EUROPEAN UROLOGY欧洲泌尿外科

EUROPEAN UROLOGY(英文缩写 EUR UROL),ISSN 0302-2838,eISSN 1873-7560,中文译名:欧洲泌尿外科 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
29.100
JCR 分区
Q1
CAS 分区
B1
近一年发文量
449
本站 PubMed 收录统计

发文量统计区间:2025-11-01 至 2026-10-31,按本站收录文献的发表日期统计。

ISSN: 0302-2838 · eISSN: 1873-7560 · 缩写: EUR UROL ·中文: 欧洲泌尿外科

期刊介绍

选择期刊介绍栏目

期刊简介

European Urology 是欧洲泌尿外科学会官方期刊,聚焦泌尿系统疾病的基础、临床与转化研究,涵盖肿瘤、结石、感染、排尿功能障碍及男科等领域。读者群主要为泌尿外科医师、肿瘤学家及相关科研人员。该刊以发表高影响力临床 trials、系统综述和指南类文章著称,在国际泌尿学界具有权威地位,常被视作该领域前沿成果的重要发布平台。

研究方向

主要方向包括泌尿肿瘤(前列腺癌、膀胱癌、肾癌等)、腔镜与机器人手术、结石病、尿路感染、神经泌尿学、男科与性医学。论文类型涵盖原创临床研究、随机对照试验、系统综述与荟萃分析、实践指南及专家共识,也接受具有转化意义的基础研究。

期刊特色

研究取向强调临床相关性与方法学严谨性,偏好大样本、多中心或前瞻性设计,统计分析与报告规范要求较高。论文通常需具备改变临床实践或启发后续研究的潜力。适合已完成高质量临床研究、希望在国际顶级泌尿学期刊展示成果的资深临床医生与研究者。

投稿难度

投稿难度很高,对创新性、样本量、随访完整性和统计严谨性均有严格要求。建议在投稿前充分评估研究的新颖性与临床意义,完善试验注册、伦理审批和报告规范,并针对该刊读者群凝练信息。若被拒稿,可考虑同领域其他高影响力期刊。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202124.344Q1
202223.400Q1
202325.300Q1
202425.200Q1
202529.100Q1

EUROPEAN UROLOGY 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    1. {"_":"Re: Sobia Khan, Nathan Papa, Andrew Kneebone, et al. Prospective Comparison of Copper [Cu]SAR-bisPSMA vs Gallium [Ga] PSMA-11 PET/CT for Biochemical Recurrence of Prostate Cancer Following Radical Prostatectomy (Co-PSMA Trial). Eur Urol 2026;89:512-20.","sup":["64","64","68","68"]}

    1. {"_":"回复:Sobia Khan、Nathan Papa、Andrew Kneebone等。铜[Cu]SAR-bisPSMA与镓[Ga]PSMA-11 PET/CT在根治性前列腺切除术后前列腺癌生化复发中的前瞻性比较(Co-PSMA试验)。Eur Urol 2026;89:512-20。","sup":["64","64","68","68"]}
    作者:
    Elif Hindié, Aurélien Callaud, Clément Morgat
    日期:
    2026-10-03

    该文献暂无摘要。

  2. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    2. Accumulating Evidence Supports NECTIN4 as a Predictive Biomarker for Enfortumab Vedotin: The Compartment Still Matters.

    2. 不断积累的证据支持NECTIN4作为恩诺单抗维多汀的预测性生物标志物:区室仍然重要
    作者:
    Niklas Klümper, Jonathan E Rosenberg, David H Aggen, Markus Eckstein
    日期:
    2026-10-03

    Accumulating data support nectin-4, particularly membranous expression, as a predictive biomarker of enfortumab vedotin activity. Low expression identifies patients with poorer outcomes but not absence of benefit, underscoring the need for standardized prospective validation before clinical implementation.

