Oncologia Medica, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Largo Agostino Gemelli 8, 00158, Rome, Italy.
Oncologia Medica, Facoltà di Medicina e Chirurgia, Università Cattolica del Sacro Cuore, Rome, Italy.
Target Oncol. 2020 Aug;15(4):495-501. doi: 10.1007/s11523-020-00732-y.
Angiogenesis has been recognized as the most important factor for tumor invasion, proliferation, and progression in metastatic renal cell carcinoma (mRCC). However, few clinical data are available regarding the efficacy of cabozantinib following immunotherapy.
To describe the outcome of cabozantinib in patients previously treated with immunotherapy.
Patients with mRCC who received cabozantinib immediately after nivolumab were included. The primary endpoint was to assess the outcome in terms of efficacy and activity.
Eighty-four mRCC patients met the criteria to be included in the final analysis. After a median follow-up of 9.4 months, median overall survival was 17.3 months. According to the IMDC criteria, the rates of patients alive at 12 months in the good, intermediate, and poor prognostic groups were 100%, 74%, and 33%, respectively (p < 0.001). The median progression-free survival (PFS) was 11.5 months (95% CI 8.3-14.7); no difference was found based on duration of previous first-line therapy or nivolumab PFS. The overall response rate was 52%, stable disease was found as the best response in 25.3% and progressive disease in 22.7% of patients. Among the 35 patients with progressive disease on nivolumab, 26 (74.3%) patients showed complete/partial response or stable disease with cabozantinib as best response after nivolumab. The major limitations of this study are the retrospective nature and the short follow-up.
Cabozantinib was shown to be effective and active in patients previously receiving immune checkpoint inhibitors. Therefore, cabozantinib can be considered a valid therapeutic option for previously treated mRCC patients, irrespective of the type and duration of prior therapies.
血管生成已被认为是转移性肾细胞癌(mRCC)肿瘤侵袭、增殖和进展的最重要因素。然而,关于免疫治疗后卡博替尼疗效的临床数据很少。
描述卡博替尼治疗免疫治疗后患者的结果。
纳入接受纳武单抗后立即接受卡博替尼治疗的 mRCC 患者。主要终点是评估疗效和活性方面的结果。
84 例 mRCC 患者符合最终分析标准。中位随访 9.4 个月后,中位总生存期为 17.3 个月。根据 IMDC 标准,12 个月时存活的患者在预后良好、中等和不良组的比例分别为 100%、74%和 33%(p<0.001)。中位无进展生存期(PFS)为 11.5 个月(95%CI 8.3-14.7);根据一线治疗时间或纳武单抗 PFS 长短,无差异。总缓解率为 52%,最佳缓解为 25.3%的疾病稳定和 22.7%的疾病进展。在纳武单抗进展的 35 例患者中,26 例(74.3%)患者在纳武单抗后卡博替尼治疗显示完全/部分缓解或疾病稳定为最佳反应。本研究的主要局限性是回顾性和随访时间短。
卡博替尼在接受免疫检查点抑制剂治疗的患者中显示出有效性和活性。因此,卡博替尼可被认为是先前治疗的 mRCC 患者的有效治疗选择,而与先前治疗的类型和时间长短无关。