Maiorano Mauro Francesco Pio, Loizzi Vera, Cormio Gennaro, Maiorano Brigida Anna
Unit of Obstetrics and Gynecology, Department of Interdisciplinary Medicine (DIM), University of Bari "Aldo Moro", Polyclinic of Bari, Piazza Giulio Cesare 11, 70124 Bari, Italy.
Unit of Oncologic Gynecology, IRCCS "Giovanni Paolo II" Oncologic Institute, Viale Orazio Flacco 65, 70124 Bari, Italy.
Cancers (Basel). 2025 Jul 19;17(14):2392. doi: 10.3390/cancers17142392.
: Advanced and recurrent vulvar squamous cell carcinoma (VSCC) presents a major therapeutic challenge with limited treatment options and poor outcomes. Immune checkpoint inhibitors (ICIs) have shown efficacy in other HPV-associated malignancies, but their role in VSCC remains poorly defined due to the rarity of the disease and limited clinical trial data. : We conducted a systematic review and meta-analysis following PRISMA guidelines and registered in PROSPERO (CRD420251067565). A comprehensive literature search identified prospective clinical trials evaluating ICIs in patients with advanced, unresectable, recurrent, or metastatic VSCC. The primary outcomes included objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and safety. Risk of bias was assessed using the MINORS tool. Meta-analyses were performed using random-effects models, with subgroup analyses based on PD-L1 status and treatment regimens (monotherapy vs. combination therapy). : Six non-randomized single-arm trials involving 181 patients were included. The pooled ORR was 21%, with higher response rates observed in combination therapy (46%) compared to monotherapy (11%), though not statistically significant. Median PFS and OS were 2.2 months and 6.4 months, respectively. ORRs were similar between PD-L1-positive and PD-L1-negative subgroups. A safety analysis showed treatment-related adverse events (AEs) in 73% of patients and grade ≥ 3 AEs in 23%. The incidence of treatment-related death was 3%. : ICIs demonstrate modest but durable efficacy and an acceptable safety profile in advanced VSCC. The current evidence supports their use in selected patients. However, response variability and the lack of reliable predictive biomarkers, such as PD-L1 or HPV status, underscore the need for biomarker-driven clinical trials and improved patient selection strategies.
晚期复发性外阴鳞状细胞癌(VSCC)是一项重大的治疗挑战,治疗选择有限且预后不佳。免疫检查点抑制剂(ICI)在其他与HPV相关的恶性肿瘤中已显示出疗效,但由于该疾病罕见且临床试验数据有限,其在VSCC中的作用仍不明确。
我们按照PRISMA指南进行了系统评价和荟萃分析,并在PROSPERO(CRD420251067565)中注册。全面的文献检索确定了评估ICI在晚期、不可切除、复发或转移性VSCC患者中的前瞻性临床试验。主要结局包括客观缓解率(ORR)、无进展生存期(PFS)、总生存期(OS)和安全性。使用MINORS工具评估偏倚风险。采用随机效应模型进行荟萃分析,并根据PD-L1状态和治疗方案(单药治疗与联合治疗)进行亚组分析。
纳入了6项涉及181例患者的非随机单臂试验。汇总的ORR为21%,联合治疗(46%)的缓解率高于单药治疗(11%),尽管差异无统计学意义。中位PFS和OS分别为2.2个月和6.4个月。PD-L1阳性和PD-L1阴性亚组的ORR相似。安全性分析显示,73%的患者发生了与治疗相关的不良事件(AE),23%的患者发生了≥3级AE。治疗相关死亡的发生率为3%。
ICI在晚期VSCC中显示出适度但持久的疗效和可接受的安全性。目前的证据支持在选定的患者中使用ICI。然而,反应变异性以及缺乏可靠的预测生物标志物,如PD-L1或HPV状态,凸显了开展生物标志物驱动的临床试验和改进患者选择策略的必要性。