Updated on 2026/08/18

Information

 

写真a

 
ANDO YOHEI
 
Organization
Kyushu University Hospital Gastrointestinal Surgery (1) Assistant Professor
Title
Assistant Professor

Education

  • Kyushu University   医学部   医系学府

    2016.4 - 2020.6

  • Oita University   医学部   医学科

    2004.4 - 2010.3

Papers

  • Using Tumor Marker Gene Variants to Improve the Diagnostic Accuracy of DUPAN-2 and Carbohydrate Antigen 19-9 for Pancreatic Cancer Reviewed International journal

    Ando Y., Dbouk M., Yoshida T., Saba H., Diwan E.A., Yoshida K., Dbouk A., Blackford A.L., Lin M.T., Lennon A.M., Burkhart R.A., He J., Sokoll L., Eshleman J.R., Canto M.I., Goggins M.

    Journal of Clinical Oncology   42 ( 18 )   2196 - 2206   2024.6   ISSN:0732183X

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Journal of Clinical Oncology  

    PURPOSE Circulating carbohydrate antigen 19-9 (CA19-9) levels reflect FUT3 and FUT2 fucosyltransferase activity. Measuring the related glycan, DUPAN-2, can be useful in individuals unable to synthesize CA19-9. We hypothesized that similar to CA19-9, FUT functional groups determined by variants in FUT3 and FUT2 influence DUPAN-2 levels, and having tumor marker reference ranges for each functional group would improve diagnostic performance. MATERIALS Using a training/validation study design, FUT2/FUT3 genotypes were deter-AND METHODS mined in 938 individuals from Johns Hopkins Hospital: 607 Cancer of the Pancreas Screening (CAPS) study subjects with unremarkable pancreata and 331 with pancreatic ductal adenocarcinoma (PDAC). Serum DUPAN-2 and CA19-9 levels were measured by immunoassay. RESULTS In controls, three functional FUT groups were identified with significant differences in DUPAN-2 levels: FUT3-intact, FUT3-null/FUT2-intact, and FUT3-null/FUT2-null. DUPAN-2 training set diagnostic cutoffs for each FUT group yielded higher diagnostic sensitivity in the validation set for patients with stage I/II PDAC than uniform cutoffs (60.4% [95% CI, 50.2 to 70.0] v 39.8% [30.0 to 49.8]), at approximately 99% (96.7 to 99.6) specificity. Combining FUT/CA19-9 and FUT/DUPAN-2 tests yielded 78.4% (72.3 to 83.7) sensitivity for stage I/II PDAC, at 97.7% (95.3 to 99.1) specificity in the combined sets, with higher AUC (stage I/II: 0.960 v 0.935 for CA19-9 1 DUPAN-2 without the FUT test; P < .001); for stage I PDAC, sensitivity was 62.0% (49.1 to 73.2; AUC, 0.919 v 0.883; P 5 .03). CA19-9 levels in FUT3-null/FUT2-null PDAC subjects were higher than in FUT3-null/FUT2-intact subjects (median/IQR; 24.9/57.4 v <1/2.3 U/mL; P 5 .0044). In a simulated CAPS cohort, AUC precision recall (AUC<inf>PR</inf>) scores were 0.51 for CA19-9 alone, 0.64 for FUT/CA19-9, 0.73 for CA19-9/DUPAN-2, and 0.84 for FUT/CA19-9/DUPAN-2. CONCLUSION Using a tumor marker gene test to individualize CA19-9 and DUPAN-2 reference ranges achieves high diagnostic performance for stage I/II pancreatic cancer.

