Go Kimura

ORCID: 0000-0003-0088-9324
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About
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Research Areas
  • Renal cell carcinoma treatment
  • Bladder and Urothelial Cancer Treatments
  • Prostate Cancer Treatment and Research
  • Prostate Cancer Diagnosis and Treatment
  • Urinary and Genital Oncology Studies
  • Cancer Immunotherapy and Biomarkers
  • Renal and related cancers
  • Radiopharmaceutical Chemistry and Applications
  • Cancer Genomics and Diagnostics
  • Urological Disorders and Treatments
  • Cancer, Lipids, and Metabolism
  • Radiomics and Machine Learning in Medical Imaging
  • Bone health and treatments
  • Urologic and reproductive health conditions
  • Immune Cell Function and Interaction
  • Urinary Bladder and Prostate Research
  • Asthma and respiratory diseases
  • Economic and Financial Impacts of Cancer
  • Cancer Diagnosis and Treatment
  • Multiple and Secondary Primary Cancers
  • Immunotherapy and Immune Responses
  • Cancer Treatment and Pharmacology
  • HIV Research and Treatment
  • Cancer, Hypoxia, and Metabolism
  • Testicular diseases and treatments

Nippon Medical School
2016-2025

Nippon Medical School Hospital
2016-2025

RIKEN Center for Advanced Intelligence Project
2024

National Hospital Organization
2006-2024

Hospital Universitario Ramón y Cajal
2024

Okayama Medical Center
1993-2024

Hôpital Saint-André
2022

Japanese Urological Association
2017-2021

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori
2020

Istituti di Ricovero e Cura a Carattere Scientifico
2020

Enzalutamide is an oral androgen-receptor inhibitor that prolongs survival in men with metastatic castration-resistant prostate cancer whom the disease has progressed after chemotherapy. New treatment options are needed for patients who have not received chemotherapy, despite androgen-deprivation therapy.

10.1056/nejmoa1405095 article EN New England Journal of Medicine 2014-06-01
Thomas Powles Michiel S. van der Heijden Daniel Castellano Matthew D. Galsky Yohann Loriot and 95 more Daniel P. Petrylak Osamu Ogawa Se Hoon Park Jae‐Lyun Lee Ugo De Giorgi Martin Bögemann Aristotelis Bamias Bernhard J. Eigl Howard Gurney Som D. Mukherjee Yves Fradet Iwona Skoneczna Marinos Tsiatas A I Novikov Cristina Suárez André P. Fay Ignacio Durán Andrea Necchi Sophie Wildsmith Philip He Natasha Angra Ashok Gupta Wendy J. Levin Joaquim Bellmunt Se Hoon Park Michiel S. van der Heijden Andrea Necchi Daniel Castellano Aristotelis Bamias Jae‐Lyun Lee Ugo De Giorgi Martin Bögemann Bernhard J. Eigl Marinos Tsiatas Thomas Powles A I Novikov Iwona Skoneczna Som D. Mukherjee Cristina Suárez Hans M. Westgeest Yves Fradet Aude Fléchon Yen‐Chuan Ou Inkeun Park Vsevolod Matveev Begoña Pérez-Valderrama Susanna Cheng Stephen Jay Frank Howard Gurney Urbano Anido Alketa Hamzaj Margitta Retz Srikala S. Sridhar Giorgio V. Scagliotti Jens Voortman B. Yа. Alekseev Anna Alyasova B. K. Komyakov Herlinde Dumez Michel Pavic Go Kimura Atsushi Mizokami Susanne Osanto José Ángel Arranz Djura Piersma Sang Joon Shin O. B. Karyakin Ignacio Delgado José Luis González See‐Tong Pang Anna Tran O. N. Lipatov Wen-Pin Su Thomas W. Flaig Ajjai Alva Hwa Park Kyong Evgeny Kopyltsov Elena Almagro M. Doménech Yen‐Hwa Chang Brieuc Sautois Andre Ravaux Gerasimos Aravantinos V. Georgoulias Sasja F. Mulder Yu Jung Kim Fabio Kater Christine Chevreau Scott T. Tagawa Paweł Zalewski Florence Joly Yohann Loriot Gencay Hatiboglu Luca Gianni Franco Morelli

