Department of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Department of Urology, Akita University, Akita, Japan.
Urol Oncol. 2022 Sep;40(9):410.e11-410.e18. doi: 10.1016/j.urolonc.2022.04.005. Epub 2022 May 9.
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.
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.
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.
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.
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。
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)。
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。
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。