Adjuvant chemoradiotherapy plus pembrolizumab for locally advanced esophageal squamous cell carcinoma with high risk of recurrence following neoadjuvant chemoradiotherapy: a single-arm phase II study.

IF 4.6 2区 医学 Q2 IMMUNOLOGY Cancer Immunology, Immunotherapy Pub Date : 2024-09-09 DOI:10.1007/s00262-024-03826-y
Jhe-Cyuan Guo, Ta-Chen Huang, Hung-Yang Kuo, Chia-Chi Lin, Feng-Ming Hsu, Jason Chia-Hsien Cheng, Yen-Lin Huang, Min-Shu Hsieh, Pei-Ming Huang, Jang-Ming Lee, Shu-Ling Wu, Chih-Hung Hsu
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Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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).

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辅助化放疗加pembrolizumab治疗新辅助化放疗后复发风险高的局部晚期食管鳞癌:一项单臂II期研究。
背景新辅助化放疗和R0切除术后有病理残留的局部食管癌患者接受nivolumab辅助治疗可减少复发。然而,对于复发风险较高的患者,抗PD-1辅助治疗的疗效仍不明确:这项II期试验(ClinicalTrials.gov标识符:NCT03322267)招募了局部晚期食管鳞状细胞癌(ESCC)患者,这些患者接受了新辅助化放疗加食管切除术,但仍存在各种复发风险因素,如受累或边缘较近(≤1毫米)、受累淋巴结的结外扩展以及ypN2-3分期。患者接受的辅助治疗包括一个疗程的顺铂为基础的化放疗和pembrolizumab(200毫克,每3周静脉注射一次),共18个周期。主要终点是1年无复发生存率(RFS):25名患者入组。风险因素包括肿瘤边缘≤1毫米(18例患者)、受累淋巴结向结外扩展(9例患者)和ypN2-3分期(9例患者)。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和总生存期的中位数分别为14.3个月(95% CI:9.0-19.5)和21.6个月(95% CI:0.0-45.5)。在接受顺铂为基础的化放疗的所有患者中,56%和8%发生了任何级别的治疗突发不良事件,在接受pembrolizumab治疗的患者中,79.2%和12.5%发生了≥3级的治疗突发不良事件:在局部晚期ESCC三模式治疗后复发风险较高的患者中,辅助化放疗后使用pembrolizumab是可行的,并可提高1年RFS率。试验注册号:ClinicalTrials.gov(编号:NCT03322267)。
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来源期刊
CiteScore
10.50
自引率
1.70%
发文量
207
审稿时长
1 months
期刊介绍: Cancer Immunology, Immunotherapy has the basic aim of keeping readers informed of the latest research results in the fields of oncology and immunology. As knowledge expands, the scope of the journal has broadened to include more of the progress being made in the areas of biology concerned with biological response modifiers. This helps keep readers up to date on the latest advances in our understanding of tumor-host interactions. The journal publishes short editorials including "position papers," general reviews, original articles, and short communications, providing a forum for the most current experimental and clinical advances in tumor immunology.
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