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转变非转移性肾细胞癌围手术期治疗模式——一条可能的前进道路。

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

作者信息

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

机构信息

Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.

Division of Hematology/Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, USA.

出版信息

Kidney Cancer. 2017 Jul 26;1(1):31-40. doi: 10.3233/KCA-170010.

Abstract

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.

摘要

2017年,尚无经证实可提高非转移性肾细胞癌(RCC)总生存率的辅助全身治疗方法。抗PD-1抗体纳武单抗可提高转移性难治性RCC的总生存率,且一般耐受性良好。小鼠实体瘤模型显示,与辅助治疗相比,短疗程新辅助PD-1阻断治疗具有益处。两项正在进行的关于RCC患者围手术期使用纳武单抗的2期研究已显示出初步的可行性和安全性,未出现手术延迟或并发症。最近开展的PROSPER RCC试验(一项3期随机研究,比较围手术期纳武单抗与接受肾切除术的局限性肾细胞癌患者观察治疗的疗效;EA8143)将研究在根治性或部分肾切除术中加用围手术期纳武单抗是否能改善高危局限性和局部进展性RCC患者的临床结局。为提高非转移性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,即术前用纳武单抗进行预处理,然后进行切除和辅助性PD-1阻断治疗。我们计划在这项全球性、随机、非盲、3期国家临床试验网络研究中纳入766例任何组织学类型的临床分期≥T2或淋巴结阳性M0的RCC患者。试验组将在手术前接受两剂静脉注射240 mg纳武单抗,随后接受9个月的辅助性纳武单抗治疗。对照组将接受当前的标准治疗:手术切除后观察。患者按临床T分期、淋巴结阳性情况和组织学进行分层。该试验有能力检测出RFS主要终点的绝对获益为14.4%,即从ASSURE历史对照的5年55.8%提高到70.2%(风险比=0.70)。该研究也有能力检测出显著的总生存获益(风险比0.67)。纳入了关键的安全性、可行性和生活质量终点指标。PROSPER RCC体现了团队科学,有一系列计划中的相关性研究工作,以调查基线免疫环境以及新辅助预处理后变化对临床结局的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8f4/6179104/0e6bf056cc74/kca-1-kca170010-g001.jpg

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