Sho Sato

Dr. Sho Sato

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 July 2021 in Annals of Gastroenterological Surgery
Verified
Journal Article
Open access
PDF file
SSSho Sato
Sho Sato
YOYoko Oshima
Yoko Oshima
YMYu Matsumoto
Yu Matsumoto
YSYasuyuki Seto
Yasuyuki Seto
HYHiroharu Yamashita
Hiroharu Yamashita
HSHIDEAKI Shimada
HIDEAKI Shimada
Background: Real‐world outcomes of nivolumab treatment for gastric cancer and associated prognostic factors remain unclear; the present study aimed to evaluate both items.Methods: A total of 278 consecutive patients treated with nivolumab for gastric cancer during 2017‐2019 were enrolled in this multi‐institutional retrospective cohort study. The impact of laboratory findings, immune‐related adverse events (irAEs), and clinicopathological factors on long‐term survival was evaluated using the Cox proportional hazards model.Results: The response rate was 11.7% in patients with measurable lesions. The overall and progression‐free survival estimates were 6.77 and 2.53 months, respectively. The incidence of irAEs was 30.6% (6.8% for grade ≥3). There were no treatment‐related deaths. Multivariate analysis revealed that C‐reactive protein level of ≤0.5 mg/dL (hazard ratio = 0.476, P < .001), irAE occurrence (hazard ratio = 0.544, P < .001), albumin level of >3.5 g/dL (hazard ratio = 0.688, P = .045), performance status 0 (hazard ratio = 0.711, P = .028), lymphocyte count >1000/μL (hazard ratio = 0.686, P = .027), and differentiated histological type (hazard ratio = 0.740, P = .046) were independently associated with improved survival. The median survival of patients with four or more good prognostic factors was 18.3 months.Conclusion: Nivolumab showed safety and survival benefits in patients with previously treated unresectable or recurrent gastric cancer. Low C‐reactive protein level, irAE occurrence, high albumin level, high lymphocyte count, and differentiated histological type may affect outcomes. The presence of four or more good prognostic factors may help identify likely long‐term survivors.

14 March 2025 in Cancers
Verified
Journal Article
Open access
PDF file
MCMatteo Calì
Matteo Calì
Alberto AiolfiAlberto Aiolfi
Alberto Aiolfi
SSSho Sato
Sho Sato
JHJawon Hwang
Jawon Hwang
GBGianluca Bonitta
Gianluca Bonitta
DBDavide Bona
Davide Bona
Background: Indocyanine green-guided (ICG-guided) lymphadenectomy during gastrectomy for cancer has been proposed to enhance the accuracy of lymphadenectomy. The impact of ICG-guided lymphadenectomy on patient survival remains debated. Methods: The findings of the systematic review were reconstructed into an individual patient data (IDP) meta-analysis with restricted mean survival time difference (RMSTD). Overall survival (OS) and disease-free (DFS) survival were primary outcomes. RMSTD, standardized mead difference (SMD), and 95% confidence intervals (CI) were used as pooled effect size measures. Results: Three studies (6325 patients) were included; 42% of patients underwent ICG-guided lymphadenectomy. The patients’ age ranged from 47 to 72 years and 58% were males. Proximal, distal, and total gastrectomy were completed in 6.8%, 80.4%, and 12.8% of patients, respectively. The surgical approach was laparoscopic (62.3%) and robotic (37.7%). ICG-guided lymphadenectomy was associated with a higher number of harvested lymph nodes compared to non-ICG-guided lymphadenectomy (SMD 0.50; 95% CI 0.45–0.55). At the 42-month follow-up, OS and DFS estimates for ICG-guided vs. non-ICG-guided lymphadenectomy were 0.5 months (95% CI −0.01, 1.1) and 1.3 months (95% CI 0.39, 2.15), respectively. Conclusions: Our analysis suggests that ICG-guided lymphadenectomy offers equivalent long-term OS and DFS compared to non-ICG-guided lymphadenectomy.

9 September 2022 in European Journal of Surgical Oncology
Verified
Journal Article
Closed access
SNShinsuke Nagasawa
Shinsuke Nagasawa
TSTsutomu Sato
Tsutomu Sato
JMJunya Morita
Junya Morita
HKHiroki Kondo
Hiroki Kondo
NTNobuhiro Tsuchiya
Nobuhiro Tsuchiya
CKChikara Kunisaki
Chikara Kunisaki

23 October 2024 in European Journal of Surgical Oncology
Verified
Journal Article
Closed access
HKHiroki Kondo
Hiroki Kondo
SSSho Sato
Sho Sato
CKChikara Kunisaki
Chikara Kunisaki
YTYusaku Tanaka
Yusaku Tanaka
KSKei Sato
Kei Sato
IEItaru Endo
Itaru Endo

1 January 2026 in Asian Journal of Endoscopic Surgery
Verified
Journal Article
Closed access
RKRufuto Kubota
Rufuto Kubota
SSSho Sato
Sho Sato
YFYu Fujii
Yu Fujii
MHMinoru Homma
Minoru Homma
YTYusuke Takeshita
Yusuke Takeshita
IEItaru Endo
Itaru Endo

25 May 2026 in Annals of Surgical Oncology
Verified
Journal Article
Closed access
HWHayato Watanabe
Hayato Watanabe
SSSho Sato
Sho Sato
HKHiroki Kondo
Hiroki Kondo
IHItaru Hashimoto
Itaru Hashimoto
YMYukio Maezawa
Yukio Maezawa
ASAya Saito
Aya Saito