γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:Lifileucel, an Autologous Tumor-Infiltrating Lymphocyte Monotherapy, in Patients with Advanced Non-Small Cell Lung Cancer Resistant to Immune Checkpoint Inhibitors.
客观缓解率为21.4%(6/28)。
在这项2期多中心研究中,我们评估了lifileucel(LN-145)——一种自体TIL(肿瘤浸润淋巴细胞)细胞疗法——在既往接受过免疫治疗且最近一次治疗进展的转移性非小细胞肺癌(mNSCLC)患者中的疗效和安全性。既往全身治疗的中位数为2线(范围,1-6)。Lifileucel使用来自不同解剖部位(主要为肺)的肿瘤组织成功制备。客观缓解率为21.4%(6/28)。缓解出现在通常对免疫治疗耐药的肿瘤特征中,如PD-L1阴性、低肿瘤突变负荷和STK11突变。截至数据截止时,有两例缓解仍在持续,包括一例PD-L1阴性肿瘤中的完全代谢缓解。不良事件总体符合预期且可管理。两例患者死于治疗中出现的不良事件:心力衰竭和多器官衰竭。Lifileucel是既往治疗难治的mNSCLC患者的一种潜在治疗选择。意义:自体TIL(肿瘤浸润淋巴细胞)疗法lifileucel被用于28例经重度预治疗的转移性非小细胞肺癌(mNSCLC)患者。在具有驱动突变以及不同肿瘤突变负荷和PD-L1表达的患者中观察到了缓解,可能满足既往治疗难治的mNSCLC患者中未被满足的医疗需求。参见Lotze等人的相关评论,第1366页。
In this phase 2 multicenter study, we evaluated the efficacy and safety of lifileucel (LN-145), an autologous tumor-infiltrating lymphocyte cell therapy, in patients with metastatic non-small cell lung cancer (mNSCLC) who had received prior immunotherapy and progressed on their most recent therapy. The median number of prior systemic therapies was 2 (range, 1-6). Lifileucel was successfully manufactured using tumor tissue from different anatomic sites, predominantly lung. The objective response rate was 21.4% (6/28). Responses occurred in tumors with profiles typically resistant to immunotherapy, such as PD-L1-negative, low tumor mutational burden, and STK11 mutation. Two responses were ongoing at the time of data cutoff, including one complete metabolic response in a PD-L1-negative tumor. Adverse events were generally as expected and manageable. Two patients died of treatment-emergent adverse events: cardiac failure and multiple organ failure. Lifileucel is a potential treatment option for patients with mNSCLC refractory to prior therapy. Significance: Autologous tumor-infiltrating lymphocyte therapy lifileucel was administered to 28 patients with heavily pretreated metastatic non-small cell lung cancer (mNSCLC). Responses were observed in patients with driver mutations, and various tumor mutational burdens and PD-L1 expression, potentially addressing an unmet medical need in patients with mNSCLC refractory to prior therapy. See related commentary by Lotze et al., p. 1366.
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