Interim report on engineered NK cell trial in lung cancer refractory to immune checkpoint inhibitors.

IF 6.1 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL JCI insight Pub Date : 2025-02-04 DOI:10.1172/jci.insight.186890
Miguel A Villalona-Calero, Lei Tian, Xiaochen Li, Joycelynne M Palmer, Claudia Aceves, Hans Meisen, Catherine Cortez, Timothy W Synold, Colt Egelston, Jeffrey VanDeusen, Ivone Bruno, Lei Zhang, Eliezer Romeu-Bonilla, Omer Butt, Stephen J Forman, Michael A Caligiuri, Jianhua Yu
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Abstract

Background: Non-small cell lung cancer (NSCLC) remains the leading cause of cancer-related mortality, necessitating the exploration of alternate therapeutic approaches. Tumor-reactive or activated-by-cytokine killers (TRACK) are PD-L1+, highly cytolytic NK cells derived from umbilical cord blood NK cells and engineered to express soluble IL-15 (sIL15), and these cells show promise in preclinical studies against NSCLC.

Methods: We assessed safety, persistence, homing, and cytotoxic activity in 6 patients with advanced, refractory, and progressing NSCLC who received a low dose of unmatched, allogeneic, off-the-shelf sIL15_TRACK NK cells. We evaluated NK cell presence and persistence with droplet digital PCR (ddPCR), flow cytometry, and immunofluorescence staining.

Results: sIL15_TRACK NK cells had peak measurements at 1 hour and became undetectable 4 hours after each infusion. Cognate ligands to activating NK cell receptors were found in NSCLC. sIL15_TRACK NK cells were observed in a lung tumor biopsy 7 days after the final infusion, confirming their sustainment and tumor-homing ability. They retained cytolytic function following isolation from the lung tumor. Three of 6 patients achieved disease stabilization on repeat imaging, while the others progressed.

Conclusion: Unmatched, allogeneic, cryopreserved, off-the-shelf sIL15_TRACK NK cells express activating receptors, home to tumor sites that express their cognate ligands, and retain cytolytic activity after infusion, underscoring their potential as a therapeutic approach in solid tumors. At low doses, the therapy was safely administered and showed preliminary evidence of activity in 3 of 6 patients with advanced and progressive NSCLC. Additional dose escalation cohorts and coadministration with atezolizumab are planned.

Trial registration:

Clinicaltrials: gov NCT05334329.

Funding: Funding was provided by CytoImmune Therapeutics and grants from the National Cancer Institute (CA266457, CA033572, and CA210087).

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对免疫检查点抑制剂难治的肺癌的工程NK细胞的首次人体试验。
背景:非小细胞肺癌(NSCLC)仍然是癌症相关死亡的主要原因,需要探索替代治疗方法。肿瘤反应性或细胞因子激活型杀伤细胞(TRACK)是PD-L1+高细胞溶解性自然杀伤细胞(NK),来源于脐带血NK细胞,经过改造表达可溶性il - 15 (sIL15),在非小细胞肺癌的临床前研究中显示出前景。方法:我们评估了6例晚期、难治性和进展性NSCLC患者的安全性、持久性、归家和细胞毒性活性,这些患者接受了低剂量的不匹配的、同种异体的、现成的sIL15_TRACK NK细胞。我们用液滴数字(dd) PCR、流式细胞术和免疫荧光染色来评估NK细胞的存在和持久性。结果:sIL15_TRACK NK细胞在1小时达到峰值,在每次融合后4小时无法检测到。在非小细胞肺癌中发现了活化NK细胞受体的同源配体。最后一次输注7天后,在肺肿瘤活检中观察到sIL15_TRACK NK细胞,证实了它们的维持和肿瘤归巢能力。从肺肿瘤分离后,它们保留了细胞溶解功能。6名患者中有3名在重复成像中达到疾病稳定,而其他患者则进展。结论:不匹配的,异体的,冷冻保存的,现成的sIL15_TRACK NK细胞表达激活受体,肿瘤位点表达同源配体,并在输注后保持细胞溶解活性,强调了它们作为实体肿瘤治疗方法的潜力。在低剂量下,治疗是安全的,并且在6例晚期和进展性NSCLC患者中有3例显示出初步的活性证据。计划增加剂量递增队列并与atezolizumab共同给药。试验注册:Clinicaltrials: gov nct05334329资金由CytoImmune Therapeutics提供;CA266457;CA033572;CA210087。
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来源期刊
JCI insight
JCI insight Medicine-General Medicine
CiteScore
13.70
自引率
1.20%
发文量
543
审稿时长
6 weeks
期刊介绍: JCI Insight is a Gold Open Access journal with a 2022 Impact Factor of 8.0. It publishes high-quality studies in various biomedical specialties, such as autoimmunity, gastroenterology, immunology, metabolism, nephrology, neuroscience, oncology, pulmonology, and vascular biology. The journal focuses on clinically relevant basic and translational research that contributes to the understanding of disease biology and treatment. JCI Insight is self-published by the American Society for Clinical Investigation (ASCI), a nonprofit honor organization of physician-scientists founded in 1908, and it helps fulfill the ASCI's mission to advance medical science through the publication of clinically relevant research reports.
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