10.1016/s1470-2045(20)30541-6 article EN The Lancet Oncology 2020-09-21
Thomas Powles Piotr Tomczak Se Hoon Park Balaji Venugopal Thomas Ferguson and 95 more Stefan N. Symeonides Jaroslav Hájek Howard Gurney Yen‐Hwa Chang Jae‐Lyun Lee Naveed Sarwar Antoine Thiery-Vuillemin Marine Gross‐Goupil Mauricio Mahave Naomi B. Haas Piotr Sawrycki Joseph E. Burgents Lei Xu Kentaro Imai David I. Quinn Toni K. Choueiri Piotr Tomczak Toni K. Choueiri Se Hoon Park Balaji Venugopal Thomas Ferguson Jaroslav Hájek Tzu-Ping Lin Stefan N. Symeonides Jae‐Lyun Lee Piotr Sawrycki Naomi B. Haas Howard Gurney Mauricio Mahave Naveed Sarwar Antoine Thiery-Vuillemin Marine Gross‐Goupil Christine Chevreau John M. Burke Gurjyot K. Doshi Bohuslav Melichar Delphine Topart Stéphane Oudard Evgeniy Kopyltsov H. Hammers David I. Quinn Ajjai Alva Juliana de Menezes Adriano Goncalves e Silva Eric Winquist Alketa Hamzaj Giuseppe Procopio Boguslawa Karaszewska Ewa M. Nowakowska-Zajdel B. Yа. Alekseev Rustem Gafanov А. А. Измайлов Andrey Semenov S. G. Afanasyev O. N. Lipatov T.B. Powles Sandy Srinivas David F. McDermott Samith T. Kochuparambil Ian D. Davis Katriina Peltola Roberto Sabbatini Jinsoo Chung М. I. Shkolnik В. Б. Матвеев P. Gajate Borau Steven McCune Thomas E. Hutson Alejandro Dri Silvio Correia Sales Carrie Yeung Carmen Marcela Alcala Castro Peter J. Boström Brigitte Laguerre Consuelo Buttigliero Ugo De Giorgi Eugeniy A. Fomin Yousef Zakharia Clara Hwang Eric A. Singer Jeffrey T. Yorio David Waterhouse Rubén Dario Kowalyszyn Margarita Sonia Alfie Eduardo Yañez Ruiz Tomáš Büchler Krista Kankaanranta G. Ferretti Go Kimura Kazuo Nishimura Naoya Masumori Satoshi Tamada Haruaki Kato Hiroshi Kitamura Iwona Danielewicz

The first interim analysis of the KEYNOTE-564 study showed improved disease-free survival with adjuvant pembrolizumab compared placebo after surgery in patients clear cell renal carcinoma at an increased risk recurrence. reported here, additional 6 months follow-up, was designed to assess longer-term efficacy and safety versus placebo, as well secondary exploratory endpoints.In multicentre, randomised, double-blind, placebo-controlled, phase 3 trial, adults aged 18 years or older recurrence...

10.1016/s1470-2045(22)00487-9 article EN cc-by-nc-nd The Lancet Oncology 2022-08-30

Abstract Deep learning algorithms have been successfully used in medical image classification. In the next stage, technology of acquiring explainable knowledge from images is highly desired. Here we show that deep algorithm enables automated acquisition features diagnostic annotation-free histopathology images. We compare prediction accuracy prostate cancer recurrence using our algorithm-generated with diagnosis by expert pathologists established criteria on 13,188 whole-mount pathology...

