The Society for Immunotherapy of Cancer statement on best practices for multiplex immunohistochemistry (IHC) and immunofluorescence (IF) staining and validation

Janis M. Taube(Bloomberg (United States)), Güray Aktürk(Icahn School of Medicine at Mount Sinai), Michael Angelo(Stanford University), Elizabeth L. Engle(Bloomberg (United States)), Sacha Gnjatic(Icahn School of Medicine at Mount Sinai), Shirley Greenbaum(Stanford University), Noah F. Greenwald(Stanford University), Cyrus V. Hedvat(Bristol-Myers Squibb (United States)), Travis J. Hollmann(Memorial Sloan Kettering Cancer Center), Jonathan Juco(Merck & Co., Inc., Rahway, NJ, USA (United States)), Edwin R. Parra(The University of Texas MD Anderson Cancer Center), Marlon C. Rebelatto(AstraZeneca (United States)), David L. Rimm(Yale University), Jaime Rodriguez‐Canales(AstraZeneca (United States)), Kurt A. Schalper(Yale University), Edward C. Stack, Cláudia S. Ferreira(Roche Pharma AG (Germany)), Konstanty Korski(Roche Pharma AG (Germany)), Ana Lako(Harvard University), Scott J. Rodig(Harvard University), Emanuel Schenck(AstraZeneca (United States)), Keith E. Steele(AstraZeneca (United States)), Michael Surace(AstraZeneca (United States)), Michael T. Tetzlaff(The University of Texas MD Anderson Cancer Center), Katharina von Loga(Royal Marsden NHS Foundation Trust), Ignacio I. Wistuba(The University of Texas MD Anderson Cancer Center), Carlo Bifulco(Providence Portland Medical Center)
Journal for ImmunoTherapy of Cancer
May 1, 2020
Cited by 285Open Access
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Abstract

OBJECTIVES: The interaction between the immune system and tumor cells is an important feature for the prognosis and treatment of cancer. Multiplex immunohistochemistry (mIHC) and multiplex immunofluorescence (mIF) analyses are emerging technologies that can be used to help quantify immune cell subsets, their functional state, and their spatial arrangement within the tumor microenvironment. METHODS: The Society for Immunotherapy of Cancer (SITC) convened a task force of pathologists and laboratory leaders from academic centers as well as experts from pharmaceutical and diagnostic companies to develop best practice guidelines for the optimization and validation of mIHC/mIF assays across platforms. RESULTS: Representative outputs and the advantages and disadvantages of mIHC/mIF approaches, such as multiplexed chromogenic IHC, multiplexed immunohistochemical consecutive staining on single slide, mIF (including multispectral approaches), tissue-based mass spectrometry, and digital spatial profiling are discussed. CONCLUSIONS: mIHC/mIF technologies are becoming standard tools for biomarker studies and are likely to enter routine clinical practice in the near future. Careful assay optimization and validation will help ensure outputs are robust and comparable across laboratories as well as potentially across mIHC/mIF platforms. Quantitative image analysis of mIHC/mIF output and data management considerations will be addressed in a complementary manuscript from this task force.


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