    DOI: 10.1200/JCO.23.01573

    Scopus

  • Perioperative Outcomes of Robotic Versus Conventional Laparoscopic Pelvic Exenteration for Anteriorly Invaded Primary Colorectal Cancer: A Retrospective Study Reviewed International journal

    Manabe, T; Takesue, S; Fujimoto, T; Mizuuchi, Y; Ando, Y; Hiraki, M; Nakamura, M; Noshiro, H

    SURGICAL LAPAROSCOPY ENDOSCOPY & PERCUTANEOUS TECHNIQUES   36 ( 1 )   2026.2   ISSN:1530-4515 eISSN:1534-4908

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Surgical Laparoscopy Endoscopy and Percutaneous Techniques  

    Background: – Robot-assisted surgery has been widely adopted in digestive, urological, and gynecologic procedures, leading to its application in complex operations such as pelvic exenteration (PE). However, limited data are available regarding the perioperative outcomes of robotic PE compared directly to conventional laparoscopic PE in the treatment of colorectal cancer. Methods: – To assess the feasibility of robotic PE compared with laparoscopic PE for locally advanced colorectal cancer invading the anterior pelvic organs, we retrospectively reviewed patients who underwent either robotic or laparoscopic PE with curative intent (R0 resection) between May 2012 and August 2024. Results: – A total of 24 patients were included in the study (12 in the robotic group and 12 in the laparoscopic group). Patient characteristics revealed that the robotic group had an older median age and a lower prognostic nutritional index. In terms of surgical outcomes, no significant differences were observed in PE type, total operative time, estimated blood loss, or the number of retrieved lymph nodes. Conversion to open surgery occurred in 3 patients in the laparoscopic group, whereas no conversions were noted in the robotic group (P = 0.032). The reasons for conversion in the laparoscopic group included uncontrollable bleeding and technical difficulty due to large tumor size. Conclusions: – Robotic surgery may offer greater suitability for complex procedures such as PE, compared with conventional laparoscopic surgery, particularly in challenging cases involving large tumors.

    DOI: 10.1097/SLE.0000000000001424

    Web of Science

    Scopus

    PubMed

  • 局所進行および再発直腸癌に対する腹腔鏡下骨盤内臓器全摘術の短期転帰の評価(Evaluating the short-term outcome of laparoscopic pelvic exenteration in locally advanced and recurrent rectal cancer) Reviewed International journal

    Ozaki Kosuke, Mukai Toshiki, Ando Yohei, Noguchi Tatsuki, Sakamoto Takashi, Matsui Shimpei, Yamaguchi Tomohiro, Akiyoshi Takashi

    Surgery Today   55 ( 11 )   1621 - 1628   2025.11   ISSN:0941-1291

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:シュプリンガー・ジャパン(株)  

    局所再発直腸癌(LRRC)に対する腹腔鏡下骨盤内臓器全摘術(Lap PE)の技術的安全性を検討した。2013~2023年の当施設63例を原発群41例と再発群22例に分類し後ろ向きに比較した。再発群では他臓器合併切除を要する症例が14例(63.6%)と原発群10例(24.4%)より有意に多かった。手術時間は再発群(633分)と原発群(714分)に有意差は認めず、術中出血量にも有意な群間差は認めなかった(580 vs. 650g)。開腹移行はいずれも認めなかった。R0切除率は再発群(81.8%)、原発群(95.1%)で有意差は認めなかった。Clavien-Dindo分類GradeIII以上の合併症は再発群18.2%、原発群29.3%で有意差は認めなかった。以上より、原発と再発で短期成績は概ね同等であった。

  • Evaluating the short-term outcome of laparoscopic pelvic exenteration in locally advanced and recurrent rectal cancer Reviewed International journal

    Ozaki K., Mukai T., Ando Y., Noguchi T., Sakamoto T., Matsui S., Yamaguchi T., Akiyoshi T.

