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Lenvatinib with or Without Everolimus in Patients with Metastatic Renal Cell Carcinoma After Immune Checkpoint Inhibitors and Vascular Endothelial Growth Factor Receptor-Tyrosine Kinase Inhibitor Therapies

机译:Lenvatinib在免疫检查点抑制剂和血管内皮生长因子受体 - 酪氨酸激酶抑制剂治疗后,Lenvatinib有或没有everolimus的转移性肾细胞癌

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Introduction Lenvatinib (Len) plus everolimus (Eve) is an approved therapy for metastatic renal cell carcinoma (mRCC) after first-line vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFR-TKIs), but limited data exist on the efficacy of Len ± Eve after progression on immune checkpoint inhibitors (ICIs) and VEGFR-TKIs. Methods We retrospectively reviewed the records of patients with mRCC at our institution who were treated with Len ± Eve after ICI and VEGFR-TKI. A blinded radiologist assessed objective response as defined by RECIST version 1.1. Descriptive statistics and the Kaplan-Meier method were used. Results Fifty-five patients were included in the analysis. Of these patients, 81.8% had clear-cell histology (ccRCC), and 76.4% had International Metastatic RCC Database Consortium intermediate-risk disease. Median number of prior therapies was four (range, 2–10); all patients had prior ICIs and VEGFR-TKIs, and 80% were previously treated with ICI and at least two VEGFR-TKIs, including cabozantinib. One patient (1.8%) achieved a complete response, and 11 patients (20.0%) achieved a partial response, for an overall response rate (ORR) of 21.8%; 35 patients (63.6%) achieved stable disease. In all patients, median progression-free survival (PFS) was 6.2 months (95% confidence interval [CI], 4.8–9.4) and median overall survival (OS) was 12.1 months (95% CI, 8.8–16.0). In patients with ccRCC, ORR was 24.4%, PFS was 7.1 months (95% CI, 5.0–10.5), and OS was 11.7 months (95% CI, 7.9–16.1). 50.9% of patients required dose reductions and 7.3% discontinued treatment because of toxicity. Conclusion Len ± Eve demonstrated meaningful clinical activity and tolerability in heavily pretreated patients with mRCC after disease progression with prior ICIs and VEGFR-TKIs. Implications for Practice As the therapeutic landscape for patients with metastatic renal cell carcinoma continues to evolve, this single-center, retrospective review highlights the real-world efficacy of lenvatinib with or without everolimus in heavily pretreated patients. This article supports the use of lenvatinib with or without everolimus as a viable salvage strategy for patients whose disease progresses after treatment with immune checkpoint inhibitors and vascular endothelial growth factor receptor-tyrosine kinase inhibitor therapies, including cabozantinib.
机译:简介Lenvatinib(LEN)加卓洛米斯(前夕)是一系列批准的转移性肾细胞癌(MRCC)的批准治疗一线血管内皮生长因子受体 - 酪氨酸激酶抑制剂(VEGFR-TKIS),但数据存在有限的数据对LEN的疗效存在在免疫检查点抑制剂(ICIS)和VEGFR-TKIS上进行±前夜。方法我们回顾性地审查了在ICI和VEGFR-TKI之后用LEN±EVE治疗的机构MRCC患者的记录。盲声放射科医生评估了RECIST版本1.1所定义的客观响应。使用描述性统计和Kaplan-Meier方法。结果分析中包含五十五名患者。在这些患者中,81.8%具有透明细胞组织学(CCRCC),76.4%具有国际转移性RCC数据库联盟中间风险疾病。中间疗法数为四(范围,2-10);所有患者均有先前的ICIS和VEGFR-TKI,先前用ICI和至少两种VEGFR-TKIS治疗了80%,包括Cabozantib。一名患者(1.8%)达到了完全反应,11名患者(20.0%)达到了部分反应,总体反应率(ORR)为21.8%; 35例患者(63.6%)取得了稳定的疾病。在所有患者中,中位进展生存期(PFS)为6.2个月(95%置信区间[CI],4.8-9.4)和中位整体存活(OS)为12.1个月(95%CI,8.8-16.0)。在CCRCC患者中,ORR为24.4%,PFS为7.1个月(95%CI,5.0-10.5),OS为11.7个月(95%CI,7.9-16.1)。 50.9%的患者需要剂量减少和7.3%因毒性而停止治疗。结论LEN±EVE在疾病进展和VEGFR-TKIS患者疾病进展后,LEN±EVE在严重预处理患者中展示了有意义的临床活性和耐受性。这种单一中心的转移肾细胞癌患者的练习的影响,这一单一中心的持续发展突出了Lenvatinib在重预处理患者中具有或没有Everolimus的现实世界疗效。本文支持使用Lenvatinib的使用或没有everolimus作为疾病在用免疫检查点抑制剂和血管内皮生长因子受体 - 酪氨酸激酶抑制剂治疗(包括Cabozantinib)的患者进行疾病进展的患者的可行性抢救策略。

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