  3. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    3. Reply to Paolo Zaurito's Letter to the Editor re: Robert M. Meier, Nima Aghdam, Alan C. Beckman, et al. 10-yr Survival and Toxicity Outcomes of Stereotactic Body Radiotherapy for Prostate Cancer: A Nonrandomized Clinical Trial. Eur Urol. In press. http://dx.doi.org/10.1016/j.eururo.2026.04.029.

    3. 回复Paolo Zaurito致编辑的信,关于Robert M. Meier、Nima Aghdam、Alan C. Beckman等人的文章:前列腺癌立体定向体部放疗的10年生存和毒性结局:一项非随机临床试验。Eur Urol。出版中。http://dx.doi.org/
    作者:
    Robert Meier, Nima Aghdam, Irving Kaplan
    日期:
    2026-10-03

    该文献暂无摘要。

  4. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    4. Reply to Riccardo Lombardo's Letter to the Editor re: Bi-Ming He, Keqin Zhang, Zhien Zhou, et al. Cognitive Versus Software-based Fusion targeted Biopsy for the Diagnosis of Clinically Significant Prostate Cancer: A Multicenter, Randomized, Noninferiority Trial (IMAGINATION). Eur Urol. In press. http://dx.doi.org/10.1016/j.eururo.2026.06.020.

    4. 回复Riccardo Lombardo致编辑的信,关于:Bi-Ming He、Keqin Zhang、Zhien Zhou等人。认知融合与基于软件融合的靶向穿刺活检对临床显著性前列腺癌诊断的比较:一项多中心、随机、非劣效性试验(IMAGINATION)。Eur Urol。印刷中。http://dx.doi.org/
    作者:
    Bi-Ming He, Hai-Feng Wang
    日期:
    2026-10-03

    该文献暂无摘要。

  5. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    5. PSMA-PET/CT-guided Intensification of Radiation Therapy for Prostate Cancer (PSMAgRT): 5-yr Analysis of a Phase 2 Randomized Controlled Trial.

    5. 前列腺特异性膜抗原PET/CT引导下的前列腺癌放疗强化(PSMAgRT):一项2期随机对照试验的5年分析
    作者:
    Colin Belliveau, Fred Saad, Danny Duplan, Claire Petit, Guila Delouya, Carole Lambert, Daniel Taussky, Maroie Barkati, Marie-Claude Beauchemin, Sebastien Clavel, Gary Mok, Anne-Sophie Gauthier-Paré, Levon Igidbashian, Marjory Jolicoeur, Thu-Van Nguyen, Pierre-Yves McLaughlin, Philip Wong, Khun Visith Keu, Jean N DaSilva, Daniel Juneau, Cynthia Ménard
    日期:
    2026-10-03

    Prostate-specific membrane antigen positron emission tomography (PSMA-PET) improves lesion detection, leading to treatment intensification via PSMA-guided radiotherapy (PSMAgRT), but its impact on patient outcomes remains undefined. We evaluated whether PSMAgRT improves failure-free survival (FFS). This phase 2, two-center, open-label randomized trial enrolled patients planned for standard-of-care (SOC) radiotherapy (RT). Patients were randomized 1:1 to SOC or PSMAgRT to all detected sites across four strata: salvage post-radical prostatectomy (RP), high-risk, oligometastatic, and salvage post-RT. Between 2018 and 2021, 262 patients were randomized (253 treated/analyzed). The primary FFS end point (measured from RT completion) comprised prostate-specific antigen (PSA)/radiological progression, next-line therapy, or death. Secondary end points included freedom from biochemical progression (FFBP; PSA rise ≥0.2 ng/ml post-RP or ≥2 ng/ml above nadir in other strata). Prespecified analyses used a one-sided threshold of p < 0.10, whereas post hoc analyses used two-sided p < 0.05 thresholds and 95% confidence intervals (CIs). Among 253 patients, median follow-up was 66 mo (range 9-91). The 5-yr primary FFS was 66% with PSMAgRT versus 62% in controls (hazard ratio [HR] = 0.80; one-sided 90% CI, upper bound 1.04; p = 0.14). FFBP favored PSMAgRT: 72% versus 65% overall (subdistribution HR [sHR] 0.70, one-sided 90% CI upper bound 0.92; p = 0.048), 81% versus 66% in patients with high-risk disease (sHR 0.54; p = 0.07), and 80% versus 68% in patients in post-RP stratum (sHR 0.54; p = 0.037). In an exploratory, post hoc analysis combining patients with high-risk disease and those in the post-RP stratum, FFBP favored PSMAgRT (sHR 0.54, 95% CI = 0.32-0.91; two-sided p = 0.02). Only one grade ≥3 event was possibly related to dose escalation. Limitations include a phase 2 design with a heterogeneous population. Although the primary FFS end point was not met in the overall population, treatment-effect estimates favored PSMAgRT in the high-risk and post-RP strata. These findings provide a meaningful rationale for the target populations currently being evaluated in the definitive phase 3 PATRON trial. ClinicalTrials.gov NCT03525288.

