[预测 T3a 非转移性肾细胞癌患者的 3 年肿瘤特异性生存率]。

Q3 Medicine 北京大学学报(医学版) Pub Date : 2024-08-18
Zezhen Zhou, Shaohui Deng, Ye Yan, Fan Zhang, Yichang Hao, Liyuan Ge, Hongxian Zhang, Guoliang Wang, Shudong Zhang
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引用次数: 0

摘要

目的:预测非转移性T3a肾细胞癌患者术后3年癌症特异性生存率(CSS预测非转移性T3a肾细胞癌患者术后3年癌症特异性生存率(CSS):回顾性收集2013年3月至2021年2月在北京大学第三医院泌尿外科接受手术治疗的病理确诊T3a N0-1M0肾细胞癌(RCC)患者共336例。这些患者按 4 ∶ 1 的比例随机分为 268 例训练队列和 68 例内部验证队列。通过双向拉索回归法,选择变量构建了预测T3aN0-1M0 RCC患者3年癌症特异性生存率(CSS)的提名图。提名图的性能评估包括判别和校准能力评估,以及使用一致性指数(C-index)、随时间变化的接收者工作特征曲线下面积[随时间变化的曲线下面积(AUC)]、校准曲线和决策曲线分析(DCA)等指标进行临床实用性评估。根据提名图评分确定风险分层,并采用卡普兰-梅耶生存分析和对数秩检验比较不同风险组患者的无进展生存期(PFS)和癌症特异性生存期(CSS):根据Lasso回归筛选结果,用肿瘤最大直径、组织学分级、肉瘤样分化、T3a特征和淋巴结转移五个变量构建了提名图。训练集和验证集的基线数据无统计学差异(P>0.05)。训练集和内部验证集的柱状图一致性指数分别为 0.808(0.708- 0.907)和 0.903(0.838-0.969)。两组 3 年癌症特异性生存率的 AUC 值分别为 0.843(0.725-0.961)和 0.923(0.844-1.002)。两组数据的校准曲线显示,实际 CSS 与预测概率高度一致。决策曲线分析(DCA)曲线显示,柱状图在临床实践中具有良好的净效益。研究共纳入 336 例患者,其中 35 例因癌症死亡,69 例术后复发。根据柱状图,患者被分为低风险组(评分 0-117)和高风险组(评分 119-284)。在低风险组中,282 例病例中有 16 例肿瘤特异性死亡,282 例病例中有 36 例术后复发。在高风险组中,54 个病例中有 19 例肿瘤特异性死亡,54 个病例中有 33 例术后复发。低危组和高危组的无进展生存期(PFS)和癌症特异性生存期(CSS)有明显差异(P < 0.000 1):本研究成功构建并验证了预测非转移性T3a肾细胞癌患者3年CSS的提名图模型。该提名图有助于临床医生准确评估此类患者的长期预后。
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[Predicting the 3-year tumor-specific survival in patients with T3a non-metastatic renal cell carcinoma].

Objective: To predict the 3-year cancer-specific survival (CSS) of patients with non-metastatic T3a renal cell carcinoma after surgery.

Methods: A total of 336 patients with pathologically confirmed T3a N0-1M0 renal cell carcinoma (RCC) who underwent surgical treatment at the Department of Urology, Peking University Third Hospital from March 2013 to February 2021 were retrospectively collected. The patients were randomly divided into a training cohort of 268 cases and an internal validation cohort of 68 cases at an 4 ∶ 1 ratio. Using two-way Lasso regression, variables were selected to construct a nomogram for predicting the 3-year cancer-specific survival (CSS) of the patients with T3aN0-1M0 RCC. Performance assessment of the nomogram included evaluation of discrimination and calibration ability, as well as clinical utility using measures such as the concordance index (C-index), time-dependent area under the receiver operating characteristic curve [time-dependent area under the curve (AUC)], calibration curve, and decision curve analysis (DCA). Risk stratification was determined based on the nomogram scores, and Kaplan-Meier survival analysis and Log-rank tests were employed to compare progression-free survival (PFS) and cancer-specific survival (CSS) among the patients in the different risk groups.

Results: Based on the Lasso regression screening results, the nomogram was constructed with five variables: tumor maximum diameter, histological grading, sarcomatoid differentiation, T3a feature, and lymph node metastasis. The baseline data of the training and validation sets showed no statistical differences (P>0.05). The consistency indices of the column diagram were found to be 0.808 (0.708- 0.907) and 0.903 (0.838-0.969) for the training and internal validation sets, respectively. The AUC values for 3-year cancer-specific survival were 0.843 (0.725-0.961) and 0.923 (0.844-1.002) for the two sets. Calibration curves of both sets demonstrated a high level of consistency between the actual CSS and predicted probability. The decision curve analysis (DCA) curves indicated that the column diagram had a favorable net benefit in clinical practice. A total of 336 patients were included in the study, with 35 cancer-specific deaths and 69 postoperative recurrences. According to the line chart, the patients were divided into low-risk group (scoring 0-117) and high-risk group (scoring 119-284). Within the low-risk group, there were 16 tumor-specific deaths out of 282 cases and 36 postoperative recurrences out of 282 cases. In the high-risk group, there were 19 tumor-specific deaths out of 54 cases and 33 post-operative recurrences out of 54 cases. There were significant differences in progression-free survival (PFS) and cancer-specific survival (CSS) between the low-risk and high-risk groups (P < 0.000 1).

Conclusion: A nomogram model predicting the 3-year CSS of non-metastatic T3a renal cell carcinoma patients was successfully constructed and validated in this study. This nomogram can assist clinicians in accurately assessing the long-term prognosis of such patients.

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来源期刊
北京大学学报(医学版)
北京大学学报(医学版) Medicine-Medicine (all)
CiteScore
0.80
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0.00%
发文量
9815
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