改变非转移性 RCC 的围手术期治疗范式--一条可能的前进之路。

L C Harshman, C G Drake, N B Haas, J Manola, M Puligandla, S Signoretti, D Cella, R T Gupta, R Bhatt, E Van Allen, P Lara, T K Choueiri, A Kapoor, D Y C Heng, B Shuch, M Jewett, D George, D Michaelson, M A Carducci, D McDermott, M Allaf
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引用次数: 0

摘要

2017 年,没有任何辅助系统疗法被证实能提高非转移性肾细胞癌(RCC)的总生存率。抗PD-1抗体nivolumab可提高转移性治疗难治性RCC的总生存率,且一般可耐受。小鼠实体瘤模型显示,与辅助治疗相比,短疗程的新辅助 PD-1 阻断治疗更有疗效。目前正在进行的两项关于 RCC 患者围手术期使用 nivolumab 的 2 期研究显示了初步的可行性和安全性,没有出现手术延迟或并发症。最近开始的 PROSPER RCC 试验(比较接受肾切除术的局部肾细胞癌患者围手术期使用尼妥珠单抗与观察治疗的 3 期 RandOmized 研究;EA8143)将研究在根治性或局部肾切除术中增加围手术期使用尼妥珠单抗是否能改善高风险局部和局部晚期 RCC 患者的临床预后。为了提高非转移性 RCC 的治愈率和无复发生存率 (RFS),我们正在实施一种三管齐下的多学科方法,即术前先使用 nivolumab,然后进行切除和 PD-1 阻断辅助治疗。我们计划招募 766 名临床分期≥T2 或结节阳性的任何组织学类型的 M0 RCC 患者参与这项全球性、随机、非盲的国家临床试验网络 3 期研究。研究组将在手术前接受两剂240毫克的尼夫单抗静脉注射,然后接受为期9个月的尼夫单抗辅助治疗。对照组将接受目前的标准治疗:手术切除,然后进行观察。患者按临床T分期、结节阳性和组织学进行分层。该试验的作用是检测主要终点RFS的14.4%绝对获益,即5年后RFS从ASSURE历史对照组的55.8%提高到70.2%(HR = 0.70)。该研究还能检测到显著的总生存期获益(HR 0.67)。关键的安全性、可行性和生活质量终点均已纳入。PROSPER RCC是团队科学的典范,计划开展一系列相关工作,研究基线免疫环境和新辅助治疗后的变化对临床结果的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transforming the Perioperative Treatment Paradigm in Non-Metastatic RCC-A Possible Path Forward.

Transforming the Perioperative Treatment Paradigm in Non-Metastatic RCC-A Possible Path Forward.

Transforming the Perioperative Treatment Paradigm in Non-Metastatic RCC-A Possible Path Forward.

In 2017, there is no adjuvant systemic therapy proven to increase overall survival in non-metastatic renal cell carcinoma (RCC). The anti-PD-1 antibody nivolumab improves overall survival in metastatic treatment refractory RCC and is generally tolerable. Mouse solid tumor models have revealed a benefit with a short course of neoadjuvant PD-1 blockade compared to adjuvant therapy. Two ongoing phase 2 studies of perioperative nivolumab in RCC patients have shown preliminary feasibility and safety with no surgical delays or complications. The recently opened PROSPER RCC trial (A Phase 3 RandOmized Study Comparing PERioperative Nivolumab vs. Observation in Patients with Localized Renal Cell Carcinoma Undergoing Nephrectomy; EA8143) will examine if the addition of perioperative nivolumab to radical or partial nephrectomy can improve clinical outcomes in patients with high risk localized and locally advanced RCC. With the goal of increasing cure and recurrence-free survival (RFS) rates in non-metastatic RCC, we are executing a three-pronged, multidisciplinary approach of presurgical priming with nivolumab followed by resection and adjuvant PD-1 blockade. We plan to enroll 766 patients with clinical stage ≥T2 or node positive M0 RCC of any histology in this global, randomized, unblinded, phase 3 National Clinical Trials Network study. The investigational arm will receive two doses of nivolumab 240 mg IV prior to surgery followed by adjuvant nivolumab for 9 months. The control arm will undergo the current standard of care: surgical resection followed by observation. Patients are stratified by clinical T stage, node positivity, and histology. The trial is powered to detect a 14.4% absolute benefit in the primary endpoint of RFS from the ASSURE historical control of 55.8% to 70.2% at 5 years (HR = 0.70). The study is also powered to detect a significant overall survival benefit (HR 0.67). Key safety, feasibility, and quality of life endpoints are incorporated. PROSPER RCC exemplifies team science with a host of planned correlative work to investigate the impact of the baseline immune milieu and changes after neoadjuvant priming on clinical outcomes.

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