首页 > 最新文献

BJUI compass最新文献

英文 中文
Anatomical distribution of disease in pN1 prostate cancer with BCR post-RP: A PSMA-PET/CT-based analysis pN1前列腺癌术后BCR的解剖分布:PSMA-PET/ ct分析
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-10 DOI: 10.1002/bco2.70123
Lotte G. Zuur, Katelijne C. C. de Bie, Lieke Wever, Anne-Claire Berrens, Jean-Paul A. van Basten, Harm H. E. van Melick, Maarten L. Donswijk, Daniela E. Oprea-Lager, Wouter V. Vogel, Henk G. van der Poel, André N. Vis, Pim J. van Leeuwen

Objectives

To explore the distribution of metastatic disease in pN1 patients with biochemical recurrence (BCR) assessed by Prostate-Specific Membrane Antigen-Positron-Emission/Computed Tomography (PSMA-PET/CT).

Patients and Methods

This multicentre, retrospective cohort study included 130 pN1 PCa patients with BCR (PSA ≥ 0.2 ng/ml) post-RP with ePLND (2015–2022). All were preoperatively staged as molecular imaging (mi)N0M0 and underwent restaging PSMA-PET/CT at BCR. Clinical and imaging data were analysed using Mann–Whitney U, chi-square tests and Cox regression.

Results

Median time to BCR was 9 months (IQR 3–18). Biochemical persistence (BCP) (PSA ≥ 0.1 ng/ml at first follow-up) occurred in 66/130 (51%). At restaging PSMA-PET/CT, median PSA was 0.33 ng/ml (IQR 0.24–0.65). PSMA-PET/CT identified metastases in 63/130 (48%), with 37/63 (59%) having lymph node metastases (LNMs) limited to the ePLND template – 16/37 (43%) on the ipsilateral side of the positive resected node. Additionally, 26/63 (41%) had disease beyond the nodal template (miM+). Univariate Cox regression identified BCP as a predictor for any PSMA-PET/CT-detected recurrence, while a higher ISUP grade group at RP predicted miM+ disease.

Conclusion

PSMA-PET/CT identified PSMA-expressing recurrent disease in nearly half of pN1 PCa patients at early BCR, with about half confined to the pelvis and a quarter beyond the pelvis. These anatomical patterns indicate that PSMA-PET/CT can inform risk-adapted salvage strategies, including pelvic radiotherapy for nodal recurrences and systemic treatment when disease extends beyond the pelvis.

目的:探讨前列腺特异性膜抗原-正电子发射/计算机断层扫描(PSMA-PET/CT)评估pN1生化复发(BCR)患者转移性疾病的分布。患者和方法:这项多中心、回顾性队列研究纳入了130例pN1 PCa患者,rp后BCR (PSA≥0.2 ng/ml)合并ePLND(2015-2022)。所有患者术前均进行分子成像(mi)N0M0分期,并在BCR进行PSMA-PET/CT再分期。临床和影像学资料采用Mann-Whitney U检验、卡方检验和Cox回归分析。结果:达到BCR的中位时间为9个月(IQR 3-18)。生化持久性(BCP)(首次随访时PSA≥0.1 ng/ml)为66/130(51%)。再分期PSMA-PET/CT时,中位PSA为0.33 ng/ml (IQR 0.24-0.65)。PSMA-PET/CT发现转移63/130(48%),其中37/63(59%)的淋巴结转移(LNMs)仅限于ePLND模板,16/37(43%)在阳性切除淋巴结的同侧。此外,26/63(41%)的患者有超过淋巴结模板(miM+)的疾病。单因素Cox回归发现BCP是任何PSMA-PET/ ct检测到的复发的预测因子,而RP较高的ISUP分级组预测miM+疾病。结论:PSMA-PET/CT在近一半的早期BCR pN1 PCa患者中发现了表达psma的复发性疾病,其中约一半局限于骨盆,四分之一超出骨盆。这些解剖模式表明PSMA-PET/CT可以为风险适应的挽救策略提供信息,包括淋巴结复发的盆腔放疗和疾病扩展到骨盆以外的全身治疗。
{"title":"Anatomical distribution of disease in pN1 prostate cancer with BCR post-RP: A PSMA-PET/CT-based analysis","authors":"Lotte G. Zuur,&nbsp;Katelijne C. C. de Bie,&nbsp;Lieke Wever,&nbsp;Anne-Claire Berrens,&nbsp;Jean-Paul A. van Basten,&nbsp;Harm H. E. van Melick,&nbsp;Maarten L. Donswijk,&nbsp;Daniela E. Oprea-Lager,&nbsp;Wouter V. Vogel,&nbsp;Henk G. van der Poel,&nbsp;André N. Vis,&nbsp;Pim J. van Leeuwen","doi":"10.1002/bco2.70123","DOIUrl":"10.1002/bco2.70123","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>To explore the distribution of metastatic disease in pN1 patients with biochemical recurrence (BCR) assessed by Prostate-Specific Membrane Antigen-Positron-Emission/Computed Tomography (PSMA-PET/CT).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Patients and Methods</h3>\u0000 \u0000 <p>This multicentre, retrospective cohort study included 130 pN1 PCa patients with BCR (PSA ≥ 0.2 ng/ml) post-RP with ePLND (2015–2022). All were preoperatively staged as molecular imaging (mi)N0M0 and underwent restaging PSMA-PET/CT at BCR. Clinical and imaging data were analysed using Mann–Whitney U, chi-square tests and Cox regression.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Median time to BCR was 9 months (IQR 3–18). Biochemical persistence (BCP) (PSA ≥ 0.1 ng/ml at first follow-up) occurred in 66/130 (51%). At restaging PSMA-PET/CT, median PSA was 0.33 ng/ml (IQR 0.24–0.65). PSMA-PET/CT identified metastases in 63/130 (48%), with 37/63 (59%) having lymph node metastases (LNMs) limited to the ePLND template – 16/37 (43%) on the ipsilateral side of the positive resected node. Additionally, 26/63 (41%) had disease beyond the nodal template (miM+). Univariate Cox regression identified BCP as a predictor for any PSMA-PET/CT-detected recurrence, while a higher ISUP grade group at RP predicted miM+ disease.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>PSMA-PET/CT identified PSMA-expressing recurrent disease in nearly half of pN1 PCa patients at early BCR, with about half confined to the pelvis and a quarter beyond the pelvis. These anatomical patterns indicate that PSMA-PET/CT can inform risk-adapted salvage strategies, including pelvic radiotherapy for nodal recurrences and systemic treatment when disease extends beyond the pelvis.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12690614/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145745874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
MRI performance to identify clinically significant prostate cancer following focal cryo-ablation MRI表现鉴别局灶性冷冻消融后临床意义重大的前列腺癌。
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-10 DOI: 10.1002/bco2.70120
Herbert Lepor, Samuel Parry, Majlinda Tafa, Eli Rapoport, James S. Wysock

Objectives

To determine the performance of MRI for detecting clinically significant prostate cancer (csPCa) recurrence following focal cryo-ablation over five years of oncological surveillance.

Subjects and Methods

A total of 305 men with intermediate-risk prostate cancer undergoing focal cryo-ablation (FCA) at our referral centre between 03/2017 and 03/2024 were prospectively enrolled in an outcomes registry. Selection criteria, treatment planning and oncological surveillance were standardized. The initial surveillance protocol included MRI at six months, two, 3.5, five years, and surveillance prostate biopsy at six months, two and five years. The surveillance protocol biopsy at six months and two years was abandoned for a negative MRI in May 2019 and November 2020. Performance statistics of MRI for detecting csPCa recurrence were assessed among mandatory MRI and biopsy dyads at six months and two years. Clinically significant prostate cancer detection rates for suspicious (positive) and negative MRI included all subjects.

