Hepatocellular Carcinoma Clinical Trial
Official title:
Establishing a Correlation Between Pre-treatment CT Perfusion Parameter Values and Post-treatment PET/CT Dosimetry to Aid in Tumor-specific Y-90 Radioembolization Treatment Planning for Hepatocellular Carcinoma
NCT number | NCT02558205 |
Other study ID # | 14100902 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | July 2015 |
Est. completion date | July 2020 |
Verified date | October 2020 |
Source | Rush University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to see if it is possible to establish a relationship between the
blood flow and blood volume of liver tumors from CT body perfusion and the radiation dose
deposited in the tumors from the radioembolization treatment as measured by PET/CT.
The study will do this by:
1. Measuring the blood flow and blood volume of tumors in the imaging data from a CT body
perfusion
2. Measuring the radioactivity in the tumors after the radioembolization treatment using
PET/CT and then calculating the dose deposited in the tumor
3. Using statistical analysis to assess the relationship between the dose and the perfusion
parameters
In addition, the research may help develop a method for calculating the dose of
radioembolization to be delivered to a liver tumor(s) using blood volume and blood flow data
obtained from the CT body perfusion scans.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | July 2020 |
Est. primary completion date | July 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Hepatocellular Carcinoma diagnosis - Candidate for Trans-Arterial Radioembolization treatment Exclusion Criteria: - Less than 18 years old - Pregnant - Iodinated Contrast Agent Allergy |
Country | Name | City | State |
---|---|---|---|
United States | Rush University Medical Center | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Rush University Medical Center | Swim Across America |
United States,
Bourgeois AC, Chang TT, Bradley YC, Acuff SN, Pasciak AS. Intraprocedural yttrium-90 positron emission tomography/CT for treatment optimization of yttrium-90 radioembolization. J Vasc Interv Radiol. 2014 Feb;25(2):271-5. doi: 10.1016/j.jvir.2013.11.004. — View Citation
D'Arienzo M, Filippi L, Chiaramida P, Chiacchiararelli L, Cianni R, Salvatori R, Scopinaro F, Bagni O. Absorbed dose to lesion and clinical outcome after liver radioembolization with 90Y microspheres: a case report of PET-based dosimetry. Ann Nucl Med. 2013 Aug;27(7):676-80. doi: 10.1007/s12149-013-0726-4. Epub 2013 Apr 20. — View Citation
Frampas E, Lassau N, Zappa M, Vullierme MP, Koscielny S, Vilgrain V. Advanced Hepatocellular Carcinoma: early evaluation of response to targeted therapy and prognostic value of Perfusion CT and Dynamic Contrast Enhanced-Ultrasound. Preliminary results. Eur J Radiol. 2013 May;82(5):e205-11. doi: 10.1016/j.ejrad.2012.12.004. Epub 2012 Dec 28. — View Citation
Lea WB, Tapp KN, Tann M, Hutchins GD, Fletcher JW, Johnson MS. Microsphere localization and dose quantification using positron emission tomography/CT following hepatic intraarterial radioembolization with yttrium-90 in patients with advanced hepatocellular carcinoma. J Vasc Interv Radiol. 2014 Oct;25(10):1595-603. doi: 10.1016/j.jvir.2014.06.028. Epub 2014 Aug 23. — View Citation
Morsbach F, Sah BR, Spring L, Puippe G, Gordic S, Seifert B, Schaefer N, Pfammatter T, Alkadhi H, Reiner CS. Perfusion CT best predicts outcome after radioembolization of liver metastases: a comparison of radionuclide and CT imaging techniques. Eur Radiol. 2014 Jul;24(7):1455-65. doi: 10.1007/s00330-014-3180-3. Epub 2014 May 12. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Correlation of CT perfusion metrics to radiation dose deposition of Y-90 as measured by PET/CT | 1 year | ||
Secondary | Correlation between CT perfusion metrics and post treatment response as measured by RECIST 1.0 criteria | 2 years |
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