Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Aarhus University Hospital, Aarhus, Denmark.
Eur Urol. 2014 Apr;65(4):723-30. doi: 10.1016/j.eururo.2013.10.013. Epub 2013 Oct 26.
Hyponatremia has been associated with poor survival in many solid tumors and more recently found to be of prognostic and predictive value in metastatic renal cell cancer (mRCC) patients treated with immunotherapy.
To investigate the influence of baseline hyponatremia in mRCC patients treated with targeted therapy in the International Metastatic Renal Cell Carcinoma Database Consortium.
DESIGN, SETTING, AND PARTICIPANTS: Data on 1661 patients treated with first-line vascular endothelial growth factor (VEGF) or mammalian target of rapamycin (mTOR) targeted therapy for mRCC were available from 18 cancer centers to study the impact of hyponatremia (serum sodium level <135 mmol/l) on clinical outcomes.
The primary objective was overall survival (OS) and secondary end points included time to treatment failure (TTF) and the disease control rate (DCR). The chi-square test was used to compare the DCR in patients with and without hyponatremia. OS and TTF were estimated with the Kaplan-Meier method and differences between groups were examined by the log-rank test. Multivariable logistic regression (for DCR) and Cox regression (for OS and TTF) were undertaken adjusted for prognostic risk factors.
Median OS after treatment initiation was 18.5 mo (95% confidence interval [CI], 17.5-19.8 mo), with 552 (33.2%) of patients remaining alive on a median follow-up of 22.1 mo. Median baseline serum sodium was 138 mmol/l (range: 122-159 mmol/l), and hyponatremia was found in 14.6% of patients. On univariate analysis, hyponatremia was associated with shorter OS (7.0 vs 20.9 mo), shorter TTF (2.9 vs 7.4 mo), and lower DCR rate (54.9% vs 78.8%) (p<0.0001 for all comparisons). In multivariate analysis, these effects remain significant (hazard ratios: 1.51 [95% CI, 1.26-1.80] for OS, and 1.57 [95% CI, 1.34-1.83] for TTF; odds ratio: 0.50 [95% CI, 34-0.72] for DCR; adjusted p<0.001). Results were similar if sodium was analyzed as a continuous variable (adjusted p<0.0001 for OS, TTF, and DCR).
This is the largest multi-institutional report to show that hyponatremia is independently associated with a worse outcome in mRCC patients treated with VEGF- and mTOR-targeted agents.
低钠血症与许多实体瘤患者的生存不良有关,最近在接受免疫治疗的转移性肾细胞癌(mRCC)患者中发现其具有预后和预测价值。
研究在国际转移性肾细胞癌数据库联盟中接受靶向治疗的 mRCC 患者中基线低钠血症的影响。
设计、地点和参与者:来自 18 个癌症中心的 1661 名接受一线血管内皮生长因子(VEGF)或哺乳动物雷帕霉素靶蛋白(mTOR)靶向治疗的 mRCC 患者的数据可用于研究低钠血症(血清钠水平<135mmol/l)对临床结局的影响。
主要终点是总生存期(OS),次要终点包括治疗失败时间(TTF)和疾病控制率(DCR)。卡方检验用于比较低钠血症组和无低钠血症组的 DCR。采用 Kaplan-Meier 法估计 OS 和 TTF,并用对数秩检验比较组间差异。多变量逻辑回归(用于 DCR)和 Cox 回归(用于 OS 和 TTF)用于调整预后危险因素。
治疗开始后中位 OS 为 18.5 个月(95%置信区间 [CI],17.5-19.8 个月),中位随访 22.1 个月时,552 名(33.2%)患者存活。中位基线血清钠为 138mmol/l(范围:122-159mmol/l),14.6%的患者存在低钠血症。单因素分析显示,低钠血症与较短的 OS(7.0 与 20.9 个月)、较短的 TTF(2.9 与 7.4 个月)和较低的 DCR 率(54.9%与 78.8%)相关(所有比较的 p<0.0001)。多变量分析显示,这些影响仍然显著(OS 的风险比:1.51 [95%CI,1.26-1.80],TTF 的风险比:1.57 [95%CI,1.34-1.83];DCR 的比值比:0.50 [95%CI,34-0.72];调整后的 p<0.001)。如果将钠分析为连续变量,结果相似(OS、TTF 和 DCR 的调整后 p<0.0001)。
这是最大的多机构报告,表明低钠血症与接受 VEGF 和 mTOR 靶向药物治疗的 mRCC 患者的不良结局独立相关。