Cytarabine Nanotherapeutics with Increased Stability and Enhanced Lymphoma Uptake for Tailored Highly Effective Therapy of Mantle Cell Lymphoma

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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Abstract

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.
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
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。
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