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Multiplex Tissue Imaging Harmonization: A Multicenter Experience from CIMAC-CIDC Immuno-Oncology Biomarkers Network.

Authors :
Akturk G
Parra ER
Gjini E
Lako A
Lee JJ
Neuberg D
Zhang J
Yao S
Laface I
Rogic A
Chen PH
Sanchez-Espiridion B
Valle DMD
Moravec R
Kinders R
Hudgens C
Wu C
Wistuba II
Thurin M
Hewitt SM
Rodig S
Gnjatic S
Tetzlaff MT
Source :
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2021 Sep 15; Vol. 27 (18), pp. 5072-5083. Date of Electronic Publication: 2021 Jul 12.
Publication Year :
2021

Abstract

Purpose: The Cancer Immune Monitoring and Analysis Centers - Cancer Immunologic Data Commons (CIMAC-CIDC) network supported by the NCI Cancer Moonshot initiative was established to provide correlative analyses for clinical trials in cancer immunotherapy, using state-of-the-art technology. Fundamental to this initiative is implementation of multiplex IHC assays to define the composition and distribution of immune infiltrates within tumors in the context of their potential role as biomarkers. A critical unanswered question involves the relative fidelity of such assays to reliably quantify tumor-associated immune cells across different platforms.<br />Experimental Design: Three CIMAC sites compared across their laboratories: (i) image analysis algorithms, (ii) image acquisition platforms, (iii) multiplex staining protocols. Two distinct high-dimensional approaches were employed: multiplexed IHC consecutive staining on single slide (MICSSS) and multiplexed immunofluorescence (mIF). To eliminate variables potentially impacting assay performance, we completed a multistep harmonization process, first comparing assay performance using independent protocols followed by the integration of laboratory-specific protocols and finally, validating this harmonized approach in an independent set of tissues.<br />Results: Data generated at the final validation step showed an intersite Spearman correlation coefficient ( r ) of ≥0.85 for each marker within and across tissue types, with an overall low average coefficient of variation ≤0.1.<br />Conclusions: Our results support interchangeability of protocols and platforms to deliver robust, and comparable data using similar tissue specimens and confirm that CIMAC-CIDC analyses may therefore be used with confidence for statistical associations with clinical outcomes largely independent of site, antibody selection, protocol, and platform across different sites.<br /> (©2021 The Authors; Published by the American Association for Cancer Research.)

Details

Language :
English
ISSN :
1557-3265
Volume :
27
Issue :
18
Database :
MEDLINE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Publication Type :
Academic Journal
Accession number :
34253580
Full Text :
https://doi.org/10.1158/1078-0432.CCR-21-2051