Segmentation of cellular patterns in confocal images of melanocytic lesions in vivo via a multiscale encoder-decoder network (MED-Net).

Journal: Medical image analysis
Published Date:

Abstract

In-vivo optical microscopy is advancing into routine clinical practice for non-invasively guiding diagnosis and treatment of cancer and other diseases, and thus beginning to reduce the need for traditional biopsy. However, reading and analysis of the optical microscopic images are generally still qualitative, relying mainly on visual examination. Here we present an automated semantic segmentation method called "Multiscale Encoder-Decoder Network (MED-Net)" that provides pixel-wise labeling into classes of patterns in a quantitative manner. The novelty in our approach is the modeling of textural patterns at multiple scales (magnifications, resolutions). This mimics the traditional procedure for examining pathology images, which routinely starts with low magnification (low resolution, large field of view) followed by closer inspection of suspicious areas with higher magnification (higher resolution, smaller fields of view). We trained and tested our model on non-overlapping partitions of 117 reflectance confocal microscopy (RCM) mosaics of melanocytic lesions, an extensive dataset for this application, collected at four clinics in the US, and two in Italy. With patient-wise cross-validation, we achieved pixel-wise mean sensitivity and specificity of 74% and 92%, respectively, with 0.74 Dice coefficient over six classes. In the scenario, we partitioned the data clinic-wise and tested the generalizability of the model over multiple clinics. In this setting, we achieved pixel-wise mean sensitivity and specificity of 77% and 94%, respectively, with 0.77 Dice coefficient. We compared MED-Net against the state-of-the-art semantic segmentation models and achieved better quantitative segmentation performance. Our results also suggest that, due to its nested multiscale architecture, the MED-Net model annotated RCM mosaics more coherently, avoiding unrealistic-fragmented annotations.

Authors

  • Kivanc Kose
    Dermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA. Electronic address: kosek@mskcc.org.
  • Alican Bozkurt
    Electrical and Computer Engineering, Northeastern University, Boston, Massachusetts, USA.
  • Christi Alessi-Fox
    Caliber Imaging and Diagnostics, Inc, Rochester, New York, USA.
  • Melissa Gill
    Department of Pathology, SUNY Downstate Medical Center, Brooklyn, New York, USA; SkinMedical Research and Diagnostics, PLLC, Dobbs Ferry, New York, USA.
  • Caterina Longo
    Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy; Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Centro Oncologico ad Alta Tecnologia Diagnostica-Dermatologia, Reggio Emilia, Italy.
  • Giovanni Pellacani
    Facolta di Medicina et Chirugia, UNIMORE Iniversita Degli Studi di Modena e Reggio Emilia, Modena, Italy.
  • Jennifer G Dy
  • Dana H Brooks
    SPIRAL Group, ECE Dept, Northeastern University, Boston, MA, USA.
  • Milind Rajadhyaksha
    Dermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.