CheckMate 025 随机 3 期研究:纳武利尤单抗对比依维莫司治疗晚期肾细胞癌的关键基线因素和既往治疗的结局。

CheckMate 025 Randomized Phase 3 Study: Outcomes by Key Baseline Factors and Prior Therapy for Nivolumab Versus Everolimus in Advanced Renal Cell Carcinoma.

机构信息

Gustave Roussy, Villejuif, France.

MD Anderson Cancer Center, University of Texas, Houston, TX, USA.

出版信息

Eur Urol. 2017 Dec;72(6):962-971. doi: 10.1016/j.eururo.2017.02.010. Epub 2017 Mar 3.

Abstract

BACKGROUND

The randomized, phase 3 CheckMate 025 study of nivolumab (n=410) versus everolimus (n=411) in previously treated adults (75% male; 88% white) with advanced renal cell carcinoma (aRCC) demonstrated significantly improved overall survival (OS) and objective response rate (ORR).

OBJECTIVE

To investigate which baseline factors were associated with OS and ORR benefit with nivolumab versus everolimus.

DESIGN, SETTING, AND PARTICIPANTS: Subgroup OS analyses were performed using Kaplan-Meier methodology. Hazard ratios were estimated using the Cox proportional hazards model.

INTERVENTION

Nivolumab 3mg/kg every 2 wk or everolimus 10mg once daily.

RESULTS AND LIMITATIONS

The minimum follow-up was 14 mo. Baseline subgroup distributions were balanced between nivolumab and everolimus arms. Nivolumab demonstrated an OS improvement versus everolimus across subgroups, including Memorial Sloan Kettering Cancer Center (MSKCC) and International Metastatic Renal Cell Carcinoma Database Consortium risk groups; age <65 and ≥65 yr; one and two or more sites of metastases; bone, liver, and lung metastases; number of prior therapies; duration of prior therapy; and prior sunitinib, pazopanib, or interleukin-2 therapy. The benefit with nivolumab versus everolimus was noteworthy for patients with poor MSKCC risk (hazard ratio 0.48, 95% confidence interval 0.32-0.70). The mortality rate at 12 mo for all subgroups was lower with nivolumab compared with everolimus. ORR also favored nivolumab. The incidence of grade 3 or 4 treatment-related adverse events across subgroups was lower with nivolumab. Limitations include the post hoc analysis and differing sample sizes between groups.

CONCLUSION

The trend for OS and ORR benefit with nivolumab for multiple subgroups, without notable safety concerns, may help to guide treatment decisions, and further supports nivolumab as the standard of care in previously treated patients with aRCC.

PATIENT SUMMARY

We investigated the impact of demographic and pretreatment features on survival benefit and tumor response with nivolumab versus everolimus in advanced renal cell carcinoma (aRCC). Survival benefit and response were observed for multiple subgroups, supporting the use of nivolumab as a new standard of care across a broad range of patients with previously treated aRCC. The trial is registered on ClinicalTrials.gov as NCT01668784.

摘要

背景

纳武利尤单抗(n=410)与依维莫司(n=411)治疗既往治疗的晚期肾细胞癌(aRCC)的随机、3 期 CheckMate 025 研究显示,总生存期(OS)和客观缓解率(ORR)显著改善。

目的

研究纳武利尤单抗与依维莫司相比,哪些基线因素与 OS 和 ORR 获益相关。

设计、地点和参与者:使用 Kaplan-Meier 方法进行亚组 OS 分析。使用 Cox 比例风险模型估计风险比。

干预措施

纳武利尤单抗 3mg/kg,每 2 周 1 次;或依维莫司 10mg,每日 1 次。

结果和局限性

最低随访时间为 14 个月。纳武利尤单抗和依维莫司组之间的基线亚组分布平衡。纳武利尤单抗与依维莫司相比,在包括 Memorial Sloan Kettering Cancer Center(MSKCC)和国际转移性肾细胞癌数据库联盟风险组在内的所有亚组中,OS 均有改善;年龄<65 岁和≥65 岁;转移部位 1 个和 2 个或更多;骨、肝和肺转移;既往治疗次数;既往治疗持续时间;以及既往舒尼替尼、帕唑帕尼或白细胞介素-2 治疗。对于 MSKCC 风险较差的患者,纳武利尤单抗的获益显著(风险比 0.48,95%置信区间 0.32-0.70)。所有亚组的 12 个月死亡率均低于依维莫司。ORR 也有利于纳武利尤单抗。亚组之间,3 级或 4 级治疗相关不良事件的发生率较低。局限性包括事后分析和组间样本量不同。

结论

在多个亚组中,纳武利尤单抗的 OS 和 ORR 获益趋势明显,且无明显安全性问题,这可能有助于指导治疗决策,并进一步支持纳武利尤单抗作为既往治疗的晚期肾细胞癌患者的标准治疗方法。

患者概况

我们研究了在晚期肾细胞癌(aRCC)中,纳武利尤单抗与依维莫司相比,人口统计学和治疗前特征对生存获益和肿瘤反应的影响。在多个亚组中观察到生存获益和反应,支持纳武利尤单抗作为新的标准治疗方法,适用于广泛的既往治疗过的 aRCC 患者。该试验在 ClinicalTrials.gov 注册为 NCT01668784。

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