{"title":"通过微创植入 3D 打印设备对三阴性乳腺癌进行局部剂量密集化疗","authors":"Noehyun Myung, Hyun-Wook Kang","doi":"10.1016/j.ajps.2024.100884","DOIUrl":null,"url":null,"abstract":"<div><p>Dose-dense chemotherapy is the preferred first-line therapy for triple-negative breast cancer (TNBC), a highly aggressive disease with a poor prognosis. This treatment uses the same drug doses as conventional chemotherapy but with shorter dosing intervals, allowing for promising clinical outcomes with intensive treatment. However, the frequent systemic administration used for this treatment results in systemic toxicity and low patient compliance, limiting therapeutic efficacy and clinical benefit. Here, we report local dose-dense chemotherapy to treat TNBC by implanting 3D printed devices with time-programmed pulsatile release profiles. The implantable device can control the time between drug releases based on its internal microstructure design, which can be used to control dose density. The device is made of biodegradable materials for clinical convenience and designed for minimally invasive implantation via a trocar. Dose density variation of local chemotherapy using programmable release enhances anti-cancer effects <em>in vitro</em> and <em>in vivo</em>. Under the same dose density conditions, device-based chemotherapy shows a higher anti-cancer effect and less toxic response than intratumoral injection. We demonstrate local chemotherapy utilizing the implantable device that simulates the drug dose, number of releases, and treatment duration of the dose-dense AC (doxorubicin and cyclophosphamide) regimen preferred for TNBC treatment. Dose density modulation inhibits tumor growth, metastasis, and the expression of drug resistance-related proteins, including p-glycoprotein and breast cancer resistance protein. To the best of our knowledge, local dose-dense chemotherapy has not been reported, and our strategy can be expected to be utilized as a novel alternative to conventional therapies and improve anti-cancer efficiency.</p></div>","PeriodicalId":8539,"journal":{"name":"Asian Journal of Pharmaceutical Sciences","volume":"19 1","pages":"Article 100884"},"PeriodicalIF":10.7000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1818087624000011/pdfft?md5=7bbad6db8cc2163ee872827bb537c50b&pid=1-s2.0-S1818087624000011-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Local dose-dense chemotherapy for triple-negative breast cancer via minimally invasive implantation of 3D printed devices\",\"authors\":\"Noehyun Myung, Hyun-Wook Kang\",\"doi\":\"10.1016/j.ajps.2024.100884\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Dose-dense chemotherapy is the preferred first-line therapy for triple-negative breast cancer (TNBC), a highly aggressive disease with a poor prognosis. This treatment uses the same drug doses as conventional chemotherapy but with shorter dosing intervals, allowing for promising clinical outcomes with intensive treatment. However, the frequent systemic administration used for this treatment results in systemic toxicity and low patient compliance, limiting therapeutic efficacy and clinical benefit. Here, we report local dose-dense chemotherapy to treat TNBC by implanting 3D printed devices with time-programmed pulsatile release profiles. The implantable device can control the time between drug releases based on its internal microstructure design, which can be used to control dose density. The device is made of biodegradable materials for clinical convenience and designed for minimally invasive implantation via a trocar. Dose density variation of local chemotherapy using programmable release enhances anti-cancer effects <em>in vitro</em> and <em>in vivo</em>. Under the same dose density conditions, device-based chemotherapy shows a higher anti-cancer effect and less toxic response than intratumoral injection. We demonstrate local chemotherapy utilizing the implantable device that simulates the drug dose, number of releases, and treatment duration of the dose-dense AC (doxorubicin and cyclophosphamide) regimen preferred for TNBC treatment. Dose density modulation inhibits tumor growth, metastasis, and the expression of drug resistance-related proteins, including p-glycoprotein and breast cancer resistance protein. 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引用次数: 0
摘要
剂量密集化疗是治疗三阴性乳腺癌(TNBC)的首选一线疗法,TNBC 是一种侵袭性极强、预后极差的疾病。这种疗法使用的药物剂量与传统化疗相同,但给药间隔时间较短,可通过强化治疗取得良好的临床疗效。然而,该疗法频繁的全身给药会导致全身毒性和患者依从性低,从而限制了疗效和临床获益。在此,我们报告了通过植入具有时间编程脉冲释放曲线的 3D 打印装置来治疗 TNBC 的局部剂量密集化疗。这种植入式装置可根据其内部微结构设计控制药物释放的时间间隔,从而控制剂量密度。该装置由生物可降解材料制成,方便临床使用,设计用于通过套管进行微创植入。利用可编程释放技术改变局部化疗的剂量密度可增强体外和体内的抗癌效果。在相同剂量密度条件下,与瘤内注射相比,装置化疗的抗癌效果更高,毒性反应更小。我们展示了利用植入式装置进行局部化疗的效果,该装置模拟了 TNBC 治疗首选的剂量密度 AC(多柔比星和环磷酰胺)方案的药物剂量、释放次数和治疗持续时间。剂量密度调节可抑制肿瘤生长、转移和耐药相关蛋白(包括 p-糖蛋白和乳腺癌耐药蛋白)的表达。据我们所知,目前还没有关于局部剂量密度化疗的报道,我们的策略有望成为传统疗法的一种新的替代疗法,并提高抗癌效率。
Local dose-dense chemotherapy for triple-negative breast cancer via minimally invasive implantation of 3D printed devices
Dose-dense chemotherapy is the preferred first-line therapy for triple-negative breast cancer (TNBC), a highly aggressive disease with a poor prognosis. This treatment uses the same drug doses as conventional chemotherapy but with shorter dosing intervals, allowing for promising clinical outcomes with intensive treatment. However, the frequent systemic administration used for this treatment results in systemic toxicity and low patient compliance, limiting therapeutic efficacy and clinical benefit. Here, we report local dose-dense chemotherapy to treat TNBC by implanting 3D printed devices with time-programmed pulsatile release profiles. The implantable device can control the time between drug releases based on its internal microstructure design, which can be used to control dose density. The device is made of biodegradable materials for clinical convenience and designed for minimally invasive implantation via a trocar. Dose density variation of local chemotherapy using programmable release enhances anti-cancer effects in vitro and in vivo. Under the same dose density conditions, device-based chemotherapy shows a higher anti-cancer effect and less toxic response than intratumoral injection. We demonstrate local chemotherapy utilizing the implantable device that simulates the drug dose, number of releases, and treatment duration of the dose-dense AC (doxorubicin and cyclophosphamide) regimen preferred for TNBC treatment. Dose density modulation inhibits tumor growth, metastasis, and the expression of drug resistance-related proteins, including p-glycoprotein and breast cancer resistance protein. To the best of our knowledge, local dose-dense chemotherapy has not been reported, and our strategy can be expected to be utilized as a novel alternative to conventional therapies and improve anti-cancer efficiency.
期刊介绍:
The Asian Journal of Pharmaceutical Sciences (AJPS) serves as the official journal of the Asian Federation for Pharmaceutical Sciences (AFPS). Recognized by the Science Citation Index Expanded (SCIE), AJPS offers a platform for the reporting of advancements, production methodologies, technologies, initiatives, and the practical application of scientific knowledge in the field of pharmaceutics. The journal covers a wide range of topics including but not limited to controlled drug release systems, drug targeting, physical pharmacy, pharmacodynamics, pharmacokinetics, pharmacogenomics, biopharmaceutics, drug and prodrug design, pharmaceutical analysis, drug stability, quality control, pharmaceutical engineering, and material sciences.