Ultrasound Molecular Imaging to Assess Therapeutic Response

超声分子成像评估治疗反应

• 批准号: 9440982
• 负责人: Mark Andrew Borden
• 金额: $ 57.23万
• 依托单位: UNIVERSITY OF COLORADO
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-04-13 至 2021-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9440982
• 关键词: 3-Dimensional; 3D ultrasound; Acoustics; Anatomy; Animal Model; Animals; Biological Markers; Blood Circulation; Blood Vessels; Cancer Patient; Canis familiaris; Chemistry; Client; Clinical; Clinical Trials; Complement Activation; Computers; Contrast Media; Data; Diagnosis; Disease; Dose; Early treatment; Ensure; Epitopes; Europe; Evaluation; Formulation; Goals; Gold; Human; Image; Imaging Device; Imaging technology; Immunohistochemistry; Integrin alphaVbeta3; Ionizing radiation; KDR gene; Laboratories; Ligand Binding; Ligands; Lipids; Magnetic Resonance Imaging; Malignant Neoplasms; Malignant neoplasm of prostate; Measurement; Measures; Mechanics; Methods; Microbubbles; Modality; Modeling; Molecular; Molecular Target; Monitor; Morbidity - disease rate; Morphology; Motivation; Multicenter Studies; Multicenter Trials; Necrosis; Patients; Performance; Pharmacology; Physiology; Population; Prediction of Response to Therapy; Price; Process; Production; Radiation; Reporting; Research; Research Personnel; Rodent; Rodent Model; Route; Safety; Scanning; Site; Soft tissue sarcoma; Specificity; Surface; System; Techniques; Technology; Testing; Therapeutic Index; Time; Tissues; Toxic effect; Traction; Translations; Treatment Efficacy; Treatment Protocols; Tumor Angiogenesis; Tumor Markers; Tumor Volume; Ultrasonography; United States; Validation; Work; X-Ray Computed Tomography; base; cancer imaging; cancer therapy; chemotherapy; clinical application; clinical diagnostics; clinical translation; clinically relevant; contrast enhanced; contrast imaging; cost; disease phenotype; imaging detection; imaging modality; imaging study; imaging system; improved; laptop; molecular diagnostics; molecular imaging; new technology; novel strategies; nuclear imaging; oncology; personalized medicine; portability; preclinical study; prototype; public health relevance; response; safety study; systemic toxicity; tool; treatment response; tumor; tumor progression; working group

 DESCRIPTION (provided by applicant): Over the past decade, molecular imaging has gained traction as a powerful new imaging method to enhance the capabilities of ultrasound by providing assessment of physiology associated with disease on the cellular level. Our team has set out with the goal of developing contrast agents and ultrasound technology to substantially improve the utility of diagnostic molecular imaging for clinical translation. Thus far, our team ha achieved several highly significant advances: (1) we formulated a new type of targeted contrast agent, the buried-ligand microbubble, which is ultrasound-targeted, non-immunogenic and reduces the potential for nonspecific interactions; (2) we illustrated the utility of tailoring thesize distribution of contrast agents to improve imaging contrast; (3) we demonstrated the advantage of acoustic radiation force to enhance sensitivity in molecular imaging studies; (4) we performed acoustic radiation force-enhanced molecular imaging with an unmodified clinical ultrasound system; (5) we illustrated the need for 3-D in ultrasound molecular imaging; (6) we affirmed the utility of ultrasound molecular imaging in assessing tumor response to anti-angiogenic therapy in rodents; and (7) we demonstrated increased targeting specificity with the combination of acoustic radiation force and buried-ligand microbubbles. Several other groups working parallel to ours have corroborated our results, illustrating in rodents that ultrasound molecular imaging can provide an indication of tumor response to therapy significantly sooner than traditional methods, such as tumor size measurements. The significance of this result is that ultrasound molecular imaging can provide robust, low-cost, safe, bedside support for monitoring personalized medicine approaches in oncology. With these technological advances and promising results in rodent models, it is now time to evaluate the translatability of this technology for clinical application. To date, all reported molecular imaging studies in the US have been in small animals. In this project, we will validate the technology of ultrasound molecular imaging in a population of client-owned (pet) dogs with spontaneous soft tissue sarcomas. This large animal model is an ideal platform for validation of the clinical utility of ultrasound molecular imaging. Dogs receive similar radiation and chemotherapeutic treatments as humans, are of a size where clinical ultrasound systems can be utilized, and can be imaged with prototype molecularly targeted contrast agents without FDA and other regulatory hurdles. Thus, the goal of this project is to test the ability of ultrasound molecular imaging to detect eary response of tumors to therapy in canine patients. Patients undergoing chemotherapy will be monitored, and data will be correlated with the gold standards of DCE-CT and immunohistochemistry. This large animal, multi-center, pre-clinical study will be supported with studies to insure optimal performance of molecular imaging in the canine model, such as implementation of a 3-D interface for imaging, optimization of contrast agent and ultrasound parameters, and preliminary studies of toxicity in purpose-bred dogs. Accomplishment of our aims and validation of ultrasound molecular imaging as a treatment monitoring technique of clinical value for veterinary oncology will propel this promising technology toward human applications.