Results

Sensitivity, specificity, positive predictive value and negative predictive value of MRI to predict csPCa is 25%, 93%, 29% and 91%. The csPCa detection rate for positive and negative MRI was 40% and 7.0%, respectively. The area under the receiver operating characteristic curve for MRI as a predictor of csPCa was 0.60, suggesting limitations of MRI for predicting csPCa. A limitation is that a validated instrument for positive MRI was not available during the study.

Conclusions

Six-month MRI is not recommended owing to its very low csPCa detection rate. The increasing csPCa detection rates at two and five years suggest these are reasonable time points to perform MRI. Prostate biopsy should be performed on all cases with positive MRI, and can safely be deferred in most cases with negative MRI.

目的:通过5年的肿瘤监测,确定MRI检测局灶性冷冻消融后临床显著前列腺癌(csPCa)复发的性能。研究对象和方法:2017年3月至2024年3月期间,在我们的转诊中心接受局灶性冷冻消融(FCA)治疗的305名中度风险前列腺癌男性患者被前瞻性纳入结果登记。标准化了选择标准、治疗计划和肿瘤监测。最初的监测方案包括6个月、2年、3.5年、5年的MRI和6个月、2年和5年的前列腺活检监测。2019年5月和2020年11月,由于MRI阴性,放弃了6个月和2岁时的监测方案活检。在6个月和2年时对强制MRI和活检组进行MRI检测csPCa复发的性能统计。所有受试者的MRI可疑(阳性)和阴性的前列腺癌检出率均具有临床意义。结果:MRI预测csPCa的敏感性为25%,特异性为93%,阳性预测值为29%,阴性预测值为91%。MRI阳性和阴性csPCa检出率分别为40%和7.0%。MRI作为csPCa预测指标的受试者工作特征曲线下面积为0.60,提示MRI预测csPCa存在局限性。一个限制是在研究期间没有有效的MRI阳性仪器。结论:由于csPCa的检出率很低,不建议6个月MRI检查。2年和5年csPCa检出率的增加表明这是进行MRI检查的合理时间点。前列腺活检应在所有MRI阳性病例中进行,在大多数MRI阴性病例中可以安全地推迟。
{"title":"MRI performance to identify clinically significant prostate cancer following focal cryo-ablation","authors":"Herbert Lepor,&nbsp;Samuel Parry,&nbsp;Majlinda Tafa,&nbsp;Eli Rapoport,&nbsp;James S. Wysock","doi":"10.1002/bco2.70120","DOIUrl":"10.1002/bco2.70120","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>To determine the performance of MRI for detecting clinically significant prostate cancer (csPCa) recurrence following focal cryo-ablation over five years of oncological surveillance.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Subjects and Methods</h3>\u0000 \u0000 <p>A total of 305 men with intermediate-risk prostate cancer undergoing focal cryo-ablation (FCA) at our referral centre between 03/2017 and 03/2024 were prospectively enrolled in an outcomes registry. Selection criteria, treatment planning and oncological surveillance were standardized. The initial surveillance protocol included MRI at six months, two, 3.5, five years, and surveillance prostate biopsy at six months, two and five years. The surveillance protocol biopsy at six months and two years was abandoned for a negative MRI in May 2019 and November 2020. Performance statistics of MRI for detecting csPCa recurrence were assessed among mandatory MRI and biopsy dyads at six months and two years. Clinically significant prostate cancer detection rates for suspicious (positive) and negative MRI included all subjects.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Sensitivity, specificity, positive predictive value and negative predictive value of MRI to predict csPCa is 25%, 93%, 29% and 91%. The csPCa detection rate for positive and negative MRI was 40% and 7.0%, respectively. The area under the receiver operating characteristic curve for MRI as a predictor of csPCa was 0.60, suggesting limitations of MRI for predicting csPCa. A limitation is that a validated instrument for positive MRI was not available during the study.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Six-month MRI is not recommended owing to its very low csPCa detection rate. The increasing csPCa detection rates at two and five years suggest these are reasonable time points to perform MRI. Prostate biopsy should be performed on all cases with positive MRI, and can safely be deferred in most cases with negative MRI.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12690215/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145745890","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Incidence of ideal candidates for focal therapy: A scoping study following the FALCON Consensus Statements 局灶治疗理想候选者的发生率:一项遵循FALCON共识声明的范围研究
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-04 DOI: 10.1002/bco2.70121
Jae Woong Jang, Nicole Handa, Ridwan Alam, Clayton Neill, Sai Kumar, Kent T. Perry, Edward M. Schaeffer, Hiten D. Patel, Ashley E. Ross

Introduction

Ideal candidates for focal therapy (FT) for prostate cancer (PCa) have mpMRI-visible ISUP Grade Group 2–3, localized disease. Transperineal (TP) prostate biopsies provide superior positional information of PCa in the transverse axis, and possibly higher PCa detection rates—important in choosing FT modalities. Here, we describe the frequency of optimal FT candidates among a large cohort of men with proven PCa identified from MRI-guided targeted and systematic TP biopsy.

Methods

We queried the Northwestern data warehouse for men with newly diagnosed PCa who had a positive mpMRI (PI-RADS 3–5) and a TP biopsy prior to diagnosis from January 2018 to June 2024. Patients with disease optimal for FT were determined using modified FALCON consensus guidelines with emphasis on mpMRI and biopsy findings. We also explored the disparity in FT candidacy when using only target cores compared to combined target and systematic cores.

Results

We identified 1342 men diagnosed with PCa on combined targeted and systematic TP biopsy after a positive mpMRI, of which 888 men had intermediate-risk PCa. Of these 888 men, 439 patients (49.4%) had unilateral-dominant disease, while 329 patients (37%) had unilateral-dominant and anterior (106; 11.9%) or posterior-dominant (223; 25.1%) disease. Up to half of the patients considered good candidates on target cores were considered FT-ineligible on review of systematic cores.

Conclusions

FT may be considered in up to 50% of patients with intermediate risk disease, while ideal candidates for functional preservation constitute a smaller number. Review of both targeted and systematic biopsy cores is crucial in determining FT candidacy.

