Assessing Tumor-infiltrating Lymphocytes in Solid Tumors: A Practical Review for Pathologists and Proposal for a Standardized Method From the International Immunooncology Biomarkers Working Group: Part 1: Assessing the Host Immune Response, TILs in Invasive Breast Carcinoma and Ductal Carcinoma In Situ, Metastatic Tumor Deposits and Areas for Further Research

  • Shona Hendry
    Pathology
  • Roberto Salgado
    Department of Pathology and TCRU, GZA
  • Thomas Gevaert
    Laboratory of Experimental Urology, Department of Development and Regeneration, KU Leuven
  • Tom John
    Department of Medical Oncology, Austin Health
  • Bibhusal Thapa
    Medicine, University of Melbourne
  • Michael Christie
    Department of Anatomical Pathology, Royal Melbourne Hospital, Parkville
  • Koen van de Vijver
    Divisions of Diagnostic Oncology & Molecular Pathology, Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, The Netherlands
  • M.V. Estrada
    Department of Pathology, School of Medicine, University of California, San Diego
  • Paula I. Gonzalez-Ericsson
    Breast Cancer Research Program, Vanderbilt Ingram Cancer Center, Vanderbilt University
  • Melinda Sanders
    Pathology, Microbiology and Immunology
  • Benjamin Solomon
    Medical Oncology, Peter MacCallum Cancer Centre, Melbourne
  • Cinzia Solinas
    Molecular Immunology Unit
  • Gert G.G.M. Van den Eynden
    Department of Pathology, GZA Ziekenhuizen, Antwerp
  • Yves Allory
    Université Paris-Est
  • Matthias Preusser
    Department of Medicine, Clinical Division of Oncology
  • Johannes Hainfellner
    Institute of Neurology, Comprehensive Cancer Centre Vienna, Medical University of Vienna, Vienna
  • Giancarlo Pruneri
    European Institute of Oncology
  • Andrea Vingiani
    European Institute of Oncology
  • Sandra Demaria
    Departments of Radiation Oncology and Pathology, Weill Cornell Medicine, New York, NY
  • Fraser Symmans
    Department of Pathology, University of Texas M.D. Anderson Cancer Center, Houston, TX
  • Paolo Nuciforo
    Molecular Oncology Group, Vall d’Hebron Institute of Oncology, Barcelona
  • Laura Comerma
    Molecular Oncology Group, Vall d’Hebron Institute of Oncology, Barcelona
  • E.A. Thompson
    Department of Cancer Biology, Mayo Clinic, Jacksonville, FL
  • Sunil Lakhani
    Centre for Clinical Research and School of Medicine, The University of Queensland
  • Seong-Rim Kim
    National Surgical Adjuvant Breast and Bowel Project Operations Center/NRG Oncology, Pittsburgh, PA
  • Stuart Schnitt
    Cancer Research Institute and Department of Pathology, Beth Israel Deaconess Cancer Center
  • Cecile Colpaert
    Department of Pathology, GZA Ziekenhuizen, Sint-Augustinus, Wilrijk
  • Christos Sotiriou
    Department of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles
  • Stefan J. Scherer
    Academic Medical Innovation, Novartis Pharmaceuticals Corporation, East Hanover
  • Michail Ignatiadis
    Department of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles
  • Sunil Badve
    Department of Pathology and Laboratory Medicine, Indiana University, Indianapolis, IN
  • Robert H. Pierce
    Cancer Immunotherapy Trials Network, Central Laboratory and Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA
  • Giuseppe Viale
    Department of Pathology, Istituto Europeo di Oncologia, University of Milan, Milan
  • Nicolas Sirtaine
    Department of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium
  • Frederique Penault-Llorca
    Department of Surgical Pathology and Biopathology, Jean Perrin Comprehensive Cancer Centre
  • Tomohagu Sugie
    Department of Surgery, Kansai Medical School, Hirakata, Japan
  • Susan Fineberg
    Montefiore Medical Center
  • Soonmyung Paik
    Severance Biomedical Science Institute and Department of Medical Oncology, Yonsei University College of Medicine, Seoul, South Korea
  • Ashok Srinivasan
    National Surgical Adjuvant Breast and Bowel Project Operations Center/NRG Oncology, Pittsburgh, PA
  • Andrea Richardson
    Department of Pathology, Brigham and Women’s Hospital
  • Yihong Wang
    Department of Pathology and Laboratory Medicine, Rhode Island Hospital and Lifespan Medical Center
  • Ewa Chmielik
    Tumor Pathology Department, Maria Sklodowska-Curie Memorial Cancer Center
  • Jane Brock
    Department of Pathology, Brigham and Women’s Hospital
  • Douglas B. Johnson
    Department of Medicine, Vanderbilt University Medical Centre
  • Justin Balko
    Department of Medicine, Vanderbilt University Medical Centre
  • Stephan Wienert
    Institute of Pathology, Charité Universitätsmedizin Berlin
  • Veerle Bossuyt
    Department of Pathology, Yale University School of Medicine, New Haven
  • Stefan Michiels
    Service de Biostatistique et d’Epidémiologie, Gustave Roussy, CESP, Inserm U1018, Université-Paris Sud, Université Paris-Saclay
  • Nils Ternes
    Service de Biostatistique et d’Epidémiologie, Gustave Roussy, CESP, Inserm U1018, Université-Paris Sud, Université Paris-Saclay
  • Nicole Burchardi
    German Breast Group GmbH, Neu-Isenburg, Germany
  • Stephen J. Luen
    Medical Oncology, Peter MacCallum Cancer Centre, Melbourne
  • Peter Savas
    Medical Oncology, Peter MacCallum Cancer Centre, Melbourne
  • Frederick Klauschen
    Institute of Pathology, Charité Universitätsmedizin Berlin
  • Peter H. Watson
    Trev & Joyce Deeley Research Centre, British Columbia Cancer Agency
  • Brad H. Nelson
    Trev & Joyce Deeley Research Centre, British Columbia Cancer Agency
  • Carmen Criscitiello
    European Institute of Oncology
  • Sandra O’Toole
    The Cancer Research Program, Garvan Institute of Medical Research, Darlinghurst
  • Denis Larsimont
    Department of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium
  • Roland de Wind
    Department of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium
  • Giuseppe Curigliano
    European Institute of Oncology
  • Fabrice André
    INSERM Unit U981, and Department of Medical Oncology, Gustave Roussy, Villejuif
  • Magali Lacroix-Triki
    INSERM Unit U981, and Department of Medical Oncology, Gustave Roussy, Villejuif
  • Mark van de Vijver
    Department of Surgical Oncology, Netherlands Cancer Institute
  • Federico Rojo
    Pathology Department, IIS-Fundacion Jimenez Diaz, UAM, Madrid, Spain
  • Giuseppe Floris
    Department of Pathology, University Hospital Leuven, Leuven, Belgium
  • Shahinaz Bedri
    Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, Doha, Qatar
  • Joseph Sparano
    Department of Oncology, Montefiore Medical Centre, Albert Einstein College of Medicine
  • David Rimm
    Department of Pathology, Yale University School of Medicine, New Haven
  • Torsten Nielsen
    Department of Pathology and Laboratory Medicine, Genetic Pathology Evaluation Centre, University of British Columbia, Vancouver, BC
  • Zuzana Kos
    Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Canada
  • Stephen Hewitt
    Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda
  • Baljit Singh
    Department of Pathology, New York University Langone Medical Centre
  • Gelareh Farshid
    Directorate of Surgical Pathology, SA Pathology
  • Sibylle Loibl
    German Breast Group GmbH, Neu-Isenburg, Germany
  • Kimberly H. Allison
    Pathology Department, Stanford University Medical Centre, Stanford
  • Nadine Tung
    Division of Hematology-Oncology, Beth Israel Deaconess Medical Center
  • Sylvia Adams
    New York University Medical School
  • Karen Willard-Gallo
    Molecular Immunology Unit
  • Hugo M. Horlings
    Department of Pathology
  • Leena Gandhi
    Dana-Farber Cancer Institute, Boston, MA
  • Andre Moreira
    Pulmonary Pathology, New York University Center for Biospecimen Research and Development, New York University
  • Fred Hirsch
    Department of Medicine, Division of Medical Oncology, University of Colorado Anschutz Medical Campus, Aurora, CO
  • Maria V. Dieci
    Department of Surgery, Oncology and Gastroenterology, University of Padova
  • Maria Urbanowicz
    European Organisation for Research and Treatment of Cancer (EORTC) Headquarters
  • Iva Brcic
    Institute of Pathology, Medical University of Graz, Austria
  • Konstanty Korski
    Pathology and Tissue Analytics, Roche Innovation Centre Munich, Penzberg
  • Fabien Gaire
    Pathology and Tissue Analytics, Roche Innovation Centre Munich, Penzberg
  • Hartmut Koeppen
    Research Pathology, Genentech Inc., South San Francisco, CA
  • Amy Lo
    Department of Pathology, Stanford University, Palo Alto
  • Jennifer Giltnane
    Research Pathology, Genentech Inc., South San Francisco, CA
  • Marlon C. Rebelatto
    Translational Sciences, MedImmune, Gaithersberg, MD
  • Keith E. Steele
    Translational Sciences, MedImmune, Gaithersberg, MD
  • Jiping Zha
    Translational Sciences, MedImmune, Gaithersberg, MD
  • Kenneth Emancipator
    Translational Medicine, Merck & Co. Inc., Kenilworth, NJ
  • Jonathan W. Juco
    Translational Medicine, Merck & Co. Inc., Kenilworth, NJ
  • Carsten Denkert
    Institute of Pathology, Charité Universitätsmedizin Berlin
  • Jorge Reis-Filho
    Department of Pathology, Memorial Sloan-Kettering Cancer Center
  • Sherene Loi
    Medical Oncology, Peter MacCallum Cancer Centre, Melbourne

