Department of Urology, The Jikei University School of Medicine, Tokyo, Japan;
Department of Medical Informatics, Niigata University Medical and Dental Hospital, Niigata, Japan.
Anticancer Res. 2024 May;44(5):2117-2123. doi: 10.21873/anticanres.17017.
BACKGROUND/AIM: Evidence suggests that serum magnesium levels are associated with outcomes of immune checkpoint inhibitors (ICIs). However, this association remains under-explored in patients with metastatic urothelial carcinoma (UC) treated with ICIs.
This prognostic study used individual participant-level data from 1,281 patients with locally advanced or metastatic UC treated with atezolizumab (N=855) or chemotherapy (N=426) who participated in the IMvigor210 and the IMvigor211 trials. Multivariable Cox proportional hazards regression and Fine-Gray subdistribution hazards regression models were used to examine the association of baseline serum magnesium levels with overall survival (OS), progression-free survival (PFS), and immune-related adverse events (irAEs).
No evidence of an association was found between baseline serum magnesium levels and PFS or OS in patients treated with atezolizumab [PFS, hazard ratio (HR)=1.03, 95% confidence interval (CI)=0.78-1.35; OS, HR=1.13, 95%CI=0.84-1.51] or chemotherapy (PFS, HR=0.93, 95%CI=0.62-1.40; OS, HR=0.91, 95%CI=0.59-1.40). We also found no evidence of association with irAEs (subdistribution HR=1.29, 95%CI=0.81-2.07) in patients receiving atezolizumab.
This study found no evidence of an association between baseline serum magnesium levels and treatment outcomes or irAEs in patients with metastatic UC receiving atezolizumab. Contrary to previous research suggesting a role for magnesium in cancer therapy, these results indicate that serum magnesium levels may not serve as a biomarker to predict outcomes in these patients.
背景/目的:有证据表明,血清镁水平与免疫检查点抑制剂(ICI)的疗效相关。然而,在接受 ICI 治疗的转移性尿路上皮癌(UC)患者中,这一关联仍未得到充分探索。
本预后研究使用了来自接受阿替利珠单抗(N=855)或化疗(N=426)治疗的局部晚期或转移性 UC 患者的个体参与者水平数据,这些患者参加了 IMvigor210 和 IMvigor211 试验。使用多变量 Cox 比例风险回归和 Fine-Gray 亚分布风险回归模型来研究基线血清镁水平与总生存期(OS)、无进展生存期(PFS)和免疫相关不良事件(irAE)之间的关联。
在接受阿替利珠单抗治疗的患者中,基线血清镁水平与 PFS 或 OS 之间没有发现关联的证据[PFS,风险比(HR)=1.03,95%置信区间(CI)=0.78-1.35;OS,HR=1.13,95%CI=0.84-1.51]或化疗[PFS,HR=0.93,95%CI=0.62-1.40;OS,HR=0.91,95%CI=0.59-1.40]。我们还发现,在接受阿替利珠单抗治疗的患者中,基线血清镁水平与 irAE 之间也没有关联的证据(亚分布 HR=1.29,95%CI=0.81-2.07)。
本研究在接受阿替利珠单抗治疗的转移性 UC 患者中,未发现基线血清镁水平与治疗结局或 irAE 之间存在关联。与之前的研究表明镁在癌症治疗中的作用相反,这些结果表明,血清镁水平可能不能作为预测这些患者结局的生物标志物。