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纵向肿瘤信息循环肿瘤DNA状态可预测接受根治性膀胱切除术患者的疾病分期升级和预后不良。

Longitudinal Tumor-informed Circulating Tumor DNA Status Predicts Disease Upstaging and Poor Prognosis for Patients Undergoing Radical Cystectomy.

作者信息

Ben-David Reuben, Tillu Neeraja, Cumarasamy Shivaram, Alerasool Parissa, Rich Jordan M, Kaufmann Basil, Elkun Yuval, Attalla Kyrollis, Mehrazin Reza, Wiklund Peter, Sfakianos John P

机构信息

Urology Department, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Urology Department, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Eur Urol Oncol. 2024 Oct;7(5):1105-1112. doi: 10.1016/j.euo.2024.03.002. Epub 2024 Mar 22.

Abstract

BACKGROUND AND OBJECTIVE

Decision-making on the use of neoadjuvant and adjuvant treatment for patients with bladder cancer undergoing radical cystectomy (RC) currently depends on assessment of clinical and pathological features, which lack sensitivity. Circulating tumor DNA (ctDNA) has emerged as a possible novel prognostic biomarker in the field. Our aim was to assess whether ctDNA status before RC is predictive of pathological and oncological outcomes. We also evaluated the dynamic changes in ctDNA status after RC in relation to recurrence-free survival (RFS).

METHODS

We analyzed data for patients who underwent RC during 2021-2023 for whom prospective tumor-informed ctDNA analyses were conducted before and after RC. RFS was evaluated using the Kaplan-Meier method. Predictors for disease recurrence were assessed using Cox proportional-hazards models. Pathological outcomes associated with detectable ctDNA before RC were assessed in univariable and multivariable regression analyses.

KEY FINDINGS AND LIMITATIONS

We included 112 patients in the analysis. Median follow-up was 8 mo (interquartile range 4-13). ctDNA was detected before RC in 59 patients (53%) and was associated with poor RFS (log-rank p < 0.0001). Detectable ctDNA before RC was associated with poor outcomes regardless of clinical stage (<cT2 vs ≥cT2) and receipt of neoadjuvant therapy. Multivariable analyses revealed that detectable ctDNA before RC was associated with a higher risk of nodal disease (odds ratio 5.4, 95% confidence interval [CI] 1.9-18.2; p = 0.003) and locally advanced disease (odds ratio 3.6, 95% CI 1.5-9; p = 0.005). Cox regression analyses showed that detectable ctDNA before RC (hazard ratio 4.5, 95% CI 1-19; p = 0.04) and detectable ctDNA at the minimal residual disease window (hazard ratio 9.9, 95% CI 2.6-37; p < 0.001) were predictive of disease recurrence.

CONCLUSIONS AND CLINICAL IMPLICATIONS

Detectable ctDNA before definitive therapy with RC is predictive of nodal involvement, locally advanced disease, and disease recurrence in patients with bladder cancer. ctDNA status holds promise for improving clinical staging and augmenting current decision-making tools.

PATIENT SUMMARY

We found that for patients with bladder cancer undergoing radical cystectomy, a test to show the presence of tumor DNA in blood before surgery was able to predict the risk of disease relapse and adverse pathology. Use of this assay could help in decision-making by clinicians and patients for optimal personalized treatment of this disease.

摘要

背景与目的

目前,对于接受根治性膀胱切除术(RC)的膀胱癌患者,新辅助和辅助治疗的决策依赖于临床和病理特征评估,而这些评估缺乏敏感性。循环肿瘤DNA(ctDNA)已成为该领域一种可能的新型预后生物标志物。我们的目的是评估RC术前ctDNA状态是否可预测病理和肿瘤学结局。我们还评估了RC术后ctDNA状态与无复发生存期(RFS)相关的动态变化。

方法

我们分析了2021年至2023年期间接受RC的患者数据,这些患者在RC前后进行了前瞻性肿瘤知情ctDNA分析。使用Kaplan-Meier方法评估RFS。使用Cox比例风险模型评估疾病复发的预测因素。在单变量和多变量回归分析中评估与RC术前可检测到的ctDNA相关的病理结局。

主要发现与局限性

我们纳入了112例患者进行分析。中位随访时间为8个月(四分位间距4 - 13个月)。59例(53%)患者在RC术前检测到ctDNA,且与较差的RFS相关(对数秩检验p < 0.000)。无论临床分期(<cT2 vs ≥cT2)和是否接受新辅助治疗,RC术前可检测到的ctDNA均与不良结局相关。多变量分析显示,RC术前可检测到的ctDNA与淋巴结疾病风险较高相关(比值比5.4,95%置信区间[CI] 1.9 - 18.2;p = 0.003)和局部晚期疾病相关(比值比3.6,95% CI 1.5 - 9;p = 0.005)。Cox回归分析表明,RC术前可检测到的ctDNA(风险比4.5,95% CI 1 - 19;p = 0.04)和在最小残留疾病窗口可检测到的ctDNA(风险比9.9,95% CI 2.6 - 37;p < 0.001)可预测疾病复发。

结论与临床意义

在接受RC确定性治疗前可检测到的ctDNA可预测膀胱癌患者淋巴结受累、局部晚期疾病和疾病复发。ctDNA状态有望改善临床分期并增强当前的决策工具。

患者总结

我们发现,对于接受根治性膀胱切除术的膀胱癌患者,术前检测血液中肿瘤DNA的试验能够预测疾病复发风险和不良病理情况。使用该检测方法有助于临床医生和患者做出决策,以实现对该疾病的最佳个性化治疗。

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