Adjuvant immunotherapy in renal cell carcinoma: A living systematic review and network meta-analysis (NMA).

医学 易普利姆玛 肿瘤科 内科学 肾细胞癌 阿替唑单抗 彭布罗利珠单抗 无容量 佐剂 荟萃分析 危险系数 免疫疗法 癌症 置信区间
作者
Qurat Ul Ain Riaz Sipra,Irbaz Bin Riaz,Syed Arsalan Ahmed Naqvi,Huan He,Rabbia Siddiqi,Mahnoor Islam,Noureen Asghar,Waleed Ikram,Wenxin Xu,Parminder Singh,Thai H. Ho,Mehmet Asim Bilen,Yousef Zakharia,Alan H. Bryce
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:41 (6_suppl): 694-694 被引量:1
标识
DOI:10.1200/jco.2023.41.6_suppl.694
摘要

694 Background: The treatment landscape of localized renal cell carcinoma (RCC) is rapidly evolving. Recent trials have demonstrated contrasting efficacy with adjuvant immunotherapy. Therefore, we sought to assess the mixed treatment comparisons among different adjuvant treatment options using updated data from trials and quantified the absolute effect with these treatments stratified by risk categories. Methods: This living network meta-analysis was conducted using the living interactive evidence (LIvE) synthesis framework. We used stratified baseline risks of disease progression from observational data and at 5, 10, 15 years from the Leibovich risk stratification system (based on risk scores ranging from 0 to ≥15). Corresponding intervention risks were then approximated using relative effect estimates (from NMA) and baseline risks. The difference between CIRs and baseline risks were calculated to present absolute risk differences in each risk category. Results: This NMA included eight RCTs with 8480 participants and seven unique treatment options. Pembrolizumab (pembro; rank 1) was associated with improved disease-free survival (DFS) when compared to atezolizumab (atezo; rank 6; hazard ratio: 0.68; 0.49;0.93), and nivolumab-ipilimumab (nivoipi; rank 5; 0.68; 0.48-0.97). However, no statistically significant difference was observed between pembro and atezo for overall survival (0.53; 0.28-1.01). Survival data for nivoIpi was not reported. No new statistically significant differences were observed since last update. The absolute benefit of atezo and nivoipi was minimal with higher T and N patients (Table). The results were similar with increasing Leibovich risk scores. Conclusions: Current evidence favors the use of a risk adapted approach when offering adjuvant immunotherapy. Adjuvant pembrolizumab remains a preferred treatment in patients with RCC who underwent nephrectomy. [Table: see text]
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