177Lu-SN201 纳米粒子在 4T1 正位模型中显示出优于传统抗癌药物的抗肿瘤疗效。

IF 3 3区 医学 Q2 ONCOLOGY Investigational New Drugs Pub Date : 2024-08-01 Epub Date: 2024-06-05 DOI:10.1007/s10637-024-01450-2
Sujinna Lekmeechai, Kristian Pietras, Oskar Axelsson
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引用次数: 0

摘要

在目前的体内研究中,我们证明了放射性标记纳米粒子 177Lu-SN201 作为一种有效抗癌疗法的潜力,在侵袭性三阴性 4T1 小鼠乳腺癌模型中显著延长了生存期并减少了肿瘤负荷。我们的研究表明,177Lu-SN201 在抑制肿瘤生长方面不仅优于载体,而且优于常用的抗癌药物紫杉醇、尼拉帕利、卡铂,以及抗 PD-1 和抗 CTLA-4 的免疫检查点抑制剂联合疗法。标准药物的剂量是根据在各种小鼠模型中取得良好疗效的文献实例确定的。通过测量血浆样本中的谷氨酸丙酮酸丙氨酸氨基转移酶、丙氨酸氨基转移酶、血尿素氮和肌酐水平,肝肾功能的临床生化指标显示,尽管体重有所下降,但治疗的耐受性相当好。总之,177Lu-SN201 是一种很有前途的癌症治疗候选药物。
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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177Lu-SN201 nanoparticle shows superior anti-tumor efficacy over conventional cancer drugs in 4T1 orthotopic model.

In the current in-vivo study we demonstrate the potential of the radiolabeled nanoparticle 177Lu-SN201 as an effective anticancer treatment, as evidenced by significantly prolonged survival and reduced tumor burden in the aggressive, triple negative 4T1 murine breast cancer model. We show with high statistical significance that 177Lu-SN201 is superior at suppressing the tumor growth not only compared to vehicle but also to the commonly used cancer drugs paclitaxel, niraparib, carboplatin, and the combination of the immune checkpoint inhibitors anti PD-1 and anti-CTLA-4. The dosing of the standard drugs were based on examples in the literature where good effects have been seen in various mouse models. The treatment is reasonably well-tolerated, as indicated by clinical chemistry of liver and renal function through the measurement of glutamate pyruvate alanine aminotransferase, alanine amino transferase, blood urea nitrogen, and creatinine levels in plasma samples, despite some weight loss. Overall, 177Lu-SN201 presents as a promising therapeutic candidate for cancer treatment.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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