前列腺癌(PCa)局灶治疗(FT)的理想候选者有mpmri可见的ISUP分级2-3组,局限性疾病。经会阴(TP)前列腺活检提供了前列腺癌在横轴上的优越位置信息,可能有更高的前列腺癌检出率——这在选择FT模式时很重要。在这里,我们描述了通过mri引导的靶向系统性TP活检确定的前列腺癌患者的一大队列中最佳FT候选者的频率。方法:我们查询了西北大学数据仓库中2018年1月至2024年6月诊断前mpMRI阳性(PI-RADS 3-5)和TP活检阳性的新诊断PCa男性患者。采用改进的FALCON共识指南确定最适合FT的疾病患者,重点是mpMRI和活检结果。我们还探讨了当仅使用目标核心与组合目标和系统核心相比,FT候选性的差异。结果我们发现1342名男性在mpMRI阳性后通过联合靶向和系统TP活检诊断为PCa,其中888名男性为中危PCa。在这888名男性中,439名患者(49.4%)患有单侧显性疾病,329名患者(37%)患有单侧显性和前侧显性(106名,11.9%)或后侧显性(223名,25.1%)疾病。多达一半的患者被认为是目标核心的良好候选人,在系统核心的审查中被认为是不合格的。结论:高达50%的中危患者可能会考虑FT,而理想的功能保留候选者则较少。在确定FT候选资格时,对目标活检和系统活检的检查至关重要。
{"title":"Incidence of ideal candidates for focal therapy: A scoping study following the FALCON Consensus Statements","authors":"Jae Woong Jang,&nbsp;Nicole Handa,&nbsp;Ridwan Alam,&nbsp;Clayton Neill,&nbsp;Sai Kumar,&nbsp;Kent T. Perry,&nbsp;Edward M. Schaeffer,&nbsp;Hiten D. Patel,&nbsp;Ashley E. Ross","doi":"10.1002/bco2.70121","DOIUrl":"https://doi.org/10.1002/bco2.70121","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Ideal candidates for focal therapy (FT) for prostate cancer (PCa) have mpMRI-visible ISUP Grade Group 2–3, localized disease. Transperineal (TP) prostate biopsies provide superior positional information of PCa in the transverse axis, and possibly higher PCa detection rates—important in choosing FT modalities. Here, we describe the frequency of optimal FT candidates among a large cohort of men with proven PCa identified from MRI-guided targeted and systematic TP biopsy.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We queried the Northwestern data warehouse for men with newly diagnosed PCa who had a positive mpMRI (PI-RADS 3–5) and a TP biopsy prior to diagnosis from January 2018 to June 2024. Patients with disease optimal for FT were determined using modified FALCON consensus guidelines with emphasis on mpMRI and biopsy findings. We also explored the disparity in FT candidacy when using only target cores compared to combined target and systematic cores.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>We identified 1342 men diagnosed with PCa on combined targeted and systematic TP biopsy after a positive mpMRI, of which 888 men had intermediate-risk PCa. Of these 888 men, 439 patients (49.4%) had unilateral-dominant disease, while 329 patients (37%) had unilateral-dominant and anterior (106; 11.9%) or posterior-dominant (223; 25.1%) disease. Up to half of the patients considered good candidates on target cores were considered FT-ineligible on review of systematic cores.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>FT may be considered in up to 50% of patients with intermediate risk disease, while ideal candidates for functional preservation constitute a smaller number. Review of both targeted and systematic biopsy cores is crucial in determining FT candidacy.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bjui-journals.onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.70121","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145686316","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Haematuria cancer risk score as a predictor of muscle-invasive bladder cancer 血尿癌风险评分作为肌肉浸润性膀胱癌的预测因子。
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-03 DOI: 10.1002/bco2.70125
Serdar Turan, Cem Tugrul Gezmis, Nusret Can Cilesiz, Mehmet Uzut, Mustafa Satılmısoglu, Rifat Burak Ergul, Mustafa Bahadır Can Balcı

Objective

To evaluate the prognostic performance of the Haematuria Cancer Risk Score (HCRS) for predicting muscle-invasive bladder cancer (MIBC) in patients presenting with haematuria.

Methods

This retrospective study analysed newly diagnosed urothelial carcinoma cases identified during haematuria evaluations between 2018 and 2023. Pathological staging was based on the highest grade or stage from TUR or re-TUR specimens. HCRS was calculated using age, sex, haematuria type, and smoking status. The primary outcome was muscle-invasive disease (≥T2). Associations were examined using univariate logistic regression, and discriminatory performance was evaluated with ROC analysis and bootstrap-derived 95% confidence intervals.

Results

Among 162 patients, 45 (27.8%) had MIBC. The median HCRS was higher in patients with MIBC than in those with non-muscle-invasive disease (6.49 [6.08–6.96] vs. 6.16 [5.44–6.94]; p = 0.04). Univariate analysis showed a significant association between HCRS and MIBC (odds ratio = 1.78; 95% CI 1.03–3.06; p = 0.039). ROC analysis demonstrated limited discriminative performance (AUC = 0.60; 95% CI 0.53–0.67). At the Youden cut-off of 6.04, sensitivity was 77.8% and specificity 48.3%. An integer threshold of HCRS ≥6 yielded comparable performance, supporting clinical applicability.

Conclusions

Higher HCRS values were modestly associated with muscle invasion, although predictive performance was limited. The HCRS may support risk stratification in haematuria pathways by flagging patients at higher risk of muscle invasion—particularly when interpreted together with cystoscopy and imaging findings.

目的:评价血尿癌风险评分(HCRS)在血尿患者中预测肌肉浸润性膀胱癌(MIBC)的预后表现。方法:本回顾性研究分析了2018年至2023年在血尿评估中发现的新诊断尿路上皮癌病例。病理分期以TUR或再TUR标本的最高分级或分期为基础。HCRS根据年龄、性别、血尿类型和吸烟状况计算。主要终点为肌肉侵袭性疾病(≥T2)。使用单变量逻辑回归检验相关性,并使用ROC分析和bootstrap导出的95%置信区间评估歧视性表现。结果:162例患者中,45例(27.8%)有MIBC。MIBC患者的中位HCRS高于非肌肉侵袭性疾病患者(6.49[6.08-6.96]比6.16 [5.44-6.94];p = 0.04)。单因素分析显示HCRS与MIBC之间存在显著相关性(优势比= 1.78;95% CI 1.03-3.06; p = 0.039)。ROC分析显示有限的判别性能(AUC = 0.60; 95% CI 0.53-0.67)。在约登截止值为6.04时,敏感性为77.8%,特异性为48.3%。HCRS≥6的整数阈值可获得相当的性能,支持临床适用性。结论:较高的HCRS值与肌肉侵袭有一定的相关性,尽管预测性能有限。HCRS可以通过标记肌肉侵入风险较高的患者来支持血尿途径的风险分层,特别是当与膀胱镜检查和影像学结果一起解释时。
{"title":"Haematuria cancer risk score as a predictor of muscle-invasive bladder cancer","authors":"Serdar Turan,&nbsp;Cem Tugrul Gezmis,&nbsp;Nusret Can Cilesiz,&nbsp;Mehmet Uzut,&nbsp;Mustafa Satılmısoglu,&nbsp;Rifat Burak Ergul,&nbsp;Mustafa Bahadır Can Balcı","doi":"10.1002/bco2.70125","DOIUrl":"10.1002/bco2.70125","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>To evaluate the prognostic performance of the Haematuria Cancer Risk Score (HCRS) for predicting muscle-invasive bladder cancer (MIBC) in patients presenting with haematuria.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This retrospective study analysed newly diagnosed urothelial carcinoma cases identified during haematuria evaluations between 2018 and 2023. Pathological staging was based on the highest grade or stage from TUR or re-TUR specimens. HCRS was calculated using age, sex, haematuria type, and smoking status. The primary outcome was muscle-invasive disease (≥T2). Associations were examined using univariate logistic regression, and discriminatory performance was evaluated with ROC analysis and bootstrap-derived 95% confidence intervals.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among 162 patients, 45 (27.8%) had MIBC. The median HCRS was higher in patients with MIBC than in those with non-muscle-invasive disease (6.49 [6.08–6.96] vs. 6.16 [5.44–6.94]; <i>p</i> = 0.04). Univariate analysis showed a significant association between HCRS and MIBC (odds ratio = 1.78; 95% CI 1.03–3.06; <i>p</i> = 0.039). ROC analysis demonstrated limited discriminative performance (AUC = 0.60; 95% CI 0.53–0.67). At the Youden cut-off of 6.04, sensitivity was 77.8% and specificity 48.3%. An integer threshold of HCRS ≥6 yielded comparable performance, supporting clinical applicability.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Higher HCRS values were modestly associated with muscle invasion, although predictive performance was limited. The HCRS may support risk stratification in haematuria pathways by flagging patients at higher risk of muscle invasion—particularly when interpreted together with cystoscopy and imaging findings.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12673275/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145679488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thulium fibre laser endoscopic enucleation of the prostate (THUFLEP) learning curve assessment: A retrospective analysis of the experience of a single surgeon 铥纤维激光内镜下前列腺除核术(THUFLEP)学习曲线评估:单个外科医生经验的回顾性分析
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-03 DOI: 10.1002/bco2.70116
Sulaiman Goudaimy, Louis Lenfant, Christophe Vaessen, Jérôme Parra, Emmanuel Chartier-Kastler, Aurélien Beaugerie, Pierre Mozer, Quentin Dubourg, Thomas Seisen, Morgan Roupret, Ugo Pinar

Objectives

To assess the learning curve of thulium fibre laser enucleation of the prostate (THUFLEP).

