一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Efficacy and safety of autologous CIK cell therapy plus Toripalimab with or without chemotherapy in advanced NSCLC: A phase II study.
Efficacy and safety of autologous CIK cell therapy plus Toripalimab with or without chemotherapy in advanced NSCLC: A phase II study.
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PD-L1阳性的晚期非小细胞肺癌(NSCLC)需要更有效的治疗选择。本研究旨在评估自体细胞因子诱导的杀伤(CIK)细胞疗法联合抗PD-1抗体特瑞普利单抗,联合或不联合化疗,作为晚期NSCLC一线治疗的有效性和安全性。这项II期试验于2020年7月至2022年12月期间入组了40例PD-L1阳性、驱动基因突变阴性的晚期NSCLC患者。患者被随机分配至A组(特瑞普利单抗+CIK细胞+化疗)或B组(特瑞普利单抗+CIK细胞)。评估了无进展生存期(PFS)、总生存期(OS)、总缓解率(ORR)和安全性特征。根据接受的CIK细胞周期数进行亚组分析。A组的中位PFS显著长于B组(20.0 vs. 6.0个月,p = 0.0038),而A组的中位OS未达到,B组为17.0个月(p = 0.0479)。A组ORR为47.4%,B组为60.0%。接受四个或以上周期CIK细胞治疗的患者PFS和OS显著改善。未发现新的安全性问题。CIK细胞联合特瑞普利单抗,联合或不联合化疗,在晚期PD-L1阳性NSCLC患者中显示出有前景的疗效和安全性。加用化疗可能进一步增强治疗结局,使其成为相较于CIK细胞联合抗PD-1抗体单药治疗可能更优的策略。
Advanced non-small cell lung cancer (NSCLC) with positive PD-L1 expression requires more effective therapeutic options.
This study aims to evaluate the efficacy and safety of autologous cytokine-induced killer (CIK) cell therapy combined with the anti-PD-1 antibody toripalimab, with or without chemotherapy, as a first-line treatment for advanced NSCLC. This phase II trial enrolled 40 patients with PD-L1-positive, driver mutation-negative advanced NSCLC between July 2020 and December 2022. Patients were randomly assigned to Arm A (toripalimab + CIK cells + chemotherapy) or Arm B (toripalimab + CIK cells). Progression-free survival (PFS), overall survival (OS), overall response rate (ORR), and safety profiles were evaluated. Subgroup analyses were conducted based on the number of CIK cell cycles received.
Arm A showed a significantly longer median PFS compared to Arm B (20. 0 vs. 6. 0 months, p = 0. 0038), while median OS was not reached in Arm A versus 17. 0 months in Arm B (p = 0. 0479). ORR was 47. 4% in Arm A and 60. 0% in Arm B. Patients receiving four or more cycles of CIK cells had significantly improved PFS and OS. No new safety concerns were identified.
The combination of CIK cells and toripalimab, with or without chemotherapy, demonstrates promising efficacy and safety in patients with advanced PD-L1-positive NSCLC. The addition of chemotherapy may further enhance therapeutic outcomes, making it a potentially superior strategy compared to CIK cells combined with the anti-PD-1 antibody alone.
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