Phase II multicenter trial combining nivolumab and radiosurgery for NSCLC and RCC brain metastases

无容量 医学 临床终点 肾细胞癌 放射外科 肺癌 内科学 不利影响 临床研究阶段 肿瘤科 无进展生存期 泌尿科 随机对照试验 外科 胃肠病学 临床试验 放射治疗 免疫疗法 癌症 总体生存率
作者
Philip Wong,Laura Masucci,Marie Florescu,M.-É. Plourde,Valérie Panet-Raymond,Michel Pavic,Scott Owen,Laurence Masson‐Côté,Cynthia Ménard,Bertrand Routy,Mustapha Tehfé,Kristoff Nelson,F Guilbert,Olivier Boucher,Sareh Keshavarzi,Normand Blais,David Roberge
出处
期刊:Neuro-oncology advances [Oxford University Press]
卷期号:5 (1): vdad018-vdad018 被引量:19
标识
DOI:10.1093/noajnl/vdad018
摘要

Abstract Background Anti-PD-1 has activity in brain metastases (BM). This phase II open labeled non-randomized single arm trial examined the safety and efficacy of combining nivolumab with radiosurgery (SRS) in the treatment of patients with BM from non-small cell lung cancer (NSCLC) and renal cell carcinoma (RCC). Methods This was a multicenter trial (NCT02978404) in which patients diagnosed with NSCLC or RCC, having ≤ 10 cc of un-irradiated BM and no prior immunotherapy were eligible. Nivolumab (240 mg or 480 mg IV) was administered for up to 2 years until progression. SRS (15–21 Gy) to all un-irradiated BM was delivered within 14 days after the first dose of nivolumab. The primary endpoint was intracranial progression free survival (iPFS). Results Twenty-six patients (22 NSCLC and 4 RCC) were enrolled between August 2017 and January 2020. A median of 3 (1–9) BM were treated with SRS. Median follow-up was 16.0 months (0.43–25.9 months). Two patients developed nivolumab and SRS related grade 3 fatigue. One-year iPFS and OS were 45.2% (95% CI 29.3–69.6%) and 61.3% (95% CI 45.1–83.3%), respectively. Overall response (partial or complete) of SRS treated BM was attained in 14 out of the 20 patients with ≥1 evaluable follow-up MRI. Mean FACT-Br total scores were 90.2 at baseline and improved to 146.2 within 2–4 months (P = .0007). Conclusions The adverse event profile and FACT-Br assessments suggested that SRS during nivolumab was well tolerated. Upfront SRS with the initiation of anti-PD-1 prolonged the 1-year iPFS and achieved high intracranial control. This combined approach merits validation randomized studies.
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