Patients and methods

We conducted a retrospective study including the first 111 patients treated with THUFLEP by a single surgeon. The operator had no prior experience in prostate enucleation and performed the first two procedures under the supervision of an expert. Initial 68 cases were performed using the three-lobe technique, and the later cases were done as en bloc enucleation with early apex release (n = 43). The learning curve was analysed in terms of temporal changes in the following variables: enucleation time, morcellation time, occurrence of intraoperative complications (IOCs) and achievement of pentafecta (enucleation + morcellation <90 min, a complete enucleation without complications and stress urinary incontinence at 3 months) in four consecutive patients.

Results

A total of 111 consecutive patients were included, with a mean age of 71.5 years (SD = 10.8), a mean total PSA of 7.9 ng/ml (SD = 8.4) and a mean prostate volume of 99.1 cc (SD = 35.9). The mean enucleation and morcellation times were 65.9 min (SD = 36.2) and 15.5 min (SD = 13.5), respectively. There were 13 postoperative complications (11.7%), and only one required reoperation for clot evacuation. The pentafecta was achieved in 66 patients (59.5%) and was reached in four consecutive patients after the 38th case. Operative time reached a plateau after approximately 60 procedures. The average enucleation efficiency was 1.1 g/min (SD = 0.7), and the plateau had not yet been reached after 111 patients.

Conclusions

In our experience, we observed a learning curve of 40–60 cases for THUFLEP. This plateau was reached after a relatively long learning curve; a more structured and supervised training programme may help improve these learning curves. Lastly, the complication rate was low from the beginning of the surgical experience, and the pentafecta was achieved in more than half of the patients.

