Division of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO; Department of Medicine, Saint Louis University School of Medicine, St Louis, MO.
Division of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Clin Genitourin Cancer. 2020 Aug;18(4):252-257.e2. doi: 10.1016/j.clgc.2020.03.003. Epub 2020 Mar 14.
Patients with primary refractory metastatic renal cell carcinoma (mRCC) have a dismal prognosis and poor response to subsequent treatments. While there are several approved second-line therapies, it remains critical to choose the most effective treatment regimen.
We identified 7 patients with clear cell mRCC who had primary resistance to vascular endothelial growth factor (VEGF)-targeted tyrosine kinase inhibitors (TKIs) or immune checkpoint inhibitor (ICI) combination therapy. The patients were treated with lenvatinib (a multitargeted TKI) plus everolimus (a mammalian target of rapamycin inhibitor). Among these 7 patients, 2 had prior TKI therapy, 3 had prior ICI therapy, and 2 had prior TKI and ICI therapy. We collected the patients' clinical characteristics, molecular profiles, treatment durations, and toxicity outcomes.
The median time to progression on prior therapies was 1.5 months. Lenvatinib plus everolimus was used either as a second-line (n = 4) or third-line (n = 3) therapy. As best responses, 3 patients had partial responses and 3 achieved stable disease. Patients were followed for ≥17 months; progression-free survival ranged from 3 to 15 months, and overall survival ranged from 4 to 17 months.
These 7 cases provide real-world data for the use of lenvatinib plus everolimus in patients with mRCC with primary resistance to first-line VEGF-targeted TKIs or ICI combination therapy.
原发性耐药转移性肾细胞癌(mRCC)患者预后极差,对后续治疗反应不佳。虽然有几种已批准的二线治疗方法,但选择最有效的治疗方案仍然至关重要。
我们确定了 7 名患有透明细胞 mRCC 的患者,他们对血管内皮生长因子(VEGF)靶向酪氨酸激酶抑制剂(TKI)或免疫检查点抑制剂(ICI)联合治疗具有原发性耐药性。这些患者接受了仑伐替尼(一种多靶点 TKI)加依维莫司(一种雷帕霉素靶蛋白抑制剂)治疗。在这 7 名患者中,有 2 名患者有 TKI 治疗史,3 名患者有 ICI 治疗史,2 名患者有 TKI 和 ICI 治疗史。我们收集了患者的临床特征、分子谱、治疗持续时间和毒性结局。
先前治疗的中位无进展时间为 1.5 个月。仑伐替尼加依维莫司用于二线(n = 4)或三线(n = 3)治疗。作为最佳反应,3 名患者有部分缓解,3 名患者疾病稳定。患者随访≥17 个月;无进展生存期为 3 至 15 个月,总生存期为 4 至 17 个月。
这 7 例为仑伐替尼加依维莫司用于一线 VEGF 靶向 TKI 或 ICI 联合治疗原发性耐药的 mRCC 患者提供了真实世界的数据。