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在有和没有支持性护理的情况下,对小鼠进行最大耐受剂量的细胞毒性化疗的系统研究。

A systematic investigation of the maximum tolerated dose of cytotoxic chemotherapy with and without supportive care in mice.

机构信息

National Centre for Asbestos Related Diseases, University of Western Australia, 5th Floor, QQ Block, 6 Verdun Street, Nedlands, WA, 6009, Australia.

Faculty of Health and Medical Science, The University of Western Australia, 35 Stirling Highway, Crawley, WA, 6009, Australia.

出版信息

BMC Cancer. 2017 Oct 16;17(1):684. doi: 10.1186/s12885-017-3677-7.

Abstract

BACKGROUND

Cytotoxic chemotherapeutics form the cornerstone of systemic treatment of many cancers. Patients are dosed at maximum tolerated dose (MTD), which is carefully determined in phase I studies. In contrast, in murine studies, dosages are often based on customary practice or small pilot studies, which often are not well documented. Consequently, research groups need to replicate experiments, resulting in an excess use of animals and highly variable dosages across the literature. In addition, while patients often receive supportive treatments in order to allow dose escalation, mice do not. These issues could affect experimental results and hence clinical translation.

METHODS

To address this, we determined the single-dose MTD in BALB/c and C57BL/6 mice for a range of chemotherapeutics covering the canonical classes, with clinical score and weight as endpoints.

RESULTS

We found that there was some variation in MTDs between strains and the tolerability of repeated cycles of chemotherapy at MTD was drug-dependent. We also demonstrate that dexamethasone reduces chemotherapy-induced weight loss in mice.

CONCLUSION

These data form a resource for future studies using chemotherapy in mice, increasing comparability between studies, reducing the number of mice needed for dose optimisation experiments and potentially improving translation to the clinic.

摘要

背景

细胞毒性化疗药物是许多癌症系统治疗的基石。患者以最大耐受剂量(MTD)给药,这在 I 期研究中被仔细确定。相比之下,在小鼠研究中,剂量通常基于常规实践或小型试点研究,这些研究往往记录不完整。因此,研究小组需要复制实验,导致动物过度使用和文献中剂量高度可变。此外,尽管患者经常接受支持性治疗以允许剂量递增,但小鼠没有。这些问题可能会影响实验结果,从而影响临床转化。

方法

为了解决这个问题,我们以临床评分和体重为终点,确定了一系列涵盖经典类别的化疗药物在 BALB/c 和 C57BL/6 小鼠中的单次剂量 MTD。

结果

我们发现,不同品系之间的 MTD 存在一些差异,并且在 MTD 下重复化疗周期的耐受性是药物依赖性的。我们还证明地塞米松可减少小鼠化疗引起的体重减轻。

结论

这些数据为未来在小鼠中使用化疗药物的研究提供了资源,增加了研究之间的可比性,减少了剂量优化实验所需的小鼠数量,并有可能提高向临床的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea05/5644108/2c6389a16ba4/12885_2017_3677_Fig1_HTML.jpg

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