Division of Solid Tumor Oncology, Department of Medicine, Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Clinical Research Division, Department of Medicine, Fred Hutchinson Cancer Center, Seattle, Washington.
Cancer Discov. 2024 Aug 2;14(8):1389-1402. doi: 10.1158/2159-8290.CD-23-1334.
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.
在这项 2 期多中心研究中,我们评估了 lifileucel(LN-145),一种自体肿瘤浸润淋巴细胞细胞疗法,在先前接受过免疫治疗且最近的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。先前系统治疗的中位数为 2(范围,1-6)。使用来自不同解剖部位的肿瘤组织成功制造了 lifileucel,主要是肺。客观缓解率为 21.4%(28 例中有 6 例)。在免疫治疗通常耐药的肿瘤中发生了反应,例如 PD-L1 阴性、低肿瘤突变负担和 STK11 突变。数据截止时,有 2 个缓解仍在持续,包括 PD-L1 阴性肿瘤中的一个完全代谢缓解。不良事件通常如预期的那样且可管理。两名患者因治疗出现的不良事件死亡:心力衰竭和多器官衰竭。Lifileucel 是先前治疗难治性 mNSCLC 患者的潜在治疗选择。意义:自体肿瘤浸润淋巴细胞疗法 lifileucel 被施用于 28 名先前接受过大量治疗的转移性非小细胞肺癌(mNSCLC)患者。在有驱动突变的患者中观察到了反应,并且有各种肿瘤突变负担和 PD-L1 表达,这可能满足了先前治疗难治性 mNSCLC 患者的未满足的医疗需求。见相关评论 Lotze 等人,第 1366 页。