Tucker Matthew, Chen Yu-Wei, Voss Martin H, McGregor Bradley A, Bilen Mehmet A, Grimm Marc-Oliver, Nathan Paul, Kollmannsberger Christian, Tomita Yoshihiko, Huang Bo, Amezquita Robert, Mariani Mariangela, di Pietro Alessandra, Rini Brian
Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Alabama Oncology, Grandview Cancer Center, Birmingham, Alabama, USA.
BMJ Oncol. 2024 Jun 12;3(1):e000181. doi: 10.1136/bmjonc-2023-000181. eCollection 2024.
We report post hoc analyses of efficacy with first-line avelumab plus axitinib or sunitinib according to baseline neutrophil-to-eosinophil ratio (NER) in patients with advanced renal cell carcinoma (aRCC) from the JAVELIN Renal 101 phase 3 trial.
Progression-free survival (PFS), overall survival (OS) and objective response per baseline NER were analysed in the overall population and in patients with programmed death ligand 1 (PD-L1+) tumours. Multivariable Cox regression analyses to assess the effect of NER after adjustment for other baseline variables were conducted.
In NER <median versus ≥median subgroups of the avelumab plus axitinib arm, HRs for PFS and OS were 0.81 (95% CI 0.630 to 1.035) and 0.67 (95% CI 0.481 to 0.940), and objective response rates (ORRs) were 63.9% vs 55.2%, respectively. The HR for PFS in the PD-L1+ subgroup was 0.72 (95% CI 0.520 to 0.986). Comparing NER-defined subgroups in the sunitinib arm, HRs for PFS and OS were 0.93 (95% CI 0.728 to 1.181) and 0.57 (95% CI 0.424 to 0.779), and ORRs were 32.8% versus 30.8%, respectively. Within NER subgroups, analyses of PFS, OS and ORR favoured avelumab plus axitinib versus sunitinib treatment. Interaction tests that assessed the association between treatment and NER yielded conflicting results when NER was assessed as a dichotomised variable (median cut-off) or continuous variable.
Hypothesis-generating analyses suggest that baseline NER may be prognostic for longer OS irrespective of treatment. Analyses of the association between NER level and treatment outcomes with avelumab plus axitinib versus sunitinib were inconclusive.
NCT02684006.
我们对JAVELIN Renal 101 3期试验中晚期肾细胞癌(aRCC)患者根据基线中性粒细胞与嗜酸性粒细胞比值(NER)使用一线阿维鲁单抗加阿昔替尼或舒尼替尼的疗效进行事后分析。
在总体人群以及程序性死亡配体1(PD-L1+)肿瘤患者中,分析了无进展生存期(PFS)、总生存期(OS)以及根据基线NER得出的客观缓解率。进行了多变量Cox回归分析,以评估在对其他基线变量进行调整后NER的影响。
在阿维鲁单抗加阿昔替尼组NER<中位数与≥中位数亚组中,PFS和OS的HR分别为0.81(95%CI 0.630至1.035)和0.67(95%CI 0.481至0.940),客观缓解率(ORR)分别为63.9%和55.2%。PD-L1+亚组中PFS的HR为0.72(95%CI 0.520至0.986)。比较舒尼替尼组中由NER定义的亚组,PFS和OS的HR分别为0.93(95%CI 0.728至1.181)和0.57(95%CI 0.424至0.779),ORR分别为32.8%和30.8%。在NER亚组内,PFS、OS和ORR的分析表明阿维鲁单抗加阿昔替尼治疗优于舒尼替尼治疗。当将NER评估为二分变量(中位数截断)或连续变量时,评估治疗与NER之间关联的交互检验得出了相互矛盾的结果。
假设生成分析表明,无论治疗如何,基线NER可能对更长的OS具有预后价值。关于NER水平与阿维鲁单抗加阿昔替尼和舒尼替尼治疗结果之间关联的分析尚无定论。
NCT02684006。