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帕博利珠单抗治疗晚期尿路上皮癌伴严重肾功能不全患者的耐受性和治疗结局。

Tolerability and treatment outcome of pembrolizumab in patients with advanced urothelial carcinoma and severe renal dysfunction.

机构信息

Department of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Department of Urology, Akita University, Akita, Japan.

出版信息

Urol Oncol. 2022 Sep;40(9):410.e11-410.e18. doi: 10.1016/j.urolonc.2022.04.005. Epub 2022 May 9.

Abstract

OBJECTIVES

Pembrolizumab, an anti-PD-1 monoclonal antibody, revolutionized the treatment of advanced urothelial carcinoma. However, the tolerability and outcomes of pembrolizumab in patients with severe renal dysfunction [creatinine clearance (CrCl) <30 ml/min] are unclear because no clinical trials included such patients. We analyzed the safety profile and outcomes of these patients in the real world.

METHODS

We extracted data for 739 pembrolizumab-treated patients from a Japanese nationwide cohort of platinum-refractory metastatic urothelial carcinoma. Using propensity score matching, the overall survival (OS) and adverse events (AEs) of patients with CrCl <30 and ≥30 were compared.

RESULTS

Ninety-two patients (12.4%) had CrCl <30 ml/min. The median number of doses was similar between the CrCl ≥ 30 and CrCl <30 groups (5 and 4, respectively), and there was no difference in the frequency of grade ≥2 treatment-related AEs between the groups (35.5% vs. 35.7%). The overall response rate was similar between the groups (27.2% vs. 29.7%, P = 0.184). Using propensity score matching, the median OS times in the CrCl ≥30 and CrCl <30 groups were 10.3 (95% confidence interval [CI] = CI 7.3-13.0) and 8.1 months (95% CI = 5.4-14.6, P = 0.626), respectively. The 1-year OS rates in these groups were 41.5% and 38.2%, respectively, and the 2-year OS rates were 21.3% and 20.2%, respectively. In multivariate Cox regression analysis, performance status ≥2 (hazard ratio [HR] = 5.56, 95% CI = 2.64-11.71, P < 0.0001) and neutrophil-to-lymphocyte ratio ≥3 (HR = 2.20, 95% CI =1.15-4.19, P = 0.013) were independently associated with patient prognosis in the CrCl <30 group.

CONCLUSIONS

This report illustrated that pembrolizumab can be safely administered to patients with severe renal dysfunction, who had similar outcomes as patients without severe renal dysfunction.

摘要

目的

抗 PD-1 单克隆抗体 pembrolizumab 彻底改变了晚期尿路上皮癌的治疗方式。然而,由于没有临床试验纳入此类患者,因此对于严重肾功能障碍(肌酐清除率[CrCl] <30 ml/min)患者使用 pembrolizumab 的耐受性和结果尚不清楚。我们分析了这些患者在真实世界中的安全性和结局。

方法

我们从日本铂类难治性转移性尿路上皮癌全国队列中提取了 739 例接受 pembrolizumab 治疗的患者的数据。采用倾向评分匹配,比较了 CrCl <30 和 CrCl ≥30 患者的总生存期(OS)和不良事件(AE)。

结果

92 例患者(12.4%)CrCl <30 ml/min。CrCl ≥30 和 CrCl <30 组的中位剂量数相似(分别为 5 剂和 4 剂),两组间≥2 级治疗相关 AE 的频率无差异(分别为 35.5%和 35.7%)。两组间总缓解率相似(分别为 27.2%和 29.7%,P=0.184)。采用倾向评分匹配,CrCl ≥30 和 CrCl <30 组的中位 OS 时间分别为 10.3 个月(95%置信区间[CI]:7.3-13.0)和 8.1 个月(95% CI:5.4-14.6,P=0.626)。两组 1 年 OS 率分别为 41.5%和 38.2%,2 年 OS 率分别为 21.3%和 20.2%。多变量 Cox 回归分析显示,体能状态≥2(危险比[HR]:5.56,95% CI:2.64-11.71,P<0.0001)和中性粒细胞与淋巴细胞比值≥3(HR:2.20,95% CI=1.15-4.19,P=0.013)与 CrCl <30 组患者的预后独立相关。

结论

本报告表明,pembrolizumab 可安全用于严重肾功能障碍患者,且其结局与无严重肾功能障碍患者相似。

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