Department of Medical Oncology, National Taiwan University Cancer Center, Taipei, Taiwan.
Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
Cancer Immunol Immunother. 2024 Sep 9;73(11):230. doi: 10.1007/s00262-024-03826-y.
Adjuvant nivolumab reduces recurrence in patients with locoregional esophageal cancer who had pathological residual disease after neoadjuvant chemoradiotherapy and R0 resection. However, the efficacy of adjuvant anti-PD-1 therapy in patients at higher risk of recurrence remains unclear.
This phase II trial (ClinicalTrials.gov identifier: NCT03322267) enrolled patients with locally advanced esophageal squamous cell carcinoma (ESCC) received neoadjuvant chemoradiotherapy plus esophagectomy but still had various risk factors for recurrence, such as involved or close margins (≤ 1 mm), extranodal extension of the involved lymph nodes, and the ypN2-3 stage. Patients received adjuvant therapy composed of a course of cisplatin-based chemoradiotherapy and pembrolizumab (200 mg, IV every 3 weeks) for 18 cycles. The primary endpoint was 1-year relapse-free survival (RFS) rate.
Twenty-five patients were enrolled. The risk factors were tumor margins of ≤ 1 mm (18 patients), extranodal extension of the involved lymph nodes (9 patients), and the ypN2-3 stage (9 patients). The median follow-up duration was 21.6 months (95% CI: 18.7-33.2). The rate of 1-year RFS was 60.0%. The median duration of RFS and overall survival was 14.3 (95% CI: 9.0-19.5) and 21.6 (95% CI: 0.0-45.5) months, respectively. Treatment-emergent adverse events of any grade and those of ≥ 3 grade occurred in 56% and 8% of all patients receiving cisplatin-based chemoradiotherapy and in 79.2% and 12.5% of those receiving pembrolizumab.
Adjuvant chemoradiotherapy followed by pembrolizumab is feasible and may be associated with improved 1-year RFS rate in patients at high risk of recurrence after trimodality therapy for locally advanced ESCC. Trial registration number ClinicalTrials.gov (No. NCT03322267).
辅助 nivolumab 可降低新辅助放化疗和 R0 切除术后病理残留疾病的局部区域食管癌患者的复发率。然而,辅助抗 PD-1 治疗在复发风险较高的患者中的疗效尚不清楚。
这是一项 II 期临床试验(ClinicalTrials.gov 标识符:NCT03322267),纳入了接受新辅助放化疗加食管切除术但仍存在多种复发危险因素的局部晚期食管鳞状细胞癌(ESCC)患者,这些危险因素包括受累或切缘接近(≤1mm)、受累淋巴结的结外扩展以及 ypN2-3 期。患者接受了由顺铂为基础的放化疗和 pembrolizumab(200mg,每 3 周静脉注射一次)18 个周期组成的辅助治疗。主要终点是 1 年无复发生存率(RFS)。
共纳入 25 例患者。危险因素包括肿瘤切缘≤1mm(18 例)、受累淋巴结的结外扩展(9 例)和 ypN2-3 期(9 例)。中位随访时间为 21.6 个月(95%CI:18.7-33.2)。1 年 RFS 率为 60.0%。RFS 和总生存的中位持续时间分别为 14.3(95%CI:9.0-19.5)和 21.6(95%CI:0.0-45.5)个月。所有接受顺铂为基础的放化疗的患者中有 56%和 8%发生了任何等级的治疗相关不良事件,而接受 pembrolizumab 的患者中有 79.2%和 12.5%发生了这些事件。
辅助放化疗后序贯 pembrolizumab 是可行的,可能与提高局部晚期 ESCC 三模态治疗后复发风险较高患者的 1 年 RFS 率相关。试验注册ClinicalTrials.gov(编号 NCT03322267)。