    Surgery Today   55 ( 11 )   1621 - 1628   2025.11   ISSN:09411291

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Surgery Today  

    Purpose: Pelvic exenteration (PE) is sometimes the only curative option for primary rectal cancer as well as locally recurrent rectal cancer (LRRC). However, data on laparoscopic PE (Lap-PE) for LRRC are limited. This study aimed to evaluate the technical safety of Lap-PE in LRRC cases. Methods: We retrospectively analyzed 63 patients who underwent Lap-PE between January 2013 and December 2023. Patients were categorized into primary (n = 41) and recurrent (n = 22) groups, and short-term outcomes, including operative details and postoperative complications, were compared. Results: The recurrent group had a significantly higher number of cases of multiple organs resected beyond PE (24.4% vs. 63.6%, p = 0.001). There were no significant differences in the operative time (714 vs. 633 min, p = 0.91) or blood loss (650 vs. 580 g, p = 0.98) between the groups. Clavien-Dindo Grade 3 complications occurred in 29.3% of primary cases and 18.2% of recurrent cases (p = 0.47). R0 resection was achieved in 95.1% of primary cases and 81.8% of recurrent cases (p = 0.10). Conclusion: Lap PE for LRRC, when performed by an experienced laparoscopic surgical team with careful patient selection, was shown to be safe, with comparable short-term outcomes to those of PE for primary rectal cancer and an acceptable R0 resection rate.

    DOI: 10.1007/s00595-025-03048-4

    Scopus

  • Germline Pathogenic Variants in Patients with Pancreatic and Periampullary Cancers Reviewed International journal

    Ando Y., Dbouk M., Yoshida T., Abou Diwan E., Saba H., Dbouk A., Yoshida K., Roberts N.J., Klein A.P., Burkhart R., He J., Hruban R.H., Goggins M.

    JCO Precision Oncology   8   2024.5

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:JCO Precision Oncology  

    PURPOSEInherited cancer susceptibility is often not suspected in the absence of a significant cancer family history. Pathogenic germline variants in pancreatic cancer are well-studied, and routine genetic testing is recommended in the guidelines. However, data on rare periampullary cancers other than pancreatic cancer are insufficient. We compared the prevalence of germline susceptibility variants in patients with pancreatic cancer and nonpancreatic periampullary cancers.MATERIALS AND METHODSSix hundred and eight patients who had undergone pancreaticoduodenal resection at a tertiary referral hospital were studied, including 213 with pancreatic ductal adenocarcinoma, 172 with ampullary cancer, 154 with distal common bile duct cancer, and 69 with duodenal adenocarcinoma. Twenty cancer susceptibility and candidate susceptibility genes were sequenced, and variant interpretation was assessed by interrogating ClinVar and PubMed.RESULTSPathogenic or likely pathogenic, moderate- to high-penetrant germline variants were identified in 46 patients (7.7%), including a similar percentage of patients with pancreatic (8.5%) and nonpancreatic periampullary cancer (7.1%). Low-penetrant variants were identified in an additional 11 patients (1.8%). Eighty-nine percent of the moderate- to high-penetrant variants involved the major cancer susceptibility genes BRCA2, ATM, BRCA1, CDKN2A, MSH2/MLH1, and PALB2; the remaining 11% involved other cancer susceptibility genes such as BRIP1, BAP1, and MSH6. Almost all pathogenic variant carriers had a family history of cancer.CONCLUSIONPatients with pancreatic and nonpancreatic periampullary cancer have a similar prevalence of pathogenic cancer susceptibility variants. Germline susceptibility testing should be considered for patients with any periampullary cancer.

    DOI: 10.1200/PO.24.00101

    Scopus

  • Using a CA19-9 Tumor Marker Gene Test to Assess Outcome After Pancreatic Cancer Surgery Reviewed International journal

    Ando Y., Dbouk M., Blackford A.L., Yoshida T., Saba H., Abou Diwan E., Yoshida K., Sokoll L., Eshleman J.R., Burkhart R., He J., Goggins M.

