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Validation of a Targeted Next-Generation Sequencing Panel for Tumor Mutation Burden Analysis: Results from the Onconetwork Immuno-Oncology Consortium.
Fenizia, Francesca; Alborelli, Ilaria; Costa, Jose Luis; Vollbrecht, Claudia; Bellosillo, Beatriz; Dinjens, Winand; Endris, Volker; Heydt, Carina; Leonards, Katharina; Merkelback-Bruse, Sabine; Pfarr, Nicole; van Marion, Ronald; Allen, Christopher; Chaudhary, Ruchi; Gottimukkala, Rajesh; Hyland, Fiona; Wong-Ho, Elaine; Jermann, Philip; Machado, Jose Carlos; Hummel, Michael; Stenzinger, Albrecht; Normanno, Nicola.
Afiliação
  • Fenizia F; Cell Biology and Biotherapy Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy.
  • Alborelli I; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Costa JL; Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
  • Vollbrecht C; Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute of Pathology, Berlin, Germany.
  • Bellosillo B; Servei de Patologia, Hospital del Mar, Barcelona, Spain.
  • Dinjens W; Department of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, the Netherlands.
  • Endris V; Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
  • Heydt C; Institute of Pathology, University Hospital Cologne, Cologne, France.
  • Leonards K; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Merkelback-Bruse S; Institute of Pathology, University Hospital Cologne, Cologne, France.
  • Pfarr N; Institute of Pathology, Technical University Munich, Munich, Germany.
  • van Marion R; Department of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, the Netherlands.
  • Allen C; Clinical Next-Generation Sequencing Division, Thermo Fisher Scientific, Waltham, Massachusetts.
  • Chaudhary R; Clinical Next-Generation Sequencing Division, Thermo Fisher Scientific, Waltham, Massachusetts.
  • Gottimukkala R; Clinical Next-Generation Sequencing Division, Thermo Fisher Scientific, Waltham, Massachusetts.
  • Hyland F; Clinical Next-Generation Sequencing Division, Thermo Fisher Scientific, Waltham, Massachusetts.
  • Wong-Ho E; Clinical Next-Generation Sequencing Division, Thermo Fisher Scientific, Waltham, Massachusetts.
  • Jermann P; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Machado JC; Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
  • Hummel M; Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute of Pathology, Berlin, Germany.
  • Stenzinger A; Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
  • Normanno N; Cell Biology and Biotherapy Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy. Electronic address: n.normanno@istitutotumori.na.it.
J Mol Diagn ; 23(7): 882-893, 2021 07.
Article em En | MEDLINE | ID: mdl-33964449
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Neoplasias Colorretais / Carga Tumoral / Instabilidade de Microssatélites / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: J Mol Diagn Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Neoplasias Colorretais / Carga Tumoral / Instabilidade de Microssatélites / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: J Mol Diagn Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália