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量化曲妥珠单抗与放射治疗联合应用对人表皮生长因子受体2阳性乳腺癌的影响

Quantifying the Effects of Combination Trastuzumab and Radiation Therapy in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer.

作者信息

Bloom Meghan J, Song Patrick N, Virostko John, Yankeelov Thomas E, Sorace Anna G

机构信息

Department of Biomedical Engineering, The University of Texas, Austin, TX 78712, USA.

Department of Radiology, The University of Alabama, Birmingham, AL 35294, USA.

出版信息

Cancers (Basel). 2022 Aug 31;14(17):4234. doi: 10.3390/cancers14174234.

Abstract

Background: Trastuzumab induces cell cycle arrest in HER2-overexpressing cells and demonstrates potential in radiosensitizing cancer cells. The purpose of this study is to quantify combination trastuzumab and radiotherapy to determine their synergy. Methods: In vitro, HER2+ cancer cells were treated with trastuzumab, radiation, or their combination, and imaged to evaluate treatment kinetics. In vivo, HER2+ tumor-bearing mice were treated with trastuzumab and radiation, and assessed longitudinally. An additional cohort was treated and sacrificed to quantify CD45, CD31, α-SMA, and hypoxia. Results: The interaction index revealed the additive effects of trastuzumab and radiation in vitro in HER2+ cell lines. Furthermore, the results revealed significant differences in tumor response when treated with radiation (p < 0.001); however, no difference was seen in the combination groups when trastuzumab was added to radiotherapy (p = 0.56). Histology revealed increases in CD45 staining in tumors receiving trastuzumab (p < 0.05), indicating potential increases in immune infiltration. Conclusions: The in vitro results showed the additive effect of combination trastuzumab and radiotherapy. The in vivo results showed the potential to achieve similar efficacy of radiotherapy with a reduced dose when combined with trastuzumab. If trastuzumab and low-dose radiotherapy induce greater tumor kill than a higher dose of radiotherapy, combination therapy can achieve a similar reduction in tumor burden.

摘要

背景

曲妥珠单抗可诱导HER2过表达细胞的细胞周期停滞,并显示出使癌细胞对放疗增敏的潜力。本研究的目的是量化曲妥珠单抗与放疗联合使用的效果,以确定它们的协同作用。方法:在体外,用曲妥珠单抗、放疗或两者联合处理HER2+癌细胞,并进行成像以评估治疗动力学。在体内,用曲妥珠单抗和放疗处理荷HER2+肿瘤的小鼠,并进行纵向评估。另外一组进行处理并牺牲,以量化CD45、CD31、α-SMA和缺氧情况。结果:相互作用指数显示曲妥珠单抗和放疗在体外对HER2+细胞系具有相加作用。此外,结果显示放疗组在肿瘤反应方面存在显著差异(p < 0.001);然而,在放疗中加入曲妥珠单抗的联合治疗组中未观察到差异(p = 0.56)。组织学显示接受曲妥珠单抗治疗的肿瘤中CD45染色增加(p < 0.05),表明免疫浸润可能增加。结论:体外结果显示曲妥珠单抗与放疗联合具有相加作用。体内结果显示,与曲妥珠单抗联合使用时,有可能以降低的剂量实现与放疗相似的疗效。如果曲妥珠单抗和低剂量放疗比高剂量放疗诱导更大的肿瘤杀伤,联合治疗可以实现类似的肿瘤负担减轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6303/9454606/5ca5377be746/cancers-14-04234-g001.jpg

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