Imaging Research-Physical Science, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, Ontario M4N 3M5, Canada.
Med Phys. 2013 Aug;40(8):082901. doi: 10.1118/1.4812683.
Currently, no clinical imaging modality is used routinely to assess tumor response to cancer therapies within hours to days of the delivery of treatment. Here, the authors demonstrate the efficacy of ultrasound at a clinically relevant frequency to quantitatively detect changes in tumors in response to cancer therapies using preclinical mouse models.
Conventional low-frequency and corresponding high-frequency ultrasound (ranging from 4 to 28 MHz) were used along with quantitative spectroscopic and signal envelope statistical analyses on data obtained from xenograft tumors treated with chemotherapy, x-ray radiation, as well as a novel vascular targeting microbubble therapy.
Ultrasound-based spectroscopic biomarkers indicated significant changes in cell-death associated parameters in responsive tumors. Specifically changes in the midband fit, spectral slope, and 0-MHz intercept biomarkers were investigated for different types of treatment and demonstrated cell-death related changes. The midband fit and 0-MHz intercept biomarker derived from low-frequency data demonstrated increases ranging approximately from 0 to 6 dBr and 0 to 8 dBr, respectively, depending on treatments administrated. These data paralleled results observed for high-frequency ultrasound data. Statistical analysis of ultrasound signal envelope was performed as an alternative method to obtain histogram-based biomarkers and provided confirmatory results. Histological analysis of tumor specimens indicated up to 61% cell death present in the tumors depending on treatments administered, consistent with quantitative ultrasound findings indicating cell death. Ultrasound-based spectroscopic biomarkers demonstrated a good correlation with histological morphological findings indicative of cell death (r2=0.71, 0.82; p<0.001).
In summary, the results provide preclinical evidence, for the first time, that quantitative ultrasound used at a clinically relevant frequency, in addition to high-frequency ultrasound, can detect tissue changes associated with cell death in vivo in response to cancer treatments.
目前,没有临床成像方式可在治疗后数小时至数天内常规评估癌症治疗的肿瘤反应。在这里,作者通过临床相关频率的超声证明了其在使用临床前小鼠模型定量检测癌症治疗反应中的肿瘤变化的有效性。
常规低频和相应高频超声(范围从 4 到 28MHz),以及来自接受化学疗法、X 射线辐射以及新型血管靶向微泡治疗的异种移植肿瘤的定量光谱和信号包络统计分析,被用于此研究。
基于超声的光谱生物标志物表明,在有反应的肿瘤中,与细胞死亡相关的参数发生了显著变化。具体来说,针对不同类型的治疗,研究了中带拟合、光谱斜率和 0-MHz 截距生物标志物的变化,并证明了与细胞死亡相关的变化。源自低频数据的中带拟合和 0-MHz 截距生物标志物显示,根据治疗方式的不同,分别增加了大约 0 到 6dBr 和 0 到 8dBr。这些数据与高频超声数据的结果一致。作为获得基于直方图的生物标志物的替代方法,对超声信号包络进行了统计分析,并提供了确认结果。肿瘤标本的组织学分析表明,根据治疗方式的不同,肿瘤中存在高达 61%的细胞死亡,这与定量超声检测到的细胞死亡结果一致。基于超声的光谱生物标志物与指示细胞死亡的组织学形态学发现具有很好的相关性(r2=0.71, 0.82;p<0.001)。
总之,这些结果首次提供了临床前证据,证明了在临床相关频率下使用的定量超声,除了高频超声之外,还可以检测与癌症治疗后体内细胞死亡相关的组织变化。