Cancer Prognostics and Health Outcomes Unit, Division of Urology, University of Montréal Health Center, Montréal, QC, Canada.
Department of Urology, Medical University of Graz, Graz, Austria.
Ann Surg Oncol. 2023 Dec;30(13):8780-8785. doi: 10.1245/s10434-023-14367-6. Epub 2023 Oct 10.
This study aimed to test the prognostic significance of pathologically confirmed lymph node invasion in metastatic renal cell carcinoma (mRCC) patients in this immunotherapy era.
Surgically treated mRCC patients were identified in the Surveillance, Epidemiology, and End Results (SEER) database between 2010 and 2018. Kaplan-Meier plots and multivariable Cox-regression models were fitted to test for differences in cancer-specific mortality (CSM) and overall mortality (OM) according to N stage (pN0 vs pN1 vs. pNx). Subgroup analyses addressing pN1 patients tested for CSM and OM differences according to postoperative systemic therapy status.
Overall, 3149 surgically treated mRCC patients were identified. Of these patients, 443 (14%) were labeled as pN1, 812 (26%) as pN0, and 1894 (60%) as pNx. In Kaplan-Meier analyses, the median CSM-free survival was 15 months for pN1 versus 40 months for pN0 versus 35 months for pNx (P < 0.001). In multivariable Cox regression analyses, pN1 independently predicted higher CSM (hazard ratio [HR], 1.88; P < 0.01) and OM (HR, 1.95; P < 0.01) relative to pN0. In sensitivity analyses addressing pN1 patients, postoperative systemic therapy use independently predicted lower CSM (HR, 0.73; P < 0.01) and OM (HR, 0.71; P < 0.01).
Pathologically confirmed lymph node invasion independently predicted higher CSM and OM for surgically treated mRCC patients. For pN1 mRCC patients, use of postoperative systemic therapy was associated with lower CSM and OM. Consequently, N stage should be considered for individual patient counseling and clinical decision-making. Consort diagram of the study population.
本研究旨在检验在免疫治疗时代,经病理证实的淋巴结侵犯对转移性肾细胞癌(mRCC)患者的预后意义。
在 2010 年至 2018 年期间,我们在监测、流行病学和最终结果(SEER)数据库中确定了接受手术治疗的 mRCC 患者。通过 Kaplan-Meier 图和多变量 Cox 回归模型,检验 N 分期(pN0 与 pN1 与 pNx)对癌症特异性死亡率(CSM)和总死亡率(OM)的影响。针对 pN1 患者的亚组分析,根据术后全身治疗情况,检验 CSM 和 OM 的差异。
共确定了 3149 例接受手术治疗的 mRCC 患者。其中,443 例(14%)被标记为 pN1,812 例(26%)为 pN0,1894 例(60%)为 pNx。在 Kaplan-Meier 分析中,pN1 组的中位 CSM 无复发生存期为 15 个月,pN0 组为 40 个月,pNx 组为 35 个月(P<0.001)。在多变量 Cox 回归分析中,pN1 独立预测更高的 CSM(风险比 [HR],1.88;P<0.01)和 OM(HR,1.95;P<0.01),与 pN0 相比。在针对 pN1 患者的敏感性分析中,术后全身治疗的使用独立预测了更低的 CSM(HR,0.73;P<0.01)和 OM(HR,0.71;P<0.01)。
经病理证实的淋巴结侵犯独立预测了接受手术治疗的 mRCC 患者的更高 CSM 和 OM。对于 pN1 mRCC 患者,术后全身治疗的使用与更低的 CSM 和 OM 相关。因此,应考虑 N 分期以进行个体患者咨询和临床决策。
研究人群的 Consort 图。