目的探讨铥纤维激光前列腺摘除(THUFLEP)的学习曲线。患者和方法我们进行了一项回顾性研究,包括由一名外科医生治疗的首批111名患者。操作者没有前列腺摘除的经验,在专家的监督下进行了前两次手术。最初的68例采用三瓣技术,随后的43例采用早期心尖释放的整体去核术。根据以下变量的时间变化来分析学习曲线:连续4例患者的去核时间、碎化时间、术中并发症(IOCs)的发生以及五感的实现(去核+碎化& 90分钟,完全去核无并发症,3个月时压力性尿失禁)。结果共纳入111例患者,平均年龄71.5岁(SD = 10.8),平均总PSA为7.9 ng/ml (SD = 8.4),平均前列腺体积为99.1 cc (SD = 35.9)。平均去核和分块时间分别为65.9 min (SD = 36.2)和15.5 min (SD = 13.5)。术后并发症13例(11.7%),仅1例需要再次手术进行血块清除。66例患者(59.5%)达到五肛,第38例后连续4例患者达到五肛。大约60次手术后,手术时间达到平稳期。平均去核效率为1.1 g/min (SD = 0.7), 111例患者未达到平台期。根据我们的经验,我们观察到40-60例THUFLEP的学习曲线。这个平台是在经历了相对较长的学习曲线之后达到的;一个更有组织、更有监督的培训项目可能有助于改善这些学习曲线。最后,从手术开始,并发症发生率就很低,超过一半的患者达到了五肛。
{"title":"Thulium fibre laser endoscopic enucleation of the prostate (THUFLEP) learning curve assessment: A retrospective analysis of the experience of a single surgeon","authors":"Sulaiman Goudaimy,&nbsp;Louis Lenfant,&nbsp;Christophe Vaessen,&nbsp;Jérôme Parra,&nbsp;Emmanuel Chartier-Kastler,&nbsp;Aurélien Beaugerie,&nbsp;Pierre Mozer,&nbsp;Quentin Dubourg,&nbsp;Thomas Seisen,&nbsp;Morgan Roupret,&nbsp;Ugo Pinar","doi":"10.1002/bco2.70116","DOIUrl":"https://doi.org/10.1002/bco2.70116","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>To assess the learning curve of thulium fibre laser enucleation of the prostate (THUFLEP).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Patients and methods</h3>\u0000 \u0000 <p>We conducted a retrospective study including the first 111 patients treated with THUFLEP by a single surgeon. The operator had no prior experience in prostate enucleation and performed the first two procedures under the supervision of an expert. Initial 68 cases were performed using the three-lobe technique, and the later cases were done as en bloc enucleation with early apex release (<i>n</i> = 43). The learning curve was analysed in terms of temporal changes in the following variables: enucleation time, morcellation time, occurrence of intraoperative complications (IOCs) and achievement of pentafecta (enucleation + morcellation &lt;90 min, a complete enucleation without complications and stress urinary incontinence at 3 months) in four consecutive patients.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>A total of 111 consecutive patients were included, with a mean age of 71.5 years (SD = 10.8), a mean total PSA of 7.9 ng/ml (SD = 8.4) and a mean prostate volume of 99.1 cc (SD = 35.9). The mean enucleation and morcellation times were 65.9 min (SD = 36.2) and 15.5 min (SD = 13.5), respectively. There were 13 postoperative complications (11.7%), and only one required reoperation for clot evacuation. The pentafecta was achieved in 66 patients (59.5%) and was reached in four consecutive patients after the 38th case. Operative time reached a plateau after approximately 60 procedures. The average enucleation efficiency was 1.1 g/min (SD = 0.7), and the plateau had not yet been reached after 111 patients.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>In our experience, we observed a learning curve of 40–60 cases for THUFLEP. This plateau was reached after a relatively long learning curve; a more structured and supervised training programme may help improve these learning curves. Lastly, the complication rate was low from the beginning of the surgical experience, and the pentafecta was achieved in more than half of the patients.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bjui-journals.onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.70116","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145686109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multivariable model integrating PHI and mpMRI for detecting csPCa in biopsy-naïve men 整合PHI和mpMRI的多变量模型检测biopsy-naïve男性csPCa。
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-12-02 DOI: 10.1002/bco2.70101
Mario Dominguez Esteban, Ester Fernandez Guzman, Enrique Ramos Barselo, Ernesto Herrero Blanco, Sergio Zubillaga Guerrero, Roberto Ballestero Diego, Alejandro Fernandez Florez, Jose Javier Gomez Roman, Jaime Garcia Herrero, Marina Sanchez Gil, Guillermo Velilla Diez, Felix Campos Juanatey, Maria Teresa Garcia Unzueta, Jose Luis Gutierrez Baños
<div> <section> <h3> Background</h3> <p>The integration of blood-based biomarkers and multiparametric magnetic resonance imaging (mpMRI) has been proposed to improve prostate cancer (PCa) diagnosis. However, few validated models combine both tools to support risk-adapted clinical decision-making.</p> </section> <section> <h3> Objective</h3> <p>The study's aim is to evaluate and internally validate a multivariable model integrating clinical, analytical and imaging parameters—including the Prostate Health Index (PHI) and mpMRI—for predicting clinically significant prostate cancer (csPCa) in biopsy-naïve men.</p> </section> <section> <h3> Design, setting and participants</h3> <p>This prospective observational study included 183 biopsy-naïve men aged 50–75 years with PSA levels of 4–10 ng/mL and/or abnormal digital rectal examination. All patients underwent PHI testing, and 47.5% received prebiopsy mpMRI. All underwent systematic biopsy; targeted cognitive fusion biopsy was performed for PIRADS ≥ 3 lesions.</p> </section> <section> <h3> Outcome measurements and statistical analysis</h3> <p>A multivariable logistic regression model was constructed using PHI, PSA density, PSA free/total ratio, PIRADS score and age. The model was internally validated with bootstrap resampling and converted into a clinical nomogram. Diagnostic accuracy (AUC, sensitivity, specificity, NPV and PPV) was assessed and compared with simplified strategies using PHI or PIRADS alone, as well as a sequential approach (PHI → PIRADS).</p> </section> <section> <h3> Results and limitations</h3> <p>The model achieved an AUC of 0.841 (95% CI 0.76–0.91), with 100% sensitivity and 66.7% specificity for csPCa in the mpMRI cohort at the optimal 17% risk threshold (65.5 points). It safely avoided 49.4% of biopsies without missing any csPCa cases. Simpler strategies using PHI or PIRADS alone showed lower efficiency, particularly in balancing sensitivity and biopsy reduction. As an additional analysis, the PHI–mpMRI nomogram by Siddiqui et al. (2023) was externally validated in our cohort, confirming robust diagnostic accuracy (AUC 0.89, 95% CI 0.82–0.95). Limitations include the modest size of the mpMRI cohort and the historical nature of recruitment (2014–2018), although PHI and mpMRI remain standard in contemporary practice.</p> </section> <section> <h3> Conclusions</h3> <p>This model accurat
背景:基于血液的生物标志物和多参数磁共振成像(mpMRI)的整合已被提出用于改善前列腺癌(PCa)的诊断。然而,很少有经过验证的模型将这两种工具结合起来,以支持适应风险的临床决策。目的:该研究的目的是评估和内部验证一个多变量模型,该模型整合了临床、分析和影像学参数,包括前列腺健康指数(PHI)和mpmri,用于预测biopsy-naïve男性的临床显著性前列腺癌(csPCa)。设计背景和参与者:这项前瞻性观察性研究包括183名年龄在50-75岁、PSA水平为4-10 ng/mL和/或直肠指检异常的biopsy-naïve男性。所有患者都进行了PHI检测,47.5%的患者接受了活检前mpMRI检查。所有患者均行系统活检;PIRADS≥3个病灶行定向认知融合活检。结果测量与统计分析:采用PHI、PSA密度、PSA游离/总比、PIRADS评分和年龄构建多变量logistic回归模型。该模型通过bootstrap重新采样进行内部验证,并转换为临床nomogram。评估诊断准确性(AUC、敏感性、特异性、NPV和PPV),并与单独使用PHI或PIRADS的简化策略以及顺序方法(PHI→PIRADS)进行比较。结果和局限性:该模型的AUC为0.841 (95% CI 0.76-0.91),在最佳17%风险阈值(65.5点)下,mpMRI队列中csPCa的敏感性为100%,特异性为66.7%。它安全地避免了49.4%的活组织检查,没有遗漏任何csPCa病例。单独使用PHI或PIRADS的简单策略效率较低,特别是在平衡敏感性和活检减少方面。作为另一项分析,Siddiqui等人(2023)的pi - mpmri图在我们的队列中进行了外部验证,证实了强大的诊断准确性(AUC 0.89, 95% CI 0.82-0.95)。尽管PHI和mpMRI在当代实践中仍然是标准的,但其局限性包括mpMRI队列的适度规模和招募的历史性质(2014-2018年)。结论:该模型准确预测csPCa,优于单独使用PHI或PIRADS等单独工具。它的应用可以提高诊断效率,减少不必要的程序。患者总结:结合血液检查(PHI)和MRI的模型可以帮助避免不必要的前列腺活检,同时可靠地检测侵袭性癌症。
{"title":"Multivariable model integrating PHI and mpMRI for detecting csPCa in biopsy-naïve men","authors":"Mario Dominguez Esteban,&nbsp;Ester Fernandez Guzman,&nbsp;Enrique Ramos Barselo,&nbsp;Ernesto Herrero Blanco,&nbsp;Sergio Zubillaga Guerrero,&nbsp;Roberto Ballestero Diego,&nbsp;Alejandro Fernandez Florez,&nbsp;Jose Javier Gomez Roman,&nbsp;Jaime Garcia Herrero,&nbsp;Marina Sanchez Gil,&nbsp;Guillermo Velilla Diez,&nbsp;Felix Campos Juanatey,&nbsp;Maria Teresa Garcia Unzueta,&nbsp;Jose Luis Gutierrez Baños","doi":"10.1002/bco2.70101","DOIUrl":"10.1002/bco2.70101","url":null,"abstract":"&lt;div&gt;\u0000 \u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Background&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;The integration of blood-based biomarkers and multiparametric magnetic resonance imaging (mpMRI) has been proposed to improve prostate cancer (PCa) diagnosis. However, few validated models combine both tools to support risk-adapted clinical decision-making.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Objective&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;The study's aim is to evaluate and internally validate a multivariable model integrating clinical, analytical and imaging parameters—including the Prostate Health Index (PHI) and mpMRI—for predicting clinically significant prostate cancer (csPCa) in biopsy-naïve men.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Design, setting and participants&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;This prospective observational study included 183 biopsy-naïve men aged 50–75 years with PSA levels of 4–10 ng/mL and/or abnormal digital rectal examination. All patients underwent PHI testing, and 47.5% received prebiopsy mpMRI. All underwent systematic biopsy; targeted cognitive fusion biopsy was performed for PIRADS ≥ 3 lesions.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Outcome measurements and statistical analysis&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;A multivariable logistic regression model was constructed using PHI, PSA density, PSA free/total ratio, PIRADS score and age. The model was internally validated with bootstrap resampling and converted into a clinical nomogram. Diagnostic accuracy (AUC, sensitivity, specificity, NPV and PPV) was assessed and compared with simplified strategies using PHI or PIRADS alone, as well as a sequential approach (PHI → PIRADS).&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Results and limitations&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;The model achieved an AUC of 0.841 (95% CI 0.76–0.91), with 100% sensitivity and 66.7% specificity for csPCa in the mpMRI cohort at the optimal 17% risk threshold (65.5 points). It safely avoided 49.4% of biopsies without missing any csPCa cases. Simpler strategies using PHI or PIRADS alone showed lower efficiency, particularly in balancing sensitivity and biopsy reduction. As an additional analysis, the PHI–mpMRI nomogram by Siddiqui et al. (2023) was externally validated in our cohort, confirming robust diagnostic accuracy (AUC 0.89, 95% CI 0.82–0.95). Limitations include the modest size of the mpMRI cohort and the historical nature of recruitment (2014–2018), although PHI and mpMRI remain standard in contemporary practice.&lt;/p&gt;\u0000 &lt;/section&gt;\u0000 \u0000 &lt;section&gt;\u0000 \u0000 &lt;h3&gt; Conclusions&lt;/h3&gt;\u0000 \u0000 &lt;p&gt;This model accurat","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12672186/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145679476","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Flexible ureteroscopy with a flexible and navigable suction ureteral access sheath versus mini-percutaneous nephrolithotomy for 1–2 cm lower pole renal stones: Protocol for an international, multicentre, randomized non-inferiority trial (FLAME trial) 柔性输尿管镜与柔性可导航的吸引输尿管通路鞘对1-2厘米肾结石的微创经皮肾镜取石术:一项国际、多中心、随机、非效性试验方案(FLAME试验)
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-11-29 DOI: 10.1002/bco2.70114
Wei Zhu, Jinghua Zhong, Kefeng Wang, Guangming Yin, Chi-Ho Leung, Nariman Gadzhiev, Mehmet Ilker Gökce, Jaisukh Kalathia, Vineet Gauhar, Guangyuan Zhang, Gang Wu, Mingyong Li, Li Fang, Shaohua Zeng, Peide Bai, Ji Li, Zhenhua Zhao, Ming Xi, Xin Mai, Xianzhong Duan, Kehua Jiang, Jianwei Cao, Xianghu Meng, Shusheng Liu, Aram Aloyan, Peng Yuan, Xiaorui Zhu, Ting Huang, Jianhui Xing, Jingzeng Du, Wenqi Wu, Jinxiang Ma, Wen Zhong, Zhijian Zhao, Yongda Liu, Chi Fai Ng, Jean de la Rosette, Bhaskar Somani, Shiyong Qi, Guohua Zeng, Steffi Kar Kei Yuen

Background

Lower pole renal stones measuring 1–2 cm remain challenging to treat. While mini-percutaneous nephrolithotomy (mini-PCNL) provides high stone-free rates (SFRs), it carries tract-related morbidity. Flexible ureteroscopy (f-URS) is less invasive but limited in SFR. The flexible and navigable suction ureteral access sheath (FANS) has shown promise in improving stone evacuation and intrarenal pressure control. We hypothesize that FANS f-URS is non-inferior to mini-PCNL for patients with 1–2 cm lower pole stones in SFR.

