Curriculum Vitaes
Profile Information
- Affiliation
- School of Medicine Faculty of Medicine, Fujita Health University
- Degree
- 医学博士(慶應義塾大学)
- J-GLOBAL ID
- 200901043674612973
- researchmap Member ID
- 5000066271
Research Areas
1Research History
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Apr, 2025 - Present
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Apr, 2025 - Present
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Apr, 2010 - Present
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Apr, 2022 - Mar, 2025
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Feb, 2022 - Mar, 2025
Education
1-
Apr, 1981 - Mar, 1987
Committee Memberships
10-
Nov, 2024 - Present
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Oct, 2021 - Present
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Sep, 2018 - Present
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May, 2014 - Present
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Oct, 2010 - Present
Papers
437-
Clinical neurology and neurosurgery, 265 109371-109371, Mar 2, 2026OBJECTIVE: Central nervous system (CNS) solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms with a high propensity for local recurrence and extracranial metastasis. Although surgery and radiotherapy are the mainstays of treatment, systemic therapeutic options for recurrent disease remain limited. Pazopanib, a multitargeted tyrosine kinase inhibitor, has demonstrated clinical activity in extracranial SFTs; however, evidence in CNS SFTs is scarce. METHODS: We conducted a retrospective, single-institution study of patients with recurrent CNS SFTs treated with pazopanib. Clinical data, including prior treatments, imaging responses, treatment duration, and adverse events, were collected from medical records. Exploratory next-generation sequencing-based cancer panel testing was performed in two patients. RESULTS: Four patients with recurrent CNS SFTs were included. All had undergone prior surgical resection and radiotherapy. Pazopanib achieved partial response in one patient and stable disease in three patients, with treatment durations ranging from 7 months to over 2 years. One patient experienced disease progression after an initial period of response. Adverse events, including fatigue, gastrointestinal symptoms, and hypertension, were observed in all patients but were generally manageable with supportive care or dose adjustment. Exploratory molecular profiling identified various genomic alterations in two patients. CONCLUSIONS: In this single-institution retrospective series, pazopanib provided durable disease control with acceptable tolerability in selected patients with recurrent CNS SFTs. These findings support considering pazopanib as a systemic treatment option when further local therapies are not feasible, while highlighting the need for larger multicenter studies.
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Acta neurochirurgica, 167(1) 228-228, Aug 26, 2025The lateralized efficacy of vagus nerve stimulation (VNS) remains insufficiently explored. We report a case of drug-resistant epilepsy with bilateral frontal lobe seizure onset, treated with left cervical VNS. Preoperative video- electroencephalogram revealed predominant interictal discharges in the right hemisphere and frequent seizures from both hemispheres. Following VNS, overall seizure frequency decreased. Notably, stereo-electroencephalography performed 15 months postoperatively showed a marked reduction in right-sided seizures, while left-sided seizures remained frequent. This case highlights the potential lateralized effect of VNS in a single patient with bilateral frontal lobe epilepsy, suggesting that VNS may preferentially suppress seizures originating from the right hemisphere.
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Brain tumor pathology, Jul 27, 2025Compared to oligodendrogliomas, astrocytomas may have a relatively higher frequency of intracranial remote recurrence, despite generally favorable prognoses. Previous studies identified 8q gain, particularly in the terminal region, as a poor prognostic factor. This study evaluated MYC expression and its relationship with copy number gain at 8q24.21, in relation to recurrence patterns in astrocytomas, with a particular focus on intracranial remote recurrence. A retrospective analysis was conducted on 27 patients treated between 2006 and 2019. MYC expression was assessed by immunohistochemistry (IHC), and copy number status by metaphase comparative genomic hybridization and next-generation sequencing. Recurrence patterns were categorized as local or remote.Among 43 specimens analyzed by IHC, MYC expression was observed in 72%, with higher positivity in recurrent (80%) than initial (61%) specimens, though the difference was not statistically significant (p = 0.30). Copy number analysis showed a significant increase in 8q24.21 copy number in specimens from cases with remote recurrence compared to those with local recurrence (p = 0.033). However, no significant correlation was found between MYC copy number and protein expression (p = 0.055). These findings suggest that MYC is frequently expressed in astrocytomas, but its expression does not significantly reflect 8q gain or recurrence pattern.
