Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy

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Standard

Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy. / Jepsen, Dea Natalie Munch; Høeg, Henrik; Bzorek, Michael; Orhan, Adile; Eriksen, Jens Ole; Gögenur, Ismail; Reiss, Björn; Fiehn, Anne Marie Kanstrup.

I: Human Pathology, Bind 144, 2024, s. 61-70.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jepsen, DNM, Høeg, H, Bzorek, M, Orhan, A, Eriksen, JO, Gögenur, I, Reiss, B & Fiehn, AMK 2024, 'Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy', Human Pathology, bind 144, s. 61-70. https://doi.org/10.1016/j.humpath.2023.12.010

APA

Jepsen, D. N. M., Høeg, H., Bzorek, M., Orhan, A., Eriksen, J. O., Gögenur, I., Reiss, B., & Fiehn, A. M. K. (2024). Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy. Human Pathology, 144, 61-70. https://doi.org/10.1016/j.humpath.2023.12.010

Vancouver

Jepsen DNM, Høeg H, Bzorek M, Orhan A, Eriksen JO, Gögenur I o.a. Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy. Human Pathology. 2024;144:61-70. https://doi.org/10.1016/j.humpath.2023.12.010

Author

Jepsen, Dea Natalie Munch ; Høeg, Henrik ; Bzorek, Michael ; Orhan, Adile ; Eriksen, Jens Ole ; Gögenur, Ismail ; Reiss, Björn ; Fiehn, Anne Marie Kanstrup. / Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy. I: Human Pathology. 2024 ; Bind 144. s. 61-70.

Bibtex

@article{2b1ee02d28cc4926bfd1d561b022c608,
title = "Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy",
abstract = "A frequently used treatment strategy in locally advanced rectal cancer (RC) is neoadjuvant therapy followed by surgery. Patients treated with neoadjuvant therapy achieve varying pathological response, and currently, predicting the degree of response is challenging. This study examined the association between digitally assessed histopathological features in the diagnostic biopsies and pathological response to neoadjuvant therapy, aiming to find potential predictive biomarkers. 50 patients with RC treated with neoadjuvant chemotherapy and/or radiotherapy followed by surgery were included. Deep learning-based digital algorithms were used to assess the epithelium tumor area percentage (ETP) based on H&E-stained slides, and to quantify the density of CD3+ and CD8+ lymphocytes, as well as the CD8+/CD3+ lymphocyte percentage, based on immunohistochemically stained slides, from the diagnostic tumor biopsies. Pathological response was assessed according to the Mandard method. A good pathological response was defined as tumor regression grade (TRG) 1–2, and a complete pathological response was defined as Mandard TRG 1. Associations between the ETP and lymphocyte densities in the diagnostic biopsies and the pathological response were examined. The density of CD8+ lymphocytes, and the CD8+/CD3+ lymphocyte percentage, were associated with both good and complete response to neoadjuvant therapy, while the density of CD3+ lymphocytes was associated with complete response. The ETP did not correlate with response to neoadjuvant therapy. It is well-known that infiltration of lymphocytes in colorectal cancer is a prognostic biomarker. However, assessment of CD8+ and CD3+ lymphocytes in the diagnostic tumor biopsies of patients with RC may also be useful in predicting response to neoadjuvant therapy.",
keywords = "Deep learning, Digital image analysis, Lymphocyte infiltration, Neoadjuvant therapy, Pathological response, Rectal cancer",
author = "Jepsen, {Dea Natalie Munch} and Henrik H{\o}eg and Michael Bzorek and Adile Orhan and Eriksen, {Jens Ole} and Ismail G{\"o}genur and Bj{\"o}rn Reiss and Fiehn, {Anne Marie Kanstrup}",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors",
year = "2024",
doi = "10.1016/j.humpath.2023.12.010",
language = "English",
volume = "144",
pages = "61--70",
journal = "Human Pathology",
issn = "0046-8177",
publisher = "W.B.Saunders Co.",

}

RIS

TY - JOUR

T1 - Digitally assessed lymphocyte infiltration in rectal cancer biopsies is associated with pathological response to neoadjuvant therapy

