研究者業績

suda koichi

  (須田 康一)

Profile Information

Affiliation
Professor, Schoolo of Medicine Department of Gastroenterological Surgery, Fujita Health University
Degree
MD, PhD, FACS

J-GLOBAL ID
200901017395279643
researchmap Member ID
5000105427

Papers

 525
  • Ichiro Takemasa, Hiroyuki Yamamoto, Tatsuto Nishigori, Takeo Fujita, Tomoki Makino, Yusuke Taniyama, Masanori Terashima, Masanori Tokunaga, Takatoshi Matsuyama, Tomohiro Yamaguchi, Noriko Iwata, Hidetoshi Katsuno, Koichi Suda, Yusuke Kinugasa, Kazutaka Obama, Takashi Kamei, Ichiro Uyama, Masahiko Watanabe, Yoshiharu Sakai, Yuko Kitagawa
    Asian Journal of Endoscopic Surgery, 19(1), Jan 22, 2026  
    ABSTRACT Aim The adoption of robot‐assisted surgery (RAS) in Japan has progressed significantly since its initial approval in 2009. RAS gradually expanded into various surgical fields with 35 procedures now covered under Japan's national health insurance. This study provides an inaugural assessment of RAS outcomes for seven digestive procedures introduced in 2018. Methods The Japanese Society for Endoscopic Surgery working group established an RAS registry integrating data from the National Clinical Database and additional RAS‐specific records. The analysis focused on three major gastrointestinal fields: the esophagus, stomach, and rectum. Results In 2019, 530 esophagectomies, 2295 gastrectomies, and 3269 proctectomies were performed. RAS for these procedures was characterized by relatively long operative times, low intraoperative blood loss, and very low conversion rates to open surgery (< 1%). Postoperative morbidity rates Grade IIIa or higher were 23.2% for esophagectomy, 4.9% for gastrectomy, and 9.4% for proctectomy. Length of postoperative hospital stay correlated with morbidity, though readmission (1.3%–3.1%) and postoperative mortality rates (0.3%–0.6%) remained low. The early nationwide implementation of RAS in Japan was marked by a high surgeon qualification rate (98.9%) and meticulous case selection; the DVSS Xi model accounted for 66.3% of robotic platforms used. Conclusion These findings underscore the need for ongoing surveillance and data‐driven evaluation to ensure safe and effective implementation of RAS. Future longitudinal analyses will refine surgical quality, optimize resource allocation, and advance minimally invasive techniques. This study highlights the transformative potential of RAS in Japanese surgical practice and its alignment with global trends.
  • Yutaka Hattori, Tadashi Fujii, Takumi Tochio, Tsutomu Kumamoto, Junichiro Hiro, Hiroshi Matsuoka, Koji Masumori, Kohei Funasaka, Eizaburo Ohno, Yoshiki Hirooka, Koichi Suda, Koki Otsuka
    Journal of the Anus, Rectum and Colon, 9(4) 447-454, Oct 25, 2025  
  • Nanaho Hiraga, Yosuke Ando, Hiroshi Matsuoka, Seira Nishibe-Toyosato, Tomohiro Mizuno, Hidetoshi Katsuno, Yoshiaki Ikeda, Kenji Kawada, Zenichi Morise, Koichi Suda, Shigeki Yamada
    International journal of clinical oncology, 30(8) 1602-1609, Aug, 2025  
    BACKGROUND: The incidence of chemotherapy-induced nausea and vomiting (CINV) when using an oxaliplatin-based regimen may vary according to the cancer type. This study compared the occurrence of CINV in patients with gastric or colorectal cancers. METHODS: This retrospective study included patients who received oxaliplatin-containing regimens for gastric or colorectal cancer. The incidence of CINV during the first treatment course was evaluated. Propensity score matching (PSM) was performed between gastric cancer (GC) and colorectal cancer (CRC) groups to compare the complete response (CR) and total control (TC) rates as indicators of antiemetic efficacy. The impact of primary tumor resection history, surgical procedure, and antiemetic agents was analyzed in the group with a higher incidence of CINV. RESULTS: The GC group included 99 patients and the CRC group included 180 patients, with 60 patients per group, after PSM. The CR rate was significantly lower in the GC group (75.0%) than in the CRC group (95.0%) (P < 0.01). Before PSM, the TC rate varied significantly by resection type in patients with GC (P = 0.012), indicating that tumor resection influenced the TC rate (P = 0.015). In patients with GC who underwent tumor resection, neither dopamine 2 receptor antagonists (P = 0.090) nor neurokinin 1 receptor antagonist (P = 0.66) use was associated with a significant difference in the CR rate. CONCLUSION: Patients with GC have a higher incidence of CINV than those with CRC. In patients with GC, tumor resection significantly influenced the total control rate of CINV.
