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Molecular characteristics and clinical outcomes of elderly patients with IDH-wildtype glioblastomas: comparative study of older and younger cases in Kansai Network cohort.
Fukai, Junya; Arita, Hideyuki; Umehara, Toru; Yoshioka, Ema; Shofuda, Tomoko; Kanematsu, Daisuke; Kodama, Yoshinori; Mano, Masayuki; Kinoshita, Manabu; Okita, Yoshiko; Nonaka, Masahiro; Uda, Takehiro; Tsuyuguchi, Naohiro; Sakamoto, Daisuke; Uematsu, Yuji; Nakao, Naoyuki; Mori, Kanji; Kanemura, Yonehiro.
Afiliación
  • Fukai J; Department of Neurological Surgery, Wakayama Medical University School of Medicine, Kimiidera 811-1, Wakayama, 641-0012, Japan. junfukai@wakayama-med.ac.jp.
  • Arita H; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan. junfukai@wakayama-med.ac.jp.
  • Umehara T; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Yoshioka E; Department of Neurosurgery, Takatsuki General Hospital, Takatsuki, Osaka, 569-1192, Japan.
  • Shofuda T; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Kanematsu D; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan.
  • Kodama Y; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Mano M; Division of Stem Cell Research, Department of Biomedical Research and Innovation, Institute for Clinical Research, National Hospital Organization Osaka National Hospital, Osaka, 540-0006, Japan.
  • Kinoshita M; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Okita Y; Division of Stem Cell Research, Department of Biomedical Research and Innovation, Institute for Clinical Research, National Hospital Organization Osaka National Hospital, Osaka, 540-0006, Japan.
  • Nonaka M; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Uda T; Division of Regenerative Medicine, Department of Biomedical Research and Innovation, Institute for Clinical Research, National Hospital Organization Osaka National Hospital, Osaka, 540-0006, Japan.
  • Tsuyuguchi N; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Sakamoto D; Department of Diagnostic Pathology, Kobe University Graduate School of Medicine, Kobe, Hyogo, 650-0017, Japan.
  • Uematsu Y; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Nakao N; Department of Central Laboratory and Surgical Pathology, National Hospital Organization Osaka National Hospital, Osaka, 540-0006, Japan.
  • Mori K; Kansai Molecular Diagnosis Network for CNS Tumors, Osaka, 540-0006, Japan.
  • Kanemura Y; Department of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan.
Brain Tumor Pathol ; 37(2): 50-59, 2020 Apr.
Article en En | MEDLINE | ID: mdl-32361941
Aging is a known negative prognostic factor in glioblastomas (GBM). Whether particular genetic backgrounds are a factor in poor outcomes of elderly patients with GBM warrants investigation. We aim to elucidate any differences between older and younger adult patients with IDH-wildtype GBM regarding both molecular characteristics and clinical outcomes. We collected adult cases diagnosed with IDH-wildtype GBM from the Kansai Network. Clinical and pathological characteristics were analyzed retrospectively and compared between older (≥ 70 years) and younger (≤ 50 years) cases. Included were 92 older vs. 33 younger cases. The older group included more patients with preoperative Karnofsky performance status score < 70 and had a shorter survival time than the younger group. MGMT promoter was methylated more frequently in the older group. TERT promoter mutation was more common in the older group. There were significant differences in DNA copy-number alteration profiles between age groups in PTEN deletion and CDK4 amplification/gain. In the older group, no molecular markers were identified, but surgical resection was an independent prognostic factor. Age-specific survival difference was significant in the MGMT methylated and TERT wildtype subgroup. Elderly patients have several potential factors in poor prognosis of glioblastomas. Varying molecular profiles may explain differing rates of survival between generations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Isocitrato Deshidrogenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Brain Tumor Pathol Asunto de la revista: CEREBRO / NEOPLASIAS / PATOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma / Isocitrato Deshidrogenasa Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Brain Tumor Pathol Asunto de la revista: CEREBRO / NEOPLASIAS / PATOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Japón