Results From First-in-Human Phase I Dose-Escalation Study of a Novel Bicycle Toxin Conjugate Targeting EphA2 (BT5528) in Patients With Advanced Solid Tumors.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-09-04 DOI:10.1200/JCO.23.01107
Babar Bashir, Judy S Wang, Gerald Falchook, Elisa Fontana, Hendrik-Tobias Arkenau, Louise Carter, Rachel Galot, Bristi Basu, Alastair Greystoke, Vivek Subbiah, Debra L Richardson, Hanna Orr, Gavin Bennett, Rajiv Sharma, Hongmei Xu, Paola Paganoni, Cong Xu, Carly Campbell, Meredith McKean
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Abstract

Purpose: BT5528 is a Bicycle Toxin Conjugate, a novel class of chemically synthesized molecules, comprising a bicyclic peptide targeting EphA2 tumor antigen, linked to a cytotoxin (monomethyl auristatin E [MMAE]). EphA2 is overexpressed in many solid tumors and contributes to oncogenesis, tumor-associated angiogenesis, and metastasis.

Materials and methods: The primary objectives were to investigate the safety and tolerability of BT5528 and to define the maximum-tolerated dose, if observed, and recommended phase II dose (RP2D)/expansion dose. Dose escalation exploring once every week or once every 2 weeks administration of BT5528 employed a 3 + 3 dose-escalation design for the first two dose levels, followed by a Bayesian logistic regression model. Secondary and exploratory end points included preliminary efficacy and the pharmacokinetics of BT5528 and MMAE.

Results: Forty-five patients were enrolled and received BT5528 doses between 2.2 mg/m2 once every week to 10.0 mg/m2 once every 2 weeks within the dose-escalation stage of the study. The most frequent BT5528-related adverse events (AEs) were nausea (44.4%), diarrhea (35.6%), and fatigue (33.3%), and the most common grade ≥3 BT5528-related AE was neutropenia/neutrophil count decrease (22.2%). Dose level 6.5 mg/m2 once every 2 weeks was selected as a RP2D. At 6.5 mg/m2 once every 2 weeks, the overall response rate was 6.7%, and the disease control rate was 20.0%. BT5528 and MMAE pharmacokinetics are generally dose proportional. BT5528 has a short half-life (0.4-0.7 hours), and the half-life of MMAE is longer (35-47 hours).

Conclusion: BT5528 was well tolerated and demonstrated favorable and preliminary antitumor activity. We believe these data provide preliminary validation of a Bicycle Toxin Conjugate approach to EphA2 tumor antigen. The study is ongoing and is evaluating BT5528 as monotherapy at a RP2D of 6.5 mg/m2 once every 2 weeks.

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靶向 EphA2 的新型自行车毒素共轭物 (BT5528) 在晚期实体瘤患者中的首次人体 I 期剂量放大研究结果。
目的:BT5528 是一种自行车毒素共轭物,它是一类化学合成的新型分子,由靶向 EphA2 肿瘤抗原的双环肽与细胞毒素(单甲基乌司他丁 E [MMAE])连接而成。EphA2 在许多实体瘤中过度表达,有助于肿瘤发生、肿瘤相关血管生成和转移:主要目的是研究BT5528的安全性和耐受性,并确定最大耐受剂量(如果观察到)和II期推荐剂量(RP2D)/扩大剂量。剂量升级探索每周一次或每两周一次服用BT5528,前两个剂量水平采用3 + 3剂量升级设计,然后采用贝叶斯逻辑回归模型。次要和探索性终点包括初步疗效以及 BT5528 和 MMAE 的药代动力学:45名患者入组,在研究的剂量递增阶段,他们接受的BT5528剂量从每周一次的2.2 mg/m2到每两周一次的10.0 mg/m2不等。最常见的BT5528相关不良事件(AEs)是恶心(44.4%)、腹泻(35.6%)和疲劳(33.3%),最常见的≥3级BT5528相关AE是中性粒细胞减少/中性粒细胞计数减少(22.2%)。剂量水平为 6.5 mg/m2,每 2 周一次,被选为 RP2D。6.5毫克/平方米、每两周一次的剂量水平下,总反应率为6.7%,疾病控制率为20.0%。BT5528 和 MMAE 的药代动力学一般与剂量成正比。BT5528的半衰期较短(0.4-0.7小时),而MMAE的半衰期较长(35-47小时):BT5528的耐受性良好,并显示出良好的初步抗肿瘤活性。我们相信,这些数据初步验证了针对 EphA2 肿瘤抗原的 "自行车毒素共轭物 "方法。这项研究正在进行中,目前正在评估 BT5528 作为单药治疗的效果,RP2D 为 6.5 mg/m2,每 2 周一次。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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