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TRK-950(一种针对CAPRIN-1的IgG1抗体)在晚期实体瘤患者中的I期首次人体研究。

Phase I First-in-Human Study of TRK-950, an IgG1 Antibody Specific to CAPRIN-1, in Patients with Advanced Solid Tumors.

作者信息

Cassier Philippe A, Borad Mitesh J, Sharma Sunil, Dubois Bertrand, Caux Christophe, Okano Fumiyoshi, Von Hoff Daniel D, Blay Jean-Yves

机构信息

Department of Medical Oncology, Centre Léon Bérard & Centre de Recherche en Cancérologie de Lyon (CRCL), Lyon, France.

Department of Hematology-Oncology, Mayo Clinic Arizona, Mayo Clinic Comprehensive Cancer Center, Phoenix, Arizona.

出版信息

Cancer Res Commun. 2025 Jul 1;5(7):1119-1128. doi: 10.1158/2767-9764.CRC-25-0123.

Abstract

PURPOSE

TRK-950 is a first-in-class humanized antibody targeting cytoplasmic activation/proliferation-associated protein-1, which is strongly expressed on the cell membrane surface in or on most solid tumors but not in or on normal tissues. This first-in-human study investigated the safety profile, pharmacokinetics (PK), and preliminary antitumor activity.

PATIENTS AND METHODS

Patients with treatment-refractory, locally advanced, or metastatic solid tumors were enrolled in a dose escalation/expansion study. TRK-950 was administered intravenously weekly for 3 weeks in a 28-day cycle, with doses ranging from 3 to 30 mg/kg. Dose expansion included 10 mg/kg weekly and 30 mg/kg biweekly for colorectal cancer and 10 mg/kg weekly for cholangiocarcinoma. The primary objective of this study was to determine its safety, tolerability, and maximum tolerated dose. The secondary objectives were PK, preliminary antitumor activity, and identification of potential biomarkers.

RESULTS

Thirty-six patients received at least one dose of TRK-950. In the dose escalation cohort, the maximum tolerated dose was not reached, and no dose-limiting toxicities were observed up to 30 mg/kg. Common adverse events included abdominal pain, fatigue, constipation, back pain, nausea, and decreased appetite. TRK-950 exhibited a PK profile similar to that of other IgG subclass 1 therapeutic antibodies, with linear PK parameters over the 3 to 30 mg/kg dose range. The best response was stable disease. Notably, one patient with cholangiocarcinoma showed signs of cavitation after approximately 8 months, suggesting potential antitumor activity.

CONCLUSIONS

TRK-950 is safe and well tolerated, has a favorable PK profile, and should be further investigated as a monotherapy and in combination with standard treatment for various types of solid tumors.

SIGNIFICANCE

TRK-950, a humanized antibody targeting CAPRIN-1, demonstrated good tolerability, no dose-limiting toxicities, a favorable PK profile, and potential antitumor activity in this first-in-human study. Currently, TRK-950 is undergoing Phase Ib and II trials for various cancers, showing promising development potential.

摘要

目的

TRK - 950是一种靶向细胞质激活/增殖相关蛋白-1的首创人源化抗体,该蛋白在大多数实体瘤的细胞膜表面或内部强烈表达,但在正常组织中不表达。这项首次人体研究调查了其安全性、药代动力学(PK)和初步抗肿瘤活性。

患者与方法

治疗难治性、局部晚期或转移性实体瘤患者参加了剂量递增/扩展研究。TRK - 950在28天周期内每周静脉注射1次,共3周,剂量范围为3至30mg/kg。剂量扩展包括结直肠癌每周10mg/kg和每两周30mg/kg,胆管癌每周10mg/kg。本研究的主要目的是确定其安全性、耐受性和最大耐受剂量。次要目的是药代动力学、初步抗肿瘤活性以及识别潜在生物标志物。

结果

36例患者接受了至少一剂TRK - 950。在剂量递增队列中,未达到最大耐受剂量,在30mg/kg时未观察到剂量限制性毒性。常见不良事件包括腹痛、疲劳、便秘、背痛、恶心和食欲下降。TRK - 950的药代动力学特征与其他IgG1亚类治疗性抗体相似,在3至30mg/kg剂量范围内药代动力学参数呈线性。最佳反应为病情稳定。值得注意的是,1例胆管癌患者在大约8个月后出现空洞形成迹象,提示有潜在抗肿瘤活性。

结论

TRK - 950安全且耐受性良好,具有良好的药代动力学特征,应作为单一疗法以及与标准治疗联合用于各类实体瘤的进一步研究。

意义

TRK - 950,一种靶向CAPRIN - 1的人源化抗体,在这项首次人体研究中显示出良好的耐受性、无剂量限制性毒性、良好的药代动力学特征和潜在抗肿瘤活性。目前,TRK - 950正在针对多种癌症进行Ib期和II期试验,显示出有前景的发展潜力。

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