Fibre-based fluorescence-lifetime imaging microscopy: a real-time biopsy guidance tool for suspected lung cancer

Susan Fernandes, Elvira Williams, Neil Finlayson, Hazel Stewart, Catharine Dhaliwal, David A. Dorward, William A. Wallace, Ahsan R. Akram, James Stone, Kevin Dhaliwal, Gareth O.S. Williams

Research output: Contribution to journalArticlepeer-review

Abstract

Lung cancer is the most common cause of cancer-related deaths worldwide. Early detection improves outcomes, however, existing sampling techniques are associated with suboptimal diagnostic yield and procedure-related complications. Autofluorescence-based fluorescence-lifetime imaging microscopy (FLIM), a technique which measures endogenous fluorophore decay rates, may aid identification of optimal biopsy sites in suspected lung cancer. Our fibre-based fluorescence-lifetime imaging system, utilising 488 nm excitation, which is deliverable via existing diagnostic platforms, enables real-time visualisation and lifetime analysis of distal alveolar lung structure. We evaluated the diagnostic accuracy of the fibre-based fluorescence-lifetime imaging system to detect changes in fluorescence lifetime in freshly resected ex vivo lung cancer and adjacent healthy tissue as a first step towards future translation. The study compares paired non-small cell lung cancer (NSCLC) and non-cancerous tissues with gold standard diagnostic pathology to assess the performance of the technique. Paired NSCLC and non-cancerous lung tissues were obtained from thoracic resection patients (N=21). A clinically compatible 488 nm fluorescence-lifetime endomicroscopy platform was used to acquire simultaneous fluorescence intensity and lifetime images. Fluorescence lifetimes were calculated using a computationally-lightweight, rapid lifetime determination method. Fluorescence lifetime was significantly reduced in ex vivo lung cancer, compared with non-cancerous lung tissue [mean ± standard deviation (SD), 1.79±0.40 vs. 2.15±0.26 ns, P<0.0001], and fluorescence intensity images demonstrated distortion of alveolar elastin autofluorescence structure. Fibre-based fluorescence-lifetime imaging demonstrated good performance characteristics for distinguishing lung cancer, from adjacent noncancerous tissue, with 81.0% sensitivity and 71.4% specificity. Our novel fibre-based fluorescence-lifetime imaging system, which enables label-free imaging and quantitative lifetime analysis, discriminates ex vivo lung cancer from adjacent healthy tissue. This minimally invasive technique has potential to be translated as a real-time biopsy guidance tool, capable of optimising diagnostic accuracy in lung cancer.

Original languageEnglish
Pages (from-to)355-361
Number of pages7
JournalTranslational Lung Cancer Research
Volume13
Issue number2
Early online date1 Feb 2024
DOIs
Publication statusPublished - 1 Feb 2024

Funding

This work was supported by Medical Research Council (grant No. MR/R017794/1 to S.F.); Engineering and Physical Sciences Research Council (grants Nos. EP/ K03197X/1 and EP/S025987/1 to K.D.).

FundersFunder number
The Wellcome Trust
Medical Research CouncilMR/R017794/1
Engineering and Physical Sciences Research CouncilEP/ K03197X/1, EP/S025987/1

Keywords

  • diagnostic imaging
  • fibre-optics
  • interventional pulmonology
  • Lung cancer
  • optical imaging

ASJC Scopus subject areas

  • Oncology

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