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Journal of NeuroInterventional Surgery, Jun 20, 2025
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Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 135 111192-111192, May, 2025BACKGROUND: This study aimed to determine the efficacy of flow diverters (FDs) for small/medium (≤10 mm) aneurysms and analyzed the factors that prevent aneurysm occlusion. METHODS: This retrospective single-center study evaluated the angiographic and clinical data of consecutive patients between June 2020 and February 2023. RESULTS: Overall, 121 small/medium aneurysms were observed in 106 patients treated with FDs. The median dome diameter was 6.1 (5.1-7.2) mm. Symptomatic thromboembolic complications were observed in four (3.7 %) patients, and none showed a major ischemic stroke. Intracranial hemorrhage was detected using postprocedural computed tomography in one (0.9 %) patient with asymptomatic subarachnoid hemorrhage. The rate of permanent neurological deficits was 1.8 %, and the mortality rate was 0 %. No delayed ischemic or hemorrhagic complications were observed during follow-up. Angiographic follow-up revealed complete and adequate occlusion (O'Kelly-Marotta grades C and D) rates of 77.5 % and 90.8 %, respectively. On multivariate analysis, incomplete occlusion was only associated with the presence of a branch vessel from the aneurysm dome (P < 0.01). In aneurysms with incorporated branch vessels, univariate analysis revealed that coil usage was a predictor of complete occlusion (P = 0.03). Moreover, even without using coils, effective occlusion was achieved when the branch vessel diameter was small (P = 0.03). CONCLUSIONS: FDs are an effective and safe treatment option for small/medium aneurysms. The presence of incorporated branch vessels can predict incomplete occlusion. Even in aneurysms with incorporated branch vessels, FD can obtain therapeutic effects by adding coil embolization or treating with only FD if the branch vessel diameter is small.
Misc.
206-
Brain Tumor Pathology, 29(Suppl.) 113-113, May, 2012
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Brain Tumor Pathology, 29(Suppl.) 171-171, May, 2012
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EUROPEAN SPINE JOURNAL, 21(5) 946-955, May, 2012 Peer-reviewed
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Japanese journal of neurosurgery, 21(3) 200-206, Mar 20, 2012With the introduction of temozolomide (TMZ), a drug treatment for malignant gliomas has been developed and the importance of chemotherapy has been validated. Nonetheless, these tumors are still incurable, and many issues remain to be solved. Recent advances in tumor genetics have enabled us to better predict each patient's prognosis, and, especially in the TMZ era, methylation of the O^6-methylguanine-DNA methyltransferase (MGMT) promoter has been thoroughly investigated. This DNA repair enzyme catalyzes the O^6-methylguanine that TMZ creates and theoretically promotes TMZ resistance, and clinical studies have revealed that MGMT-proficient gliomas indeed showed a poorer prognosis. Thus many studies were carried out in an effort to inhibit MGMT in gliomas and to overcome TMZ resistance, but unfortunately, none have yielded a successful result, which leads to the conclusion that TMZ-resistance is not promoted solely by MGMT. Since medical treatment for malignant gliomas using DNA damaging agents could show limited efficacy, a new concept of molecular-targeted therapy has been developed. However, clinical studies using various molecular-targeted compounds did not make remarkable improvement in patients' prognosis either. New problems that have emerged from various clinical studies are discussed in this text to open novel prospects for medical treatment of malignant gliomas.