10.1038/s41467-019-13647-8 article EN cc-by Nature Communications 2019-12-18

LBA1^ Background: Enzalutamide, an orally administered androgen receptor inhibitor, improved overall survival (OS) in men with mCRPC who had received prior docetaxel therapy (Scher et al, NEJM 367:13, 2012). This study examined whether enzalutamide could prolong OS and radiographic progression-free (rPFS) asymptomatic or mildly symptomatic chemotherapy-naive mCRPC. Methods: In this randomized, double-blind, placebo-controlled, multinational phase 3 (NCT01212991), patients were stratified by...

10.1200/jco.2014.32.4_suppl.lba1 article EN Journal of Clinical Oncology 2014-02-01

Abstract Background In patients with renal cell carcinoma (RCC) enrolled in the phase III KEYNOTE-564 trial (NCT03142334), disease-free survival (DFS) following nephrectomy was prolonged use of adjuvant pembrolizumab therapy versus placebo. Patient-reported outcomes (PROs) provide an important measure health-related quality life (HRQoL) and can complement efficacy safety results. Patients Methods KEYNOTE-564, 994 were randomly assigned to receive 200 mg (n = 496) or placebo 498)...

10.1093/oncolo/oyad231 article EN cc-by-nc The Oncologist 2023-08-09

This study presents the enfortumab vedotin (EV) treatment analysis at our institution. We retrospectively analyzed patients with metastatic urothelial cancer (mUC) treated EV between January 2021 and October 2023. was administered 1.25 mg/kg on days 1, 8, 15 in a 28-day cycle. Whole-body computed tomography scans were performed to assess response. Patient characteristics, histories, response rates, progression-free survival, adverse events evaluated. Response rates determined, recorded....

10.3390/curroncol31020056 article EN cc-by Current Oncology 2024-01-29

Evidence has been accumulating that in many tumors, insulin-like growth factors (IGFs) promote cancer cell an autocrine/paracrine manner via the IGF-I receptor. In effort to understand role of IGFs prostate growth, we characterized IGF system components produced by human prostatic cell-lines, LNCaP, DU145, and PC-3, grown serum-free medium.IGFs, their receptors, binding proteins (IGFBPs) three lines were reverse transcriptase-polymerase chain reaction (RT-PCR), radioimmunoassay (RIA),...

10.1111/j.1442-2042.1996.tb00628.x article EN International Journal of Urology 1996-01-01

Nivolumab improved overall survival (OS) and objective response rate (ORR) versus everolimus in previously treated patients with advanced renal cell carcinoma the phase III CheckMate 025 study (minimum follow-up: 14 months). We report efficacy safety global Japanese populations 26 months).Patients were randomized 1:1 to receive nivolumab 3 mg/kg intravenously every 2 weeks or 10-mg tablet orally once daily. Primary endpoint: OS, key secondary endpoints: ORR, progression-free safety.Of 410...

10.1093/jjco/hyx049 article EN cc-by-nc Japanese Journal of Clinical Oncology 2017-04-05

Nivolumab treatment resulted in superior efficacy and safety versus everolimus the 2-year follow-up of CheckMate 025 Phase III study, with consistent results global population Japanese population. Here, we report 3-year both groups. Patients were randomized 1:1 to nivolumab 3 mg/kg intravenously every 2 weeks or 10 mg orally once daily until progression/intolerable toxicity. The primary endpoint was overall survival (OS). Key secondary endpoints included objective response rate,...

10.1093/jjco/hyz026 article EN Japanese Journal of Clinical Oncology 2019-02-22

Nivolumab plus ipilimumab (NIVO+IPI) demonstrated superior efficacy over sunitinib (SUN) for previously untreated advanced renal cell carcinoma (aRCC) in CheckMate 214, with a manageable safety profile. We report and extended follow-up amongst Japanese patients.CheckMate 214 patients received NIVO (3 mg/kg) IPI (1 every 3 weeks four doses, then 2 weeks; or SUN (50 mg) once daily 4 (6-week cycle). This subgroup analysis assessed overall survival (OS), objective response rate (ORR)...

