Emerging role of deep learning‐based artificial intelligence in tumor pathology DOI Creative Commons
Yahui Jiang, Meng Yang, Shuhao Wang

et al.

Cancer Communications, Journal Year: 2020, Volume and Issue: 40(4), P. 154 - 166

Published: April 1, 2020

Abstract The development of digital pathology and progression state‐of‐the‐art algorithms for computer vision have led to increasing interest in the use artificial intelligence (AI), especially deep learning (DL)‐based AI, tumor pathology. DL‐based been developed conduct all kinds work involved pathology, including diagnosis, subtyping, grading, staging, prognostic prediction, as well identification pathological features, biomarkers genetic changes. applications AI not only contribute improve diagnostic accuracy objectivity but also reduce workload pathologists subsequently enable them spend additional time on high‐level decision‐making tasks. In addition, is useful meet requirements precision oncology. However, there are still some challenges relating implementation issues algorithm validation interpretability, computing systems, unbelieving attitude pathologists, clinicians patients, regulators reimbursements. Herein, we present an overview how AI‐based approaches could be integrated into workflow discuss perspectives

Language: Английский

Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease DOI
Giampaolo Bianchini, Justin M. Balko, Ingrid A. Mayer

et al.

Nature Reviews Clinical Oncology, Journal Year: 2016, Volume and Issue: 13(11), P. 674 - 690

Published: May 17, 2016

Language: Английский

Citations

2409

Breast cancer DOI
Nadia Harbeck, Frédérique Penault‐Llorca, Javier Cortés

et al.

Nature Reviews Disease Primers, Journal Year: 2019, Volume and Issue: 5(1)

Published: Sept. 23, 2019

Language: Английский

Citations

2303

Tumour-infiltrating lymphocytes and prognosis in different subtypes of breast cancer: a pooled analysis of 3771 patients treated with neoadjuvant therapy DOI
Carsten Denkert,

Gϋnter von Minckwitz,

Silvia Darb‐Esfahani

et al.

The Lancet Oncology, Journal Year: 2017, Volume and Issue: 19(1), P. 40 - 50

Published: Dec. 8, 2017

Language: Английский

Citations

1727

Tertiary lymphoid structures in the era of cancer immunotherapy DOI
Catherine Sautès‐Fridman, Florent Petitprez, Julien Caldéraro

et al.

Nature reviews. Cancer, Journal Year: 2019, Volume and Issue: 19(6), P. 307 - 325

Published: May 15, 2019

Language: Английский

Citations

1329

Tumor microenvironment as a therapeutic target in cancer DOI
Yi Xiao, Dihua Yu

Pharmacology & Therapeutics, Journal Year: 2020, Volume and Issue: 221, P. 107753 - 107753

Published: Nov. 28, 2020

Language: Английский

Citations

1295

Single-cell profiling of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis DOI
Peter Savas, Balaji Virassamy, Chengzhong Ye

et al.

Nature Medicine, Journal Year: 2018, Volume and Issue: 24(7), P. 986 - 993

Published: June 22, 2018

Language: Английский

Citations

850

Molecular alterations in triple-negative breast cancer—the road to new treatment strategies DOI
Carsten Denkert,

Cornelia Liedtke,

Andrew Tutt

et al.

The Lancet, Journal Year: 2016, Volume and Issue: 389(10087), P. 2430 - 2442

Published: Dec. 6, 2016

Language: Английский

Citations

761

Breast Cancer Immunotherapy: Facts and Hopes DOI Open Access
Leisha A. Emens

Clinical Cancer Research, Journal Year: 2017, Volume and Issue: 24(3), P. 511 - 520

Published: Aug. 12, 2017

Abstract Immunotherapy is revolutionizing the management of multiple solid tumors, and early data have revealed clinical activity programmed cell death-1/programmed death ligand-1 (PD-1/PD-L1) antagonists in small numbers patients with metastatic breast cancer. Clinical appears more likely if tumor triple negative, PD-L1+, and/or harbors higher levels tumor-infiltrating leukocytes. Responses to atezolizumab pembrolizumab appear be durable triple-negative cancer (TNBC), suggesting that these agents may transform lives responding patients. Current efforts are focused on developing immunotherapy combinations convert nonresponders responders, deepen those responses do occur, surmount acquired resistance immunotherapy. Identifying biomarkers can predict potential for response single-agent immunotherapy, identify best a particular patient, guide salvage progressive disease high priorities development. Smart trials testing rational include robust biomarker evaluations will accelerate progress, moving us closer effective almost all Clin Cancer Res; 24(3); 511–20. ©2017 AACR.

