Evidence map›Paper›PMID 35991912›Full record

ArticleBiomedical optics express2022

Clinical label-free endoscopic imaging of biochemical and metabolic autofluorescence biomarkers of benign, precancerous, and cancerous oral lesions.

Elvis Duran-Sierra, Shuna Cheng, Rodrigo Cuenca, Beena Ahmed, Jim Ji, Vladislav V Yakovlev, Mathias Martinez, Moustafa Al-Khalil, Hussain Al-Enazi, Javier A Jo

Open access · goldAbstract read
In one paragraph

Article in Biomedical optics express, 2022. 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 21% 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, 9 citations in OpenAlex.

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

10 authors at 5 institutions in 3 countries.

Elvis Duran-SierraDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Shuna ChengDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Rodrigo CuencaSchool of Electrical and Computer Engineering, University of Oklahoma, Norman, OK 73019, USA.
Beena AhmedSchool of Electrical Engineering and Telecommunications, University of New South Wales, Sydney 2052, Australia.
Jim JiDepartment of Electrical and Computer Engineering, Texas A&M University at Qatar, Doha 23874, Qatar.
Vladislav V YakovlevDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID https://orcid.org/0000-0002-4557-1013
Mathias MartinezDepartment of Cranio-Maxillofacial Surgery, Hamad Medical Corporation, Doha 3050, Qatar.
Moustafa Al-KhalilDepartment of Cranio-Maxillofacial Surgery, Hamad Medical Corporation, Doha 3050, Qatar.
Hussain Al-EnaziDepartment of Otorhinolaryngology Head and Neck Surgery, Hamad Medical Corporation, Doha 3050, Qatar.
Javier A JoSchool of Electrical and Computer Engineering, University of Oklahoma, Norman, OK 73019, USA.
Hamad Medical Corporation · QAMitchell Institute · USUniversity of Oklahoma · USTexas A&M University at Qatar · QAUNSW Sydney · AU

Funding

Endogenous fluorescence lifetime endoscopy for early detection of oral cancer and dysplasiaR01CA218739 · NCI · UNIVERSITY OF OKLAHOMA · PI JO, JAVIER ANTONIO · 2018 to 2023
$2.5M
NCI NIH HHS R01 CA218739
6 · The paper itself

Abstract

Early detection is critical for improving the survival rate and quality of life of oral cancer patients; unfortunately, dysplastic and early-stage cancerous oral lesions are often difficult to distinguish from oral benign lesions during standard clinical oral examination. Therefore, there is a critical need for novel clinical technologies that would enable reliable oral cancer screening. The autofluorescence properties of the oral epithelial tissue provide quantitative information about morphological, biochemical, and metabolic tissue and cellular alterations accompanying carcinogenesis. This study aimed to identify novel biochemical and metabolic autofluorescence biomarkers of oral dysplasia and cancer that could be clinically imaged using novel multispectral autofluorescence lifetime imaging (maFLIM) endoscopy technologies. In vivo maFLIM clinical endoscopic images of benign, precancerous, and cancerous lesions from 67 patients were acquired using a novel maFLIM endoscope. Widefield maFLIM feature maps were generated, and statistical analyses were applied to identify maFLIM features providing contrast between dysplastic/cancerous vs. benign oral lesions. A total of 14 spectral and time-resolved maFLIM features were found to provide contrast between dysplastic/cancerous vs. benign oral lesions, representing novel biochemical and metabolic autofluorescence biomarkers of oral epithelial dysplasia and cancer. To the best of our knowledge, this is the first demonstration of clinical widefield maFLIM endoscopic imaging of novel biochemical and metabolic autofluorescence biomarkers of oral dysplasia and cancer, supporting the potential of maFLIM endoscopy for early detection of oral cancer.

Identifiers

PMID35991912
PMCPMC9352301
OpenAlexW4281486611

What OpenQuestion holds

Textmetadata
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.