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SH003 草药治疗实体瘤患者的安全性:一项多中心、单臂、开放标签、剂量递增的 I 期研究。

Safety of the Herbal Medicine SH003 in Patients With Solid Cancer: A Multi-Center, Single-Arm, Open-Label, Dose-Escalation Phase I Study.

机构信息

Kyung Hee University, Dongdaemun-gu, Seoul, Republic of Korea.

Ajou University Hospital, Suwon-si, Gyeonggi-do, Republic of Korea.

出版信息

Integr Cancer Ther. 2024 Jan-Dec;23:15347354241293451. doi: 10.1177/15347354241293451.

Abstract

BACKGROUND

SH003, a novel herbal medicine comprising Huang-Qi, Dang-Gui, and Gua-Lou-Gen, has historical roots in traditional medicine with reported anticancer properties. The need to explore safe and effective treatments in oncology underlines the importance of this study.

METHODS

This phase I trial, conducted at Ajou University Hospital and Gachon University Gil Medical Center in Korea, adopted a single-arm, open-label, dose-escalation design. It aimed to evaluate the safety of escalated doses of SH003 in patients with various solid cancers, focusing on determining its maximum tolerated dose. Participants with confirmed solid cancers, unresponsive to standard treatments, were enrolled. The dosage of SH003 was escalated from 4800 to 9600 mg per day, using a 3 + 3 design. Safety was assessed based on the Common Terminology Criteria for Adverse Events ver. 5.0.

RESULTS

The study established that the maximum tolerated dose of SH003 is 9600 mg/day. Most adverse events were mild, primarily including dizziness and nausea, indicating the tolerability of SH003 at this dosage.

CONCLUSIONS

SH003 demonstrates safety and promises as an anticancer treatment at doses up to 9600 mg/day. This research supports further investigation into its efficacy for cancer therapy, emphasizing the significance of natural products in oncology, particularly concerning patient safety and tolerance.

摘要

背景

SH003 是一种由黄芪、当归和瓜蒌根组成的新型草药,在传统医学中有抗癌作用的历史渊源。在肿瘤学中探索安全有效的治疗方法突显了这项研究的重要性。

方法

这项在韩国的亚洲大学医院和加图立大学圣心医疗院进行的 I 期试验采用单臂、开放标签、剂量递增设计。目的是评估各种实体瘤患者中递增剂量 SH003 的安全性,重点确定其最大耐受剂量。纳入标准为经证实患有对标准治疗无反应的实体瘤的患者。SH003 的剂量从每天 4800 毫克递增至 9600 毫克,采用 3+3 设计。根据不良事件常用术语标准 5.0 评估安全性。

结果

本研究确定 SH003 的最大耐受剂量为每天 9600 毫克。大多数不良事件为轻度,主要包括头晕和恶心,表明在该剂量下 SH003 具有可耐受性。

结论

SH003 在高达 9600 毫克/天的剂量下表现出安全性和抗癌治疗的潜力。这项研究支持进一步研究其在癌症治疗中的疗效,强调了天然产物在肿瘤学中的重要性,特别是考虑到患者的安全性和耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/11528795/cabe88707648/10.1177_15347354241293451-fig1.jpg

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