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纳武利尤单抗对比依维莫司用于晚期肾细胞癌患者:随机、开放标签、III 期 CheckMate 025 试验的长期随访更新结果。

Nivolumab versus everolimus in patients with advanced renal cell carcinoma: Updated results with long-term follow-up of the randomized, open-label, phase 3 CheckMate 025 trial.

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Department of Medical Oncology, Gustave Roussy, Villejuif, France.

出版信息

Cancer. 2020 Sep 15;126(18):4156-4167. doi: 10.1002/cncr.33033. Epub 2020 Jul 16.

Abstract

BACKGROUND

CheckMate 025 has shown superior efficacy for nivolumab over everolimus in patients with advanced renal cell carcinoma (aRCC) along with improved safety and tolerability. This analysis assesses the long-term clinical benefits of nivolumab versus everolimus.

METHODS

The randomized, open-label, phase 3 CheckMate 025 trial (NCT01668784) included patients with clear cell aRCC previously treated with 1 or 2 antiangiogenic regimens. Patients were randomized to nivolumab (3 mg/kg every 2 weeks) or everolimus (10 mg once a day) until progression or unacceptable toxicity. The primary endpoint was overall survival (OS). The secondary endpoints were the confirmed objective response rate (ORR), progression-free survival (PFS), safety, and health-related quality of life (HRQOL).

RESULTS

Eight hundred twenty-one patients were randomized to nivolumab (n = 410) or everolimus (n = 411); 803 patients were treated (406 with nivolumab and 397 with everolimus). With a minimum follow-up of 64 months (median, 72 months), nivolumab maintained an OS benefit in comparison with everolimus (median, 25.8 months [95% CI, 22.2-29.8 months] vs 19.7 months [95% CI, 17.6-22.1 months]; hazard ratio [HR], 0.73; 95% CI, 0.62-0.85) with 5-year OS probabilities of 26% and 18%, respectively. ORR was higher with nivolumab (94 of 410 [23%] vs 17 of 411 [4%]; P < .001). PFS also favored nivolumab (HR, 0.84; 95% CI, 0.72-0.99; P = .0331). The most common treatment-related adverse events of any grade were fatigue (34.7%) and pruritus (15.5%) with nivolumab and fatigue (34.5%) and stomatitis (29.5%) with everolimus. HRQOL improved from baseline with nivolumab but remained the same or deteriorated with everolimus.

CONCLUSIONS

The superior efficacy of nivolumab over everolimus is maintained after extended follow-up with no new safety signals, and this supports the long-term benefits of nivolumab monotherapy in patients with previously treated aRCC.

LAY SUMMARY

CheckMate 025 compared the effects of nivolumab (a novel immunotherapy) with those of everolimus (an older standard-of-care therapy) for the treatment of advanced kidney cancer in patients who had progressed on antiangiogenic therapy. After 5 years of study, nivolumab continues to be better than everolimus in extending the lives of patients, providing a long-lasting response to treatment, and improving quality of life with a manageable safety profile. The results demonstrate that the clinical benefits of nivolumab versus everolimus in previously treated patients with advanced kidney cancer continue in the long term.

摘要

背景

CheckMate 025 研究结果表明,与依维莫司相比,纳武利尤单抗可为晚期肾细胞癌(aRCC)患者带来更优的疗效,且安全性和耐受性更好。本分析评估了纳武利尤单抗对比依维莫司的长期临床获益。

方法

这是一项随机、开放标签、III 期 CheckMate 025 研究(NCT01668784),纳入了既往接受过 1 或 2 种抗血管生成治疗方案的透明细胞 aRCC 患者。患者随机接受纳武利尤单抗(3 mg/kg,每 2 周 1 次)或依维莫司(10 mg,每日 1 次)治疗,直至疾病进展或出现不可耐受的毒性。主要终点为总生存期(OS)。次要终点包括确认的客观缓解率(ORR)、无进展生存期(PFS)、安全性和健康相关生活质量(HRQOL)。

结果

821 例患者被随机分配至纳武利尤单抗组(n=410)或依维莫司组(n=411);803 例患者接受了治疗(纳武利尤单抗组 406 例,依维莫司组 397 例)。随访时间至少 64 个月(中位随访时间 72 个月),与依维莫司相比,纳武利尤单抗维持了 OS 获益(中位 OS:25.8 个月[95%CI,22.2-29.8 个月] vs 19.7 个月[95%CI,17.6-22.1 个月];风险比[HR],0.73;95%CI,0.62-0.85),5 年 OS 率分别为 26%和 18%。纳武利尤单抗的 ORR 更高(410 例患者中 94 例[23%] vs 411 例患者中 17 例[4%];P<0.001)。纳武利尤单抗组的 PFS 也更优(HR,0.84;95%CI,0.72-0.99;P=0.0331)。最常见的任何等级治疗相关不良事件为疲乏(34.7%)和瘙痒(15.5%),与纳武利尤单抗相关;疲乏(34.5%)和口腔炎(29.5%),与依维莫司相关。纳武利尤单抗治疗后 HRQOL 从基线改善,而依维莫司则保持不变或恶化。

结论

在无新安全性信号的情况下,纳武利尤单抗的疗效优于依维莫司,这支持纳武利尤单抗单药治疗既往接受过治疗的 aRCC 患者的长期获益。

简而言之

CheckMate 025 研究比较了纳武利尤单抗(一种新型免疫疗法)与依维莫司(一种标准治疗药物)在治疗抗血管生成治疗后进展的晚期肾细胞癌患者中的效果。研究进行 5 年后,与依维莫司相比,纳武利尤单抗在延长患者生命、提供持久的治疗反应以及改善生活质量方面仍具有优势,且安全性可控。这些结果表明,纳武利尤单抗对比依维莫司在既往接受治疗的晚期肾细胞癌患者中的临床获益在长期持续存在。

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本文引用的文献

3
Second-Line Treatment Landscape for Renal Cell Carcinoma: A Comprehensive Review.
Oncologist. 2018 May;23(5):540-555. doi: 10.1634/theoncologist.2017-0534. Epub 2018 Feb 27.
5
Immunomodulatory Activity of Nivolumab in Metastatic Renal Cell Carcinoma.
Clin Cancer Res. 2016 Nov 15;22(22):5461-5471. doi: 10.1158/1078-0432.CCR-15-2839. Epub 2016 May 11.
6
Nivolumab versus Everolimus in Advanced Renal-Cell Carcinoma.
N Engl J Med. 2015 Nov 5;373(19):1803-13. doi: 10.1056/NEJMoa1510665. Epub 2015 Sep 25.
7
Survival, Durable Response, and Long-Term Safety in Patients With Previously Treated Advanced Renal Cell Carcinoma Receiving Nivolumab.
J Clin Oncol. 2015 Jun 20;33(18):2013-20. doi: 10.1200/JCO.2014.58.1041. Epub 2015 Mar 30.
8
Nivolumab for Metastatic Renal Cell Carcinoma: Results of a Randomized Phase II Trial.
J Clin Oncol. 2015 May 1;33(13):1430-7. doi: 10.1200/JCO.2014.59.0703. Epub 2014 Dec 1.
10
Development and validation of a scale to measure disease-related symptoms of kidney cancer.
Value Health. 2007 Jul-Aug;10(4):285-93. doi: 10.1111/j.1524-4733.2007.00183.x.

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