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Completed

NCT Number: NCT00910572

Radioembolization With Yttrium-90 Microspheres for Intermediate or Advanced Hepatocellular Carcinoma

Rationale: Patients diagnosed with hepatocellular carcinoma (HCC) at an intermediate or advanced stage (according to the BCLC classification system) are not amenable of curative treatment. According to EASL and AASLD guidelines patients with an intermediate stage HCC are treated with trans-arterial chemoembolization (TACE) while patients with an advanced stage HCC are treated with molecular targeted drugs or other combinations according to their liver function. The median survival expected for patients in intermediate-advanced stages ranges from 11 to 20 months.

Purpose of the Study: The purpose of this prospective phase II study is to determine whether or not Radioembolization with Yttrium-90 microspheres (TheraSphere®) provides an anti-tumoral effect and a sensible benefit in terms of time-to-progression (TTP) and survival in patients with good liver function (Child A-B7) and a confirmed diagnosis of Intermediate or Advanced (because of the presence of neoplastic portal thrombosis) Hepatocellular Carcinoma (HCC).

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Milan, 20133, Italy

About this study

Patients at an intermediate stage (BCLC-B) are currently offered trans-arterial chemoembolisation (TACE) as the standard of care. A recent meta-analysis showed that radioembolization with beta-emitting Yttrium-90-loaded glass microspheres (TheraSphere®) in patients with HCC achieves a median objective response in 79% of cases (range 29-88%) and median survival exceeding 15 months has been reported in patients at intermediate stages who have been treated with TheraSphere®.

In patients with HCC at an advanced stage (BCLC-C) the single treatment that has shown a statistical advantage on overall survival and disease progression is sorafenib, that provides a median survival of 10.7 months. Based on the results reported in literature, the estimated median expected survival of patients with advanced HCC treated by TheraSphere® can be as long as 12 months.

After approval on July 2007 of a treatment protocol of Y-90 for compassionate use by the institutional IRB, at the National Cancer Institute of Milan 40 consecutive patients have been treated with radioembolization with Yttrium-90 microspheres (Theraspheres®) according to the same guidelines of the present prospective phase II protocol. The initial series of 40 patients treated according to a compassionate use of Y-90 has been instrumental for the assessment of the procedure's safety and tolerability. The present study has been targeted to 60 cases including the fist series of 40 "compassionate" patients, due to their adherence to the same inclusion/exclusion criteria of the proposed phase II study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of HCC confirmed by histology or non-invasive criteria (EASL/AASLD)
  • Intermediate stage (BCLC-B) HCC: patients with a large or multinodular HCC (single HCC > 5 cm or multiple HCC defined as > 3 nodules > 3 cm), a Child Pugh class A or B7 and no cancer related symptoms (PS=0-1).
  • Advanced stage (BCLC-C) HCC: patients with hepatic vascular involvement (at any tumor number and diameter), a Child Pugh class A or B7, no cancer related symptoms (PS=0-1) and absence of extra-hepatic tumor spread.
  • Cancer-related symptoms within the ECOG 0-1 score
  • Liver function within Child B-7 class
  • Platelets > 50.000/µL
  • WBC > 1500/µL
  • AST/ALT < 5 times the upper limit of normal (U/L)
  • Creatinine < 2.0 mg /dL
  • No indication for any possible curative treatment after multidisciplinary assessment (resection, ablation, transplantation)
  • Signed informed consent

Exclusion criteria

  • Child-Pugh class higher than B-7 at entry
  • ECOG performance score ≥ 2 at entry
  • Tumor volume ≥ 50% of liver volume
  • Extrahepatic tumor spread
  • Pulmonary insufficiency
  • Life expectancy of less than 3 months due to HCC or less than 6 months due to any other disease
  • Previous chemoembolization procedure (TACE)
  • Evidence on 99mTc-MAA scan of vascular shunts that can not be corrected by angiographic coil embolization
  • Evidence on 99mTc-MAA scan of lung shunting, with a potential absorbed dose of radiation to the lungs > 30 Gy

Treatment and study plan

Yttrium-90 microspheres (Therasphere MDS Nordion)

Device

Y-90 is incorporated into very tiny glass beads (microspheres: Therasphere MDS Nordion) and is injected into the liver tumor through the hepatic arteries, which are responsible for the feeding of the neoplastic liver tissue. Since the microspheres are unable to pass through the micro-vasculature of the liver parenchyma and tumor they are trapped at those sites and exert a local radio-therapeutic effect.

Other names: Therasphere, produced by MDS Nordion, Ottawa, Canada

Primary outcomes

  1. Time to progression (TTP)

    Time frame: At 1, 3, 6, 12 months and every 6 months thereafter

Secondary outcomes

  1. Tumor Response according to RECIST, WHO, EASL and Choi criteria

    Time frame: At 3, 6, 12 months and every 6 months thereafter

  2. Overall survival

    Time frame: At 1, 3, 6, 12 months and every 6 months thereafter

  3. Safety: documentation of all adverse events

    Time frame: At 1, 3, 6, 12 months and every 6 months thereafter

  4. Time-to-symptomatic progression (TTSP)

    Time frame: At 1, 3, 6, 12 months and every 6 months thereafter

Sponsors and collaborators

Lead sponsor

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Other

Collaborators

  • Gastro Intestinal Surgery and Liver Transplantation
  • The Hepato-Oncology Group: Department of Surgery, Medicine and Radiology

Registry information

Official study title

Radioembolization With Yttrium-90 Microspheres for Intermediate or Advanced HCC (Hepatocellular Carcinoma) Not Eligible to Curative Approach. A Phase II-b Study.

Important dates

Study start
2007
Primary completion
2009
Study completion
2010
First posted
Jun 1, 2009
Registry last updated
Jul 1, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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