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奥希替尼每周给药可防止注定归巢至小鼠肺部的EGFR突变肿瘤细胞。

Weekly osimertinib dosing prevents EGFR mutant tumor cells destined to home mouse lungs.

作者信息

Butle Ashwin, Joshi Asim, Noronha Vanita, Prabhash Kumar, Dutt Amit

机构信息

Integrated Cancer Genomics Laboratory, Advanced Centre for Treatment Research Education In Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, Maharashtra, India 410210.

Integrated Cancer Genomics Laboratory, Advanced Centre for Treatment Research Education In Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, Maharashtra, India 410210; Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai, India 400094.

出版信息

Transl Oncol. 2021 Aug;14(8):101111. doi: 10.1016/j.tranon.2021.101111. Epub 2021 May 13.

DOI:10.1016/j.tranon.2021.101111
PMID:33993094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8236545/
Abstract

The recently conducted ADAURA trial concludes daily dosing of adjuvant osimertinib, a third-generation EGFR tyrosine kinase inhibitor (TKI), improves disease-free survival with stage IB/II/IIIA EGFR -mutated non-small cell lung cancer patients in comparison to placebo. We have developed a preclinical orthotopic mouse model, using luciferase tagged lung adenocarcinoma cells harboring EGFR TKI sensitive exon 19 deletion to model and extend trial implications comparing a weekly vs daily dosing outcome of osimertinib to a first-generation TKI- erlotinib. We find that 100% of mice in both the groups receiving osimertinib daily or weekly before injection of cells show a complete absence of homing of cells in mice's lungs from day three until day 18 post-injection of cells. On the other hand, 25% and 75% of mice receiving erlotinib daily and weekly before injecting cells show homing of cells to the lungs. The tumors observed in the lungs, when dissected at day 30, confirmed the colonization of the injected cells homing to the organ. Thus, our study establishes the efficacy of pretreatment with osimertinib in reducing tumor cells' homing to mouse lungs in an in vivo mouse model.

摘要

最近进行的ADAURA试验得出结论,对于IB/II/IIIA期表皮生长因子受体(EGFR)突变的非小细胞肺癌患者,每日服用第三代EGFR酪氨酸激酶抑制剂(TKI)奥希替尼,与服用安慰剂相比,可提高无病生存率。我们利用携带对EGFR TKI敏感的19号外显子缺失的荧光素酶标记的肺腺癌细胞,建立了一种临床前原位小鼠模型,以模拟并扩展试验意义,比较奥希替尼每日和每周给药方案与第一代TKI厄洛替尼的给药结果。我们发现,在注射细胞前每日或每周接受奥希替尼治疗的两组小鼠中,从注射细胞后的第三天到第十八天,100%的小鼠肺部完全没有细胞归巢现象。另一方面,在注射细胞前每日和每周接受厄洛替尼治疗的小鼠中,分别有25%和75%出现细胞归巢至肺部的现象。在第30天解剖时,在肺部观察到的肿瘤证实了注射的细胞在该器官中定植。因此,我们的研究证实了在体内小鼠模型中,用奥希替尼进行预处理在减少肿瘤细胞归巢至小鼠肺部方面的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/3217bf626554/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/0fd6cd276881/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/2051181cf772/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/3217bf626554/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/0fd6cd276881/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/2051181cf772/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d135/8236545/3217bf626554/gr2.jpg

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本文引用的文献

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奥希替尼用于携带低频表皮生长因子受体(EGFR)T790M突变的肺癌细胞。
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