AI Article Synopsis

  • Fluorescence-guided oncology using indocyanine green (ICG) may improve the detection and treatment of colorectal cancer by studying its distribution in human tumors.
  • The research involved 50 patients, analyzing near-infrared video and imagery from both early and late post-administration of ICG, revealing notable fluorescence patterns in malignant versus benign tissue.
  • Results showed that early fluorescence primarily appeared in tissue stroma and not in malignant or healthy glands, while later stages displayed uneven fluorescence in malignant cells, suggesting potential uses for ICG in diagnosing and targeting cancerous tissues.

Article Abstract

Unlabelled: Fluorescence-guided oncology promises to improve both the detection and treatment of malignancy. We sought to investigate the temporal distribution of indocyanine green (ICG), an exogenous fluorophore in human colorectal cancer. This analysis aims to enhance our understanding of ICG's effectiveness in current tumour detection and inform potential future diagnostic and therapeutic enhancements.

Methods: Fifty consenting patients undergoing treatment for suspected/confirmed colorectal neoplasia provided near infrared (NIR) video and imagery of transanally recorded and ex vivo resected rectal lesions following intravenous ICG administration (0.25 mg/kg), with a subgroup providing tissue samples for microscopic (including near infrared) analysis. Computer vision techniques detailed macroscopic 'early' (<15 min post ICG administration) and 'late' (>2 h) tissue fluorescence appearances from surgical imagery with digital NIR scanning (Licor, Lincoln, NE, USA) and from microscopic analysis (Nikon, Tokyo, Japan) undertaken by a consultant pathologist detailing tissue-level fluorescence distribution over the same time.

Results: Significant intra-tumoural fluorescence heterogeneity was seen 'early' in malignant versus benign lesions. In all 'early' samples, fluorescence was predominantly within the tissue stroma, with uptake within plasma cells, blood vessels and lymphatics, but not within malignant or healthy glands. At 'late' stage observation, fluorescence was visualised non-uniformly within the intracellular cytoplasm of malignant tissue but not retained in benign glands. Fluorescence also accumulated within any present peritumoural inflammatory tissue.

Conclusion: This study demonstrates the time course diffusion patterns of ICG through both benign and malignant tumours in vivo in human patients at both macroscopic and microscopic levels, demonstrating important cellular drivers and features of geolocalisation and how they differ longitudinally after exposure to ICG.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10887825PMC
http://dx.doi.org/10.3390/curroncol31020063DOI Listing

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