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依维莫司α(可溶性 LAG3 蛋白)联合帕博利珠单抗作为转移性头颈部鳞状细胞癌二线治疗药物。

Eftilagimod Alpha (Soluble LAG3 Protein) Combined with Pembrolizumab as Second-Line Therapy for Patients with Metastatic Head and Neck Squamous Cell Carcinoma.

机构信息

UCL Cancer Institute/University College London Hospitals NHS Foundation, London, United Kingdom.

Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, Barcelona, Spain.

出版信息

Clin Cancer Res. 2024 Sep 3;30(17):3726-3734. doi: 10.1158/1078-0432.CCR-24-0473.

Abstract

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.

摘要

目的

eftilagimod alpha(efti)是一种可溶性 LAG3 蛋白,可激活抗原呈递细胞(APC)和下游 T 细胞。TACTI-002(第 C 部分)评估了在二线复发或转移性头颈部鳞状细胞癌(R/M HNSCC)患者中,efti 联合 pembrolizumab 是否能导致强烈的抗肿瘤反应,同时表现出良好的耐受性。

方法

这是一项多中心的 II 期试验,采用西蒙两阶段设计,入组的患者为 PD-L(1)-初治的 R/M HNSCC 患者,在铂类治疗失败后,未选择 PD-L1,接受静脉注射 pembrolizumab(200mg,每 2 周一次)联合皮下 efti(30mg,每 2 周一次,共 24 周,此后每 3 周一次)。主要终点是研究者评估的基于免疫疗法的 RECIST 1.1 改良的客观缓解率。其他终点包括缓解持续时间、无进展生存期、总生存期和耐受性。在液体活检中评估了药效学效应(绝对淋巴细胞计数)和 Th1 细胞因子生物标志物(IFNγ/CXCL10)。

结果

在 2019 年 3 月至 2021 年 1 月期间,共纳入 39 例患者,37 例患者可评估疗效。所有患者均接受过化疗,40.5%的患者曾接受过西妥昔单抗治疗,53.1%的患者 PD-L1 联合阳性评分<20。中位随访 38.8 个月时,客观缓解率为 29.7%,包括 13.5%的完全缓解者。缓解持续时间未达到。在有客观缓解的患者中,观察到快速和持续的绝对淋巴细胞计数增加。首次治疗后,Th1 生物标志物持续增加。未观察到意外的安全性信号。

结论

efti 联合 pembrolizumab 安全,并在二线头颈部鳞状细胞癌(HNSCC)患者中显示出令人鼓舞的抗肿瘤活性和药效学效应,因此支持在更早期的治疗线中进一步评估该联合用药。

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