Clinical Application of Super-resolution Ultrasound(SR-US) Imaging in Solid Tumors

Sponsor

Chinese PLA General Hospital (Other)

Overall Status

Recruiting

CT.gov ID

NCT06018142

Collaborator

(none)

100

Enrollment

Location

Anticipated Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

It has well accepted that tumor angiogenesis present aberrant vascular architecture and functional abnormalities, which is associated with tumorigenesis, tumor propagation and progression. By locating, separating and tracking microbubbles, the recently introduced and upgraded Ultrasound Localization Microscopy (ULM) surpassed classical wave diffraction limit. However, the acquisition of structural and functional parameters of microcirculation in vivo for ULM is still confined by the compromise between the resolution and penetration depth. The relatively long acquisition time induced the difficulty of motion correction potentially, which hampers the preclinical to clinical application in organs with distinct tissue motion such as the liver. Therefore, we take the lead in studying human liver lesion microvasculature, which remains a challenge for noninvasive, quantitative and functional intravital imaging especially due to its deep-seated location and strong motion. We developed a Super-resolution Ultrasound (SR-US) imaging technique based on ULM to assess its feasibility of visualizing and quantifying microvasculature in human organs.

Condition or Disease	Intervention/Treatment	Phase
Neoplasms, Liver Neoplasms Malignant Neoplasm Metastasis Ultrasound Microvessels

Detailed Description

In this study, 7 indexes were obtained by ultrasonic acquisition. These 7 indicators are used to describe and evaluate the microvessels in the tumor, so as to achieve the early identification and diagnosis of the tumor, and to monitor the growth of the tumor for a long time and evaluate the treatment of the tumor. This is not available with other ultrasound devices.

Based on contrast-enhanced ultrasound, this technology can provide information of smaller blood vessels, which will certainly contribute to the early diagnosis and real-time evaluation of solid tumors during treatment, and play an important role in clinical application.

Study Design

Study Type:

Observational [Patient Registry]

Anticipated Enrollment :

100 participants

Observational Model:

Case-Only

Time Perspective:

Prospective

Official Title:

Clinical Application of Super-resolution Ultrasound(SR-US) Imaging in Solid Tumors

Actual Study Start Date :

Jun 1, 2022

Anticipated Primary Completion Date :

Oct 28, 2024

Anticipated Study Completion Date :

Feb 28, 2025

Outcome Measures

Primary Outcome Measures

Perfusion index [30 minutes]
The product of the average speed of microbubbles in region of interest (ROI) and the ROI area
Vessel diameter [30 minutes]
To describe the diameters of the tiniest blood vessels that can be explored
Vessel density [30 minutes]
To describe the ratio of the number of blood vessels in the tumor to the cross-sectional area of the tumor
Vessel density ratio [30 minutes]
The ratio of blood vessel density between the core and peripheral areas of the tumor
Mean flow velocity [30 minutes]
The average velocity in the region of interest
Distance metric [30 minutes]
The ratio of the total length of the curve path to the straight line distance from the beginning to the end of the curve
Perfusion ratio [30 minutes]
Perfusion ratio of tumor core to peripheral area

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Age over 18 years old, gender unlimited;
Patients with solid organ tumors with a maximum diameter > 1cm;
No contraindications with contrast ultrasound agents;
It can improve the pathological results of the tumor or the diagnostic results supported by other relevant imaging tests.
Patients can understand the purpose of the examination, voluntarily participate and sign the informed consent.

Exclusion Criteria:

The subject is known to be allergic to any component of the contrast agent Sonovue;
Lesions were diffuse or borderless on contrast ultrasound;
Patients who underwent previous anti-angiogenesis and chemotherapy, or other local treatment of the tumor;
Poor image display or deep position in conventional ultrasound evaluation (<10 cm from skin),
The researchers determined that there were any other factors that were not suitable for inclusion or affected participants' participation in the study
Patients with severe heart disease or lung disease;
Patients who are pregnant, may be pregnant or breastfeeding;
No enhanced MRI or enhanced CT results can be obtained;
The investigator considers the subjects unfit to participate in this study.