Department of Thoracic Surgery.
Department of Pathology.
Int J Surg. 2024 Mar 1;110(3):1430-1440. doi: 10.1097/JS9.0000000000000978.
Neoadjuvant administration of immune checkpoint inhibitors (ICIs) combined with chemotherapy demonstrated promising efficacy and manageable safety in locally advanced esophageal squamous cell carcinoma (ESCC). This prospective, single-arm, phase 2 study evaluated the efficacy and safety of neoadjuvant therapy with camrelizumab plus paclitaxel and nedaplatin for 2-4 cycles in ESCC.
Patients with locally advanced stage IIa-IIIb ESCC were enrolled in the study and received camrelizumab (200 mg), paclitaxel (155 mg/m 2 ), and nedaplatin (80 mg/m 2 ) intravenously on day one every 3 weeks. Patients underwent surgery after 2-4 cycles of treatment. The primary endpoint was the pathological complete response (pCR) rate. Secondary endpoints included the major pathological response (MPR) rate, R0 resection rate, tumor regression, objective response rate (ORR), and disease-free survival (DFS). Programmed cell death 1 ligand 1 (PD-L1) expression in tumor tissues was measured and quantified using immunohistochemistry staining and combined positive score (CPS), respectively.
In total, 75 patients were enrolled and received neoadjuvant treatment. Of them, 45 (60%) received two cycles, 18 (24%) received three cycles, and 10 patients (13.3%) received four cycles of neoadjuvant therapy. Ultimately, 62 patients (82.7%) underwent surgery. The patients achieved a pCR of 27.4% (95% CI: 16.9-40.2), an MPR of 45.2% (95% CI: 33.1-59.2), and an ORR of 48.4% (95% CI: 35.5-61.4); all patients had an R0 resection. T and N downstaging occurred in 39 (62.9%) and 19 (30.6%) patients Moreover, patients with CPS ≥10 tended to have enhanced ORR, pCR, and MPR compared to those with CPS <10. Treatment-related adverse events (TRAEs) of grade 1-2 occurred in 59 (78.7%) patients, grade 3 TRAEs in four (5.3%), and one patient (1.3%) experienced a grade 4 TRAE.
Neoadjuvant camrelizumab combined with chemotherapy showed promising efficacy in locally advanced ESCC, with a manageable safety profile, when administered flexibly in two to four cycles.
新辅助免疫检查点抑制剂(ICI)联合化疗在局部晚期食管鳞状细胞癌(ESCC)中显示出有希望的疗效和可管理的安全性。这项前瞻性、单臂、2 期研究评估了卡瑞利珠单抗联合紫杉醇和奈达铂在 ESCC 患者中进行 2-4 个周期新辅助治疗的疗效和安全性。
入组的局部晚期 IIa-IIIb 期 ESCC 患者接受卡瑞利珠单抗(200mg)、紫杉醇(155mg/m 2 )和奈达铂(80mg/m 2 )静脉输注,每 3 周一次,在治疗的第 2-4 周期后进行手术。主要终点为病理完全缓解(pCR)率。次要终点包括主要病理缓解(MPR)率、R0 切除率、肿瘤退缩、客观缓解率(ORR)和无病生存(DFS)。使用免疫组织化学染色和联合阳性评分(CPS)分别测量和定量肿瘤组织中程序性死亡配体 1(PD-L1)的表达。
共纳入 75 例患者接受新辅助治疗,其中 45 例(60%)接受 2 个周期,18 例(24%)接受 3 个周期,10 例(13.3%)接受 4 个周期。最终,62 例(82.7%)患者接受了手术。患者的 pCR 率为 27.4%(95%CI:16.9-40.2),MPR 率为 45.2%(95%CI:33.1-59.2),ORR 率为 48.4%(95%CI:35.5-61.4);所有患者均行 R0 切除术。39 例(62.9%)和 19 例(30.6%)患者的 T 和 N 分期下降。此外,与 CPS<10 的患者相比,CPS≥10 的患者的 ORR、pCR 和 MPR 均有提高。59 例(78.7%)患者出现 1-2 级治疗相关不良事件(TRAEs),4 例(5.3%)患者出现 3 级 TRAEs,1 例(1.3%)患者出现 4 级 TRAE。
在局部晚期 ESCC 患者中,灵活应用 2-4 个周期的卡瑞利珠单抗联合化疗新辅助治疗具有较好的疗效,安全性可控。