Study Design

The FLAME trial is an international, multicentre, randomized, non-inferiority study directly comparing FANS-f-URS with mini-PCNL in this setting.

Endpoints

The primary outcome is immediate SFR within 72 hours on low-dose CT. Secondary outcomes include SFR at 1 month, operative time, postoperative pain, hospital stay, complications (Clavien–Dindo) and quality-of-life changes.

Patients and Methods

A total of 640 adults with CT-confirmed 1–2 cm lower pole renal stones will be randomized 1:1 to undergo FANS-f-URS or mini-PCNL across 20 high-volume urology centres worldwide. Randomization is centralized and stratified by site. Radiologists and statisticians will remain blinded to allocation. Sample size was calculated assuming an 85% SFR for both arms, an 8.5% non-inferiority margin, 80% power and 15% attrition. Analyses will follow both intention-to-treat and per-protocol principles.

Trial registration

ClinicalTrials.gov NCT07159035.

背景:1-2厘米的下极肾结石的治疗仍然具有挑战性。虽然微型经皮肾镜取石术(mini-PCNL)提供了高的结石清除率(SFRs),但它具有与尿道相关的发病率。柔性输尿管镜(f-URS)侵入性较小,但仅限于SFR。柔性和可导航的输尿管吸入鞘(FANS)已显示出改善结石排出和肾内压力控制的希望。我们假设fan - f-URS对SFR患者1-2 cm下极结石的疗效不低于mini-PCNL。FLAME试验是一项国际、多中心、随机、非劣效性研究,在这种情况下直接比较FANS-f-URS和mini-PCNL。主要终点是低剂量CT治疗72小时内立即发生SFR。次要结局包括1个月时SFR、手术时间、术后疼痛、住院时间、并发症(Clavien-Dindo)和生活质量变化。患者和方法640例ct确诊1-2 cm下极肾结石的成年人将在全球20个大容量泌尿外科中心按1:1随机分组,接受FANS-f-URS或mini-PCNL。随机化按地点集中分层。放射科医生和统计学家将继续对分配不知情。样本量的计算假设两个组的SFR为85%,非劣效性边际为8.5%,药效为80%,损耗率为15%。分析将遵循意向治疗原则和协议原则。试验注册ClinicalTrials.gov NCT07159035。
{"title":"Flexible ureteroscopy with a flexible and navigable suction ureteral access sheath versus mini-percutaneous nephrolithotomy for 1–2 cm lower pole renal stones: Protocol for an international, multicentre, randomized non-inferiority trial (FLAME trial)","authors":"Wei Zhu,&nbsp;Jinghua Zhong,&nbsp;Kefeng Wang,&nbsp;Guangming Yin,&nbsp;Chi-Ho Leung,&nbsp;Nariman Gadzhiev,&nbsp;Mehmet Ilker Gökce,&nbsp;Jaisukh Kalathia,&nbsp;Vineet Gauhar,&nbsp;Guangyuan Zhang,&nbsp;Gang Wu,&nbsp;Mingyong Li,&nbsp;Li Fang,&nbsp;Shaohua Zeng,&nbsp;Peide Bai,&nbsp;Ji Li,&nbsp;Zhenhua Zhao,&nbsp;Ming Xi,&nbsp;Xin Mai,&nbsp;Xianzhong Duan,&nbsp;Kehua Jiang,&nbsp;Jianwei Cao,&nbsp;Xianghu Meng,&nbsp;Shusheng Liu,&nbsp;Aram Aloyan,&nbsp;Peng Yuan,&nbsp;Xiaorui Zhu,&nbsp;Ting Huang,&nbsp;Jianhui Xing,&nbsp;Jingzeng Du,&nbsp;Wenqi Wu,&nbsp;Jinxiang Ma,&nbsp;Wen Zhong,&nbsp;Zhijian Zhao,&nbsp;Yongda Liu,&nbsp;Chi Fai Ng,&nbsp;Jean de la Rosette,&nbsp;Bhaskar Somani,&nbsp;Shiyong Qi,&nbsp;Guohua Zeng,&nbsp;Steffi Kar Kei Yuen","doi":"10.1002/bco2.70114","DOIUrl":"https://doi.org/10.1002/bco2.70114","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Lower pole renal stones measuring 1–2 cm remain challenging to treat. While mini-percutaneous nephrolithotomy (mini-PCNL) provides high stone-free rates (SFRs), it carries tract-related morbidity. Flexible ureteroscopy (f-URS) is less invasive but limited in SFR. The flexible and navigable suction ureteral access sheath (FANS) has shown promise in improving stone evacuation and intrarenal pressure control. We hypothesize that FANS f-URS is non-inferior to mini-PCNL for patients with 1–2 cm lower pole stones in SFR.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Study Design</h3>\u0000 \u0000 <p>The FLAME trial is an international, multicentre, randomized, non-inferiority study directly comparing FANS-f-URS with mini-PCNL in this setting.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Endpoints</h3>\u0000 \u0000 <p>The primary outcome is immediate SFR within 72 hours on low-dose CT. Secondary outcomes include SFR at 1 month, operative time, postoperative pain, hospital stay, complications (Clavien–Dindo) and quality-of-life changes.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Patients and Methods</h3>\u0000 \u0000 <p>A total of 640 adults with CT-confirmed 1–2 cm lower pole renal stones will be randomized 1:1 to undergo FANS-f-URS or mini-PCNL across 20 high-volume urology centres worldwide. Randomization is centralized and stratified by site. Radiologists and statisticians will remain blinded to allocation. Sample size was calculated assuming an 85% SFR for both arms, an 8.5% non-inferiority margin, 80% power and 15% attrition. Analyses will follow both intention-to-treat and per-protocol principles.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Trial registration</h3>\u0000 \u0000 <p>ClinicalTrials.gov NCT07159035.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bjui-journals.onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.70114","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145619244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Post-operative recovery of quality-of-life following percutaneous nephrolithotomy: The impact on pain intensity and interference and the ability to participate in social roles 经皮肾镜取石术后生活质量的恢复:对疼痛强度、干扰和参与社会角色能力的影响
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-11-29 DOI: 10.1002/bco2.70102
Justin B. Ziemba, Amanda Jones, Hanna Stambakio, Gregory E. Tasian, Jing Huang

Objectives

To prospectively capture patient-reported outcomes in the post-operative period to better understand the quality-of-life impact of percutaneous nephrolithotomy (PNL).

Subjects and Methods

Adults undergoing PNL for renal/ureteral stones were eligible for inclusion (11/2020–8/2022). Patients prospectively completed PROMIS – Pain Intensity, Pain Interference and Ability to participate in social roles and activities in-person pre-operatively (POD 0) and via email on POD 1, 7, 14 and 30. Scores are reported as T-scores (normalized to US pop., mean = 50) with a change of 5 (0.5 SD) considered clinically significant.

Results

A total of 62 participants enrolled at POD 0 (POD 1 = 28, POD 7 = 29, POD 14 = 20, POD 30 = 23). There was a worsening of quality of life from POD 0 to POD 1 for pain intensity (median difference 7.9, p = 0.005) and pain interference (median difference 11.9, p = 0.0003), but not for the ability to participate in social roles (median difference −5.3, p = 0.07). This was also observed for POD 0 to POD 7, but only for the dimension of pain interference (median difference 7.2, p = 0.02). All three dimensions then improved until POD 30. In multivariable analysis, there were no variables associated with severe symptomatology for any of the three dimensions.

