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 Nivolumab Monotherapy in Patients with High PD-1-Positive CD8/Treg Ratio in Advanced NSCLC and Gastric Cancer: A Phase II, Multicenter Study.
Efficacy and Safety of Nivolumab Monotherapy in Patients with High PD-1-Positive CD8/Treg Ratio in Advanced NSCLC and Gastric Cancer: A Phase II, Multicenter Study.
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尽管 TIL 生物标志物的低阳性率限制了结果解读,但令人鼓舞的 ORR 提示 TIL 生物标志物对纳武利尤单抗单药治疗具有预测性。
如何筛选适合接受抗PD-1/PD-L1单药治疗的患者仍具挑战。为预测这类治疗的疗效,本开放标签II期研究(ONO-4538-88)评估TIL(肿瘤浸润淋巴细胞)生物标志物的潜力,即细胞毒性T细胞与调节性T细胞之间的平衡。
2021年3月至2022年1月筛查晚期非小细胞肺癌(NSCLC)或胃癌患者。符合预设TIL生物标志物标准的患者接受纳武利尤单抗单药治疗。主要终点为客观缓解率(ORR),次要终点包括总生存期和无进展生存期。研究还探索性分析常规生物标志物(肿瘤比例评分、综合阳性评分、肿瘤突变负荷和微卫星不稳定性),并评估安全性。
37例NSCLC和127例胃癌患者符合TIL分析条件,分别有6例(16.2%)和15例(11.8%)符合TIL标志物标准,其中部分患者接受评估。NSCLC和胃癌患者的ORR分别为80%(5例中4例)和36.4%(11例中4例);分别有5例及11例中的5例肿瘤缩小。两组总生存期中位数均未达到(胃癌组25个月);无进展生存期中位数分别未达到和5.59个月。总体19例患者中13例发生治疗相关不良事件:NSCLC患者6例中5例,胃癌患者13例中8例。
TIL标志物阳性率较低,限制了结果解读;但令人鼓舞的ORR提示该标志物可能具有预测纳武利尤单抗单药疗效的能力。
本II期研究评估了TIL标志物预测纳武利尤单抗单药疗效的价值。尽管标志物阳性患者有限,其疗效和安全性表现较好,提示该标志物具有潜在应用价值。
It is challenging to identify the appropriate patients who benefit from anti-PD-1/PD-L1 monotherapy. For predicting effectiveness of anti-PD-1/PD-L1 monotherapy, this open-label phase II study (ONO-4538-88) evaluated the potential of the tumor-infiltrating lymphocyte (TIL) biomarker: the balance between cytotoxic T cells and regulatory T cells.
Patients with advanced non-small cell lung cancer (NSCLC) or gastric cancer were screened between March 2021 and January 2022. Eligible patients who met the prespecified TIL biomarker criteria received nivolumab monotherapy. The primary endpoint was objective response rate (ORR). The secondary endpoints included overall survival and progression-free survival. Conventional biomarkers (tumor proportion score, combined positive score, tumor mutation burden, and microsatellite instability) were exploratorily analyzed, and safety was also assessed.
Thirty-seven patients with NSCLC and 127 patients with gastric cancer were eligible for TIL analysis: 6 (16.2%) and 15 patients (11.8%) met the TIL biomarker criteria, respectively; a part of them were assessed. For NSCLC and gastric cancer, the ORR was 80% (4/5 patients) and 36.4% (4/11 patients), respectively; all the five patients and 5/11 patients had a reduction in tumor size, respectively; the median overall survival was not reached and 25 months, respectively; and the median progression-free survival was not reached and 5.59 months, respectively. Treatment-related adverse events occurred in 13/19 patients overall: 5/6 patients for NSCLC and 8/13 patients for gastric cancer.
Although the low positive rate of the TIL biomarker limits interpretation, the promising ORRs suggest signs of the TIL biomarker's predictability for nivolumab monotherapy. SIGNIFICANCE: In this phase II study, we examined the predictive utility of the TIL biomarker for nivolumab monotherapy. Although the positivity of the TIL biomarker was limited, the promising efficacy and safety profile in the TIL biomarker-positive patients may suggest the potential utility of the TIL biomarker.
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