedical optics2017

Detection of precancerous lesions in the oral cavity using oblique polarized reflectance spectroscopy: a clinical feasibility study.

Maria J Bailey, Nishant Verma, Leonid Fradkin, Sylvia Lam, Calum MacAulay, Catherine Poh, Mia K Markey, Konstantin Sokolov

Open access · goldAbstract read
In one paragraph

Article in Journal of biomedical optics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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

8 authors at 2 institutions in 2 countries.

Maria J BaileyUniversity of Texas M.D. Anderson Cancer Center, Department of Imaging Physics, Houston, Texas, United StatesbUniversity of Texas at Austin, Department of Biomedical Engineering, Austin, Texas, United States.
Nishant VermaUniversity of Texas at Austin, Department of Biomedical Engineering, Austin, Texas, United States.
Leonid FradkinUniversity of Texas at Austin, Department of Biomedical Engineering, Austin, Texas, United States.
Sylvia LamBritish Columbia Cancer Agency, Integrative Oncology Department, Vancouver, British Columbia, Canada.
Calum MacAulayBritish Columbia Cancer Agency, Integrative Oncology Department, Vancouver, British Columbia, Canada.
Catherine PohBritish Columbia Cancer Agency, Integrative Oncology Department, Vancouver, British Columbia, Canada.
Mia K MarkeyUniversity of Texas M.D. Anderson Cancer Center, Department of Imaging Physics, Houston, Texas, United StatesbUniversity of Texas at Austin, Department of Biomedical Engineering, Austin, Texas, United States.
Konstantin SokolovUniversity of Texas M.D. Anderson Cancer Center, Department of Imaging Physics, Houston, Texas, United StatesbUniversity of Texas at Austin, Department of Biomedical Engineering, Austin, Texas, United StatesdRice University, Department of Bioengineering, Houston, Texas, United States.
BC Cancer Agency · CAThe University of Texas at Austin · US

Funding

Optical Systems for In Vivo Molecular Imaging of CancerR01CA103830 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI RICHARDS-KORTUM, REBECCA R. · 2004 to 2015
$12.4M
Comprehensive Training Program in Imaging Science and InformaticsT32EB007507 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI MARKEY, MIA K, RYLANDER, HENRY GRADY · 2009 to 2024
$2.7M
Polarization Spectroscopy and Imaging of Pre-CancerR01EB003540 · NIBIB · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOKOLOV, KONSTANTIN V · 2005 to 2008
$975k
NCI NIH HHS R01 CA103830NIBIB NIH HHS R01 EB003540NIBIB NIH HHS T32 EB007507
6 · The paper itself

Abstract

We developed a multifiber optical probe for oblique polarized reflectance spectroscopy (OPRS) in vivo and evaluated its performance in detection of dysplasia in the oral cavity. The probe design allows the implementation of a number of methods to enable depth resolved spectroscopic measurements including polarization gating, source–detector separation, and differential spectroscopy; this combination was evaluated in carrying out binary classification tasks between four major diagnostic categories: normal, benign, mild dysplasia (MD), and severe dysplasia (SD). Multifiber OPRS showed excellent performance in the discrimination of normal from benign, MD, SD, and MD plus SD yielding sensitivity/specificity values of 100%/93%, 96%/95%, 100%/98%, and 100%/100%, respectively. The classification of benign versus dysplastic lesions was more challenging with sensitivity and specificity values of 80%/93%, 71%/93%, and 74%/80% in discriminating benign from SD, MD, and SD plus MD categories, respectively; this challenge is most likely associated with a strong and highly variable scattering from a keratin layer that was found in these sites. Classification based on multiple fibers was significantly better than that based on any single detection pair for tasks dealing with benign versus dysplastic sites. This result indicates that the multifiber probe can perform better in the detection of dysplasia in keratinized tissues.

Indexed as

Spectrum AnalysisFeasibility StudiesHumansMouthPrecancerous ConditionsSensitivity and Specificity

Identifiers

PMID28609512
PMCPMC5469421
OpenAlexW2626544072

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.