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Assessment of the Diagnostic Utility of Serum MicroRNA Classification in Patients With Diffuse Glioma.
Ohno, Makoto; Matsuzaki, Juntaro; Kawauchi, Junpei; Aoki, Yoshiaki; Miura, Junichiro; Takizawa, Satoko; Kato, Ken; Sakamoto, Hiromi; Matsushita, Yuko; Takahashi, Masamichi; Miyakita, Yasuji; Ichimura, Koichi; Narita, Yoshitaka; Ochiya, Takahiro.
Afiliação
  • Ohno M; Department of Neurosurgery and Neuro-oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Matsuzaki J; Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
  • Kawauchi J; Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
  • Aoki Y; Toray Industries, Inc, Tebiro, Kamakura, Japan.
  • Miura J; Dynacom Co, Ltd, Chiba, Japan.
  • Takizawa S; Dynacom Co, Ltd, Chiba, Japan.
  • Kato K; Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
  • Sakamoto H; Toray Industries, Inc, Tebiro, Kamakura, Japan.
  • Matsushita Y; Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Takahashi M; Department of Biobank and Tissue Resources, National Cancer Center Research Institute, Tokyo, Japan.
  • Miyakita Y; Department of Neurosurgery and Neuro-oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Ichimura K; Department of Neurosurgery and Neuro-oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Narita Y; Department of Neurosurgery and Neuro-oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Ochiya T; Division of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.
JAMA Netw Open ; 2(12): e1916953, 2019 12 02.
Article em En | MEDLINE | ID: mdl-31808923
ABSTRACT
Importance A blood-based screening tool for detecting diffuse glioma is necessary to improve clinical outcomes.

Objectives:

To establish models using serum microRNAs to distinguish patients with diffuse glioma from control individuals without cancer (the Glioma Index) and to differentiate glioblastoma (GBM), primary central nervous system lymphoma (PCNSL), and metastatic brain tumors (the 3-Tumor Index). Design, Setting, and

Participants:

This retrospective, case-control diagnostic study included 157 patients with diffuse glioma and 109 patients with central nervous system (CNS) diseases other than diffuse glioma diagnosed from August 1, 2008, through May 1, 2016, and 314 sex- and age-matched controls without cancer. Samples of patients with diffuse glioma and controls were randomly divided into training and validation set 1, and those of patients with CNS diseases other than diffuse glioma were allocated to an exploratory set. Samples of patients with GBM, PCNSL, and metastatic brain tumors were randomly divided into training and validation set 2. Data were analyzed from April 1, 2018, to March 31, 2019. Main Outcomes and

Measures:

The expression of 2565 microRNAs was assessed, and the diagnostic performance was evaluated by calculating the area under the receiver operating characteristics curve (AUC), sensitivity, specificity, and accuracy.

Results:

A total of 580 patients were included in the analysis (309 [53.3%] male; median age, 57 years [range, 10-87 years]). In training set 1, 100 patients with diffuse glioma (median age, 56 years [range, 14-87 years]; 55 male [55.0%]) were compared with 200 control patients (median age, 56 years [range, 14-87 years]; 105 male [52.5%]), and the Glioma Index was constructed using 3 microRNAs (miR-4763-3p, miR-1915-3p, and miR-3679-5p). In validation set 1, the AUC was 0.99 (95% CI, 0.99-1.00); sensitivity, 0.95 (95% CI, 0.89-1.00); and specificity, 0.97 (95% CI, 0.93-1.00). The Glioma Index classified 39 of 42 PCNSL samples (92.9%) and 25 of 28 metastatic brain tumor samples (89.3%) as positive and 2 of 2 spinal tumors (100%) as negative in the exploratory set. In training set 2, 68 patients with GBM, 34 with PCNSL, and 23 with metastatic brain tumor were compared, and the 3-Tumor Index was constructed using 48 microRNAs. The 3-Tumor Index had an accuracy of 0.80, positively detecting 16 of 17 GBM samples (94.1%), 4 of 5 metastatic brain tumor samples (80.0%), and 4 of 8 PCNSL samples (50.0%) in validation set 2. Conclusions and Relevance This study appears to have identified promising serum microRNA combinations for detecting diffuse glioma and for assessing histologic features of brain tumors.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias do Sistema Nervoso Central / Glioblastoma / MicroRNAs / Glioma / Linfoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias do Sistema Nervoso Central / Glioblastoma / MicroRNAs / Glioma / Linfoma Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article