    Annals of Surgical Oncology   31 ( 5 )   2902 - 2912   2024.5

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Annals of Surgical Oncology  

    BACKGROUND: Cancer antigen 19-9 (CA19-9) is widely used as a marker of pancreatic cancer tumor burden and response to therapy. Synthesis of CA19-9 and its circulating levels are determined by variants encoding the fucosyltransferases, FUT2 and FUT3. Individuals can be grouped into one of four functional FUT groups (FUT3-null, FUT-low, FUT-intermediate, FUT-high), each with its own CA19-9 reference range based on its predicted capacity to produce CA19-9. The authors hypothesized that a FUT variant-based CA19-9 tumor marker gene test could improve the prognostic performance of CA19-9. METHODS: Preoperative and pre-treatment CA19-9 levels were measured, and FUT variants were determined in 449 patients who underwent surgery for pancreatic ductal adenocarcinoma (PDAC) at Johns Hopkins Hospital between 2010 and 2020, including 270 patients who underwent neoadjuvant therapy. Factors associated with recurrence-free and overall survival were determined in Cox proportional hazards models. RESULTS: Higher preoperative CA19-9 levels were associated with recurrence and mortality for patients in the higher-FUT groups (FUT-intermediate, FUT-high for mortality, with adjustment for other prognostic factors; hazard ratio [HR], 1.34 and 1.58, respectively; P < 0.001), but not for those in the lower-FUT groups (FUT3-null, FUT-low). As a tumor marker, CA19-9 levels of 100 U/ml or lower after neoadjuvant therapy and normalization of CA19-9 based on FUT group were more sensitive but less specific predictors of evidence for a major pathologic response to therapy (little/no residual tumor) and of early recurrence (within 6 months). CONCLUSION: Among patients undergoing pancreatic cancer resection, a CA19-9 tumor marker gene test modestly improved the prognostic performance of CA19-9.

    DOI: 10.1245/s10434-024-14942-5

    Scopus

  • ASO Author Reflections: Using a CA19-9 Tumor Marker Gene Test to Assess Outcome after Pancreatic Cancer Surgery Reviewed International journal

    Ando Y., Goggins M.

    Annals of Surgical Oncology   31 ( 5 )   2961 - 2962   2024.5   ISSN:10689265

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    Authorship:Lead author   Publisher:Annals of Surgical Oncology  

    DOI: 10.1245/s10434-024-14974-x

    Scopus

  • Diagnostic Performance of a Tumor Marker Gene Test to Personalize Serum CA19–9 Reference Ranges Reviewed International journal

    Dbouk M., Abe T., Koi C., Ando Y., Saba H., Diwan E.A., MacGregor-Das A., Blackford A.L., Mocci E., Beierl K., Dbouk A., He J., Burkhart R., Lennon A.M., Sokoll L., Canto M.I., Eshleman J.R., Goggins M.

    Clinical Cancer Research   29 ( 20 )   4178 - 4185   2023.10   ISSN:10780432

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    Publishing type:Research paper (scientific journal)   Publisher:Clinical Cancer Research  

    Purpose: CA19–9 synthesis is influenced by common variants in the fucosyltransferase (FUT) enzymes FUT3 and FUT2. We developed a clinical test to detect FUT variants, and evaluated its diagnostic performance for pancreatic ductal adenocarcinoma (PDAC). Experimental Design: A representative set of controls from the Cancer of the Pancreas Screening study was identified for each FUT functional group. Diagnostic sensitivity was determined first in a testing set of 234 PDAC cases, followed by a 134-case validation set, all of whom had undergone resection with curative intent without neoadjuvant therapy. Tumor marker gene testing was performed in the Johns Hopkins Molecular Diagnostics Laboratory. CA19–9 levels were measured in the Hopkins Clinical Chemistry lab. Receiver operating characteristic (ROC) curve analysis was used to evaluate the discriminative ability of CA19–9 alone versus with the gene test. Results: Applying the CA19–9 standard cutoff (<36 U/mL) to all 716 subjects yielded a 68.8% sensitivity in the test set of cases, 67.2% in the validation set, at 91.4% specificity. Applying 99th percentile cutoffs according to each individual’s FUT group (3, 34.9, 41.8, and 89.2, for the FUT3-null, FUT-low, FUT-intermediate, and FUT-high groups, respectively) yielded a diagnostic sensitivity for CA19–9 in the first set of cases of 66.7%, 65.7% in the validation set, at 98.9% specificity. ROC analysis for CA19–9 alone yielded an AUC of 0.84; with the tumor marker gene test, AUC improved to 0.92 (P < 0.001). Conclusions: Using a tumor marker gene test to personalize an individual’s CA19–9 reference range significantly improves diagnostic accuracy.