  6. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    6. Re: Perioperative Apalutamide in High-risk Localized Prostate Cancer.

    6. 回复:高危局限性前列腺癌的围手术期阿帕他胺治疗
    作者:
    Gregory M Hemenway, Daniel M Geynisman
    日期:
    2026-10-03

    该文献暂无摘要。

  7. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    7. Re: Microultrasonography-guided Versus MRI-guided Biopsy for Prostate Cancer Diagnosis: The OPTIMUM Randomized Clinical Trial.

    7. 关于微超声引导与MRI引导前列腺癌诊断活检的比较:OPTIMUM随机临床试验
    作者:
    Rossano Girometti, Francesco Giganti
    日期:
    2026-10-03

    该文献暂无摘要。

  8. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    8. Re: Pierre-Etienne Gabriel, Alec Zhu, Paolo Gontero, Morgan Rouprêt, Evanguelos Xylinas, John P Sfakianos. BCG-unresponsive NMIBC: An Obsolete Definition in a Multimodal and Evolving Therapeutic Landscape. Eur Urol. In press. http://dx.doi.org/10.1016/j.eururo.2026.03.028.

    8. 回复:Pierre-Etienne Gabriel,Alec Zhu,Paolo Gontero,Morgan Rouprêt,Evanguelos Xylinas,John P Sfakianos。BCG无应答非肌层浸润性膀胱癌:在多模式且不断演变的治疗格局中一个过时的定义。《欧洲泌尿外科学》。出版中。http://dx.doi.org/
    作者:
    Marie-Pier St-Laurent, Peter C Black
    日期:
    2026-10-01

    该文献暂无摘要。

  9. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    9. Re: Twelve-month Results from the CISTO Study Comparing Radical Cystectomy Versus Bladder-Sparing Therapy for Recurrent High-grade Non-muscle-invasive Bladder Cancer.

    9. 回复:CISTO研究比较根治性膀胱切除术与保留膀胱疗法治疗复发性高级别非肌层浸润性膀胱癌的12个月结果
    作者:
    Laura E Davis, Spyridon P Basourakos, Adam C Calaway
    日期:
    2026-10-01

    该文献暂无摘要。

  10. JCR分区: Q1 CAS分区: B1 影响因子: 29.1

    10. Re: Stockholm3 Versus Prostate-specific Antigen in Prostate Cancer Screening: 9 yr Outcomes Demonstrating Improved Detection of Aggressive Cancers and Reduced Overdiagnosis from the STHLM3 Trial.

    10. 关于斯德哥尔摩3与前列腺特异性抗原在前列腺癌筛查中的比较:STHLM3试验9年结果显示侵袭性癌症检出率提高且过度诊断减少
    作者:
    Roman Gulati, Ruth Etzioni
    日期:
    2026-10-01

    该文献暂无摘要。

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