 描述（由申请人提供）：在过去的十年中，分子成像作为一种强大的新成像方法，通过在细胞水平上提供与疾病相关的生理学评估，增强了超声的能力。我们的团队已经着手开发造影剂和超声技术的目标，以大大提高诊断分子成像的临床翻译的效用。到目前为止，我们的团队已经取得了几个非常重要的进展：（1）我们配制了一种新型的靶向造影剂，埋藏配体微泡，它是超声靶向的，非免疫原性的，并减少了非特异性相互作用的可能性;（2）我们说明了定制造影剂的尺寸分布以提高成像对比度的实用性;（3）我们证明了声辐射力在提高分子成像研究灵敏度方面的优势：（4）我们用未经改进的临床超声系统进行了声辐射力增强的分子成像：（5）我们说明了超声分子成像中三维的必要性;（6）我们确认了超声分子成像在评估啮齿动物中肿瘤对抗血管生成治疗的反应中的实用性;（7）我们证明了声辐射力和埋藏配体微泡的组合增加了靶向特异性。与我们平行工作的其他几个小组已经证实了我们的结果，在啮齿动物中说明超声分子成像可以比传统方法（如肿瘤大小测量）更快地提供肿瘤对治疗反应的指示。这一结果的意义在于，超声分子成像可以为监测肿瘤学中的个性化医疗方法提供稳健、低成本、安全的床边支持。随着这些技术的进步和在啮齿动物模型中的有希望的结果，现在是时候评估该技术在临床应用中的可转化性了。迄今为止，美国所有报道的分子成像研究都是在小动物中进行的。在这个项目中，我们将在患有自发性软组织肉瘤的客户（宠物）犬群中验证超声分子成像技术。这种大型动物模型是验证超声分子成像临床实用性的理想平台。狗接受与人类相似的放射和化学治疗，具有可以使用临床超声系统的尺寸，并且可以用原型分子靶向造影剂成像，而没有FDA和其他监管障碍。因此，本项目的目标是测试超声分子成像检测犬患者肿瘤对治疗的早期反应的能力。将对接受化疗的患者进行监测，并将数据与DCE-CT和免疫组化的金标准相关联。这项大型动物、多中心、临床前研究将得到研究的支持，以确保犬模型中分子成像的最佳性能，例如成像的3-D界面的实现、造影剂和超声参数的优化以及目的饲养犬中毒性的初步研究。我们目标的实现和超声分子成像作为兽医肿瘤学临床价值的治疗监测技术的验证将推动这一有前途的技术向人类应用。

项目成果

Vaporizable endoskeletal droplets via tunable interfacial melting transitions

• DOI: 10.1126/sciadv.aaz7188
• 发表时间: 2020-04-01
• 期刊: SCIENCE ADVANCES
• 影响因子: 13.6
• 作者: Shakya, Gazendra;Hoff, Samuel E.;Borden, Mark A.
• 通讯作者: Borden, Mark A.

Click Conjugation of Cloaked Peptide Ligands to Microbubbles.

• DOI: 10.1021/acs.bioconjchem.8b00084
• 发表时间: 2018-04
• 期刊: Bioconjugate chemistry
• 影响因子: 4.7
• 作者: Connor Slagle;D. Thamm;E. Randall;M. Borden

Microbubble Radiation Force-Induced Translation in Plane-Wave Versus Focused Transmission Modes.

平面波与聚焦传输模式中微泡辐射力诱导的平移。

• DOI: 10.1109/tuffc.2019.2937158
• 发表时间: 2019
• 期刊: IEEE transactions on ultrasonics, ferroelectrics, and frequency control
• 作者: Guidi,Francesco;Supponen,Outi;Upadhyay,Awaneesh;Vos,HendrikJ;Borden,MarkAndrew;Tortoli,Piero
• 通讯作者: Tortoli,Piero

Changes in microbubble dynamics upon adhesion to a solid surface.

粘附到固体表面后微泡动力学的变化。

• DOI: 10.1063/1.5135017
• 发表时间: 2020
• 期刊: Applied physics letters
• 影响因子: 4
• 作者: Lum,JordanS;Daeichin,Verya;Kienle,DanielF;Schwartz,DanielK;Murray,ToddW;Borden,MarkA
• 通讯作者: Borden,MarkA