  • Yuichiro Uchida, Kosei Takagi, Takeshi Takahara, Tomokazu Fuji, Daiki Kimura, Kazuya Yasui, Ayaka Ito, Akihiro Nishimura, Hirotaka Fukuoka, Shinichi Taniwaki, Hideaki Iwama, Masayuki Kojima, Ichiro Uyama, Toshiyoshi Fujiwara, Koichi Suda
    Surgical endoscopy, Jul 18, 2025  
    BACKGROUND: Late biliary complications, consisting of anastomotic stricture and cholangitis, are known to impair long-term quality of life and significantly impact patient outcomes following robot-assisted pancreaticoduodenectomy (RPD). The role of stent placement in HJ remains debatable. This study aimed to investigate the incidence of late biliary complications and the impact of stent placement on long-term outcomes after RPD. METHODS: This retrospective observational study included patients who underwent RPD from November 2009 to April 2024 at two institutions. Patients were categorized into no-stent, internal stent, and external stent groups. The incidence of late biliary complications was analyzed with Kaplan-Meier estimates and Cox proportional hazards models. RESULTS: The analysis included 157 patients. Late biliary stricture occurred in 20 (13%) cases, with 17 (11%) cases being nontumor-related. No cases of late biliary stricture were observed in patients with a preoperative bile duct diameter of ≥ 15 mm. Internal stent placement was determined as an independent protective factor against late biliary stricture compared to no-stent placement among patients with a bile duct diameter of < 15 mm (hazard ratio: 0.310, 95% confidence interval: 0.096-0.999, p = 0.050). Spontaneous dislocation of internal stents occurred in 71% of cases at 6 months postoperatively. The incidence of postoperative late cholangitis in the internal stent group was 17% (15/89), which was not significantly different compared with the no-stent group (30%, 12/40; p = 0.237). External stent placement prolonged hospitalization and was not superior in biliary complication prevention. CONCLUSIONS: Internal stent placement may decrease the incidence of late biliary stricture after RPD and should be considered a preferred strategy for biliary reconstruction, except in cases with significant bile duct dilatation.
  • Yosuke Ando, Hiroshi Matsuoka, Hanaho Orito, Takuma Ishihara, Tomohiro Mizuno, Nanaho Hiraga, Hidetoshi Katsuno, Zenichi Morise, Akihiko Horiguchi, Koichi Suda, Takahiro Hayashi, Shigeki Yamada
    Japanese journal of clinical oncology, Jul 8, 2025  
    BACKGROUND: Trifluridine/tipiracil (FTD/TPI) plus bevacizumab (BEV) is a standard third-line therapy for unresectable advanced or recurrent colorectal cancer. The standard dosing schedule (5 days of administration followed by 2 days off) is associated with a high incidence of severe neutropenia. Conversely, a biweekly dosing schedule (5 days of administration followed by 9 days off) reportedly reduces this incidence. However, no direct comparison of these regimens has been made. In this study, we retrospectively compared the efficacy and safety of these two dosing schedules. METHODS: We analyzed data from patients who received FTD/TPI + BEV treatment between June 2016 and January 2024 at three hospitals affiliated with Fujita Health University. The effects of the dosing schedules on hematological toxicity, overall survival (OS), and time to treatment failure (TTF) were assessed. RESULTS: Among the 125 patients, 26 and 99 were classified into the standard and biweekly groups, respectively. Grade ≥ 3 neutropenia occurred in 50.0% of patients in the standard group and 29.3% of those in the biweekly group (P = .062), with multivariable analysis confirming the dosing schedule impact (P = .048). Median TTF was 5.4 and 7.0 months, while median OS was 16.4 and 14.5 months (P = .908, 0.947) in the standard and biweekly groups, respectively. CONCLUSION: The biweekly regimen of FTD/TPI + BEV resulted in a lower tendency for severe neutropenia than that in the standard regimen, while maintaining comparable OS and TTF in patients with unresectable advanced or recurrent colorectal cancer.

