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Immune subtyping of melanoma whole slide images using multiple instance learning

Godson, Lucy (författare)
Univ Leeds, England
Alemi, Navid (författare)
Univ Leeds, England
Nsengimana, Jeremie (författare)
Newcastle Univ, England
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Cook, Graham P. (författare)
Leeds Teaching Hosp NHS Trust, England
Clarke, Emily L. (författare)
Leeds Teaching Hosp NHS Trust, England; Univ Leeds, England
Treanor, Darren (författare)
Linköpings universitet,Avdelningen för inflammation och infektion,Medicinska fakulteten,Centrum för medicinsk bildvetenskap och visualisering, CMIV,Region Östergötland, Klinisk patologi,Leeds Teaching Hosp NHS Trust, England; Univ Leeds, England
Bishop, D. Timothy (författare)
Univ Leeds, England
Newton-Bishop, Julia (författare)
Univ Leeds, England
Gooya, Ali (författare)
Univ Glasgow, Scotland
Magee, Derek (författare)
Univ Leeds, England
visa färre...
 (creator_code:org_t)
ELSEVIER, 2024
2024
Engelska.
Ingår i: Medical Image Analysis. - : ELSEVIER. - 1361-8415 .- 1361-8423. ; 93
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Determining early-stage prognostic markers and stratifying patients for effective treatment are two key challenges for improving outcomes for melanoma patients. Previous studies have used tumour transcriptome data to stratify patients into immune subgroups, which were associated with differential melanoma specific survival and potential predictive biomarkers. However, acquiring transcriptome data is a time-consuming and costly process. Moreover, it is not routinely used in the current clinical workflow. Here, we attempt to overcome this by developing deep learning models to classify gigapixel haematoxylin and eosin (H&E) stained pathology slides, which are well established in clinical workflows, into these immune subgroups. We systematically assess six different multiple instance learning (MIL) frameworks, using five different image resolutions and three different feature extraction methods. We show that pathology-specific self-supervised models using 10x resolution patches generate superior representations for the classification of immune subtypes. In addition, in a primary melanoma dataset, we achieve a mean area under the receiver operating characteristic curve (AUC) of 0.80 for classifying histopathology images into 'high' or 'low immune' subgroups and a mean AUC of 0.82 in an independent TCGA melanoma dataset. Furthermore, we show that these models are able to stratify patients into 'high' and 'low immune' subgroups with significantly different melanoma specific survival outcomes (log rank test, P < 0.005). We anticipate that MIL methods will allow us to find new biomarkers of high importance, act as a tool for clinicians to infer the immune landscape of tumours and stratify patients, without needing to carry out additional expensive genetic tests.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Radiologi och bildbehandling (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Radiology, Nuclear Medicine and Medical Imaging (hsv//eng)

Nyckelord

Multiple instance learning; Self-supervised learning; Computational pathology; Melanoma; Histopathology; Image classification

Publikations- och innehållstyp

ref (ämneskategori)
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