研究概要
Cinrebafusp alfa 在既往接受过 HER2 靶向方案后进展的 HER2 阳性恶性肿瘤患者中显示出有前景的活性。其可接受的安全性特征表明,它可能成为对现有 HER2 导向治疗无应答患者的一种治疗选择。参见 Eguren-Santamaría 等人的相关评论,第 231 页。
研究思路结论见上方概要
目的
4-1BB(CD137)是一种表达于活化T细胞、活化B细胞、NK细胞和TIL(肿瘤浸润淋巴细胞)上的共刺激免疫受体,使其成为癌症免疫治疗的一个有前景的靶点。Cinrebafusp alfa是一种靶向HER2和4-1BB的类单克隆抗体双特异性蛋白,旨在将4-1BB激活定位至HER2阳性肿瘤。本研究评估了cinrebafusp alfa在既往接受过治疗的HER2阳性恶性肿瘤患者中的安全性、耐受性和初步疗效。
方法
这是一项多中心剂量递增研究,纳入既往接受过治疗的HER2阳性恶性肿瘤患者。研究评估了cinrebafusp alfa在不同剂量水平下的安全性和疗效。患者被分配至不同队列,并评估抗肿瘤反应。研究旨在确定MTD,并观察不同剂量水平下的临床活性。
结果
在“活性剂量”疗效队列的40例可评估患者中,5例显示出抗肿瘤反应,总体缓解率为12.5%,疾病控制率为52.5%。在8和18 mg/kg剂量水平观察到临床活性,确认的客观缓解率分别为28.6%和25.0%。Cinrebafusp alfa安全且可耐受,≤2级输注相关反应是最常见的治疗相关不良事件。研究期间未达到MTD。
展开英文摘要原文
PURPOSE: 4-1BB (CD137) is a costimulatory immune receptor expressed on activated T cells, activated B cells, NK cells, and tumor-infiltrating lymphocytes, making it a promising target for cancer immunotherapy. Cinrebafusp alfa, a monoclonal antibody-like bispecific protein targeting HER2 and 4-1BB, aims to localize 4-1BB activation to HER2-positive tumors. This study evaluated the safety, tolerability, and preliminary efficacy of cinrebafusp alfa in patients with previously treated HER2-positive malignancies.
PATIENTS AND METHODS: This was a multicenter dose-escalation study involving patients with HER2-positive malignancies who received prior treatment. The study assessed the safety and efficacy of cinrebafusp alfa across various dose levels. Patients were assigned to different cohorts, and antitumor responses were evaluated. The study aimed to determine the MTD and to observe any clinical activity at different dose levels.
RESULTS: Of 40 evaluable patients in the "active dose" efficacy cohorts, five showed an antitumor response, resulting in an overall response rate of 12.5% and a disease-control rate of 52.5%. Clinical activity was observed at the 8 and 18 mg/kg dose levels, with confirmed objective response rates of 28.6% and 25.0%, respectively. Cinrebafusp alfa was safe and tolerable, with grade ≤2 infusion-related reactions being the most frequent treatment-related adverse event. MTD was not reached during the study.
CONCLUSIONS: Cinrebafusp alfa demonstrates promising activity in patients with HER2-positive malignancies who have progressed on prior HER2-targeting regimens. Its acceptable safety profile suggests it could be a treatment option for patients not responding to existing HER2-directed therapies. See related commentary by Eguren-Santamaría et al., p. 231.
论文信息
- 作者
- Piha-Paul S、Olwill SA、Hamilton E、Tolcher A、Pohlmann P、Liu SV、Wurzenberger C、Hasenkamp LC
- 第一作者单位
- Department of Investigational Cancer Therapeutics (A Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.United States
- 通讯作者单位
- Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.United States
- 文献类型
- 多中心研究 · I 期临床试验
- 期刊
- Clinical cancer research : an official journal of the American Association for Cancer Research2025 Jan 17