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Status unknownNCT03273608Updated Sep 6, 2017

Observation Study: Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients

An observational study in Hepatocellular Carcinoma, sponsored by Taipei Veterans General Hospital, Taiwan. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2017-09-06.

Sponsored by Taipei Veterans General Hospital, Taiwan · Observational

The sponsor has not verified this record recently (last verified Sep 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
120
Ages
20 Years and older
Sex
All
01

Study summary

The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence in HCC management to physicians in the region, and to support the application of deTACE in treating advanced HCC patients.

Read the detailed description

The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence on deTACE in HCC management to physicians in the region, and to support the application of in treating advanced HCC patients.

  1. Primary Objective:

    To collect 1-year overall survival of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients in Taiwan.

  2. Secondary Objectives:

    1. To evaluate the overall tumor response of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients. The tumor response is according to Modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria.
    2. To evaluate the local tumor response (in the tumor(s) treated with drug-eluting microsphere) by chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
    3. To evaluate the safety profile of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
  3. Exploratory Objectives:

    1. To evaluate the downstaging and downsizing potential of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients to within Milan Criteria and to within Resection margin.
    2. To collect time-to-progression (TTP) and progress-free-survival (PFS) data of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
02

Conditions studied

  • Hepatocellular Carcinoma

Keywords

  • Hepatocellular Carcinoma
  • Advanced HCC
  • Unresectable
  • deTACE
  • HepaSphere
03

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients.

Eligibility criteria

Inclusion Criteria:Patients must meet all of the following inclusion criteria in order to be entered into the study:

  • Age 20 or older.
  • Patient has signed informed consent.
  • Patient must have a diagnosis of hepatocellular cancer confirmed by AASLD and at least one of the following method:

    • Magnetic resonance imaging (MRI) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
    • Contrast enhanced computed tomography (CT) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
    • Histological confirmation is required for lesions with inconclusive features.
  • Patient must not be suitable for treatment by resection or percutaneous ablation at time of study entry.

    • Patients not suitable for ablation due to lesion location may be enrolled.
    • Patients with HCC recurrence but not suitable for resection or ablation maybe enrolled.
  • Patient MUST be with either BCLC stage B OR C, and meet the following criteria:

    • Stage Child-Pugh A or B AND
    • Performance status ECOG ≤ 1 WITH Vascular Invasion or WITHOUT Vascular invasion.
  • Patient has a life expectancy of at least 6 months.

Exclusion Criteria:If patients meet any of the following criteria they may not be entered into the study:

  • Current or previous treatment with chemo- or radiation therapy or sorafenib or drug-eluting chemoembolization (deTACE).
  • Patients with concurrent cancer except non-melanomatous skin cancer.
  • Female patients who are pregnant, breastfeeding, or premenopausal and not using an effective method of contraceptive.
  • Performance status ECOG > 1.
  • Child-Pugh Class C.
  • Occlusive tumor thrombus to the main portal trunk.
  • Active gastrointestinal bleeding.
  • Evidence of uncorrectable bleeding diathesis.
  • Extra-Hepatic spread of the HCC.
  • Encephalopathy not adequately controlled medically.
  • Presence of ascites not controlled medically.
  • Any contraindication for MRI/ CT (eg. metallic implants).
  • Allergy to contrast media that cannot be managed with prophylaxis.
  • Any contraindication to arteriography.
  • Any contraindication for doxorubicin administration.
  • Any contraindication for hepatic embolization. Porto-systemic shunt, or an arteriovenous shunt that cannot be adequately closed prior to chemoembolization. Hepatofugal blood flow. Serum creatinine > 2mg/dL. Other condition deemed exclusionary by physician. Uncorrectable impaired clotting.
04

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
120 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes
05

What researchers measure

Primary outcomes

  1. Overall survival

    To define all participants from the day of the first HepaSphere Treatment until end of study or death is reported, whichever comes first.

    Time frame: 1 year

Secondary outcomes

  1. Tumor Response

    Tumor response will be assessed using modified Response Evaluation Criteria In Solid Tumors (mRECIST) criteria to evaluate tumor necrosis under CT/ MRI and will be presented as %.

    Time frame: 1 year

  2. Adverse Event (AE)

    Adverse event will be accessed according to CTCAE 4.0 after treatments until end of study or death.

    Time frame: 1 year

Other outcomes

  1. Exploratory Objectives, Time-To-Progression (TTP)

    To define all participants from the day of the first HepaSphere Treatment until tumor progression or death is first reported, whichever comes first.

    Time frame: 1 year

  2. Exploratory Objectives, Downstaging

    Tumor staging will be accessed according to BCLC staging system and Milan criteria, and will be reviewed at follow-up until end of study or death.

    Time frame: 1 year

06

Study locations

1 of 1 sites recruiting
  • Taipei Veterans General Hospital
    Taipei, 11217, Taiwan
    Recruiting
07

Registry details

Key details

Study ID
NCT03273608
Lead sponsor
Taipei Veterans General Hospital, Taiwan
Collaborators
National Taiwan University Hospital, Tri-Service General Hospital, China Medical University Hospital, Chang Gung Memorial Hospital
Responsible party
vghtpe user (Professor Yi-Hsiang Huang, Taipei Veterans General Hospital, Taiwan) — Principal investigator
First posted
Sep 6, 2017
Start date
Sep 14, 2016
Primary completion
Sep 30, 2019 (estimated)
Completion
Sep 30, 2019 (estimated)
Last update
Sep 6, 2017

Study contacts

Yi-Hsiang Huang, M.D. Ph.D.
Contact
yhhhuang@vghtpe.gov.tw
+886-2-28757506
Yi-Hsiang Huang, M.D. Ph.D.
principal investigator · Taipei Veterans General Hospital, Taiwan

Oversight

Data monitoring committee
No
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This study is status unknown, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

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