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Nivolumab in Combination with Stereotactic Body Radiotherapy in Pretreated Patients with Metastatic Renal Cell Carcinoma. Results of the Phase II NIVES Study

医学 无容量 肾细胞癌 内科学 实体瘤疗效评价标准 肿瘤科 置信区间 临床终点 泌尿科 外科 放射治疗 临床试验 临床研究阶段 免疫疗法 癌症
作者
Cristina Masini,C. Iotti,Ugo De Giorgi,Roberto Salvatore Bellia,Sebastiano Buti,Francesco Salaroli,Ilaria Zampiva,Renzo Mazzarotto,Claudia Mucciarini,Maria Giuseppa Vitale,Alessio Bruni,Frank Lohr,Giuseppe Procopio,Orazio Caffo,Franco Nolè,Franco Morelli,Susanne Baier,Consuelo Buttigliero,Patrizia Ciammella,Giorgia Timon
出处
期刊:European Urology [Elsevier BV]
卷期号:81 (3): 274-282 被引量:83
标识
DOI:10.1016/j.eururo.2021.09.016
摘要

Nivolumab showed an overall survival (OS) benefit in pretreated metastatic renal cell carcinoma (mRCC). The role of stereotactic body radiotherapy (SBRT) in mRCC remains to be defined.Our aim was to evaluate the efficacy and safety of SBRT in combination with nivolumab in second- and third-line mRCC patients.The NIVES study was a phase II, single-arm, multicenter trial in patients with mRCC with measurable metastatic sites who progressed after antiangiogenic therapy, of whom at least one was suitable for SBRT.The patients received SBRT to a lesion at a dose of 10 Gy in three fractions for 7 d from the first infusion of nivolumab. Nivolumab was given at an initial dose of 240 mg every 14 d for 6 mo and then 480 mg q4-weekly in responding patients.We hypothesized that nivolumab plus SBRT improves the objective response rate (ORR) compared with nivolumab alone from 25% (derived from historical controls) to 40%. Secondary endpoints were progression-free survival (PFS), OS, disease control rate (DCR) of irradiated and nonirradiated metastases, and safety.Sixty-nine patients were enrolled from July 2017 to March 2019. The ORR was 17% and the DCR was 55%. The median PFS was 5.6 mo (95% confidence interval [CI], 2.9-7.1) and median OS 20 mo (95% CI, 17-not reached). After 1.5 yr of follow-up, 23 patients died. The median time to treatment response was 2.8 mo and median duration of response was 14 mo. No new safety concerns arose.We did not find sufficient evidence to suggest that nivolumab in combination with SBRT provides an added benefit in pretreated mRCC patients; it should however be evaluated in patients with oligometastatic or oligoprogressive disease.Nivolumab in combination with stereotactic body radiotherapy does not provide evidence of increased outcomes in metastatic renal cell carcinoma patients. However this approach was safe and showed a good response of the irradiated lesions.
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