Dana-Farber Cancer Institute, Boston, MA.
International Agency for Research on Cancer, Lyon, France.
J Clin Oncol. 2024 Aug 1;42(22):2691-2701. doi: 10.1200/JCO.23.00699. Epub 2024 May 3.
Both clear cell and papillary renal cell carcinomas (RCCs) overexpress kidney injury molecule-1 (KIM-1). We investigated whether plasma KIM-1 (pKIM-1) may be a useful risk stratification tool among patients with suspicious renal masses.
Prenephrectomy pKIM-1 was measured in two independent cohorts of patients with renal masses. Cohort 1, from the prospective K2 trial, included 162 patients found to have clear cell RCC (cases) and 162 patients with benign renal masses (controls). Cohort 2 included 247 patients with small (cT1a) renal masses from an academic biorepository, of whom 184 had RCC. We assessed the relationship between pKIM-1, surgical pathology, and clinical outcomes.
In Cohort 1, pKIM-1 distinguished RCC versus benign masses with area under the receiver operating curve (AUC-ROC, 0.81 [95% CI, 0.76 to 0.86]). In Cohort 2 (cT1a only), pKIM-1 distinguished RCC versus benign masses (AUC-ROC, 0.74 [95% CI, 0.67 to 0.80]) and the addition of pKIM-1 to an established nomogram for predicting malignancy improved the model AUC-ROC (0.65 [95% CI, 0.57 to 0.74] 0.78 [95% CI, 0.72 to 0.85]). A pKIM-1 cutpoint identified using Cohort 2 demonstrated sensitivity of 92.5% and specificity of 60% for identifying RCC in Cohort 1. In long-term follow-up of RCC cases (Cohort 1), higher prenephrectomy pKIM-1 was associated with worse metastasis-free survival (multivariable MFS hazard ratio [HR] 1.29 per unit increase in log pKIM-1, 95% CI, 1.10 to 1.53) and overall survival (multivariable OS HR 1.31 per unit increase in log pKIM-1, 95% CI, 1.10 to 1.54). In long-term follow-up of Cohort 2, no metastatic events occurred, consistent with the favorable prognosis of resected cT1a RCC.
Among patients with renal masses, pKIM-1 is associated with malignant pathology, worse MFS, and risk of death. pKIM-1 may be useful for selecting patients with renal masses for intervention versus surveillance.
透明细胞和乳头状肾细胞癌 (RCC) 均过度表达肾损伤分子-1 (KIM-1)。我们研究了血浆 KIM-1 (pKIM-1) 是否可作为疑似肾肿块患者的有用风险分层工具。
在两个独立的肾肿块患者队列中测量了术前 pKIM-1。队列 1 来自前瞻性 K2 试验,包括 162 例透明细胞 RCC(病例)和 162 例良性肾肿块患者(对照组)。队列 2 包括来自学术生物库的 247 例小 (cT1a) 肾肿块患者,其中 184 例为 RCC。我们评估了 pKIM-1 与手术病理和临床结果之间的关系。
在队列 1 中,pKIM-1 可区分 RCC 与良性肿块,其受试者工作特征曲线下面积 (AUC-ROC,0.81 [95% CI,0.76 至 0.86])。在队列 2(仅 cT1a)中,pKIM-1 可区分 RCC 与良性肿块 (AUC-ROC,0.74 [95% CI,0.67 至 0.80]),并且将 pKIM-1 添加到用于预测恶性肿瘤的既定列线图中可提高模型 AUC-ROC(0.65 [95% CI,0.57 至 0.74] 0.78 [95% CI,0.72 至 0.85])。使用队列 2 确定的 pKIM-1 切点在队列 1 中可识别出 92.5%的 RCC 病例的敏感性和 60%的特异性。在 RCC 病例的长期随访中(队列 1),术前较高的 pKIM-1 与无转移生存不良相关(多变量 MFS 危险比 [HR] 每单位 log pKIM-1 增加 1.29,95% CI,1.10 至 1.53)和总生存(多变量 OS HR 每单位 log pKIM-1 增加 1.31,95% CI,1.10 至 1.54)。在队列 2 的长期随访中,未发生转移事件,这与切除的 cT1a RCC 的良好预后一致。
在肾肿块患者中,pKIM-1 与恶性病理、较差的 MFS 和死亡风险相关。pKIM-1 可能有助于选择肾肿块患者进行干预或监测。