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Automated next-generation profiling of genomic alterations in human cancers.
Keefer, Laurel A; White, James R; Wood, Derrick E; Gerding, Kelly M R; Valkenburg, Kenneth C; Riley, David; Gault, Christopher; Papp, Eniko; Vollmer, Christine M; Greer, Amy; Hernandez, James; McGregor, Paul M; Zingone, Adriana; Ryan, Bríd M; Deak, Kristen; McCall, Shannon J; Datto, Michael B; Prescott, James L; Thompson, John F; Cerqueira, Gustavo C; Jones, Siân; Simmons, John K; McElhinny, Abigail; Dickey, Jennifer; Angiuoli, Samuel V; Diaz, Luis A; Velculescu, Victor E; Sausen, Mark.
Afiliação
  • Keefer LA; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • White JR; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Wood DE; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Gerding KMR; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Valkenburg KC; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Riley D; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Gault C; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Papp E; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Vollmer CM; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Greer A; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Hernandez J; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • McGregor PM; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Zingone A; Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20850, USA.
  • Ryan BM; Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20850, USA.
  • Deak K; Department of Pathology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • McCall SJ; Department of Pathology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Datto MB; Department of Pathology, Duke University School of Medicine, Durham, NC, 27710, USA.
  • Prescott JL; PathGroup, Nashville, TN, 37217, USA.
  • Thompson JF; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Cerqueira GC; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Jones S; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Simmons JK; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • McElhinny A; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Dickey J; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Angiuoli SV; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA.
  • Diaz LA; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
  • Velculescu VE; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
  • Sausen M; Personal Genome Diagnostics Inc., Baltimore, MD, 21224, USA. msausen@pgdx.com.
Nat Commun ; 13(1): 2830, 2022 05 20.
Article em En | MEDLINE | ID: mdl-35595835
ABSTRACT
The lack of validated, distributed comprehensive genomic profiling assays for patients with cancer inhibits access to precision oncology treatment. To address this, we describe elio tissue complete, which has been FDA-cleared for examination of 505 cancer-related genes. Independent analyses of clinically and biologically relevant sequence changes across 170 clinical tumor samples using MSK-IMPACT, FoundationOne, and PCR-based methods reveals a positive percent agreement of >97%. We observe high concordance with whole-exome sequencing for evaluation of tumor mutational burden for 307 solid tumors (Pearson r = 0.95) and comparison of the elio tissue complete microsatellite instability detection approach with an independent PCR assay for 223 samples displays a positive percent agreement of 99%. Finally, evaluation of amplifications and translocations against DNA- and RNA-based approaches exhibits >98% negative percent agreement and positive percent agreement of 86% and 82%, respectively. These methods provide an approach for pan-solid tumor comprehensive genomic profiling with high analytical performance.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos