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Role of Perfusion CT in Pancreatic Cancer

Evaluation of Diagnostic Efficacy of Perfusion CT Using Wide Detector for Staging and Response Prediction After Chemotherapy in Pancreatic Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01703650
Enrollment
48
Registered
2012-10-10
Start date
2012-11-30
Completion date
2021-09-30
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenocarcinoma, Pancreas, Neuroendocrine Carcinoma of Pancreas

Keywords

CT, pancreas adenocarcinoma, RECIST, perfusion

Brief summary

The purpose of this study is 1. to determine whether the perfusion parameters in the normal pancreas and the pancreas cancer (adenocarcinoma or neuroendocrine tumor) are different on perfusion CT 2. to determine whether initial perfusion parameters as well as perfusion parameter change in pancreas adenocarcinoma before and after chemotherapy are different between chemotherapy response group (CR, PR according to RECIST 1.1) and non response group (SD, PD according to RECIST 1.1).

Detailed description

1. Performance of preoperative perfusion CT for preoperative staging is assessed by comparing with operative finding and histologic disease staging 2. Estimation of initial or change of pancreas cancer perfusion parameters and whether those can provide cut-off value for predicting response of chemotherapy in patients with pancreas adenocarcinoma

Interventions

1. iopromide (370mgI/mL) enhanced perfusion CT will be performed within 14 days of operation. 2. In patients who are planned to receive chemotherapy, iopromide enhanced perfusion CT was performed twice; within 14 days before starting 1st cycle and within 14 days after finishing 2nd cycle. 3. iopromide (370mgI/mL) will be administered intravenously with an amount of 30mL (body weight\[BW\] \<50kg) or 35 mL (50kg ≤BW \<70kg) or 40 mL (70 kg≤BW \<90kg) or 50 mL (90≤BW), followed by saline infusion (30mL). 4. Injection rate is as follows; 6.0mL/sec if BW is \<50kg, 7.0 mL/sec if BW is 50kg≤and \<70kg, 8.0 mL/sec if BW is 70≤and\<90kg and 9.0mL/sec if BW is 90kg≤.

PROCEDURECT

1. Perfusion CT will be performed by using a 320 channel MDCT 2. Patients are requested for fasting for at least 8 hours before CT scan. 3. Patients are requested for doing shallow breathing as slow as possible and wide strap is applied during CT scan. 4. Scan range is limited to the whole pancreas and it focuses to the pancreas tumor lesion. 5. During perfusion CT, 19 phases (ten phases with two seconds interval and six phases with three seconds interval and three phases with five seconds interval) are obtained in fifty three seconds. 6. ADIR 3D and SURE EXPOSURE 3D are applied during perfusion CT to minimize radiation dose.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients who are older than eighteen years * patients in whom operation and preoperative computed tomography are scheduled for resectable pancreas adenocarcinoma or pancreas neuroendocrine tumor * patients in whom chemotherapy is scheduled for histologically confirmed pancreas adenocarcinoma * patients in whom chemotherapy is planned for highly suspicious pancreas adenocarcinoma on imaging workup * patients who agree with the study and whose informed consent is obtained.

Exclusion criteria

* patients who are younger than eighteen years old * patients in whom previously radiation therapy was performed and the RTx field includes pancreas * patients with recurred pancreas adenocarcinoma * patient who are pregnant or nursing patients * patients with renal failure (GFR\<30mL/min) * patients with history of malignancy, except malignancy is in complete remission after operation or iodine therapy for at least five years) * patients with hypersensitivity for iodine or contrast media or other causes of contraindication of contrast-media enhanced CT scan * Any other condition which, in the opinion of the Investigator, would make the patient unsuitable for enrollment or could interfere with the completion of the study.

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of the correlation between the initial perfusion parameters of the tumor and response of the chemotherapyafter 6 cycles of the planned chemotherapyInitial perfusion parameters (blood volume, blood flow and permeability) are compared between CTx-responder and non-responders after 6 cycle of the scheduled chemotherapy, using RECIST 1.1 criteria.

Secondary

MeasureTime frameDescription
Correlation between change of perfusion parameters and the chemotherapy responseafter 6 cycles of the chemotherapyPerfusion parameters (blood volume, blood flow, and permeability) change between initial perfusion CT and second perfusion CT (which is taken after 2 cycle of the CTx) are compared between CTx-responder and non-responder after finishing 6 cycles of CTx according to RECIST 1.1 criteria.
Perfusion parameters among different pancreas tumorswithin 2 months after finishing enrollmentPerfusion parameters (blood volume, blood flow and permeability) are compared among the different types of the pancreas tumors to investigate perfusion parameters can help characterization of the tumors.
comparison of perfusion parameters among the pancreas tumors and parenchymawithin three weeks before pancreas tumor surgeryblood volume, blood flow and permeability are compared between the tumor and the pancreas parenchyma.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026