2025/05/12 更新

写真a

ゴトウ シユンスケ
後藤 駿介
GOTO SHUNSUKE
所属
九州大学病院 泌尿器・前立腺・腎臓・副腎外科 助教
医学部 医学科(併任)
職名
助教
プロフィール
泌尿器科における臨床業務 泌尿器科癌に関する基礎および臨床研究 臨床泌尿器科領域に関する講義、実習等での指導
外部リンク

学位

  • 医学博士

論文

  • Enhanced anti-tumor efficacy of IL-7/CCL19-producing human CAR-T cells in orthotopic and patient-derived xenograft tumor models 査読 国際誌

    Shunsuke Goto, Yukimi Sakoda, Keishi Adachi, Yoshitaka Sekido, Seiji Yano, Masatoshi Eto, Koji Tamada

    CANCER IMMUNOLOGY IMMUNOTHERAPY   70 ( 9 )   2503 - 2515   2021年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    Chimeric antigen receptor (CAR)-T cell therapy has impressive efficacy in hematological malignancies, but its application in solid tumors remains a challenge. Multiple hurdles associated with the biological and immunological features of solid tumors currently limit the application of CAR-T cells in the treatment of solid tumors. Using syngeneic mouse models, we recently reported that CAR-T cells engineered to concomitantly produce interleukin (IL)-7 and chemokine (C-C motif) ligand 19 (CCL19)-induced potent anti-tumor efficacy against solid tumors through an improved ability of migration and proliferation even in an immunosuppressive tumor microenvironment. In this study, for a preclinical evaluation preceding clinical application, we further explored the potential of IL-7/CCL19-producing human CAR-T cells using models that mimic the clinical features of solid tumors. Human anti-mesothelin CAR-T cells producing human IL-7/CCL19 achieved complete eradication of orthotopic pre-established malignant mesothelioma and prevented a relapse of tumors with downregulated antigen expression. Moreover, mice with patient-derived xenograft of mesothelin-positive pancreatic cancers exhibited significant inhibition of tumor growth and prolonged survival following treatment with IL-7/CCL19-producing CAR-T cells, compared to treatment with conventional CAR-T cells. Transfer of IL-7/CCL19-producing CAR-T cells resulted in an increase in not only CAR-T cells but also non-CAR-T cells within the tumor tissues and downregulated the expression of exhaustion markers, including PD-1 and TIGIT, on the T cells. Taken together, our current study elucidated the exceptional anti-tumor efficacy of IL-7/CCL19-producing human CAR-T cells and their potential for clinical application in the treatment of patients with solid tumors.

    DOI: 10.1007/s00262-021-02853-3

  • Novel immune drug combination induces tumour microenvironment remodelling and reduces the dosage of anti-PD-1 antibody

    Ozasa, T; Nakajima, M; Tsunedomi, R; Goto, S; Adachi, K; Takahashi, H; Tamada, K; Nagano, H

    SCIENTIFIC REPORTS   15 ( 1 )   8956   2025年3月   ISSN:2045-2322

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    記述言語:英語   出版者・発行元:Scientific Reports  

    Immune checkpoint inhibitors (ICIs) are effective in clinical settings; however, they present immune-related adverse effects and financial burden. Although dose reduction of ICIs may mitigate these limitations, it could compromise therapeutic efficacy. Using two adjuvants (poly(I:C) and LAG-3-Ig) combined with three neoantigen peptides (Comb), we examined whether Comb could enhance the efficacy of reduced dose of αPD-1 monoclonal antibody (RD-αPD-1 mAb), which has limited efficacy. In a murine colorectal cancer model using an MC38 cell line, Comb addition to RD-αPD-1 mAb enhanced treatment efficacy. Analysis of the tumour microenvironment (TME) in mice treated with Comb using flow cytometry and single-cell RNA sequencing revealed decreased macrophages with highly expressing immunosuppressive genes and increased plasmacytoid dendritic cells with highly expressing antigen-presenting genes. A potent infiltration of CD8+ tumour-infiltrating lymphocytes (TILs) with an effector profile was only observed in RD-αPD-1 mAb with Comb. Additionally, single-cell T cell receptor repertoire analysis underscored an oligoclonal expansion of CD8+ TILs following treatment with RD-αPD-1 mAb with Comb. This novel immune drug combination may be a promising strategy for reducing αPD-1 mAb dosage while preserving antitumour efficacy through modulating the TME.

    DOI: 10.1038/s41598-025-87344-6

    Web of Science

    Scopus

    PubMed

  • Laparoscopic Retroperitoneal Lymph Node Dissection After Chemotherapy for Nonseminomatous Testicular Germ-Cell Tumor at a Single Center

    Shiota, M; Tanegashima, T; Tsukahara, S; Mutaguchi, J; Goto, S; Kobayashi, S; Matsumoto, T; Eto, M

    ASIAN JOURNAL OF ENDOSCOPIC SURGERY   18 ( 1 )   e13416   2025年1月   ISSN:1758-5902 eISSN:1758-5910

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    記述言語:英語   出版者・発行元:Asian Journal of Endoscopic Surgery  

    Objective: This study investigated the perioperative and oncological outcomes of laparoscopic retroperitoneal lymph node dissection (RPLND) procedures for post-chemotherapy patients with nonseminomatous testicular germ-cell tumor at a single center. Methods: This study included patients with nonseminomatous testicular cancer who underwent RPLND after chemotherapy at the Kyushu University Hospital between 2016 and 2024. The preoperative clinicopathological characteristics, perioperative outcomes, and oncological outcomes were investigated. Results: A total of 13 patients underwent laparoscopic RPLND. Median maximum retroperitoneal tumor size at post-chemotherapy before RPLND was 11 mm (range, 2–30 mm). RPLND template was one side and both sides in nine and four patients. Median operative time was 272 min (range, 129–490 min), and median estimated blood loss was 27 mL (range, 0–100 mL). Median time from operation to discharge was 8 days (range, 5–15 days). There was no severe perioperative and postoperative complication. Residual cancer and teratoma were detected in one and seven patients. During median follow-up of 18.6 months (range, 1.0–95.7 months), no case presented recurrence. Conclusion: Laparoscopic RPLND presented safety in perioperative outcomes and favorable oncological outcomes. Thus, it was confirmed that laparoscopic RPLND is a feasible minimally invasive procedure for selected cases.

    DOI: 10.1111/ases.13416

    Web of Science

    Scopus

    PubMed

  • Independent validation of genetic risk model to progression after intravesical BCG therapy for NMIBC

    Nagakawa, S; Shiota, M; Tsukahara, S; Tanegashima, T; Ueda, S; Mutaguchi, J; Goto, S; Kobayashi, S; Matsumoto, T; Eto, M

    CANCER SCIENCE   116   1513 - 1513   2025年1月   ISSN:1347-9032 eISSN:1349-7006

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  • Analysis of Tumor Immune Microenvironment in the Upper Tract Urothelial Carcinoma with Intravesical Recurrence

    Ito, D; Tanegashima, T; Okumura, G; Itahashi, K; Tsukahara, S; Mutaguchi, J; Goto, S; Kobayashi, S; Matsumoto, T; Shiota, M; Koyama, S; Nishikawa, H; Eto, M

    CANCER SCIENCE   116   55 - 55   2025年1月   ISSN:1347-9032 eISSN:1349-7006

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▼全件表示

講演・口頭発表等

▼全件表示

MISC

  • 九州大学泌尿器科学教室における2021年から2023年の3年間の臨床統計

    辻田 次郎, 種子島 時祥, 塚原 茂大, 牟田口 淳, 後藤 駿介, 小林 聡, 松元 崇, 塩田 真己, 江藤 正俊

    西日本泌尿器科   87 ( 3 )   110 - 114   2025年2月   ISSN:0029-0726

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    記述言語:日本語   出版者・発行元:(一社)西日本泌尿器科学会  

    九州大学泌尿器科学教室における2021年から2023年の3年間の外来,入院および手術術式に関する統計をまとめた.1)外来患者総数は47,054人で新来2,706人,再来44,348人であり,外来新来患者疾患別頻度では,尿路性器悪性腫瘍1,514人(55.9%),悪性腫瘍等による尿路通過障害207人(7.6%),前立腺肥大症203人(7.5%),神経因性膀胱140人(5.2%),炎症性疾患103人(3.8%),尿路結石症87人(3.2%)の順であった.2)入院患者総数は3,265人で男性2,609人,女性656人で60~70歳代の男性患者が全入院患者の過半数を占めた(57.2%).入院患者疾患別では,尿路性器腫瘍が2,172人(66.5%)と最も多く,膀胱癌,前立腺癌,腎癌,腎盂尿管癌の順であった.次いで前立腺生検目的526人(16.1%),尿路結石症129人(4.0%),副腎腫瘍75人(2.3%)の順であった.3)総手術例数は1,732例で,開放手術32例(1.8%),腹腔鏡手術745例(43.0%)(うちロボット支援下手術503(29.0%)),内視鏡手術例896例(51.7%),その他74例(4.3%)であった.(著者抄録)

  • 【臨床腎・泌尿器癌(上)-基礎・臨床研究の進歩-】腎癌の治療 腎癌治療の歴史と現況

    後藤 駿介, 江藤 正俊

    日本臨床   82 ( 増刊8 臨床腎・泌尿器癌(上) )   189 - 193   2024年10月   ISSN:0047-1852

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    記述言語:日本語   出版者・発行元:(株)日本臨床社  

  • Current status and future perspective of immunotherapy for renal cell carcinoma(タイトル和訳中)

    Blas Leandro, Monji Keisuke, Mutaguchi Jun, Kobayashi Satoshi, Goto Shunsuke, Matsumoto Takashi, Shiota Masaki, Inokuchi Junichi, Eto Masatoshi

    International Journal of Clinical Oncology   29 ( 8 )   1105 - 1114   2024年8月   ISSN:1341-9625

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    記述言語:英語   出版者・発行元:シュプリンガー・ジャパン(株)  

  • 【泌尿器科の未来を拓く基礎研究】固形がんに対するCAR-T細胞療法の可能性

    後藤 駿介

    泌尿器科   15 ( 4 )   345 - 350   2022年4月   ISSN:2435-192X

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    記述言語:日本語   出版者・発行元:(有)科学評論社  

教育活動概要

  • 医学部学生講義、学生実習指導

学内運営に関わる各種委員・役職等

  • 2022年4月 - 2023年3月   部門 がん薬物療法委員会

専門診療領域

  • 生物系/医歯薬学/外科系臨床医学/泌尿器科学学

臨床医資格

  • 専門医

    日本癌治療学会、日本泌尿器内視鏡・ロボティクス学会、日本泌尿器腫瘍学会

  • 専門医

    日本泌尿器科学会

医師免許取得年

  • 2011年