Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
Clin Genitourin Cancer. 2019 Jun;17(3):e678-e688. doi: 10.1016/j.clgc.2019.03.018. Epub 2019 Apr 1.
Sarcomatoid features (SF) in renal cell carcinoma (RCC) denote poor prognosis. Data for metastatic chromophobe RCC (ChRCC) with SF are limited. We studied clinical outcomes and genomic features in this setting.
We performed a retrospective review of newly diagnosed metastatic ChRCC patients; end points included overall survival (OS), time to treatment failure (TTF), and time to metastatic recurrence (TTR) after nephrectomy for localized disease. A subset of patients underwent next-generation sequencing (NGS). Outcomes were compared using nonparametric tests.
One hundred nine patients with metastatic ChRCC were identified including 29 with SF. Median TTR after nephrectomy was shorter for patients with versus without SF (2.7 months [95% confidence interval (CI), 0.7-6.9] versus 48.8 months [95% CI, 30.8-80.7], log rank P < .001). Median TTF during first-line therapy was shorter for patients with versus without SF (1.8 months [95% CI, 0.9-2.7] vs. 8.0 months [95% CI, 5.1-13.0]; log rank P < .001). No responses were observed in 6 patients treated with nivolumab including 4 with SF. Median OS was inferior for patients with versus without SF (38 months vs.7.5 months; hazard ratio, 4.7 [95% CI, 2.7-8.2]; P < .001). NGS, performed in 22 patients, showed that 64% and 45% harbored tumor protein P53 and phosphatase and tensin homolog alterations, respectively. Microsatellite instability high status was identified in 3 patients.
Metastatic ChRCC patients with SF had worse outcomes compared with those without SF. Median TTR < 3 months for this subgroup supports close surveillance after nephrectomy for localized tumors. Lack of benefit with various systemic regimens warrants studying underlying biology and investigating novel agents.
肉瘤样特征(SF)在肾细胞癌(RCC)中表示预后不良。转移性嫌色细胞 RCC(ChRCC)伴 SF 的数据有限。我们在此背景下研究了临床结局和基因组特征。
我们对新诊断的转移性 ChRCC 患者进行了回顾性研究;终点包括总生存(OS)、局部疾病肾切除术后治疗失败时间(TTF)和转移复发时间(TTR)。一部分患者接受了下一代测序(NGS)。使用非参数检验比较结局。
共确定了 109 例转移性 ChRCC 患者,其中 29 例伴 SF。与无 SF 患者相比,肾切除术后 TTR 更短(2.7 个月[95%置信区间(CI),0.7-6.9]与 48.8 个月[95%CI,30.8-80.7],对数秩 P<.001)。一线治疗中 TTF 更短(1.8 个月[95%CI,0.9-2.7]与 8.0 个月[95%CI,5.1-13.0];对数秩 P<.001)。6 例接受nivolumab 治疗的患者中未观察到任何反应,其中 4 例伴 SF。与无 SF 患者相比,中位 OS 更差(38 个月 vs.7.5 个月;风险比,4.7[95%CI,2.7-8.2];P<.001)。22 例患者进行了 NGS,分别有 64%和 45%的患者存在肿瘤蛋白 P53 和磷酸酶和张力蛋白同源物改变。3 例患者存在微卫星不稳定高状态。
与无 SF 的患者相比,转移性 ChRCC 伴 SF 的患者结局更差。该亚组的中位 TTR<3 个月支持对局部肿瘤进行肾切除术后的密切监测。各种系统治疗方案无效,需要研究潜在生物学并研究新型药物。