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Digital Image Analysis for Estimating Stromal CD8+ Tumor-Infiltrating Lymphocytes in Lung Adenocarcinoma.
Jhun, Iny; Shepherd, Daniel; Hung, Yin P; Madrigal, Emilio; Le, Long P; Mino-Kenudson, Mari.
Afiliação
  • Jhun I; Department of Pathology, Stanford Health Care, Palo Alto, CA, USA.
  • Shepherd D; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Hung YP; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Madrigal E; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Le LP; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Mino-Kenudson M; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
J Pathol Inform ; 12: 28, 2021.
Article em En | MEDLINE | ID: mdl-34447608
BACKGROUND: Stromal CD8+ tumor-infiltrating lymphocytes (TILs) are an important prognostic and predictive indicator in non-small cell lung cancer (NSCLC). In this study, we aimed to develop and test the feasibility of a digital image analysis (DIA) workflow for estimating stromal CD8+ TIL density. METHODS: A DIA workflow developed in a software platform (QuPath) was applied to a specified region of interest (ROI) within the stromal compartment of dual PD-L1/CD8 immunostained slides from 50 lung adenocarcinoma patients. A random tree classifier was trained from 25 training cases and applied to 25 test cases. The DIA-estimated CD8+ TIL densities were compared to manual estimates of three pathologists, who independently quantitated the percentage of CD8+ TILs from predefined ROIs in QuPath. RESULTS: The average estimated total stromal cell count per case was 520 (range: 282-816) by QuPath and 551 (range: 265-744) by pathologists. The DIA-estimated CD8+ TIL density (mean = 16.9%) was comparable to pathologists' manual estimates (mean = 15.9%). A paired t-test showed no statistically significant difference between DIA and pathologist estimates of CD8+ TIL density among both training (n = 25, P = 0.55) and test (n = 25, P = 0.34) cases. There was an almost perfect agreement between QuPath and each pathologist's estimates of CD8+ TIL density (κ = 0.85-0.86). CONCLUSIONS: These findings demonstrate the feasibility of applying a DIA workflow for estimating stromal CD8+ TIL density in NSCLC. DIA has the potential to provide an efficient and standardized approach for estimating stromal CD8+ TIL density.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Pathol Inform Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Pathol Inform Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos