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阿维鲁单抗联合阿昔替尼与舒尼替尼对比在晚期肾细胞癌中按基线 IMDC 风险因素和靶肿瘤部位个数的疗效:JAVELIN Renal 101 的长期随访结果。

Efficacy of avelumab plus axitinib versus sunitinib by numbers of IMDC risk factors and target tumor sites at baseline in advanced renal cell carcinoma: long-term follow-up results from JAVELIN Renal 101.

机构信息

Departments of Urology and Molecular Oncology, Niigata University Graduate School of Medicine, Niigata, Japan.

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

出版信息

ESMO Open. 2023 Dec;8(6):102034. doi: 10.1016/j.esmoop.2023.102034. Epub 2023 Oct 20.

Abstract

BACKGROUND

In the phase III JAVELIN Renal 101 trial, first-line avelumab + axitinib improved progression-free survival (PFS) and objective response rate versus sunitinib in patients with advanced renal cell carcinoma across all International Metastatic RCC Database Consortium (IMDC) risk groups (favorable, intermediate, and poor); analyses of overall survival (OS) remain immature. Here, we report post hoc analyses of efficacy from the third interim analysis (data cut-off, April 2020) by the numbers of IMDC risk factors and target tumor sites at baseline.

METHODS

Efficacy endpoints assessed were PFS, objective response, and best overall response per investigator assessment (RECIST v1.1) and OS. Best percentage change and percentage change from baseline in target tumor size over time during the study were also assessed.

RESULTS

In patients with 0, 1, 2, 3, or 4-6 IMDC risk factors, hazard ratios [HRs; 95% confidence interval (CIs)] for OS with avelumab + axitinib versus sunitinib were 0.660 (0.356-1.223), 0.745 (0.524-1.059), 0.973 (0.668-1.417), 0.718 (0.414-1.248), and 0.443 (0.237-0.829), and HRs (95% CIs) for PFS were 0.706 (0.490-1.016), 0.709 (0.540-0.933), 0.711 (0.527-0.960), 0.501 (0.293-0.854), and 0.395 (0.214-0.727), respectively. In patients with 1, 2, 3, or ≥4 target tumor sites, HRs (95% CIs) for OS with avelumab + axitinib versus sunitinib were 0.912 (0.640-1.299), 0.715 (0.507-1.006), 0.679 (0.442-1.044), and 0.747 (0.346-1.615), and HRs (95% CIs) for PFS were 0.706 (0.548-0.911), 0.552 (0.422-0.723), 0.856 (0.589-1.244), and 0.662 (0.329-1.332), respectively. Across all subgroups, analyses of objective response rate and complete response rate favored avelumab + axitinib versus sunitinib, and a greater proportion of patients treated with avelumab + axitinib had tumor shrinkage.

CONCLUSIONS

In post hoc analyses, first-line treatment with avelumab + axitinib was generally associated with efficacy benefits versus treatment with sunitinib in patients with advanced renal cell carcinoma across subgroups defined by different numbers of IMDC risk factors or target tumor sites.

摘要

背景

在 III 期 JAVELIN Renal 101 试验中,一线阿维鲁单抗+阿昔替尼相较于舒尼替尼改善了所有国际转移性肾细胞癌数据库联盟(IMDC)风险组(有利、中间和差)患者的无进展生存期(PFS)和客观缓解率;总生存期(OS)的分析仍不成熟。在这里,我们根据基线时 IMDC 风险因素和靶肿瘤部位的数量,报告了第三次中期分析(数据截止日期为 2020 年 4 月)的疗效事后分析。

方法

评估的疗效终点是 PFS、客观缓解和研究者评估的最佳总体缓解(RECIST v1.1)以及 OS。还评估了研究期间靶肿瘤大小随时间的最佳百分比变化和基线百分比变化。

结果

在 IMDC 风险因素为 0、1、2、3 或 4-6 的患者中,阿维鲁单抗+阿昔替尼与舒尼替尼相比的 OS 风险比(HR;95%置信区间(CI))分别为 0.660(0.356-1.223)、0.745(0.524-1.059)、0.973(0.668-1.417)、0.718(0.414-1.248)和 0.443(0.237-0.829),PFS 的 HR(95% CI)分别为 0.706(0.490-1.016)、0.709(0.540-0.933)、0.711(0.527-0.960)、0.501(0.293-0.854)和 0.395(0.214-0.727)。在靶肿瘤部位为 1、2、3 或≥4 的患者中,阿维鲁单抗+阿昔替尼与舒尼替尼相比的 OS HR(95% CI)分别为 0.912(0.640-1.299)、0.715(0.507-1.006)、0.679(0.442-1.044)和 0.747(0.346-1.615),PFS 的 HR(95% CI)分别为 0.706(0.548-0.911)、0.552(0.422-0.723)、0.856(0.589-1.244)和 0.662(0.329-1.332)。在所有亚组中,客观缓解率和完全缓解率的分析均有利于阿维鲁单抗+阿昔替尼与舒尼替尼,并且接受阿维鲁单抗+阿昔替尼治疗的患者中有更大比例的肿瘤缩小。

结论

在事后分析中,一线使用阿维鲁单抗+阿昔替尼与舒尼替尼相比,在不同数量的 IMDC 风险因素或靶肿瘤部位定义的亚组中,通常与晚期肾细胞癌患者的疗效获益相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eb5/10774904/a9baaf580494/gr1.jpg

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