University Hospitals Seidman Cancer Center, Cleveland, OH.
SWOG Statistics and Data Management Center, Seattle, WA.
J Clin Oncol. 2024 Nov 20;42(33):3911-3916. doi: 10.1200/JCO.24.00767. Epub 2024 Sep 10.
JCO Mesenchymal-epithelial transition (MET) signaling pathway plays a role in the pathogenesis of selected patients with papillary renal cell carcinoma (PRCC). In the phase II PAPMET trial (ClinicalTrials.gov identifier: NCT02761057), cabozantinib significantly prolonged progression-free survival and improved objective response rate compared with sunitinib in patients with advanced PRCC. Here, we present the final overall survival (OS) analysis. In this multicenter, randomized phase II, open-label trial, 147 patients with advanced PRCC who have received up to one previous therapy (excluding vascular endothelial growth factor-directed agents) were assigned to sunitinib, cabozantinib, crizotinib, or savolitinib. Ultimately, savolitinib and crizotinib arms were closed because of futility. With a median follow-up of 17.5 months, the median OS was 21.5 months (95% CI, 12.0 to 28.1) with cabozantinib and 17.3 months (95% CI, 12.8 to 21.8) with sunitinib (hazard ratio, 0.83; 95% CI, 0.51 to 1.36; = .46). The OS landmark estimates for cabozantinib and sunitinib were 50% versus 39% at 24 months and 32% versus 28% at 36 months. In conclusion, we observed no significant difference in OS across treatment arms. Although cabozantinib represents a well-supported option for advanced PRCC, the lack of survival benefit underscores the need to develop novel therapies for this disease.
JCO 间质-上皮转化 (MET) 信号通路在某些患者的乳头状肾细胞癌 (PRCC) 发病机制中起作用。在 II 期 PAPMET 试验 (ClinicalTrials.gov 标识符:NCT02761057) 中,卡博替尼与舒尼替尼相比,显著延长了晚期 PRCC 患者的无进展生存期并提高了客观缓解率。在这里,我们呈现最终的总生存期 (OS) 分析。在这项多中心、随机 II 期、开放标签试验中,147 名接受过最多一次既往治疗(不包括血管内皮生长因子靶向药物)的晚期 PRCC 患者被分配接受舒尼替尼、卡博替尼、克唑替尼或 savolitinib 治疗。最终,由于无效,savolitinib 和 crizotinib 臂被关闭。中位随访 17.5 个月时,卡博替尼组的中位 OS 为 21.5 个月(95%CI,12.0 至 28.1),舒尼替尼组为 17.3 个月(95%CI,12.8 至 21.8)(风险比,0.83;95%CI,0.51 至 1.36;=.46)。卡博替尼和舒尼替尼的 OS 里程碑估计值分别为 24 个月时为 50%比 39%,36 个月时为 32%比 28%。总之,我们观察到各治疗组之间的 OS 无显著差异。尽管卡博替尼是晚期 PRCC 的一种有充分依据的选择,但缺乏生存获益突显了为这种疾病开发新疗法的必要性。