Department of Urology, University of Texas M. D. Anderson Cancer Center, Houston, Texas.
Department of Genitourinary Oncology, University of Texas M. D. Anderson Cancer Center, Houston, Texas.
J Urol. 2017 Sep;198(3):530-537. doi: 10.1016/j.juro.2017.04.067. Epub 2017 Apr 11.
We studied overall survival and prognostic factors in patients with sarcomatoid renal cell carcinoma treated with nephrectomy and systemic therapy in the cytokine and targeted therapy eras.
This is a retrospective study of patients with sarcomatoid renal cell carcinoma who underwent nephrectomy and received systemic therapy at our center in the cytokine era (1987 to 2005) or the targeted therapy era (2006 to 2015). Multivariate regression models were used to determine the association of covariables with survival.
Of the 199 patients with sarcomatoid renal cell carcinoma 167 (83.9%) died (median overall survival 16.5 months, 95% CI 15.2-20.9). Survival of patients with clear cell histology was significantly longer vs those with nonclear cell histology (p = 0.034). Patients with synchronous metastatic disease had significantly shorter survival than patients with metachronous metastatic disease (median 12.1 vs 23.3 months, p = 0.0064). Biopsy of the primary tumor or a metastatic site could detect the presence of sarcomatoid features in only 7.5% of cases. Although a significant improvement in survival rate was observed in the first year in patients treated in the targeted therapy era (p = 0.011), this effect was attenuated at year 2, disappeared at years 3 to 5 after diagnosis and was not evident in patients with poor risk features.
Patients with sarcomatoid renal cell carcinoma still have poor prognosis with no clear long-term benefit of targeted therapy. This underscores the need to develop more effective systemic therapies for these patients.
我们研究了在细胞因子和靶向治疗时代接受肾切除术和系统治疗的肉瘤样肾细胞癌患者的总生存率和预后因素。
这是一项回顾性研究,纳入了在我们中心接受肾切除术并接受系统治疗的肉瘤样肾细胞癌患者,这些患者分别来自细胞因子治疗时代(1987 年至 2005 年)和靶向治疗时代(2006 年至 2015 年)。多变量回归模型用于确定协变量与生存的关联。
在 199 名肉瘤样肾细胞癌患者中,167 名(83.9%)死亡(中位总生存期为 16.5 个月,95%CI 为 15.2-20.9)。具有透明细胞组织学的患者的生存时间明显长于具有非透明细胞组织学的患者(p=0.034)。同步转移疾病的患者的生存时间明显短于异时转移疾病的患者(中位时间分别为 12.1 个月和 23.3 个月,p=0.0064)。仅在 7.5%的病例中,通过对原发肿瘤或转移部位的活检可检测到肉瘤样特征的存在。尽管在靶向治疗时代治疗的患者在第一年的生存率显著提高(p=0.011),但这种效应在第二年减弱,在诊断后 3 至 5 年消失,并且在具有不良风险特征的患者中并不明显。
肉瘤样肾细胞癌患者的预后仍然较差,靶向治疗没有明显的长期获益。这突显了为这些患者开发更有效的全身治疗方法的必要性。