Spatial Characterization of Tumor-Infiltrating Lymphocytes and Breast Cancer Progression.

TILs breast cancer computational pathology machine learning risk of recurrence

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
26 Apr 2022
Historique:
received: 17 03 2022
revised: 09 04 2022
accepted: 15 04 2022
entrez: 14 5 2022
pubmed: 15 5 2022
medline: 15 5 2022
Statut: epublish

Résumé

Tumor-infiltrating lymphocytes (TILs) have been established as a robust prognostic biomarker in breast cancer, with emerging utility in predicting treatment response in the adjuvant and neoadjuvant settings. In this study, the role of TILs in predicting overall survival and progression-free interval was evaluated in two independent cohorts of breast cancer from the Cancer Genome Atlas (TCGA BRCA) and the Carolina Breast Cancer Study (UNC CBCS). We utilized machine learning and computer vision algorithms to characterize TIL infiltrates in digital whole-slide images (WSIs) of breast cancer stained with hematoxylin and eosin (H&E). Multiple parameters were used to characterize the global abundance and spatial features of TIL infiltrates. Univariate and multivariate analyses show that large aggregates of peritumoral and intratumoral TILs (forests) were associated with longer survival, whereas the absence of intratumoral TILs (deserts) is associated with increased risk of recurrence. Patients with two or more high-risk spatial features were associated with significantly shorter progression-free interval (PFI). This study demonstrates the practical utility of Pathomics in evaluating the clinical significance of the abundance and spatial patterns of distribution of TIL infiltrates as important biomarkers in breast cancer.

Identifiants

pubmed: 35565277
pii: cancers14092148
doi: 10.3390/cancers14092148
pmc: PMC9105398
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : U24CA215109
Pays : United States
Organisme : NCI NIH HHS
ID : P30CA016086
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008444
Pays : United States
Organisme : NCI NIH HHS
ID : NIH/NCI P50-CA58223
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA058223
Pays : United States
Organisme : NCI NIH HHS
ID : UH3CA225021
Pays : United States
Organisme : NCI NIH HHS
ID : P01CA151135
Pays : United States
Organisme : NCI NIH HHS
ID : F31 CA257388
Pays : United States

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Auteurs

Danielle J Fassler (DJ)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Luke A Torre-Healy (LA)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Rajarsi Gupta (R)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Alina M Hamilton (AM)

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Soma Kobayashi (S)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Sarah C Van Alsten (SC)

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Yuwei Zhang (Y)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Tahsin Kurc (T)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Richard A Moffitt (RA)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Melissa A Troester (MA)

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Katherine A Hoadley (KA)

Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Joel Saltz (J)

Department of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11790, USA.

Classifications MeSH