Chunhoo Cheon, Hyun Woo Lee, Sun Jin Sym, Seong-Gyu Ko
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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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":13734,"journal":{"name":"Integrative Cancer Therapies","volume":"23 ","pages":"15347354241293451"},"PeriodicalIF":2.9000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528795/pdf/","citationCount":"0","resultStr":"{\"title\":\"Safety of the Herbal Medicine SH003 in Patients With Solid Cancer: A Multi-Center, Single-Arm, Open-Label, Dose-Escalation Phase I Study.\",\"authors\":\"Chunhoo Cheon, Hyun Woo Lee, Sun Jin Sym, Seong-Gyu Ko\",\"doi\":\"10.1177/15347354241293451\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>SH003, a novel herbal medicine comprising Huang-Qi, Dang-Gui, and Gua-Lou-Gen, has historical roots in traditional medicine with reported anticancer properties. 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引用次数: 0
摘要
背景:SH003是一种由黄芪、当归和瓜蒌根组成的新型中药,在传统医学中具有抗癌的历史渊源。探索安全有效的肿瘤治疗方法的必要性凸显了这项研究的重要性:本 I 期试验在韩国安州大学医院和嘉泉大学吉医疗中心进行,采用单臂、开放标签、剂量递增设计。试验旨在评估SH003在各种实体瘤患者中递增剂量的安全性,重点是确定其最大耐受剂量。研究人员招募了对标准治疗无效的确诊实体瘤患者。采用3+3设计,SH003的剂量从每天4800毫克递增到9600毫克。安全性根据《不良事件通用术语标准》第 5.0 版进行评估。结果:研究确定SH003的最大耐受剂量为9600毫克/天。大多数不良反应都很轻微,主要包括头晕和恶心,这表明SH003在这个剂量下是可以耐受的:结论:SH003作为一种抗癌治疗药物,在最高剂量为9600毫克/天时具有安全性和前景。这项研究支持进一步研究其在癌症治疗中的疗效,强调了天然产品在肿瘤学中的重要性,尤其是在患者的安全性和耐受性方面。
Safety of the Herbal Medicine SH003 in Patients With Solid Cancer: A Multi-Center, Single-Arm, Open-Label, Dose-Escalation Phase I Study.
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.
期刊介绍:
ICT is the first journal to spearhead and focus on a new and growing movement in cancer treatment. The journal emphasizes scientific understanding of alternative medicine and traditional medicine therapies, and their responsible integration with conventional health care. Integrative care includes therapeutic interventions in diet, lifestyle, exercise, stress care, and nutritional supplements, as well as experimental vaccines, chrono-chemotherapy, and other advanced treatments. Contributors are leading oncologists, researchers, nurses, and health-care professionals.