Nomograms to Appraise The Risk of Chronic Kidney Disease After Radical Cystectomy: Shifting The Focus to Prevention

IF 2.3 3区 医学 Q3 ONCOLOGY Clinical genitourinary cancer Pub Date : 2024-08-13 DOI:10.1016/j.clgc.2024.102205
Alberto Artiles Medina , César Mínguez Ojeda , José Daniel Subiela Henríquez , Alfonso Muriel García , Álvaro Sánchez González , Marina Mata Alcaraz , Jennifer Brasero Burgos , Pablo Gajate Borau , Victoria Gómez Dos Santos , Miguel Ángel Jiménez Cidre , Francisco Javier Burgos Revilla
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Abstract

Introduction

Our objectives were to analyse the incidence of changes in renal function after radical cystectomy (RC) and determine the factors responsible for those changes, as a basis for rethinking strategies to ensure early detection and development of a risk-adapted approach.

Patients and methods

A single-centre retrospective study included 316 patients who underwent RC between 2010 and 2019. A competing risk Cox model, whereby death from any cause was treated as a censoring event, was used to establish nomograms to analyze the prognostic factors for CKD at 2 and 5 years. The nomograms were validated based on discrimination using the C-index, calibration plots and analysis of net benefit from decision curves.

Results

During a median follow-up of 48.73 months (0.13-156.67), 138 patients (43.7%) developed CKD. The probability of CKD development at 2 and 5 years was 41.3% (95% CI, 35.8-47.2) and 48.5% (95% CI, 42.8-54.6), respectively. Hypertension (HR 1.69, 95% CI, 1.23-2.34), prior hydronephrosis (HR 1.62, 95% CI, 1.17-2.25), acute kidney injury (AKI) during the immediate postoperative period (HR 1.88, 95% CI, 1.35-2.61) and readmission due to urinary tract infection (HR 1.41, 95% CI, 1.01-1.96) were predictors of 2-year CKD. Hydronephrosis at follow-up computed tomography (HR 2.21, 95% CI, 1.60-3.07), prior hydronephrosis (HR 1.54, 95% CI, 1.09-2.15), AKI during the immediate postoperative period (HR 1.77, 95% CI, 1.27-2.46) and hypertension (HR 1.60, 95% CI, 1.16-2.21) were predictors for 5-year CKD. Prior eGFR ≥ 90 mL/min/1.73 m2 was a protective factor (HR 0.50, 95% CI, 0.32-0.80 and HR 0.48, 95% CI, 0.30-0.78 for 2- and 5-year CKD, respectively). The resulting nomograms were based on these prognostic factors.

Conclusion

Almost half of the patients had developed CKD at 5 years. Thus, it is crucial to identify patients at risk of developing CKD in order to initiate renal function-sparing measures and tailor follow-up protocols. The proposed nomograms effectively predicted CKD in these patients.

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评估根治性膀胱切除术后慢性肾病风险的提名图:将重点转向预防
我们的目的是分析根治性膀胱切除术(RC)后肾功能变化的发生率,并确定导致这些变化的因素,以此为基础重新思考确保早期发现的策略,并制定适应风险的方法。这项单中心回顾性研究纳入了2010年至2019年期间接受根治性膀胱切除术的316名患者。该研究采用竞争风险 Cox 模型,将任何原因导致的死亡作为一个普查事件,建立了代用图来分析 2 年和 5 年后 CKD 的预后因素。根据C指数、校准图和决策曲线的净效益分析对提名图进行了验证。在中位 48.73 个月(0.13-156.67 个月)的随访期间,138 名患者(43.7%)出现了 CKD。2年和5年后发生 CKD 的概率分别为 41.3% (95% CI, 35.8-47.2) 和 48.5% (95% CI, 42.8-54.6)。高血压(HR 1.69,95% CI,1.23-2.34)、既往肾积水(HR 1.62,95% CI,1.17-2.25)、术后即刻急性肾损伤(AKI)(HR 1.88,95% CI,1.34-2.61)和因尿路感染再次入院(HR 1.41,95% CI,1.01-1.96)是预测 2 年 CKD 的因素。随访计算机断层扫描时的肾积水(HR 1.54,95% CI,1.09-2.15)、术后即刻出现的 AKI(HR 1.77,95% CI,1.27-2.46)和高血压(HR 1.60,95% CI,1.16-2.21)是 5 年 CKD 的预测因素。之前的 eGFR ≥ 90 mL/min/1.73 m 是一个保护因素(2 年和 5 年 CKD 的 HR 分别为 0.50,95% CI,0.32-0.80 和 HR 0.48,95% CI,0.30-0.78)。根据这些预后因素得出了提名图。近一半的患者在 5 年后出现了 CKD。因此,识别有发展成慢性肾功能衰竭风险的患者,以便启动保护肾功能的措施和制定后续治疗方案至关重要。所提出的提名图能有效预测这些患者的慢性肾功能衰竭。
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来源期刊
Clinical genitourinary cancer
Clinical genitourinary cancer 医学-泌尿学与肾脏学
CiteScore
5.20
自引率
6.20%
发文量
201
审稿时长
54 days
期刊介绍: Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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