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光学分子成像引导的放射治疗 第 2 部分:X 射线与荧光分子断层融合成像。

Optical molecular imaging-guided radiation therapy part 2: Integrated x-ray and fluorescence molecular tomography.

机构信息

Department of Radiation Oncology, School of Medicine, University of Miami, Miami, FL, 33136, USA.

出版信息

Med Phys. 2017 Sep;44(9):4795-4803. doi: 10.1002/mp.12414. Epub 2017 Jul 21.

Abstract

PURPOSE

Differentiating tumor from its surrounding soft tissues is challenging for x-ray computed tomography (CT). Fluorescence molecular tomography (FMT) can directly localize the internal tumors targeted with specific fluorescent probes. A FMT system was developed and integrated onto a CT-guided irradiator to improve tumor localization for image-guided radiation.

METHODS

The FMT system was aligned orthogonal to the cone-beam CT onboard our previously developed image-guided small animal arc radiation treatment system (iSMAART). Through rigorous physical registration, the onboard CT provides accurate surface contour which is used to generate three-dimensional mesh for FMT reconstruction. During FMT experiments, a point laser source perpendicular to the rotating axis was used to excite the internal fluorophores. The normalized optical images from multiple projection angles were adopted for tomographic reconstruction. To investigate the accuracy of the FMT in locating the tumor and recovering its volume, in vivo experiments were conducted on two breast cancer models: MDA-MB-231 cancer xenograft on nude mice and 4T1 cancer xenograft on white mice. Both cancer cell lines overexpress the epidermal growth factor receptor (EGFR). A novel fluorescent poly(lactic-co-glycolic) acid (PLGA) nanoparticle conjugated with anti-EGFR was intravenously injected to specifically target the breast cancer cells. Another ex vivo experiment on a mouse bearing a surgically implanted Indocyanine Green-containing glass tube was conducted, to additionally validate the precision of FMT-guided radiation therapy.

RESULTS

The FMT can accurately localize the single-nodule breast tumors actively targeted with fluorescent nanoparticles with localization error < 0.5 mm calculated between the centers of mass of tumors in FMT and CT. The reconstructed tumor volume in FMT was significantly correlated with that in the iodinated contrast-enhanced CT (R = 0.94, P < 0.001). The FMT was able to guide focal radiation delivery with submillimeter accuracy.

CONCLUSION

Using the tumor-targeting fluorescent probes, the iSMAART with onboard FMT system can accurately differentiate tumors from their surrounding soft tissue, guide precise focal radiation delivery, and potentially assess tumor response in cancer research.

摘要

目的

X 射线计算机断层扫描(CT)很难区分肿瘤与其周围的软组织。荧光分子断层扫描(FMT)可以直接定位用特定荧光探针靶向的内部肿瘤。我们开发了一种 FMT 系统,并将其集成到 CT 引导的辐照器上,以提高肿瘤定位能力,从而实现图像引导的放射治疗。

方法

FMT 系统与我们之前开发的图像引导小动物弧形放射治疗系统(iSMAART)上的锥形束 CT 正交对准。通过严格的物理配准,车载 CT 提供了精确的表面轮廓,用于 FMT 重建的三维网格生成。在 FMT 实验中,使用垂直于旋转轴的点激光源来激发内部荧光团。采用来自多个投影角度的归一化光学图像进行断层扫描重建。为了研究 FMT 在定位肿瘤和恢复其体积方面的准确性,我们在两种乳腺癌模型上进行了体内实验:裸鼠 MDA-MB-231 癌症异种移植和白色小鼠 4T1 癌症异种移植。这两种癌细胞系均过度表达表皮生长因子受体(EGFR)。静脉注射一种新型抗 EGFR 荧光聚(乳酸-共-乙醇酸)(PLGA)纳米粒子,以特异性靶向乳腺癌细胞。还进行了另一个在携带手术植入的吲哚菁绿(ICG)玻璃管的小鼠上的离体实验,以进一步验证 FMT 引导放射治疗的精度。

结果

FMT 可以准确地定位用荧光纳米粒子主动靶向的单结节乳腺癌肿瘤,肿瘤中心之间的定位误差<0.5mm 是根据 FMT 和 CT 计算的。FMT 重建的肿瘤体积与碘造影增强 CT(R = 0.94,P <0.001)显著相关。FMT 能够以亚毫米精度引导焦点放射治疗。

结论

使用肿瘤靶向荧光探针,带有车载 FMT 系统的 iSMAART 可以准确地区分肿瘤与其周围的软组织,引导精确的焦点放射治疗,并在癌症研究中潜在地评估肿瘤反应。

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