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ANG1005,一种脑穿透肽-药物偶联物,在患有脑膜转移和复发性脑转移的乳腺癌患者中显示出活性。

ANG1005, a Brain-Penetrating Peptide-Drug Conjugate, Shows Activity in Patients with Breast Cancer with Leptomeningeal Carcinomatosis and Recurrent Brain Metastases.

机构信息

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

Cancer Center and Research Institute, University of Mississippi Medical Center, Jackson, Mississippi.

出版信息

Clin Cancer Res. 2020 Jun 15;26(12):2789-2799. doi: 10.1158/1078-0432.CCR-19-3258. Epub 2020 Jan 22.

Abstract

PURPOSE

ANG1005, a novel taxane derivative, consists of three paclitaxel molecules covalently linked to Angiopep-2, designed to cross the blood-brain and blood-cerebrospinal barriers and to penetrate malignant cells via LRP1 transport system. Preclinical and clinical evidence of efficacy with ANG1005 has been previously shown.

PATIENTS AND METHODS

A multicenter, open-label phase II study in adult patients with measurable recurrent brain metastases from breast cancer (BCBM), with or without leptomeningeal carcinomatosis was conducted ( = 72 BCBM; = 28 leptomeningeal carcinomatosis subset). ANG1005 was administered intravenously at 600 mg/m every 3 weeks. Tumor assessment was based on central nervous system (CNS) RECIST 1.1 for intracranial, and RECIST 1.1 for extracranial response. The primary endpoint was determination of intracranial objective response rate (iORR).

RESULTS

Median age was 47.5 years. Safety profile was similar to that of paclitaxel with myelosuppression as the predominating toxicity. Average number of prior CNS-directed therapies was 2.8 and 94% of the patients had prior taxane treatment. Patient benefit (stable disease or better) was seen in 77% (intracranial) and 86% (extracranial) of the evaluable patients, with iORR of 15% (investigator) or 8% (independent radiology facility [IRF] review). In the leptomeningeal carcinomatosis subset, 79% of the patients had intracranial disease control and estimated median overall survival of 8.0 months (95% CI, 5.4-9.4).

CONCLUSIONS

Even though the study preset rule for iORR per IRF was not met in this heavily pretreated population, a notable CNS and systemic treatment effect was seen in all patients including symptom improvement and prolonged overall survival compared to historical control for the subset of patients with leptomeningeal carcinomatosis ( = 28).

摘要

目的

ANG1005 是一种新型的紫杉烷衍生物,由三个紫杉醇分子通过化学键与 Angiopep-2 相连,旨在通过 LRP1 转运系统穿过血脑和血脑脊液屏障并穿透恶性细胞。以前已经证明了 ANG1005 的临床前和临床疗效。

患者和方法

对来自乳腺癌(BCBM)的可测量复发性脑转移瘤的成年患者进行了一项多中心、开放标签的 II 期研究,这些患者伴有或不伴有软脑膜癌病(=72 例 BCBM;=28 例软脑膜癌病亚组)。ANG1005 以 600mg/m 的剂量每 3 周静脉给药一次。根据中枢神经系统(CNS)RECIST 1.1 评估颅内肿瘤,根据 RECIST 1.1 评估颅外反应。主要终点是确定颅内客观缓解率(iORR)。

结果

中位年龄为 47.5 岁。安全性与紫杉醇相似,以骨髓抑制为主。平均既往 CNS 定向治疗次数为 2.8 次,94%的患者接受过紫杉醇治疗。77%(颅内)和 86%(颅外)的可评估患者出现疾病稳定或更好的患者获益,颅内客观缓解率为 15%(研究者)或 8%(独立放射学设施[IRF]审查)。在软脑膜癌病亚组中,79%的患者颅内疾病得到控制,估计总生存期中位数为 8.0 个月(95%CI,5.4-9.4)。

结论

即使在这个预处理人群中,IRF 设定的 iORR 规则没有达到,但在所有患者中都观察到了明显的 CNS 和全身治疗效果,包括症状改善和与软脑膜癌病亚组的历史对照相比的延长总生存期(=28)。

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