Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou, China.
State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Guangzhou, China.
BJU Int. 2023 Feb;131(2):198-207. doi: 10.1111/bju.15828. Epub 2022 Jul 7.
To evaluate the anti-tumour activity and safety of anti-programmed death receptor-1 (PD-1) antibody plus epidermal growth factor receptor blockade combined with platinum-based chemotherapy (PEP) as first-line therapy for stage IV penile squamous cell carcinoma (PSCC).
We conducted a retrospective review of 17 patients with stage IV PSCC undergoing first-line PEP at Sun Yat-sen University Cancer Center between January 2018 and September 2021. Clinical responses were assessed using the Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Adverse events (AEs) were graded according to Common Terminology Criteria for Adverse Events version 5.0.
Of 17 patients who received first-line PEP, 13 were observed to have partial responses. Twelve patients subsequently received consolidated surgery. Nine of these achieved pN0 status, of whom six with locally advanced PSCC achieved pathological complete response. The median (range) follow-up time was 24.87 (3.63-29.40) months. Median PFS and median OS were not reached, with 2-year PFS and OS rates being 68.4% (95% confidence interval [CI] 48.7-96.1) and 62.9% (95% CI 41.6-95), respectively. Eight patients experienced Grade 3 or 4 treatment-related AEs. No Grade 5 AEs or death associated with treatment was observed.
Anti-PD-1 antibody plus epidermal growth factor receptor blockade and platinum-based chemotherapy showed promising anti-tumour activity, acceptable toxicity, and satisfying long-term survival for stage IV PSCC. Larger clinical trials are needed to validate our findings.
评估抗程序性死亡受体-1(PD-1)抗体联合表皮生长因子受体阻断剂与铂类化疗(PEP)作为晚期 IV 期阴茎鳞状细胞癌(PSCC)一线治疗的抗肿瘤活性和安全性。
我们回顾性分析了中山大学肿瘤防治中心 2018 年 1 月至 2021 年 9 月期间接受一线 PEP 治疗的 17 例晚期 IV 期 PSCC 患者。采用实体瘤反应评价标准(RECIST)1.1 版评估临床反应。采用 Kaplan-Meier 法估计无进展生存期(PFS)和总生存期(OS)。根据不良事件通用术语标准 5.0 版(CTCAE v5.0)对不良事件(AE)进行分级。
17 例接受一线 PEP 治疗的患者中,13 例观察到部分缓解。12 例患者随后接受了巩固性手术。其中 9 例达到 pN0 状态,6 例局部晚期 PSCC 患者达到病理完全缓解。中位(范围)随访时间为 24.87(3.63-29.40)个月。中位 PFS 和中位 OS 均未达到,2 年 PFS 和 OS 率分别为 68.4%(95%置信区间 [CI]:48.7-96.1)和 62.9%(95% CI:41.6-95)。8 例患者发生 3 级或 4 级治疗相关 AE。未观察到 5 级 AE 或与治疗相关的死亡。
抗 PD-1 抗体联合表皮生长因子受体阻断剂与铂类化疗对晚期 IV 期 PSCC 具有良好的抗肿瘤活性、可接受的毒性和满意的长期生存。需要更大规模的临床试验来验证我们的发现。