Medical Oncology Department, CUF Tejo Hospital, Lisbon, Portugal.
START Madrid-Centro Integral Oncológico Clara Campal Hospital, Madrid, Spain.
Cancer Treat Rev. 2022 Apr;105:102374. doi: 10.1016/j.ctrv.2022.102374. Epub 2022 Mar 10.
Advanced or metastasized renal cell carcinoma (mRCC) can present with sarcomatoid features, which is considered a poor prognosis marker and a treatment challenge. Several trials in first line mRCC have included immune checkpoint inhibitors (ICI) in combination either with other ICI or tyrosine kinase inhibitors (TKI), that have led to the approval of some of these treatment strategies and their recommendation in international guidelines. The authors review all randomized phase III trials in first-line treatment with ICI for advanced or mRCC and selected prospective phase I-IV trials, that included patients with tumors with sarcomatoid features. All these trials, in first-line treatment with ICI immunotherapy in combination with another ICI or TKI, included patients with mRCC with sarcomatoid features, corresponding from 5 to 15% of the study population. The efficacy and survival end points were superior in the sarcomatoid features subgroup with ICI in combination vs TKI in monotherapy, achieving overall response rates of 50-60%. A new benchmark has been established by trials reporting over 20 months in median overall survival. Even when considering ICI in monotherapy, the efficacy has been remarkable in patients with sarcomatoid features, demonstrating a striking consistency in these groundbreaking results. No biomarkers predictive of response to ICI were identified. The toxicity profile seems similar to the general study population. Despite the limitations of the clinical trials design to infer definitive conclusions in the sarcomatoid features patients, the data overwhelmingly support that ICI-based therapy should be the preferred strategy.
高级或转移性肾细胞癌(mRCC)可表现出肉瘤样特征,这被认为是预后不良的标志物和治疗挑战。几项一线 mRCC 的临床试验包括免疫检查点抑制剂(ICI)联合其他 ICI 或酪氨酸激酶抑制剂(TKI),这导致了一些这些治疗策略的批准,并在国际指南中推荐了这些策略。作者回顾了所有用于治疗高级或 mRCC 的一线 ICI 随机 III 期试验,并选择了包括具有肉瘤样特征的肿瘤患者的前瞻性 I-IV 期试验。所有这些试验都在一线使用 ICI 免疫治疗联合另一种 ICI 或 TKI 治疗 mRCC 伴肉瘤样特征患者,占研究人群的 5%至 15%。在 ICI 联合治疗与 TKI 单药治疗的肉瘤样特征亚组中,疗效和生存终点均优于后者,总缓解率达到 50-60%。一些报告中位总生存期超过 20 个月的试验确立了新的基准。即使考虑到 ICI 单药治疗,肉瘤样特征患者的疗效也非常显著,这些突破性结果具有惊人的一致性。目前尚未确定预测对 ICI 反应的生物标志物。毒性谱似乎与一般研究人群相似。尽管临床试验设计存在局限性,无法对肉瘤样特征患者得出明确的结论,但数据压倒性地支持 ICI 为基础的治疗应成为首选策略。