    DOI: 10.1158/1078-0432.CCR-23-0655

    Scopus

  • Necroptosis in pancreatic cancer promotes cancer cell migration and invasion by release of CXCL5

    ANDO Yohei

    2020.6

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    Authorship:Lead author   Language:Japanese   Publishing type:Doctoral thesis  

    収集根拠 : 博士論文(自動収集)

    DOI: 10.1371/journal.pone.0228015

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MISC

Research Projects

  • Xeniumを用いたTLS成熟度に基づく濾胞樹状細胞を標的とした新規胃癌治療開発

    Grant number:25K19769  2025.4 - 2027.3

    Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

    安藤 陽平

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    Grant type:Scientific research funding

    本研究は、胃癌腫瘍における免疫微小環境(TME)における高度なheterogeneityを解析するため、Xeniumを用いて胃癌における三次リンパ様構造(TLS)に存在する濾胞性樹状細胞(FDC)の役割を解明し、新たな治療法の開発を目指すものである。TLSは抗腫瘍免疫活性に寄与する免疫細胞の集合体として注目されているが、FDCの機能については未解明の部分が多い。先行研究において、胃癌患者の多くがTLSを有しており、その成熟度によってFDCの局在が異なることが判明している。本研究では、未熟TLSに存在するFDCに焦点を当て、これらを活性化させることによってTLSの成熟を促進し、抗腫瘍効果を発揮する治療標的分子を同定することを目指す。

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  • Investigation and Therapeutic Exploitation of Chemotherapy-Induced Anti-Tumor Immunity in Gastric Cancer

    Grant number:21K15570  2022.12 - 2025.3

    Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

    ANDO Yohei

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    Grant type:Scientific research funding

    In recent years, immunotherapy has become a standard treatment option for gastric cancer; however, the tumor microenvironment (TME) remains incompletely understood, and the prognosis of advanced gastric cancer is still poor. In this study, we analyzed immune cell dynamics in the TME altered by neoadjuvant chemotherapy (NAC) using single-cell RNA sequencing (scRNA-seq). Tumor and adjacent normal mucosal tissues were obtained from nine gastric cancer patients who underwent gastrectomy. Comparison between the NAC and non-NAC groups revealed that CD8+ T cells in the NAC group exhibited changes in cytotoxicity and exhaustion, along with altered expression of immunosuppressive factors in tumor cells and regulatory T cells (Tregs). These findings suggest that chemotherapy may induce immune evasion mechanisms within the TME, potentially contributing to therapeutic resistance.

    CiNii Research

  • scRNA-seqを用いた化学療法による癌免疫環境改変メカニズムの解明

    Grant number:20K22957 

    安藤 陽平

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    Grant type:Scientific research funding

    ヒト胃癌検体に対しscRNAseqを用いることで、従来は認識不可能であった、細胞個々、もしくはそれに近いレベルでの腫瘍微小環境の違いを認識することで、新たな治療標的や化学療法関連の予後規定因子の発見などを目指す。さらに、PDXモデルを用いることにより、実際のヒトに近い実験系において治療実験を行い、化学療法による腫瘍免疫の変化の解明や新規標的治療の探索とその有効性の実証を行う。

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  • 大腸癌発癌過程における粘膜特異的免疫エコシステムの解明

    Grant number:24K11849 

    水内 祐介, 安藤 陽平, 藤本 崇聡, 田村 公二

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    Grant type:Scientific research funding

    大腸粘膜では、免疫系が外来物質を選別し共生もしくは排除することで生体恒常性を維持している。この部位特異的な免疫系と微生物叢の発達による独自の共生エコシステムが、発癌や癌の進展に寄与しているとされる。また近年シングルセルトランスクリプトーム解析等の手法が普及し、腫瘍微小環境の多様性、細胞間相互作用を詳細に解析可能となった。本研究では、大腸癌発癌の各段階における大腸粘膜のエコシステムの変化を、菌叢解析とsingle cell RNA sequencing (scRNA-seq)の技術を用いて解明し、発癌過程において癌細胞の免疫回避に関わる菌叢の変化やその機序を解明する。

    CiNii Research