Language: Английский

Citations

687

Assessing Tumor-Infiltrating Lymphocytes in Solid Tumors: A Practical Review for Pathologists and Proposal for a Standardized Method from the International Immuno-Oncology Biomarkers Working Group: Part 2: TILs in Melanoma, Gastrointestinal Tract Carcinomas, Non–Small Cell Lung Carcinoma and Mesothelioma, Endometrial and Ovarian Carcinomas, Squamous Cell Carcinoma of the Head and Neck, Genitourinary Carcinomas, and Primary Brain Tumors DOI
Shona Hendry, Roberto Salgado,

Thomas Gevaert

et al.

Advances in Anatomic Pathology, Journal Year: 2017, Volume and Issue: 24(6), P. 311 - 335

Published: Aug. 2, 2017

Assessment of the immune response to tumors is growing in importance as prognostic implications this are increasingly recognized, and immunotherapies evaluated implemented different tumor types. However, many approaches can be used assess describe response, which limits efforts at implementation a routine clinical biomarker. In part 1 review, we have proposed standardized methodology tumor-infiltrating lymphocytes (TILs) solid tumors, based on International Immuno-Oncology Biomarkers Working Group guidelines for invasive breast carcinoma. 2 discuss available evidence predictive value TILs common including carcinomas lung, gastrointestinal tract, genitourinary system, gynecologic head neck, well primary brain mesothelioma melanoma. The particularities emphases TIL assessment types discussed. propose adapted may standard against other compared. Standardization will help clinicians, researchers pathologists conclusively evaluate utility simple biomarker current era immunotherapy.

Language: Английский

Citations

675

Tumor-Infiltrating Lymphocytes and Prognosis: A Pooled Individual Patient Analysis of Early-Stage Triple-Negative Breast Cancers DOI
Sherene Loi, Damien Drubay, Sylvia Adams

et al.

Journal of Clinical Oncology, Journal Year: 2019, Volume and Issue: 37(7), P. 559 - 569

Published: Jan. 16, 2019

Purpose The aim of the current study was to conduct a pooled analysis studies that have investigated prognostic value tumor-infiltrating lymphocytes (TILs) in early-stage triple negative breast cancer (TNBC). Methods Participating had evaluated percentage infiltration stromally located TILs (sTILs) were quantified same manner patient diagnostic samples TNBC treated with anthracycline-based chemotherapy or without taxanes. Cox proportional hazards regression models stratified by trial used for invasive disease-free survival (iDFS; primary end point), distant (D-DFS), and overall (OS), fitting sTILs as continuous variable adjusted clinicopathologic factors. Results We collected individual data from 2,148 patients nine studies. Average age 50 years (range, 22 85 years), 33% node negative. average 23% (standard deviation, 20%), 77% 1% more sTILs. significantly lower older ( P = .001), larger tumor size .01), nodal involvement .02), histologic grade .001). A total 736 iDFS 548 D-DFS events 533 deaths observed. In multivariable model, added significant independent information all points (likelihood ratio χ 2 , 48.9 iDFS; < .001; 55.8 D-DFS; 48.5 OS; Each 10% increment corresponded an hazard 0.87 (95% CI, 0.83 0.91) iDFS, 0.79 0.88) D-DFS, 0.84 0.89) OS. node-negative ≥ 30%, 3-year 92% 89% 98%), 97% 95% 99%), OS 99% 100%). Conclusion This confirms strong role excellent high after adjuvant supports integration model TNBC. can be found at www.tilsinbreastcancer.org .

Language: Английский

Citations

660