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Detection of TP53/PIK3CA Mutations in Cell-Free Plasma DNA From Metastatic Breast Cancer Patients Using Next Generation Sequencing.
Nakauchi, Chiaki; Kagara, Naofumi; Shimazu, Kenzo; Shimomura, Atsushi; Naoi, Yasuto; Shimoda, Masafumi; Kim, Seung Jin; Noguchi, Shinzaburo.
Afiliación
  • Nakauchi C; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kagara N; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan. Electronic address: kagaran@onsurg.med.osaka-u.ac.jp.
  • Shimazu K; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Shimomura A; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Naoi Y; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Shimoda M; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Kim SJ; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Noguchi S; Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Clin Breast Cancer ; 16(5): 418-423, 2016 10.
Article en En | MEDLINE | ID: mdl-27265061
ABSTRACT

BACKGROUND:

Circulating tumor DNA (ctDNA) within a liquid biopsy is a promising marker for genotyping metastatic tumors. MATERIALS AND

METHODS:

We performed next generation whole exon sequencing of TP53 and PIK3CA genes, which are the 2 most common genetic alterations in breast cancer, in plasma DNA (pDNA) of 17 metastatic breast cancer (MBC) patients and in tumor DNA (tDNA) from their primary tumors.

RESULTS:

We identified 11 mutations (6 in TP53 and 5 in PIK3CA) in tDNA from 8 patients (47%) and 13 mutations (6 in TP53 and 7 in PIK3CA) in pDNA from 7 patients (41%). Six mutations in pDNA were also identified in tDNA but seven were not. Six MBC patients with TP53 and/or PIK3CA mutations in pDNA had a significantly worse survival rate (P < .05) after recurrence than that of the other 8 MBC patients without these mutations. Carcinoembryonic antigen and cancer antigen 15-3 levels did not correlate with prognosis (P = .675 and P = .877, respectively).

CONCLUSION:

These results suggest that mutations in ctDNA can be detected with next generation sequencing in MBC patients and could be a more useful prognostic factor for survival after recurrence than conventional tumor markers.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / ADN de Neoplasias / Proteína p53 Supresora de Tumor / Fosfatidilinositol 3-Quinasas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Clin Breast Cancer Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: Japón Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / ADN de Neoplasias / Proteína p53 Supresora de Tumor / Fosfatidilinositol 3-Quinasas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Clin Breast Cancer Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article País de afiliación: Japón Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA