TY - JOUR
T1 - Validation of a Targeted Next-Generation Sequencing Panel for Tumor Mutation Burden Analysis
T2 - Results from the Onconetwork Immuno-Oncology Consortium
AU - Fenizia, Francesca
AU - Alborelli, Ilaria
AU - Costa, Jose Luis
AU - Vollbrecht, Claudia
AU - Bellosillo, Beatriz
AU - Dinjens, Winand
AU - Endris, Volker
AU - Heydt, Carina
AU - Leonards, Katharina
AU - Merkelback-Bruse, Sabine
AU - Pfarr, Nicole
AU - van Marion, Ronald
AU - Allen, Christopher
AU - Chaudhary, Ruchi
AU - Gottimukkala, Rajesh
AU - Hyland, Fiona
AU - Wong-Ho, Elaine
AU - Jermann, Philip
AU - Machado, Jose Carlos
AU - Hummel, Michael
AU - Stenzinger, Albrecht
AU - Normanno, Nicola
N1 - Copyright © 2021 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Tumor mutation burden (TMB) is evaluated as a biomarker of response to immunotherapy. We present the efforts of the Onconetwork Immuno-Oncology Consortium to validate a commercial targeted sequencing test for TMB calculation. A three-phase study was designed to validate the Oncomine Tumor Mutational Load (OTML) assay at nine European laboratories. Phase 1 evaluated reproducibility and accuracy on seven control samples. In phase 2, six formalin-fixed, paraffin-embedded samples tested with FoundationOne were reanalyzed with the OTML panel to evaluate concordance and reproducibility. Phase 3 involved analysis of 90 colorectal cancer samples with known microsatellite instability (MSI) status to evaluate TMB and MSI association. High reproducibility of TMB was demonstrated among the sites in the first and second phases. Strong correlation was also detected between mean and expected TMB in phase 1 (r2 = 0.998) and phase 2 (r2 = 0.96). Detection of actionable mutations was also confirmed. In colorectal cancer samples, the expected pattern of MSI-high/high-TMB and microsatellite stability/low-TMB was present, and gene signatures produced by the panel suggested the presence of a POLE mutation in two samples. The OTML panel demonstrated robustness and reproducibility for TMB evaluation. Results also suggest the possibility of using the panel for mutational signatures and variant detection. Collaborative efforts between academia and companies are crucial to accelerate the translation of new biomarkers into clinical research.
AB - Tumor mutation burden (TMB) is evaluated as a biomarker of response to immunotherapy. We present the efforts of the Onconetwork Immuno-Oncology Consortium to validate a commercial targeted sequencing test for TMB calculation. A three-phase study was designed to validate the Oncomine Tumor Mutational Load (OTML) assay at nine European laboratories. Phase 1 evaluated reproducibility and accuracy on seven control samples. In phase 2, six formalin-fixed, paraffin-embedded samples tested with FoundationOne were reanalyzed with the OTML panel to evaluate concordance and reproducibility. Phase 3 involved analysis of 90 colorectal cancer samples with known microsatellite instability (MSI) status to evaluate TMB and MSI association. High reproducibility of TMB was demonstrated among the sites in the first and second phases. Strong correlation was also detected between mean and expected TMB in phase 1 (r2 = 0.998) and phase 2 (r2 = 0.96). Detection of actionable mutations was also confirmed. In colorectal cancer samples, the expected pattern of MSI-high/high-TMB and microsatellite stability/low-TMB was present, and gene signatures produced by the panel suggested the presence of a POLE mutation in two samples. The OTML panel demonstrated robustness and reproducibility for TMB evaluation. Results also suggest the possibility of using the panel for mutational signatures and variant detection. Collaborative efforts between academia and companies are crucial to accelerate the translation of new biomarkers into clinical research.
UR - https://www.scopus.com/pages/publications/85109063546
U2 - 10.1016/j.jmoldx.2021.04.008
DO - 10.1016/j.jmoldx.2021.04.008
M3 - Article
C2 - 33964449
AN - SCOPUS:85109063546
SN - 1525-1578
VL - 23
SP - 882
EP - 893
JO - Journal of Molecular Diagnostics
JF - Journal of Molecular Diagnostics
IS - 7
ER -