Misc.

 160

Books and Other Publications

 7

Presentations

 725

Research Projects

 6

Other

 2
  • Jul, 2018 - Present
    ①Surgical Intelligence利活用に関連する通信、情報解析技術(AI含む) *本研究ニーズに関する産学共同研究の問い合わせは藤田医科大学産学連携推進セン ター(fuji-san@fujita-hu.ac.jp)まで
  • Jul, 2018 - Present
    ① 本邦初の内視鏡手術支援ロボット hinotori Surgical Robot Systemを核とした遠隔手術プラットフォーム開発とそこから得られる外科的医療情報(Surgical Intelligence)の利活用についての研究を本学サージカルトレーニングセンターを拠点として進めています。 *本研究シーズに関する産学共同研究の問い合わせは藤田医科大学産学連携推進セン ター(fuji-san@fujita-hu.ac.jp)まで

教育内容・方法の工夫(授業評価等を含む)

 2
  • 件名(英語)
    がんセミナー,医学部講義,大学院保健学研究科講義,医療経営情報学科講義
    開始年月日(英語)
    2012
    終了年月日(英語)
    2014
    概要(英語)
    最新のロボット支援手術も含めた食道胃悪性疾患の外科治療に関する講義
  • 件名(英語)
    慶應義塾大学リーディング大学院に対する遠隔講義
    終了年月日(英語)
    2012/01
    概要(英語)
    当院のTV会議システムを使用した.

作成した教科書、教材、参考書

 2
  • 件名(英語)
    標準外科学 第13版 p470-481
    終了年月日(英語)
    2012
    概要(英語)
    食道悪性疾患全般について執筆
  • 件名(英語)
    藤田保健衛生大学内視鏡外科手術テキスト ロボットから従来型鏡視下手術へのフィードバック
    開始年月日(英語)
    2015/10/01
    概要(英語)
    p2-16, 26-36, 40-44, 47-57, 68-71, 98-111を執筆

その他教育活動上特記すべき事項

 7
  • 件名(英語)
    藤田保健衛生大学ダヴィンチ低侵襲手術トレーニングセンター副センター長
    開始年月日(英語)
    2012/04
    終了年月日(英語)
    2016/03/31
  • 件名(英語)
    2012年度オープンキャンパスにてDTC紹介
    終了年月日(英語)
    2012/08
  • 件名(英語)
    臨床研修指導医講習会
    終了年月日(英語)
    2012/11
    概要(英語)
    第11回藤田保健衛生大学病院臨床研修指導医講習会修了
  • 件名(英語)
    医学教育ワークショップ
    終了年月日(英語)
    2013/04
    概要(英語)
    第46回藤田保健衛生大学医学部医学教育ワークショップ参加
  • 件名(英語)
    M6勉強部屋指導係
    開始年月日(英語)
    2014/06
  • 件名(英語)
    カダバーサージカルトレーニング施設施設長
    開始年月日(英語)
    2019/01/01
  • 件名(英語)
    Director, Cadaver Surgical Training Center, Fujita Health University
    開始年月日(英語)
    2019/01/01