Conclusions

Pain intensity and interference sharply increase immediately post-operatively, reducing quality of life, although the ability to participate in social roles is not impacted. The absolute magnitude of this change is significant, with a final improvement at 30 days at or above baseline. Results offer meaningful insight to assist in setting expectations for patients post-operatively.

目的前瞻性地收集术后患者报告的结果,以更好地了解经皮肾镜取石术(PNL)对生活质量的影响。受试者和方法接受PNL治疗肾/输尿管结石的成人符合入选条件(2020年11月- 2022年8月)。患者预期在术前亲自完成PROMIS -疼痛强度、疼痛干扰和参与社会角色和活动的能力(POD 0),并在POD 1、7、14和30上通过电子邮件完成。分数报告为t分数(标准化到美国流行)。,平均= 50),变化5 (0.5 SD)被认为具有临床意义。结果:共有62名参与者在POD 0 (POD 1 = 28, POD 7 = 29, POD 14 = 20, POD 30 = 23)入组。从POD 0到POD 1的生活质量在疼痛强度(中位数差7.9,p = 0.005)和疼痛干扰(中位数差11.9,p = 0.0003)方面有所恶化,但在参与社会角色的能力方面没有(中位数差- 5.3,p = 0.07)。在POD 0至POD 7中也观察到这一点,但仅在疼痛干扰维度上(中位差为7.2,p = 0.02)。所有三个维度都得到了改善,直到POD 30。在多变量分析中,在三个维度中没有与严重症状相关的变量。结论术后疼痛强度和干扰度立即急剧增加,生活质量下降,但参与社会角色的能力不受影响。这种变化的绝对幅度是显著的,最终改善是在30天达到或高于基线。结果提供了有意义的见解,以协助设定患者术后期望。
{"title":"Post-operative recovery of quality-of-life following percutaneous nephrolithotomy: The impact on pain intensity and interference and the ability to participate in social roles","authors":"Justin B. Ziemba,&nbsp;Amanda Jones,&nbsp;Hanna Stambakio,&nbsp;Gregory E. Tasian,&nbsp;Jing Huang","doi":"10.1002/bco2.70102","DOIUrl":"https://doi.org/10.1002/bco2.70102","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>To prospectively capture patient-reported outcomes in the post-operative period to better understand the quality-of-life impact of percutaneous nephrolithotomy (PNL).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Subjects and Methods</h3>\u0000 \u0000 <p>Adults undergoing PNL for renal/ureteral stones were eligible for inclusion (11/2020–8/2022). Patients prospectively completed PROMIS – Pain Intensity, Pain Interference and Ability to participate in social roles and activities in-person pre-operatively (POD 0) and via email on POD 1, 7, 14 and 30. Scores are reported as T-scores (normalized to US pop., mean = 50) with a change of 5 (0.5 SD) considered clinically significant.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>A total of 62 participants enrolled at POD 0 (POD 1 = 28, POD 7 = 29, POD 14 = 20, POD 30 = 23). There was a worsening of quality of life from POD 0 to POD 1 for pain intensity (median difference 7.9, p = 0.005) and pain interference (median difference 11.9, p = 0.0003), but not for the ability to participate in social roles (median difference −5.3, p = 0.07). This was also observed for POD 0 to POD 7, but only for the dimension of pain interference (median difference 7.2, p = 0.02). All three dimensions then improved until POD 30. In multivariable analysis, there were no variables associated with severe symptomatology for any of the three dimensions.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Pain intensity and interference sharply increase immediately post-operatively, reducing quality of life, although the ability to participate in social roles is not impacted. The absolute magnitude of this change is significant, with a final improvement at 30 days at or above baseline. Results offer meaningful insight to assist in setting expectations for patients post-operatively.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 12","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://bjui-journals.onlinelibrary.wiley.com/doi/epdf/10.1002/bco2.70102","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145619245","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pelvic organ prolapse is highly prevalent in women with spina bifida 盆腔器官脱垂在脊柱裂患者中非常普遍。
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-11-24 DOI: 10.1002/bco2.70113
Alexandre Dubois, Briac Malandain, Juliette Hascoet, Camille Haudebert, Charlène Brochard, Claire Richard, Caroline Voiry, Krystel Nyangoh Timoh, Andrea Manunta, Emmanuelle Samson, Benoit Peyronnet

Introduction

Women with spina bifida often experience neurological impairments leading to pelvic organ dysfunction, including difficulties with bladder and bowel emptying that necessitate frequent Valsalva manoeuvres. These factors, combined with pelvic floor weakness, may increase the risk of pelvic organ prolapse (POP). This study aimed to assess the prevalence of POP in women with spina bifida, identify associated risk factors and evaluate outcomes of surgical management.

Methods

We retrospectively analysed a prospectively maintained database of women with spina bifida seen at a French referral centre from 2007 to 2024. Age under 18 and congenital perineal abnormality were exclusion criteria. The primary outcome was the presence of POP grade 2 or higher (Baden-Walker classification). Secondary outcomes included symptomatic POP requiring surgery, recurrence after surgery, use of vaginal pessaries and related symptoms.

Results

POP grade ≥2 was present in 14.8% of patients. Women with POP were older (median 44 vs. 31 years; p < 0.0001) and more frequently parous (58.5% vs. 18.3%; p < 0.0001), although 41.5% of POP cases occurred in nulliparous women. Apical prolapse was predominant (64.3%). Among 11 patients who underwent POP surgery, 54.5% experienced recurrence. Multivariate analysis identified parity (OR 5.33; p = 0.005) and lower maximum urethral closure pressure (OR 0.97; p = 0.02) as independent risk factors.

Conclusions

POP is highly prevalent in young adult women with spina bifida, including many nulliparous patients. The parity status and a low maximum urethral closure pressure could be associated with an increased risk of POP in this population. High recurrence after surgery highlights the need for information, routine screening and tailored management in this population.

