Eftilagimod alpha(可溶性 LAG-3 蛋白)联合 pembrolizumab 作为转移性头颈部鳞状细胞癌患者的二线疗法。

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2024-09-03 DOI:10.1158/1078-0432.CCR-24-0473
Martin Forster, Irene Brana, Antonio L Pousa, Bernard Doger, Patricia Roxburgh, Pawan Bajaj, Julio Peguero, Matthew Krebs, Enric Carcereny, Grisma Patel, Christian Mueller, Chrystelle Brignone, Frederic Triebel
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TACTI-002 (part C) evaluated whether combining efti with pembrolizumab led to strong antitumor responses in patients with second-line recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) while demonstrating good tolerability.</p><p><strong>Patients and methods: </strong>In this multinational phase II trial using Simon's two-stage design, patients who were PD-L(1)-naïve with R/M HNSCC who had failed first-line platinum-based therapy, unselected for PD-L1, received intravenous pembrolizumab (200 mg, once every 2 weeks) combined with subcutaneous efti (30 mg once every 2 weeks for 24 weeks and once every 3 weeks thereafter). The primary endpoint was objective response rate per RECIST 1.1 modified for immune-based therapy by investigator assessment. Additional endpoints included duration of response, progression-free survival, overall survival, and tolerability. Pharmacodynamic effects (absolute lymphocyte count) and Th1 cytokine biomarkers (IFNγ/CXCL10)] were evaluated in liquid biopsies.</p><p><strong>Results: </strong>Between March 2019 and January 2021, 39 patients were enrolled; 37 were evaluated for response. All patients received prior chemotherapy, and 40.5% were pretreated with cetuximab; 53.1% of patients had PD-L1 combined positive score <20. With a median follow-up of 38.8 months, the objective response rate was 29.7%, including 13.5% complete responders. The median duration of response was not reached. Rapid and sustained absolute lymphocyte count increase was observed in patients who had an objective response. Th1 biomarkers increased sustainably after first treatment. 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引用次数: 0

摘要

目的:Eftilagimod alpha(efti)是一种可溶性LAG-3蛋白,可激活抗原递呈细胞(APC)和下游T细胞。TACTI-002(C部分)评估了在二线复发性或转移性头颈部鳞状细胞癌(R/M HNSCC)患者中将efti与pembrolizumab联合使用是否会产生强烈的抗肿瘤反应,同时显示出良好的耐受性:在这项采用西蒙两阶段设计的跨国2期试验中,一线铂类治疗失败的PD-L(1)无效的R/M HNSCC患者未经PD-L1筛选,接受静脉注射pembrolizumab(200毫克,Q3W)联合皮下注射依夫替(30毫克,Q2W,24周,此后Q3W)治疗。主要终点是研究者评估的 iRECIST 客观反应率 (ORR)。其他终点包括反应持续时间(DoR)、无进展生存期(PFS)、总生存期(OS)和耐受性。药效学效应(绝对淋巴细胞计数[ALC]和Th1细胞因子生物标志物[IFN-gamma/CXCL-10])通过液体活检进行评估:2019年3月至2021年1月,39名患者入组;37名患者接受了反应评估。所有患者均接受过化疗,40.5%的患者接受过西妥昔单抗预处理。53.1%的患者有PD-L1 CPS 结论:艾夫替尼联合pembrolizumab治疗二线HNSCC患者是安全的,并显示出令人鼓舞的抗肿瘤活性和药效学效应,因此支持在早期治疗线中进一步评估这种联合疗法。
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Eftilagimod Alpha (Soluble LAG3 Protein) Combined with Pembrolizumab as Second-Line Therapy for Patients with Metastatic Head and Neck Squamous Cell Carcinoma.

Purpose: Eftilagimod alpha (efti), a soluble LAG3 protein, activates antigen-presenting cells (APC) and downstream T cells. TACTI-002 (part C) evaluated whether combining efti with pembrolizumab led to strong antitumor responses in patients with second-line recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) while demonstrating good tolerability.

Patients and methods: In this multinational phase II trial using Simon's two-stage design, patients who were PD-L(1)-naïve with R/M HNSCC who had failed first-line platinum-based therapy, unselected for PD-L1, received intravenous pembrolizumab (200 mg, once every 2 weeks) combined with subcutaneous efti (30 mg once every 2 weeks for 24 weeks and once every 3 weeks thereafter). The primary endpoint was objective response rate per RECIST 1.1 modified for immune-based therapy by investigator assessment. Additional endpoints included duration of response, progression-free survival, overall survival, and tolerability. Pharmacodynamic effects (absolute lymphocyte count) and Th1 cytokine biomarkers (IFNγ/CXCL10)] were evaluated in liquid biopsies.

Results: Between March 2019 and January 2021, 39 patients were enrolled; 37 were evaluated for response. All patients received prior chemotherapy, and 40.5% were pretreated with cetuximab; 53.1% of patients had PD-L1 combined positive score <20. With a median follow-up of 38.8 months, the objective response rate was 29.7%, including 13.5% complete responders. The median duration of response was not reached. Rapid and sustained absolute lymphocyte count increase was observed in patients who had an objective response. Th1 biomarkers increased sustainably after first treatment. No unexpected safety signals were observed.

Conclusions: Efti plus pembrolizumab was safe and showed encouraging antitumor activity and pharmacodynamic effects in patients with second-line head and neck squamous cell carcinoma (HNSCC), thus supporting further evaluation of this combination in earlier treatment lines.

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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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