Adjuvant Pembrolizumab in Patients with Stage IIIA/N2 Non-Small Cell Lung Cancer Completely Resected after Neoadjuvant Concurrent Chemoradiation: A Prospective, Open-Label, Single-Arm, Phase 2 Trial.

IF 4.1 2区 医学 Q2 ONCOLOGY Cancer Research and Treatment Pub Date : 2024-10-01 Epub Date: 2024-04-30 DOI:10.4143/crt.2024.084
Junghoon Shin, Sehhoon Park, Kyung Hwan Kim, Eui-Cheol Shin, Hyun Ae Jung, Jong Ho Cho, Jong-Mu Sun, Se-Hoon Lee, Yong Soo Choi, Jin Seok Ahn, Jhingook Kim, Keunchil Park, Young Mog Shim, Hong Kwan Kim, Jae Myoung Noh, Yong Chan Ahn, Hongryull Pyo, Myung-Ju Ahn
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Abstract

Purpose: Optimal treatment for stage IIIA/N2 non-small cell lung cancer (NSCLC) is controversial. We aimed to assess the efficacy and safety of adjuvant pembrolizumab for stage IIIA/N2 NSCLC completely resected after neoadjuvant concurrent chemoradiation therapy (CCRT).

Materials and methods: In this open-label, single-center, single-arm phase 2 trial, patients with stage IIIA/N2 NSCLC received adjuvant pembrolizumab for up to 2 years after complete resection following neoadjuvant CCRT. The primary endpoint was disease-free survival (DFS). Secondary endpoints included overall survival (OS) and safety. As an exploratory biomarker analysis, we evaluated the proliferative response of blood CD39+PD-1+CD8+ T cells using fold changes in the percentage of proliferating Ki-67+ cells from days 1 to 7 of cycle 1 (Ki-67D7/D1).

Results: Between October 2017 and October 2018, 37 patients were enrolled. Twelve (32%) and three (8%) patients harbored EGFR and ALK alterations, respectively. Of 34 patients with programmed cell death ligand 1 assessment, 21 (62%), nine (26%), and four (12%) had a tumor proportion score of < 1%, 1%-50%, and ≥ 50%, respectively. The median follow-up was 71 months. The median DFS was 22.4 months in the overall population, with a 5-year DFS rate of 29%. The OS rate was 86% at 2 years and 76% at 5 years. Patients with tumor recurrence within 6 months had a significantly lower Ki-67D7/D1 among CD39+PD-1+CD8+ T cells than those without (p=0.036). No new safety signals were identified.

Conclusion: Adjuvant pembrolizumab may offer durable disease control in a subset of stage IIIA/N2 NSCLC patients after neoadjuvant CCRT and surgery.

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新辅助同期化疗后完全切除的 IIIA/N2 期非小细胞肺癌患者的 Pembrolizumab 辅助治疗:一项前瞻性、开放标签、单臂 2 期试验。
目的:IIIA/N2期非小细胞肺癌(NSCLC)的最佳治疗方法尚存争议。我们旨在评估新辅助同期化放疗(CCRT)后完全切除的IIIA/N2期NSCLC患者使用pembrolizumab辅助治疗的有效性和安全性:在这项开放标签、单中心、单臂的2期试验中,IIIA/N2期NSCLC患者在新辅助CCRT完全切除后接受了长达两年的pembrolizumab辅助治疗。主要终点是无病生存期(DFS)。次要终点包括总生存期(OS)和安全性。作为一项探索性生物标志物分析,我们使用第1周期第1天至第7天增殖的Ki-67+细胞百分比的折叠变化(Ki-67D7/D1)评估了血液中CD39+PD-1+CD8+ T细胞的增殖反应:2017年10月至2018年10月,37名患者入组。分别有12名(32%)和3名(8%)患者存在表皮生长因子受体(EGFR)和ALK改变。在34名进行了程序性细胞死亡配体1评估的患者中,21人(62%)、9人(26%)和4人(12%)的肿瘤比例评分为结论:在新辅助CCRT和手术后,Pembrolizumab辅助治疗可为部分IIIA/N2期NSCLC患者提供持久的疾病控制。
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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
126
审稿时长
>12 weeks
期刊介绍: Cancer Research and Treatment is a peer-reviewed open access publication of the Korean Cancer Association. It is published quarterly, one volume per year. Abbreviated title is Cancer Res Treat. It accepts manuscripts relevant to experimental and clinical cancer research. Subjects include carcinogenesis, tumor biology, molecular oncology, cancer genetics, tumor immunology, epidemiology, predictive markers and cancer prevention, pathology, cancer diagnosis, screening and therapies including chemotherapy, surgery, radiation therapy, immunotherapy, gene therapy, multimodality treatment and palliative care.
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