抄録

<jats:p>Assessment of tumor-infiltrating lymphocytes (TILs) in histopathologic specimens can provide important prognostic information in diverse solid tumor types, and may also be of value in predicting response to treatments. However, implementation as a routine clinical biomarker has not yet been achieved. As successful use of immune checkpoint inhibitors and other forms of immunotherapy become a clinical reality, the need for widely applicable, accessible, and reliable immunooncology biomarkers is clear. In part 1 of this review we briefly discuss the host immune response to tumors and different approaches to TIL assessment. We propose a standardized methodology to assess TILs in solid tumors on hematoxylin and eosin sections, in both primary and metastatic settings, based on the International Immuno-Oncology Biomarker Working Group guidelines for TIL assessment in invasive breast carcinoma. A review of the literature regarding the value of TIL assessment in different solid tumor types follows in part 2. The method we propose is reproducible, affordable, easily applied, and has demonstrated prognostic and predictive significance in invasive breast carcinoma. This standardized methodology may be used as a reference against which other methods are compared, and should be evaluated for clinical validity and utility. Standardization of TIL assessment will help to improve consistency and reproducibility in this field, enrich both the quality and quantity of comparable evidence, and help to thoroughly evaluate the utility of TILs assessment in this era of immunotherapy.</jats:p>

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