脊柱裂的女性经常经历神经损伤导致盆腔器官功能障碍,包括膀胱和肠道排空困难,需要经常进行Valsalva手术。这些因素,加上盆底无力,可能会增加盆腔器官脱垂(POP)的风险。本研究旨在评估脊柱裂女性中POP的患病率,确定相关的危险因素并评估手术治疗的结果。方法:我们回顾性分析了2007年至2024年在法国转诊中心就诊的脊柱裂女性的前瞻性数据库。年龄在18岁以下和先天性会阴异常是排除标准。主要预后指标为POP 2级或以上(Baden-Walker分级)。次要结局包括需要手术的症状性POP、手术后复发、使用阴道托及相关症状。结果:14.8%的患者存在≥2级的POP。结论:POP在患有脊柱裂的年轻成年女性中非常普遍,包括许多未生育的患者。胎次状况和较低的最大尿道闭合压力可能与该人群中POP的风险增加有关。手术后的高复发率突出了这一人群对信息、常规筛查和量身定制管理的需求。
{"title":"Pelvic organ prolapse is highly prevalent in women with spina bifida","authors":"Alexandre Dubois,&nbsp;Briac Malandain,&nbsp;Juliette Hascoet,&nbsp;Camille Haudebert,&nbsp;Charlène Brochard,&nbsp;Claire Richard,&nbsp;Caroline Voiry,&nbsp;Krystel Nyangoh Timoh,&nbsp;Andrea Manunta,&nbsp;Emmanuelle Samson,&nbsp;Benoit Peyronnet","doi":"10.1002/bco2.70113","DOIUrl":"10.1002/bco2.70113","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Women with spina bifida often experience neurological impairments leading to pelvic organ dysfunction, including difficulties with bladder and bowel emptying that necessitate frequent Valsalva manoeuvres. These factors, combined with pelvic floor weakness, may increase the risk of pelvic organ prolapse (POP). This study aimed to assess the prevalence of POP in women with spina bifida, identify associated risk factors and evaluate outcomes of surgical management.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We retrospectively analysed a prospectively maintained database of women with spina bifida seen at a French referral centre from 2007 to 2024. Age under 18 and congenital perineal abnormality were exclusion criteria. The primary outcome was the presence of POP grade 2 or higher (Baden-Walker classification). Secondary outcomes included symptomatic POP requiring surgery, recurrence after surgery, use of vaginal pessaries and related symptoms.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>POP grade ≥2 was present in 14.8% of patients. Women with POP were older (median 44 vs. 31 years; p &lt; 0.0001) and more frequently parous (58.5% vs. 18.3%; p &lt; 0.0001), although 41.5% of POP cases occurred in nulliparous women. Apical prolapse was predominant (64.3%). Among 11 patients who underwent POP surgery, 54.5% experienced recurrence. Multivariate analysis identified parity (OR 5.33; p = 0.005) and lower maximum urethral closure pressure (OR 0.97; p = 0.02) as independent risk factors.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>POP is highly prevalent in young adult women with spina bifida, including many nulliparous patients. The parity status and a low maximum urethral closure pressure could be associated with an increased risk of POP in this population. High recurrence after surgery highlights the need for information, routine screening and tailored management in this population.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 11","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12641141/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145607422","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neoadjuvant tislelizumab plus pazopanib in renal cell carcinoma with venous tumour thrombus: A retrospective study 新辅助tislelizumab加pazopanib治疗肾细胞癌伴静脉肿瘤血栓:一项回顾性研究。
IF 1.9 Q3 UROLOGY & NEPHROLOGY Pub Date : 2025-11-18 DOI: 10.1002/bco2.70095
Diliyaer Dilixiati, Houze Li, Huixiang Chen, Shiping Xie, Naifeisha Aihemaiti, Gulizhaer Abulimiti, Baihetiya Azhati

Objectives

Neoadjuvant therapy with immune checkpoint inhibitors and tyrosine kinase inhibitors has been shown to reduce the tumour size and thrombus length in patients with renal cell carcinoma with venous tumour thrombus (RCC-VTT). This study aimed to evaluate the effectiveness and safety of neoadjuvant tislelizumab plus pazopanib in patients with RCC-VTT.

Patients and Methods

From November 2021 to January 2024, nine patients with RCC-VTT were included in this retrospective study. All patients received neoadjuvant tislelizumab (200 mg intravenously every 3 weeks) and pazopanib (800 mg orally once daily), followed by surgery. Key effectiveness outcomes included the objective response rate (ORR) of the primary tumour, the percentage change in VTT length and safety.

Results

Among the nine patients with RCC-VTT, the median age was 58 years (range, 39–78). Following neoadjuvant tislelizumab plus pazopanib, six patients achieved partial response in the primary tumour and three had stable disease, yielding an ORR of 66.7%. The VTT length decreased from 4.9 cm (range, 1.1–9.3 cm) to 3.8 cm (range, 0–8.1 cm), with a median reduction of 29.2% (range, −153.1% to 100.0%). Treatment-related adverse events (TRAEs) of any grade and grade 3 were reported in 88.9% and 55.6% of patients, respectively. The common TRAEs of any grade were vomiting (77.8%), fatigue (33.3%), pruritus (33.3%), weight loss (33.3%), poor appetite (33.3%), pruritus (33.3%) and hepatic impairment (33.3%). No grade 4–5 TRAEs or deaths were observed.

Conclusion

The neoadjuvant combination of tislelizumab and pazopanib effectively reduced tumour size and thrombus length, narrowing the surgical scope and potentially leading to better postoperative outcomes.

目的:免疫检查点抑制剂和酪氨酸激酶抑制剂的新辅助治疗已被证明可以减少肾细胞癌伴静脉肿瘤血栓(RCC-VTT)患者的肿瘤大小和血栓长度。本研究旨在评估新辅助tislelizumab联合pazopanib治疗RCC-VTT患者的有效性和安全性。患者和方法:从2021年11月至2024年1月,9例RCC-VTT患者纳入回顾性研究。所有患者接受新辅助tislelizumab (200 mg静脉注射,每3周一次)和pazopanib (800 mg口服,每天一次),随后进行手术。主要疗效指标包括原发肿瘤的客观缓解率(ORR)、VTT长度变化百分比和安全性。结果:9例RCC-VTT患者中位年龄为58岁(范围39-78岁)。在新辅助治疗tislelizumab + pazopanib后,6例患者在原发肿瘤中获得部分缓解,3例病情稳定,ORR为66.7%。VTT长度从4.9 cm(范围1.1 ~ 9.3 cm)减少到3.8 cm(范围0 ~ 8.1 cm),中位减少29.2%(范围-153.1% ~ 100.0%)。88.9%和55.6%的患者分别报告了任何级别和3级治疗相关不良事件(TRAEs)。常见的trae为呕吐(77.8%)、疲劳(33.3%)、瘙痒(33.3%)、体重减轻(33.3%)、食欲不振(33.3%)、瘙痒(33.3%)和肝功能损害(33.3%)。未观察到4-5级trae或死亡。结论:新辅助联合tislelizumab和pazopanib有效缩小肿瘤大小和血栓长度,缩小手术范围,可能带来更好的术后结果。
{"title":"Neoadjuvant tislelizumab plus pazopanib in renal cell carcinoma with venous tumour thrombus: A retrospective study","authors":"Diliyaer Dilixiati,&nbsp;Houze Li,&nbsp;Huixiang Chen,&nbsp;Shiping Xie,&nbsp;Naifeisha Aihemaiti,&nbsp;Gulizhaer Abulimiti,&nbsp;Baihetiya Azhati","doi":"10.1002/bco2.70095","DOIUrl":"10.1002/bco2.70095","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>Neoadjuvant therapy with immune checkpoint inhibitors and tyrosine kinase inhibitors has been shown to reduce the tumour size and thrombus length in patients with renal cell carcinoma with venous tumour thrombus (RCC-VTT). This study aimed to evaluate the effectiveness and safety of neoadjuvant tislelizumab plus pazopanib in patients with RCC-VTT.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Patients and Methods</h3>\u0000 \u0000 <p>From November 2021 to January 2024, nine patients with RCC-VTT were included in this retrospective study. All patients received neoadjuvant tislelizumab (200 mg intravenously every 3 weeks) and pazopanib (800 mg orally once daily), followed by surgery. Key effectiveness outcomes included the objective response rate (ORR) of the primary tumour, the percentage change in VTT length and safety.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among the nine patients with RCC-VTT, the median age was 58 years (range, 39–78). Following neoadjuvant tislelizumab plus pazopanib, six patients achieved partial response in the primary tumour and three had stable disease, yielding an ORR of 66.7%. The VTT length decreased from 4.9 cm (range, 1.1–9.3 cm) to 3.8 cm (range, 0–8.1 cm), with a median reduction of 29.2% (range, −153.1% to 100.0%). Treatment-related adverse events (TRAEs) of any grade and grade 3 were reported in 88.9% and 55.6% of patients, respectively. The common TRAEs of any grade were vomiting (77.8%), fatigue (33.3%), pruritus (33.3%), weight loss (33.3%), poor appetite (33.3%), pruritus (33.3%) and hepatic impairment (33.3%). No grade 4–5 TRAEs or deaths were observed.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The neoadjuvant combination of tislelizumab and pazopanib effectively reduced tumour size and thrombus length, narrowing the surgical scope and potentially leading to better postoperative outcomes.</p>\u0000 </section>\u0000 </div>","PeriodicalId":72420,"journal":{"name":"BJUI compass","volume":"6 11","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12627238/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145566320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
BJUI compass
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1