10.1093/jjco/hyz132 article EN cc-by-nc Japanese Journal of Clinical Oncology 2019-08-29

Abstract Background The phase 3 open-label KEYNOTE-426 study demonstrated that first-line pembrolizumab plus axitinib improved overall survival (OS) and progression-free (PFS) versus sunitinib for metastatic renal cell carcinoma (mRCC) in a global population. This subgroup analysis investigated the efficacy safety of pembrolizumab-axitinib patients enrolled East Asia (Japan, South Korea, Taiwan). Methods Adults with clear mRCC were randomly assigned 1:1 to receive intravenous 200 mg every...

10.1093/jjco/hyae182 article EN cc-by-nc Japanese Journal of Clinical Oncology 2025-01-16

381 Background: Although there studies have been reported that brachytherapy (BT) for prostate cancer is associated with an increased incidence of metachronous urinary bladder (MBC), few clarified differences in the clinicopathological features (CPF) MBC between BT and prostatectomy (RP). We studied risk CPF RP groups our hospital after long-term follow-up. Methods: Five hundred four patients treated 471 referred 2006 2017 were reviewed. compared including tumor number, location within...

10.1200/jco.2025.43.5_suppl.381 article EN Journal of Clinical Oncology 2025-02-10

In a previous study (Y. Koga, M. Sasaki, H. Yoshida, Wigzell, G. Kimura, and K. Nomoto, J. Immunol. 144:94-102, 1990), we demonstrated that the expression of gp160, precursor form envelope glycoprotein human immunodeficiency virus type 1, in CD4+ cells causes downregulation surface CD4 single-cell killing by forming intracellular gp160-CD4 complex. present investigated events lead to cell death expressing gp160. We found apoptosis is induced undergoing death. Moreover, even clone, which...

10.1128/jvi.68.1.390-399.1994 article EN Journal of Virology 1994-01-01

Abstract A plasmid which has an envelope gene from the human T lymphotropic virus IIIB isolate of HIV under transcriptional control metallothionein IIA promoter was constructed and transfected into CD4+ CD4- cell lines. When expression env induced with metal ions in cloned lines such cells, viral protein precursor, gp160, produced both clones same amounts. An extensive cytopathic effect developed resulting killing; however, this occurred only not clones. The formation syncytium found those...

10.4049/jimmunol.144.1.94 article EN The Journal of Immunology 1990-01-01

Interstitial brachytherapy for localised prostate cancer may be followed by transient increases in prostate-specific antigen (PSA) that resolve without therapy. Such PSA bounces associated with an improved outcome but often cause alarm the patient and physician, have defied explanation. We developed a mathematical model to capture interactions between tumour, radiation anti-tumour immune response. The was fitted data from large cohort of patients treated exclusively interstitial...

10.1038/bjc.2016.171 article EN cc-by-nc-sa British Journal of Cancer 2016-07-01

Up to a fifth of patients diagnosed with prostate cancer (PC) will develop castration-resistant (CRPC), which has been associated poor prognosis. The aim this study was consider the patient perspective as part overall treatment decision-making process for CRPC, given that an alignment between preference and prescribing shown benefit outcomes. This examines preferences CRPC in Japan features treatments like RA-223, abiraterone, docetaxel examine extent may vary symptomatic asymptomatic...

10.1186/s12894-016-0182-2 article EN cc-by BMC Urology 2016-11-04

A CD4+ human monocytoid cell line, U937, was transfected with a constructed plasmid which has the envelope gene of immunodeficiency virus under transcriptional control metallothionein IIA promoter and cloned thereafter. These lines (EH EL cells) expressed viral gp160 in cytoplasm. The expression surface CD4 antigen examined by Leu3a OKT4 monoclonal antibodies, however, disappeared completely EH cells, produce larger amount gp160, while diminishing only partly smaller gp160. results indicate...

10.1128/jvi.63.9.3748-3754.1989 article EN Journal of Virology 1989-09-01
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