Radboud University, Nijmegen, The Netherlands.
Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Eur Urol Oncol. 2022 Oct;5(5):553-563. doi: 10.1016/j.euo.2022.02.003. Epub 2022 Mar 11.
The programmed death-1 (PD-1) inhibitor nivolumab prolongs disease-free survival in patients with muscle-invasive urothelial carcinoma (MIUC).
To evaluate the effects of nivolumab on health-related quality of life (HRQoL) after radical resection in patients with MIUC.
DESIGN, SETTING, AND PARTICIPANTS: We used data from 709 patients in CheckMate 274 (NCT02632409; 282 with programmed death ligand 1 [PD-L1] expression ≥1%), an ongoing randomized, double-blind, placebo-controlled phase 3 trial of adjuvant nivolumab.
Intravenous injection of nivolumab (240 mg) or placebo every 2 wk for ≤1 yr.
HRQoL was assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) and the EQ-5D-3L. Linear mixed-effect models for repeated measures were used to compare nivolumab and placebo on changes in HRQoL. Time to confirmed deterioration (TTCD) of HRQoL was analyzed by Cox proportional hazards regression.
In the full HRQoL evaluable population, no clinically meaningful deterioration of HRQoL was observed in either treatment arm. Moreover, nivolumab was noninferior to placebo on changes from baseline for all main outcomes. The median TTCD for fatigue was 41.0 wk for nivolumab and 44.3 wk for placebo (hazard ratio [HR]: 1.11, 95% confidence interval [CI], 0.89-1.39). For the visual analog scale, the median TTCD was not reached for nivolumab and it was 57.6 wk for placebo (HR: 0.78, 95% CI, 0.61-1.00). The median TTCD for the other main outcomes was not reached in either treatment arm. The findings were similar for patients with PD-L1 expression ≥1%.
These results demonstrate that nivolumab did not compromise the HRQoL of patients with MIUC in CheckMate 274.
Nivolumab is being researched as a new treatment for patients with bladder cancer (urothelial carcinoma). We found that nivolumab maintained quality of life while increasing the time until cancer returns in patients whose bladder cancer had spread or grown and who had unsuccessfully tried platinum-containing chemotherapy.
程序性死亡受体-1(PD-1)抑制剂纳武利尤单抗可延长肌层浸润性膀胱癌(MIUC)患者的无病生存期。
评估纳武利尤单抗对 MIUC 根治性切除术后患者健康相关生活质量(HRQoL)的影响。
设计、设置和参与者:我们使用了正在进行的随机、双盲、安慰剂对照的 III 期 CheckMate 274 试验(NCT02632409;282 例 PD-L1 表达≥1%)中 709 例患者的数据。纳武利尤单抗辅助治疗。
静脉注射纳武利尤单抗(240mg)或安慰剂,每 2 周 1 次,持续 1 年。
使用欧洲癌症研究与治疗组织生命质量问卷(EORTC QLQ-C30)和 EQ-5D-3L 评估 HRQoL。采用重复测量线性混合效应模型比较纳武利尤单抗和安慰剂对 HRQoL 变化的影响。采用 Cox 比例风险回归分析 HRQoL 确认恶化的时间(TTCD)。
在完整的 HRQoL 可评估人群中,两个治疗组均未观察到 HRQoL 有临床意义的恶化。此外,纳武利尤单抗在所有主要结局的变化上均不劣于安慰剂。纳武利尤单抗组疲劳的中位 TTCD 为 41.0 周,安慰剂组为 44.3 周(风险比[HR]:1.11,95%置信区间[CI]:0.89-1.39)。对于视觉模拟量表,纳武利尤单抗的中位 TTCD 未达到,安慰剂组为 57.6 周(HR:0.78,95%CI:0.61-1.00)。两个治疗组的其他主要结局的中位 TTCD 均未达到。在 PD-L1 表达≥1%的患者中,也观察到了类似的结果。
这些结果表明,纳武利尤单抗在 CheckMate 274 中并未降低 MIUC 患者的 HRQoL。
纳武利尤单抗正在被研究作为膀胱癌(尿路上皮癌)患者的一种新的治疗方法。我们发现,在接受过铂类化疗但无效且膀胱癌已扩散或生长的患者中,纳武利尤单抗能维持生活质量,同时延长癌症复发时间。