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TargetPlex FFPE-Direct DNA Library Preparation Kit for SiRe NGS panel: an international performance evaluation study.
Malapelle, Umberto; Pepe, Francesco; Pisapia, Pasquale; Sgariglia, Roberta; Nacchio, Mariantonia; Barberis, Massimo; Bilh, Michel; Bubendorf, Lukas; Büttner, Reinhard; Cabibi, Daniela; Castiglia, Marta; De Andrea, Carlos E; de Biase, Dario; Dumur, Catherine I; Fontanini, Gabriella; Freire, Javier; Gristina, Valerio; Hofman, Paul; Ilie, Marius; Lozano, Maria Dolores; Merkelbach-Bruse, Sabine; Pappesch, Roberto; Pelusi, Natalie; Roma, Gianluca; Russo, Antonio; Savic, Spasenija; Siemanowski, Janna; Tallini, Giovanni; Tischler, Verena; Vander Borght, Sara; Weynand, Birgit; Xu, Tom; Troncone, Giancarlo.
Afiliação
  • Malapelle U; Public Health, University of Naples Federico II, Naples, Italy.
  • Pepe F; Public Health, University of Naples Federico II, Naples, Italy.
  • Pisapia P; Public Health, University of Naples Federico II, Naples, Italy.
  • Sgariglia R; Public Health, University of Naples Federico II, Naples, Italy.
  • Nacchio M; Public Health, University of Naples Federico II, Naples, Italy.
  • Barberis M; Clinic Unit of Histopathology and Molecular Diagnostics, Istituto Europeo di Oncologia, Milano, Italy.
  • Bilh M; Department of Pathology, University Hospital Basel, Basel, Switzerland.
  • Bubendorf L; Department of Pathology, University Hospital Basel, Basel, Switzerland.
  • Büttner R; Department of Pathology, University of Cologne, Cologne, Germany.
  • Cabibi D; Health Promotion Sciences, Maternal and Infantile Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Castiglia M; Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
  • De Andrea CE; Pathology, University of Navarra, Pamplona, Spain.
  • de Biase D; Medicine (DIMES)a Hospital, Anatomic Pathology Unit, University of Bologna, Bologna, Italy.
  • Dumur CI; Molecular Diagnostic Department, Aurora Diagnostics, Jacksonville, Florida, USA.
  • Fontanini G; Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, Pisa, Italy.
  • Freire J; Pathology, Hospital Universitario Marques de Valdecilla, Santander, Spain.
  • Gristina V; Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
  • Hofman P; Pathology, INSERM, Nice, France.
  • Ilie M; Laboratory of Clinical and Experimental Pathology, Université Côte d'Azur, Nice, France.
  • Lozano MD; Pathology, Universidad de Navarra-Clínica Universidad de Navarra, Pamplona, Spain.
  • Merkelbach-Bruse S; Department of Pathology, University of Cologne, Cologne, Germany.
  • Pappesch R; Department of Pathology, University of Cologne, Cologne, Germany.
  • Pelusi N; Pathology, University of Bonn, Bonn, Germany.
  • Roma G; R&D Department, TargetPlex Genomics, Belmont, California, USA.
  • Russo A; Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy.
  • Savic S; Department of Pathology, University Hospital Basel, Basel, Switzerland.
  • Siemanowski J; Department of Pathology, University of Cologne, Cologne, Germany.
  • Tallini G; Pathology, University of Bologna, Bologna, Italy.
  • Tischler V; Pathology, University of Bonn, Bonn, Germany.
  • Vander Borght S; Department of Pathology, Katholieke Universiteit Leuven UZ Leuven, Leuven, Belgium.
  • Weynand B; Department of Pathology, Katholieke Universiteit Leuven UZ Leuven, Leuven, Belgium.
  • Xu T; R&D Department, SenseCare Medicals, Inc, Pleasanton, California, USA.
  • Troncone G; Public Health, University of Naples Federico II, Naples, Italy giancarlo.troncone@unina.it.
J Clin Pathol ; 75(6): 416-421, 2022 Jun.
Article em En | MEDLINE | ID: mdl-33766954
ABSTRACT

AIM:

Next generation sequencing (NGS) represents a key diagnostic tool to identify clinically relevant gene alterations for treatment-decision making in cancer care. However, the complex manual workflow required for NGS has limited its implementation in routine clinical practice. In this worldwide study, we validated the clinical performance of the TargetPlex FFPE-Direct DNA Library Preparation Kit for NGS analysis. Impressively, this new assay obviates the need for separate, labour intensive and time-consuming pre-analytical steps of DNA extraction, purification and isolation from formalin-fixed paraffin embedded (FFPE) specimens in the NGS workflow.

METHODS:

The TargetPlex FFPE-Direct DNA Library Preparation Kit, which enables NGS analysis directly from FFPE, was specifically developed for this study by TargetPlex Genomics Pleasanton, California. Eleven institutions agreed to take part in the study coordinated by the Molecular Cytopathology Meeting Group (University of Naples Federico II, Naples, Italy). All participating institutions received a specific Library Preparation Kit to test eight FFPE samples previously assessed with standard protocols. The analytical parameters and mutations detected in each sample were then compared with those previously obtained with standard protocols.

RESULTS:

Overall, 92.8% of the samples were successfully analysed with the TargetPlex FFPE-Direct DNA Library Preparation Kit on Thermo Fisher Scientific and Illumina platforms. Altogether, in comparison with the standard workflow, the TargetPlex FFPE-Direct DNA Library Preparation Kit was able to detect 90.5% of the variants.

CONCLUSION:

The TargetPlex FFPE-Direct DNA Library Preparation Kit combined with the SiRe panel constitutes a convenient, practical and robust cost-saving solution for FFPE NGS analysis in routine practice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genômica / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genômica / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article