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Small lung tumor biopsy samples are feasible for high quality targeted next generation sequencing.
Kage, Hidenori; Kohsaka, Shinji; Shinozaki-Ushiku, Aya; Hiraishi, Yoshihisa; Sato, Jiro; Nagayama, Kazuhiro; Ushiku, Tetsuo; Takai, Daiya; Nakajima, Jun; Miyagawa, Kiyoshi; Aburatani, Hiroyuki; Mano, Hiroyuki; Nagase, Takahide.
Afiliação
  • Kage H; Department of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Kohsaka S; Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
  • Shinozaki-Ushiku A; Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Hiraishi Y; Department of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Sato J; Department of Radiology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nagayama K; Department of Thoracic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Ushiku T; Department of Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Takai D; Department of Clinical Laboratory, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Nakajima J; Department of Thoracic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Miyagawa K; Laboratory of Molecular Radiology, Center for Disease Biology and Integrative Medicine, The University of Tokyo, Tokyo, Japan.
  • Aburatani H; Genome Science Laboratory, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
  • Mano H; Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
  • Nagase T; Department of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Cancer Sci ; 110(8): 2652-2657, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31222846
ABSTRACT
Next-generation sequencing (NGS) has been implemented in clinical oncology to analyze multiple genes and to guide therapy. In patients with advanced lung cancer, small biopsies such as computed tomography-guided needle biopsy (CTNB), endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) and transbronchial biopsy (TBB) are less invasive and are preferable to resection to make a pathological diagnosis. However, the quality of DNA/RNA and NGS from small lung tumor biopsy samples is unknown. Between April 2017 and March 2018, 107 consecutive samples were obtained from thoracic tumors or metastatic sites for targeted NGS analysis. Fifteen samples were obtained through CTNB, 11 through EBUS-TBNA, 11 through TBB and 70 through surgical resection. All samples were formalin-fixed and paraffin-embedded. DNA and RNA quality was measured using the ddCq method and the percentage of RNA fragments above 200 nucleotides (DV200), respectively. Our custommade probes were designed to capture exon sequences of 464 cancer-related genes and transcripts of 463 genes. DNA and RNA yield from the 3 biopsy methods were similar, and less than the yield obtained from resected samples. The quality of DNA and RNA was similar across all methods. Overall, 12 of 15 CTNB samples (80%), all 11 EBUS-TBNA samples, and 9 of 11 TBB samples (82%) underwent successful NGS assays from DNA. NGS analysis from RNA was successful in all 12 CTNB samples, 9 of 11 EBUS-TBNA samples (82%), and 8 of 11 TBB samples (73%). CTNB, EBUS-TBNA and TBB mostly resulted in adequate DNA and RNA quality and enabled high-quality targeted NGS analysis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pulmonares Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article