Department of Radiation Oncology, School of Medicine, University of Miami, Miami, Florida.
Department of Radiation Oncology, School of Medicine, University of Miami, Miami, Florida.
Int J Radiat Oncol Biol Phys. 2018 Nov 15;102(4):848-857. doi: 10.1016/j.ijrobp.2018.01.068. Epub 2018 Feb 2.
The image guided small animal arc radiation treatment platform has adopted onboard cone beam computed tomography and bioluminescence tomography (BLT). We used BLT to guide irradiation delivery and quantitatively assess irradiation-induced tumor response.
BLT was first validated on a tissue-simulating phantom, where the internal chemiluminescent liquid had a constant volume while its luminescence intensity gradually decayed. Then, in vivo experiments were performed on BALB/c mice orthotopically inoculated with 4T1 breast carcinoma cells expressing luciferase. Animals either received radiation treatment (radiation therapy [RT] group, n = 9) or did not (control group, n = 9). BLT was used to guide delivery of a single-fraction 5-Gy radiation dose to the tumor and to evaluate the treatment response. Terminal deoxynucleotidyl transferase deoxyuridine triphosphate (dUTP) nick end labeling (TUNEL) staining was used to evaluate irradiation-induced DNA damage and cell apoptosis.
Phantom results showed that BLT not only recovered the constant target volume with <2% deviation but also accurately monitored the decay of the chemiluminescent molecules. For the RT group of animals, there was significant reduction in both the BLT-based tumor volume (21% ± 10%, P = .001) and bioluminescence intensity (48% ± 17%, P = .0008). For the control group, a significant increase was detected in the BLT tumor volume (35% ± 12%, P < .0001) but not the BLT bioluminescence intensity (P = .4). There was a significant difference in the BLT tumor volume between the RT and control groups 7 days after irradiation (P = .03). Regression analysis suggests a strong correlation between the BLT and cone beam computed tomography tumor volume (R = 0.93). Analysis using terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling staining showed a significant difference in tumor cell apoptosis between the RT and control groups (20.6% ± 2.9% and 3.2% ± 1.7%, respectively; P < .05).
BLT onboard the image guided small animal arc radiation treatment platform can be used to accurately guide irradiation delivery and to quantitatively assess treatment response by simultaneously monitoring tumor volume and cancer cell population.
小动物弧形放射治疗平台采用了在线锥形束计算机断层扫描和生物发光断层扫描(BLT)。我们使用 BLT 来引导照射传递,并定量评估照射诱导的肿瘤反应。
BLT 首先在组织模拟体模上进行了验证,其中内部化学发光液体的体积保持不变,但其发光强度逐渐衰减。然后,在 BALB/c 小鼠中进行了原位接种表达荧光素酶的 4T1 乳腺癌细胞的体内实验。动物要么接受放射治疗(放射治疗组,n=9),要么不接受(对照组,n=9)。BLT 用于引导单次 5-Gy 剂量的照射传递,并评估治疗反应。末端脱氧核苷酸转移酶脱氧尿苷三磷酸(dUTP)缺口末端标记(TUNEL)染色用于评估照射诱导的 DNA 损伤和细胞凋亡。
体模结果表明,BLT 不仅可以以 <2%的偏差恢复恒定的目标体积,而且还可以准确监测化学发光分子的衰减。对于放射治疗组的动物,BLT 基于肿瘤体积(21%±10%,P=.001)和生物发光强度(48%±17%,P=.0008)均显著降低。对于对照组,检测到 BLT 肿瘤体积(35%±12%,P<.0001)显著增加,但 BLT 生物发光强度(P=.4)没有增加。照射后 7 天,放射治疗组和对照组之间的 BLT 肿瘤体积存在显著差异(P=.03)。回归分析表明,BLT 与锥形束计算机断层扫描肿瘤体积之间存在很强的相关性(R=0.93)。使用末端脱氧核苷酸转移酶脱氧尿苷三磷酸缺口末端标记染色的分析表明,放射治疗组和对照组之间的肿瘤细胞凋亡存在显著差异(分别为 20.6%±2.9%和 3.2%±1.7%;P<.05)。
图像引导小动物弧形放射治疗平台上的 BLT 可以用于准确地引导照射传递,并通过同时监测肿瘤体积和癌细胞数量来定量评估治疗反应。