AU - Jepsen, Dea Natalie Munch

AU - Høeg, Henrik

AU - Bzorek, Michael

AU - Orhan, Adile

AU - Eriksen, Jens Ole

AU - Gögenur, Ismail

AU - Reiss, Björn

AU - Fiehn, Anne Marie Kanstrup

N1 - Publisher Copyright: © 2024 The Authors

PY - 2024

Y1 - 2024

N2 - A frequently used treatment strategy in locally advanced rectal cancer (RC) is neoadjuvant therapy followed by surgery. Patients treated with neoadjuvant therapy achieve varying pathological response, and currently, predicting the degree of response is challenging. This study examined the association between digitally assessed histopathological features in the diagnostic biopsies and pathological response to neoadjuvant therapy, aiming to find potential predictive biomarkers. 50 patients with RC treated with neoadjuvant chemotherapy and/or radiotherapy followed by surgery were included. Deep learning-based digital algorithms were used to assess the epithelium tumor area percentage (ETP) based on H&E-stained slides, and to quantify the density of CD3+ and CD8+ lymphocytes, as well as the CD8+/CD3+ lymphocyte percentage, based on immunohistochemically stained slides, from the diagnostic tumor biopsies. Pathological response was assessed according to the Mandard method. A good pathological response was defined as tumor regression grade (TRG) 1–2, and a complete pathological response was defined as Mandard TRG 1. Associations between the ETP and lymphocyte densities in the diagnostic biopsies and the pathological response were examined. The density of CD8+ lymphocytes, and the CD8+/CD3+ lymphocyte percentage, were associated with both good and complete response to neoadjuvant therapy, while the density of CD3+ lymphocytes was associated with complete response. The ETP did not correlate with response to neoadjuvant therapy. It is well-known that infiltration of lymphocytes in colorectal cancer is a prognostic biomarker. However, assessment of CD8+ and CD3+ lymphocytes in the diagnostic tumor biopsies of patients with RC may also be useful in predicting response to neoadjuvant therapy.

AB - A frequently used treatment strategy in locally advanced rectal cancer (RC) is neoadjuvant therapy followed by surgery. Patients treated with neoadjuvant therapy achieve varying pathological response, and currently, predicting the degree of response is challenging. This study examined the association between digitally assessed histopathological features in the diagnostic biopsies and pathological response to neoadjuvant therapy, aiming to find potential predictive biomarkers. 50 patients with RC treated with neoadjuvant chemotherapy and/or radiotherapy followed by surgery were included. Deep learning-based digital algorithms were used to assess the epithelium tumor area percentage (ETP) based on H&E-stained slides, and to quantify the density of CD3+ and CD8+ lymphocytes, as well as the CD8+/CD3+ lymphocyte percentage, based on immunohistochemically stained slides, from the diagnostic tumor biopsies. Pathological response was assessed according to the Mandard method. A good pathological response was defined as tumor regression grade (TRG) 1–2, and a complete pathological response was defined as Mandard TRG 1. Associations between the ETP and lymphocyte densities in the diagnostic biopsies and the pathological response were examined. The density of CD8+ lymphocytes, and the CD8+/CD3+ lymphocyte percentage, were associated with both good and complete response to neoadjuvant therapy, while the density of CD3+ lymphocytes was associated with complete response. The ETP did not correlate with response to neoadjuvant therapy. It is well-known that infiltration of lymphocytes in colorectal cancer is a prognostic biomarker. However, assessment of CD8+ and CD3+ lymphocytes in the diagnostic tumor biopsies of patients with RC may also be useful in predicting response to neoadjuvant therapy.

KW - Deep learning

KW - Digital image analysis

KW - Lymphocyte infiltration

KW - Neoadjuvant therapy

KW - Pathological response

KW - Rectal cancer

U2 - 10.1016/j.humpath.2023.12.010

DO - 10.1016/j.humpath.2023.12.010

M3 - Journal article

C2 - 38157991

AN - SCOPUS:85183941788

VL - 144

SP - 61

EP - 70

JO - Human Pathology

JF - Human Pathology

SN - 0046-8177

ER -

ID: 382979196