Scientific Reports (Feb 2021)

Automated digital TIL analysis (ADTA) adds prognostic value to standard assessment of depth and ulceration in primary melanoma

  • Michael R. Moore,
  • Isabel D. Friesner,
  • Emanuelle M. Rizk,
  • Benjamin T. Fullerton,
  • Manas Mondal,
  • Megan H. Trager,
  • Karen Mendelson,
  • Ijeuru Chikeka,
  • Tahsin Kurc,
  • Rajarsi Gupta,
  • Bethany R. Rohr,
  • Eric J. Robinson,
  • Balazs Acs,
  • Rui Chang,
  • Harriet Kluger,
  • Bret Taback,
  • Larisa J. Geskin,
  • Basil Horst,
  • Kevin Gardner,
  • George Niedt,
  • Julide T. Celebi,
  • Robyn D. Gartrell-Corrado,
  • Jane Messina,
  • Tammie Ferringer,
  • David L. Rimm,
  • Joel Saltz,
  • Jing Wang,
  • Rami Vanguri,
  • Yvonne M. Saenger

DOI
https://doi.org/10.1038/s41598-021-82305-1
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 11

Abstract

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Abstract Accurate prognostic biomarkers in early-stage melanoma are urgently needed to stratify patients for clinical trials of adjuvant therapy. We applied a previously developed open source deep learning algorithm to detect tumor-infiltrating lymphocytes (TILs) in hematoxylin and eosin (H&E) images of early-stage melanomas. We tested whether automated digital (TIL) analysis (ADTA) improved accuracy of prediction of disease specific survival (DSS) based on current pathology standards. ADTA was applied to a training cohort (n = 80) and a cutoff value was defined based on a Receiver Operating Curve. ADTA was then applied to a validation cohort (n = 145) and the previously determined cutoff value was used to stratify high and low risk patients, as demonstrated by Kaplan–Meier analysis (p ≤ 0.001). Multivariable Cox proportional hazards analysis was performed using ADTA, depth, and ulceration as co-variables and showed that ADTA contributed to DSS prediction (HR: 4.18, CI 1.51–11.58, p = 0.006). ADTA provides an effective and attainable assessment of TILs and should be further evaluated in larger studies for inclusion in staging algorithms.