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新辅助放化疗联合序贯围手术期特瑞普利单抗治疗局部晚期食管鳞癌。

Neoadjuvant chemoradiotherapy combined with sequential perioperative toripalimab in locally advanced esophageal squamous cell cancer.

机构信息

Department of Radiation Oncology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Thoracic Surgery, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

J Immunother Cancer. 2024 Mar 7;12(3):e008631. doi: 10.1136/jitc-2023-008631.

Abstract

BACKGROUND

Programmed death 1 (PD-1) inhibitor demonstrated durable antitumor activity in advanced esophageal squamous cell carcinoma (ESCC), but the clinical benefit of perioperative immunotherapy in ESCC remains unclear. This study evaluated the efficacy and safety of neoadjuvant chemoradiotherapy (nCRT) combined with the PD-1 inhibitor toripalimab in patients with resectable ESCC.

METHODS

From July 2020 to July 2022, 21 patients with histopathologically confirmed thoracic ESCC and clinical staged as cT1-4aN1-2M0/cT3-4aN0M0 were enrolled. Eligible patients received radiotherapy (23 fractions of 1.8 Gy, 5 fractions a week) with concurrent chemotherapy of paclitaxel/cisplatin (paclitaxel 45 mg/m and cisplatin 25 mg/m) on days 1, 8, 15, 22, 29 and two cycles of toripalimab 240 mg every 3 weeks after nCRT for neoadjuvant therapy before surgery, four cycles of toripalimab 240 mg every 3 weeks for adjuvant therapy after surgery. The primary endpoint was the major pathological response (MPR) rate. The secondary endpoints were safety and survival outcomes.

RESULTS

A total of 21 patients were included, of whom 20 patients underwent surgery, 1 patient refused surgery and another patient was confirmed adenocarcinoma after surgery. The MPR and pathological complete response (pCR) rates were 78.9% (15/19) and 47.4% (9/19) for surgery ESCC patients. 21 patients (100.0%) had any-grade treatment-related adverse events, with the most common being lymphopenia (100.0%), leukopenia (85.7%), neutropenia (52.4%). 14 patients (66.7%) had adverse events of grade 3 with the most common being lymphopenia (66.7%). The maximum standardized uptake value and total lesion glycolysis of positron emission tomography/CT after neoadjuvant therapy well predicted the pathological response. The peripheral CD4+%, CD3+HLA-DR+/CD3+%, CD8+HLA-DR+/CD8+%, and IL-6 were significant differences between pCR and non-pCR groups at different times during neoadjuvant therapy. Three patients had tumor relapse and patients with MPR have longer disease-free survival than non-MPR patients.

CONCLUSIONS

nCRT combined with perioperative toripalimab is effective and safe for locally advanced resectable ESCC. Long-term survival outcomes remain to be determined.

TRIAL REGISTRATION NUMBER

NCT04437212.

摘要

背景

程序性死亡受体 1(PD-1)抑制剂在晚期食管鳞状细胞癌(ESCC)中显示出持久的抗肿瘤活性,但 ESCC 围手术期免疫治疗的临床获益仍不清楚。本研究评估了新辅助放化疗(nCRT)联合 PD-1 抑制剂特瑞普利单抗在可切除 ESCC 患者中的疗效和安全性。

方法

2020 年 7 月至 2022 年 7 月,共纳入 21 例经组织病理学证实的胸段 ESCC 且临床分期为 cT1-4aN1-2M0/cT3-4aN0M0 的患者。符合条件的患者接受放疗(23 次,每次 1.8 Gy,每周 5 次),同时在 nCRT 期间接受紫杉醇/顺铂(紫杉醇 45 mg/m2,顺铂 25 mg/m2)联合化疗,在第 1、8、15、22、29 天和第 29 天接受两个周期的特瑞普利单抗 240mg,每个周期 3 周,之后进行手术前的新辅助治疗,手术后进行四个周期的特瑞普利单抗 240mg,每个周期 3 周进行辅助治疗。主要终点是主要病理缓解(MPR)率。次要终点是安全性和生存结果。

结果

共纳入 21 例患者,其中 20 例患者接受了手术,1 例患者拒绝手术,另 1 例患者术后被确诊为腺癌。手术 ESCC 患者的 MPR 和病理完全缓解(pCR)率分别为 78.9%(15/19)和 47.4%(9/19)。21 例患者(100.0%)出现任何级别的治疗相关不良事件,最常见的是淋巴细胞减少症(100.0%)、白细胞减少症(85.7%)、中性粒细胞减少症(52.4%)。14 例患者(66.7%)出现 3 级不良事件,最常见的是淋巴细胞减少症(66.7%)。治疗前的正电子发射断层扫描/CT 的最大标准化摄取值和总病变糖酵解水平能很好地预测病理反应。新辅助治疗期间不同时间点的 pCR 组与非 pCR 组之间,外周血 CD4+%、CD3+HLA-DR+/CD3+%、CD8+HLA-DR+/CD8+%和 IL-6 有显著差异。3 例患者出现肿瘤复发,MPR 患者的无病生存率长于非 MPR 患者。

结论

nCRT 联合围手术期特瑞普利单抗治疗局部晚期可切除 ESCC 是有效和安全的。长期生存结果仍有待确定。

试验注册

NCT04437212。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12c/10921522/16cced892e28/jitc-2023-008631f01.jpg

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