...
首页> 外文期刊>Thoracic cancer. >Efficacy and safety of immune checkpoint inhibitor consolidation after chemoradiation in patients of Asian ethnicity with unresectable stage III non‐small cell lung cancer: Chinese multicenter report and literature review
【24h】

Efficacy and safety of immune checkpoint inhibitor consolidation after chemoradiation in patients of Asian ethnicity with unresectable stage III non‐small cell lung cancer: Chinese multicenter report and literature review

机译:免疫检查点抑制剂在亚洲民族患者中抑制抑制剂固结的疗效和安全性与不可切除的阶段III非小细胞肺癌:中国多中心报告和文献综述

获取原文

摘要

BACKGROUND:The PACIFIC study has defined a new standard of care for patients with unresectable stage III non-small cell lung cancer (NSCLC) in the form of immune checkpoint inhibitor (ICI) consolidation therapy. However, there is little specific data pertaining to the safety and efficacy of this approach in Chinese NSCLC patients.METHODS:This was a prospective multicenter cohort study. Between September 2018 and January 2020, patients with unresectable stage III NSCLC that had undergone chemoradiation therapy (CRT) and ICI consolidation treatment were enrolled in this study. The short-term safety, tolerability, and efficacy of ICI combination with CRT were evaluated in these patients.RESULTS:Of the 20 Chinese patients eligible for inclusion, 17 (85.0%) underwent concurrent CRT treatment. In these patients, a median period of 40.5?days (range: 1-85?days) passed between the end of CRT and initiation of consolidation therapy. Pneumonitis occurred in 80.0% of patients, with seven (35.0%) being diagnosed with grade 1 pneumonitis and nine (45.0%) with grade 2 pneumonitis. No patients experienced grade 3 or higher pneumonitis or other ICI-related toxicities. Lung V20?≥?20% was associated with higher grade 2 pneumonitis (77.8%; ≥20% vs. 18.2%; 20%, P = 0.027). The overall response rate (ORR) in these patients was 95.0%. Over a median follow-up period of 11.3 months (range: 6.2-21.8 months), 12-month PFS of these patients were 89.5% (95% CI: 76.7-100.0%), and 12 months OS was 100.0%.CONCLUSIONS:These data indicate that ICI consolidation therapy can achieve favorable short-term efficacy, while exhibiting good safety and acceptable toxicity profiles in Chinese patients with unresectable stage III NSCLC.KEY POINTS:Significant findings of the study This is the first report evaluating the safety and efficacy of ICI consolidation therapy after chemoradiotherapy in China. Our results indicate that ICI consolidation is associated with favorable efficacy and no severe pneumonitis incidence in Chinese patients undergoing both anti-PD-1 and anti-PD-L1 monoclonal antibody consolidation. What this study adds Post-hoc analysis of the Japanese subgroup in the PACIFIC study suggested that consolidation therapy may be associated with increased pneumonitis incidence in Asian patients. However, our findings indicate that consolidation therapy is safe and tolerable in Chinese patients with unresectable stage III NSCLC.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:PACIFIC研究已经定义护理的新标准的患者在免疫检查点抑制剂(ICI)巩固治疗的形式不能切除的III期非小细胞肺癌(NSCLC)。然而,有关中国在非小细胞肺癌patients.METHODS这种方法的安全性和有效性太多具体的数据:这是一个前瞻性多中心队列研究。 2018年9月和一月至2020年间,患者不能手术切除的Ⅲ期非小细胞肺癌,在经受放化疗治疗(CRT)和ICI巩固治疗的研究对象。短期安全性,耐受性和ICI组合的功效与CRT在这些patients.RESULTS评价:20名中国患者符合纳入条件中,有17(85.0%)接受并发CRT治疗。在这些患者中,40.5天(范围:1-85天?)平均期限?CRT的结束和巩固治疗的开始之间传递。肺炎的发生率为80.0%,与七(35.0%)被诊断与2级肺炎1级肺炎和九(45.0%)。没有患者出现3级以上的肺炎或其他ICI相关的毒性。 ?肺V20≥20%与较高等级2关联肺炎(77.8%;≥20%对18.2%; <20%,P = 0.027)。在这些患者的总缓解率(ORR)为95.0%。在11.3个月(范围:6.2-21.8个月)的中位随访期,这些患者中12个月的PFS分别为89.5%(95%CI:76.7-100.0%)和12个月OS为100.0%。结论:这些数据表明,ICI巩固治疗可以达到良好的短期疗效,同时表现出良好的安全性和可接受的毒性特征在中国治疗晚期阶段III NSCLC.KEY点:研究的重要结果这是第一份报告评估安全性和有效性在中国放化疗后ICI巩固治疗。我们的研究结果表明,ICI的整合与良好的疗效,无严重肺炎的发病率在中国经历的患者既抗PD-1和抗PD-L1单克隆抗体的整合有关。什么这项研究增加在太平洋研究日本亚组的事后分析表明,巩固治疗可能与亚洲患者增加发病率肺炎有关。然而,我们的研究结果表明,巩固治疗是安全,耐受性在中国患者不能手术切除的Ⅲ期NSCLC。? 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号