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JOURNAL OF THE NATIONAL CANCER INSTITUTE, 104(1) 42-55, Jan, 2012 Peer-reviewed
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Asian Journal of Neurosurgery, 7(3) 109-115, 2012 Peer-reviewed
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J. Biomedical Science and Engineering, 884-891, 2012 Peer-reviewed
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Annals of the Institute of Statistical Mathematics, 63(6) 1247-1275, Dec, 2011
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NEUROLOGY INDIA, 59(6) 829-832, Nov, 2011 Peer-reviewed
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MOLECULAR MEDICINE REPORTS, 4(6) 1101-1105, Nov, 2011 Peer-reviewed
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25(2) 130-134, Sep 25, 2011
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JOURNAL OF NEUROSURGERY, 115(2) A436-A436, Aug, 2011
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JOURNAL OF CLINICAL NEUROSCIENCE, 18(8) 1097-1100, Aug, 2011 Peer-reviewed
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Neurosurgery, 69(2) 376-90, Aug, 2011 Peer-reviewed
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Brain Tumor Pathology, 28(Suppl.) 055-055, May, 2011
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Brain Tumor Pathology, 28(Suppl.) 089-089, May, 2011
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Brain Tumor Pathology, 28(Suppl.) 122-122, May, 2011
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Japanese journal of neurosurgery, 20 85-85, Apr 10, 2011
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NEUROSURGERY, 68(1) 206-212, Jan, 2011
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MINIMALLY INVASIVE NEUROSURGERY, 53(5-6) 243-249, Oct, 2010 Peer-reviewed
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JOURNAL OF NEURO-ONCOLOGY, 98(3) 411-415, Jul, 2010 Peer-reviewed
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Japanese journal of neurosurgery, 19 54-54, Apr 20, 2010
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JOURNAL OF NEUROSURGERY, 112(1) 33-42, Jan, 2010 Peer-reviewed
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Neurosurg Rev, 33(3) 349-357, 2010 Peer-reviewed
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NEURO-ONCOLOGY, 11(6) 913-914, Dec, 2009
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NEURO-ONCOLOGY, 11(6) 904-904, Dec, 2009
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NEURO-ONCOLOGY, 11(6) 949-949, Dec, 2009
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Journal of neuro-oncology, 95(3) 307-316, Dec, 2009 Peer-reviewed
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NEURO-ONCOLOGY, 11(5) 627-627, Oct, 2009
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NEURO-ONCOLOGY, 11(5) 590-590, Oct, 2009
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NEUROSURGICAL REVIEW, 32(4) 495-498, Oct, 2009 Peer-reviewed
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JOURNAL OF NEUROSURGERY, 111(3) 492-496, Sep, 2009 Peer-reviewed
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Brain Tumor Pathology, 26(Suppl.) 52-52, May, 2009
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NEURO-ONCOLOGY, 11(2) 222-222, Apr, 2009
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JOURNAL OF NEURO-ONCOLOGY, 91(3) 251-255, Feb, 2009 Peer-reviewed
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小児がん : 小児悪性腫瘍研究会記録, 46(1) 71-71, 2009
Books and Other Publications
14Presentations
67-
The 3rd Symposium of WFNOS 2021, Jul 28, 2019 Invited
Professional Memberships
6Research Projects
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Grants-in-Aid for Scientific Research, Japan Society for the Promotion of Science, Apr, 2025 - Mar, 2028
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Grants-in-Aid for Scientific Research, Japan Society for the Promotion of Science, Apr, 2024 - Mar, 2027
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Grants-in-Aid for Scientific Research, Japan Society for the Promotion of Science, Apr, 2023 - Mar, 2026
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科学研究費助成事業, 日本学術振興会, Apr, 2022 - Mar, 2025
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科学研究費助成事業, 日本学術振興会, Apr, 2022 - Mar, 2025
教育内容・方法の工夫(授業評価等を含む)
2-
件名(英語)臨床医学への興味を喚起する教育を試みる開始年月日(英語)2010終了年月日(英語)2012概要(英語)M3「神経系」講義において、手術ビデオの供覧など臨床医学に対する興味を促進した。
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件名(英語)臨床医学への興味を喚起する教育を試みる開始年月日(英語)2010終了年月日(英語)2012概要(英語)M5臨床実習においてカルテ記載を促進し、疾患の理解を促した。