阿糖胞苷纳米治疗剂增加稳定性和增强淋巴瘤摄取,用于套细胞淋巴瘤的定制高效治疗

R. Pola, E. Pokorná, P. Vockova, E. Böhmová, M. Pechar, J. Karolová, J. Pankrác, L. Šefc, M. Trněný, T. Etrych, P. Klener
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引用次数: 0

摘要

套细胞淋巴瘤(MCL)是一种罕见的b细胞非霍奇金淋巴瘤(B-NHL)亚型,临床病程慢性复发。阿糖胞苷(araC)在诱导和挽救方案的实施成为大多数MCL患者的标准护理。在这项研究中,设计、合成了含有共价结合araC (araC共聚物)的N-(2-羟丙基)甲基丙烯酰胺(HPMA)基聚合物纳米治疗药物,并使用来自新诊断和复发/难治性(R/R) MCL的6例患者源性淋巴瘤异种移植(PDX)进行了体内抗淋巴瘤疗效评估。游离araC可暂时抑制MCL肿瘤的生长,而araC共聚物可诱导移植物淋巴瘤的长期消失,即使在高剂量araC治疗后复发的患者的PDX模型中也没有观察到毒性。该结果为在MCL患者的诱导、挽救或姑息治疗中使用基于hpma的araC共聚物提供了良好的临床前理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytarabine Nanotherapeutics with Increased Stability and Enhanced Lymphoma Uptake for Tailored Highly Effective Therapy of Mantle Cell Lymphoma
Mantle cell lymphoma (MCL) is a rare subtype of B-cell non-Hodgkin lymphoma (B-NHL) with chronically relapsing clinical course. Implementation of cytarabine (araC) into induction and salvage regimen became standard of care for majority of MCL patients. In this study, tailored N-(2-hydroxypropyl)methacrylamide (HPMA)-based polymer nanotherapeutics containing covalently bound araC (araC co-polymers) were designed, synthesized and evaluated for their anti-lymphoma efficacy in vivo using a panel of six patient-derived lymphoma xenografts (PDX) derived from newly diagnosed and relapsed / refractory (R/R) MCL. While free araC led to temporary inhibition of growth of MCL tumors, araC co-polymers induced long-term disappearance of the engrafted lymphomas with no observed toxicity even in the case of PDX models derived from patients, who relapsed after high-dose araC-based treatments. The results provide sound preclinical rationale for the use of HPMA-based araC co-polymers in induction, salvage or palliative therapy of MCL patients.
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