CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 236 enrolled / 236 target
Drug / intervention
Cisplatin +9 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00980460
NCT00980460Phase 3CompletedMonitor (1.2/mo)Completion was 72mo ago

Treatment of Children With All Stages of Hepatoblastoma With Temsirolimus (NSC#683864) Added to High Risk Stratum Treatment

National Cancer Institute (NCI)·interventional·Posted Sep 21, 2009·Updated Jun 30, 2026

In Brief

A Phase 3 clinical trial evaluating Cisplatin, Dexrazoxane, and 8 other interventions for PRETEXT I Hepatoblastoma and 3 related conditions. Completed, enrolled 236 participants across 209 sites in 6 countries.

Signals

Enrolling slower than its timeline implies

Detailed Summary

This phase III trial studies the side effects and how well risk-based therapy works in treating younger patients with newly diagnosed liver cancer. Surgery, chemotherapy drugs (cancer fighting medicines), and when necessary, liver transplant, are the main current treatments for hepatoblastoma. The stage of the cancer is one factor used to decide the best treatment. Treating patients according to the risk group they are in may help get rid of the cancer, keep it from coming back, and decrease the side effects of chemotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Brazil, Canada, Japan, Puerto Rico, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedSep 21, 2009
Enrollment StartSep 15, 2009
Primary CompletionJun 30, 2020
Study CompletionMar 31, 2026
TodayJul 2, 2026
Enrollment to primary: 10.8 yearsPosted 16.8 years ago

Arms & Interventions

High-risk group (regimen H)experimental

Patients receive up front VIT chemotherapy comprising vincristine sulfate IV over 1 minute on days 1 and 8 and irinotecan hydrochloride IV over 90 minutes on days 1-5, and temsirolimus IV over 30 minutes on days 1 and 8. Treatment with VIT repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients with disease response then receive 6 courses of C5VD with 4 courses of VIT in between each 2-course block. Patients with no disease response receive 6 courses of C5VD in the absence of disease progression or unacceptable toxicity. Patients undergo tumor resection or liver transplant after course 4 of C5VD followed by 2 courses of adjuvant C5VD. Patients may also receive dexrazoxane IV over 5-15 minutes on days 1-2 of courses 5 and 6.

Drug: CisplatinDrug: Doxorubicin HydrochlorideDrug: FluorouracilDrug: Irinotecan HydrochlorideOther: Laboratory Biomarker AnalysisProcedure: Liver TransplantationDrug: TemsirolimusProcedure: Therapeutic Conventional SurgeryDrug: Vincristine Sulfate
High-risk group (regimen W)experimental

(regimen W replaced by regimen H as of Amendment 3B) Patients receive up front VI chemotherapy comprising vincristine sulfate IV on days 1 and 8 and irinotecan hydrochloride IV over 90 minutes on days 1-5. Treatment with VI repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients with disease response then receive 6 courses of C5VD with 1 courses of VI in between each 2-course block. Patients with no disease response receive 6 courses of C5VD in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinDrug: Doxorubicin HydrochlorideDrug: FluorouracilDrug: Irinotecan HydrochlorideOther: Laboratory Biomarker AnalysisProcedure: Therapeutic Conventional SurgeryDrug: Vincristine Sulfate
Intermediate-risk group (regimen F)experimental

Patients receive C5VD chemotherapy comprising cisplatin IV over 6 hours on day 1, fluorouracil IV over 2-4 minutes on day 2, vincristine sulfate IV over 1 minute on days 2, 9, and 16, and doxorubicin hydrochloride IV over 15 minutes on days 1-2. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. Patients also undergo surgical resection after course 2 OR surgical resection or liver transplantation after course 4 of C5VD. Patients may also receive dexrazoxane IV over 5-15 minutes on days 1-2 of courses 5 and 6. (Closed to accrual as of 3/12/2012)

Drug: CisplatinDrug: DexrazoxaneDrug: Doxorubicin HydrochlorideDrug: FluorouracilOther: Laboratory Biomarker AnalysisProcedure: Liver TransplantationProcedure: Therapeutic Conventional SurgeryDrug: Vincristine Sulfate
Low-risk group (regimen T)experimental

Patients undergo surgery and then receive adjuvant cisplatin IV over 6 hours on day 1, fluorouracil IV over 2-4 minutes on day 2, and vincristine sulfate IV over 1 minute on days 2, 9, and 16. Treatment repeats every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity.

Drug: CisplatinDrug: FluorouracilOther: Laboratory Biomarker AnalysisProcedure: Therapeutic Conventional SurgeryDrug: Vincristine Sulfate
Very low-risk groupexperimental

Patients undergo surgery and then receive no further treatment.

Other: Laboratory Biomarker AnalysisProcedure: Therapeutic Conventional Surgery

Interventions

Cisplatindrug

Given IV

Dexrazoxanedrug

Given IV

Doxorubicin Hydrochloridedrug

Given IV

Fluorouracildrug

Given IV

Irinotecan Hydrochloridedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Liver Transplantationprocedure

Undergo liver transplant

Temsirolimusdrug

Given IV

Therapeutic Conventional Surgeryprocedure

Undergo surgery

Vincristine Sulfatedrug

Given IV