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Spots Global Cancer Trial Database for Irinotecan in Treating Young Patients With Refractory or Recurrent Hepatoblastoma

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Trial Identification

Brief Title: Irinotecan in Treating Young Patients With Refractory or Recurrent Hepatoblastoma

Official Title: Irinotecan Single-Drug Treatment For Children With Refractory or Recurrent Hepatoblastoma

Study ID: NCT00287976

Conditions

Liver Cancer

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as irinotecan, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. PURPOSE: This phase II trial is studying how well irinotecan works in treating young patients with refractory or recurrent hepatoblastoma.

Detailed Description: OBJECTIVES: Primary * Determine the biological activity of irinotecan hydrochloride, when given on a prolonged schedule, in terms of response rate and rate of early progression, in young patients with refractory or recurrent hepatoblastoma. Secondary * Determine the duration of response in patients showing stable disease or an objective response (partial or complete response) to this drug. * Determine the time to progression and overall survival of patients treated with this drug. * Determine the rate of resectability in patients treated with this drug. * Determine the toxicity of this drug in these patients. OUTLINE: This is a multicenter study. Patients receive irinotecan IV over 1 hour on days 1-5 and 8-12. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo evaluation for tumor resectability after courses 2, 3, or 4. Patients whose disease is considered resectable at any of these time points proceed to surgery. After completion of study treatment, patients are followed periodically. PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Our Lady's Hospital for Sick Children Crumlin, Dublin, , Ireland

Emma Kinderziekenhuis, Amsterdam, , Netherlands

Birmingham Children's Hospital, Birmingham, England, United Kingdom

Institute of Child Health at University of Bristol, Bristol, England, United Kingdom

Addenbrooke's Hospital, Cambridge, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital, Leeds, England, United Kingdom

Leicester Royal Infirmary, Leicester, England, United Kingdom

Royal Liverpool Children's Hospital, Alder Hey, Liverpool, England, United Kingdom

Royal London Hospital, London, England, United Kingdom

Great Ormond Street Hospital for Children, London, England, United Kingdom

Royal Manchester Children's Hospital, Manchester, England, United Kingdom

Sir James Spence Institute of Child Health at Royal Victoria Infirmary, Newcastle-Upon-Tyne, England, United Kingdom

Queen's Medical Centre, Nottingham, England, United Kingdom

Oxford Radcliffe Hospital, Oxford, England, United Kingdom

Children's Hospital - Sheffield, Sheffield, England, United Kingdom

Southampton General Hospital, Southampton, England, United Kingdom

Royal Marsden - Surrey, Sutton, England, United Kingdom

Royal Belfast Hospital for Sick Children, Belfast, Northern Ireland, United Kingdom

Royal Aberdeen Children's Hospital, Aberdeen, Scotland, United Kingdom

Royal Hospital for Sick Children, Edinburgh, Scotland, United Kingdom

Royal Hospital for Sick Children, Glasgow, Scotland, United Kingdom

Childrens Hospital for Wales, Cardiff, Wales, United Kingdom

Contact Details

Name: Jozsef Zsiros, MD, PhD

Affiliation: Emma Kinderziekenhuis

Role: STUDY_CHAIR

Name: Laurence Brugieres, MD

Affiliation: Gustave Roussy, Cancer Campus, Grand Paris

Role:

Name: Penelope Brock, MD, PhD

Affiliation: Great Ormond Street Hospital for Children NHS Foundation Trust

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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