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Hepatocellular CarcinomaPrimovistMRINCT01764438

Utility Study of Primovist-MRI on HCC Staging

An observational study of Hepatocellular Carcinoma, run by Inha University Hospital at 1 site in South Korea.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Gadoxetic acid (Gd-EOB-DTPA, Primovist)-enhanced MRI can affect on BCLC staging during the initial staging workups of definite HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hepatocellular Carcinoma
What is being tested?
Primovist-enhanced MRI
Type of treatment
Surgery or procedure
How many people
174 participants
Where
1 siteSouth Korea
Study dates
Aug 2012to Aug 2013
How long will I take part?
1 Year
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: HCC patients with very early (BCCLC stage 0) or early (BCLC stage A) stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT

Who may be able to join

  • 18 years ≤ age
  • Patients who are initially diagnosed as having hepatocellular carcinoma with very early or early BCLC stage by liver dynamic CT at each hospital
  • Performance status 0 or 1
  • Child-Turcotte-Pugh score ≤8

Who cannot join

  • Age of younger than 18
  • Patients with any concurrent cancer other than hepatocellular carcinoma. Any cancer curatively treated at least 3 years prior to entry is permitted.
  • Patients with BCLC B, C, or D staged HCC at initial diagnosis by liver dynamic CT
  • Patients with suspicious intrahepatic malignant lesion by liver dynamic CT
  • Patients with HIV infection
  • Female patients in pregnancy
Show all 12Show fewer
  • Clinically hemodyanmically unstable patients
  • Patients with previous life-threatening anaphylactic reaction to contrast media
  • Patients scheduled for biopsy or liver surgery within 24 h post-administration of the study
  • Patients who cannot underwent CT due to renal insufficiency (estimated GFR < 30 mL/min/1.73m2)
  • Patients who cannot perform MRI due to contraindication of MRI (e.g. an implanted cardiac pacemaker)
  • Patients in whom MRI was performed before liver dynamic CT

Trial locations and contacts

1 site in 1 country.

Young-Joo Jin, M.D contact

82-32-890-2548

jyj412@hanmail.net

South Korea1 site, 1 recruiting
  • Jin-Woo Lee

    Incheon

    Jin-Woo Lee, M.D., 82-32-8902548, jin@inha.ac.kr

    Young-Joo Jin, M.D.

    Recruiting

Other trials in South Korea

About this study

Official title: The Incidence of Change in BCLC Stage by add-on Primovist-enhanced MRI During Initial Staging Work-up in HCC Patients Who Can be Candidates for Curative Treatment by Liver Dynamic CT: A Prospective Multicenter Study

Gadoxetic acid (Gd-EOB-DTPA, Primovist)-enhanced MRI can affect on BCLC staging during the initial staging workups of definite HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT.

Read the detailed description

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer related death worldwide, and its incidence continues to rise even in the Europe and the United States. Recent advancements in early diagnosis and treatment modalities have significantly improved survival in HCC patients, but, only a small portion of them can receive curative treatments. Treatment decision making in HCC is guided by tumor stage, which can be also affected by tumor status at presentation.Thus, intrahepatic tumor status can be pivotal for treatment decision making and for determining prognosis in HCC patients, especially in possible candidates for curative treatment.

The current AASLD guideline recommends that HCC patients with typical HCC ≥1 cm by liver dynamic computed tomography (CT) do not require further investigation to confirm the presence of HCC, and that appropriate treatment can be initiated based on tumor stage. However, other intrahepatic HCC lesion which is not detected by liver dynamic CT can be additionally detected only by Primovist-enhanced MRI.Although few studies have evaluated the usefulness of Primovist-enhanced MRI in HCC patients,most of these studies have been limited by the lack of an evaluation of shift in HCC stage and by the inclusion of patients with suspicious intrahepatic HCC lesions that had been already detected by liver dynamic CT. Furthermore, given the poor prognosis of HCC patients with recurrence after curative treatments such as liver transplantation, surgical resection, or radiofrequency ablation (RFA),accurate staging workup is essential for intrahepatic HCC, especially in patients with a very early or early Barcelona Clinic Liver Cancer (BCLC) staged HCC. To date, however, no evidence based recommendations have been made regarding the benefit of add-on examination of Primovist-enhanced MRI during initial staging workups in HCC patients who are candidates for curative treatment after diagnosis by liver dynamic CT.

In this prospective multicenter study, therefore, we will assess the usefulness of Primovist-enhanced MRI during the initial staging workups of HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT. We will examine whether Primovist-enhanced MRI could provide additional information on BCLC stage, by directly comparing to liver dynamic CT in these patients. Furthermore, we assess whether add-on Primovist-enhanced MRI after a diagnosis of HCC by liver dynamic CT could aid treatment decision making in these patients.

Being tested
Primovist-enhanced MRI
Medical subject headings
Carcinoma, Hepatocellular

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Primovist-enhanced MRIProcedure or surgery

    Also called Gadoxetic acid (Gd-EOB-DTPA, Primovist)-enhancecd MRI

    Performance of Primovist-enhanced MRI in HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT.

Study groups in NCT01764438
Study groupRoleWhat they receive
very early or early staged patientsPerformance of Primovist-enhanced MRI in HCC patients with very early or early stage disease, but with no suspicious HCC by liver dynamic CT
Receives: Procedure: Primovist-enhanced MRI

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. incidence of change of BCLC stage after add-on Primovist-enhanced MRI in HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT.

    Measured: Performance of Primovist enhanced MRI within the first 7 days after liver dynamic CT

Secondary outcomes (4)
  1. Incidence of newly detected intrahepatic HCC lesionss by Primovist-enhanced MRI, but, these lesions were not detected by liver dynamic CT

    Measured: Performance of Primovist-enhacned MRI within 7 days after liver dynamic CT

  2. Incidence of newly detected intrahepatic benign lesions by Primovist-enhanced MRI, but, these lesions were not detected by liver dynamic CT

    Measured: Performance of Primovist-enhanced MRI within 7 days after liver dynamic CT

  3. Frequency of change in treatment modality in patients with change of BCLC stage after Primovist-enhanced MRI

    Measured: Performance of Primovist-enhanced MRI within 7 days after liver dynamic CT

  4. Sensitivity, specificity, false positive predictive value, false negative predictive value, and accuracy of Primovist-enhanced MRI

    Measured: after performance of Primovist-enhanced MRI and liver dynamic CT

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jan 2013 (estimated)
  2. Study startAug 2012
  3. Primary completionAug 2013 (estimated)
  4. Study completionAug 2013 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
174 participants (estimated)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT01764438
Sponsor's protocol ID
INBU study
Other IDs
INBU study group
Acronym
PrimovistMRI
Status last verified
Aug 2012
First submitted
1 Jan 2013
Last updated
9 Jan 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hepatocellular Carcinoma, run by Inha University Hospital at 1 site in South Korea.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 9 Jan 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Young-Joo Jin, M.D (82-32-890-2548, jyj412@hanmail.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

incidence of change of BCLC stage after add-on Primovist-enhanced MRI in HCC patients with very early or early stage disease, but with no suspicious intrahepatic HCC lesions by liver dynamic CT. (time frame: Performance of Primovist enhanced MRI within the first 7 days after liver dynamic CT). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2013.

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