CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 808 enrolled / 808 target
Drug / intervention
Dactinomycin +10 morebiological
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/NCT00352534
NCT00352534Phase 3CompletedMonitor (3.4/mo)Completion was 138mo ago

Treatment for Very Low and Standard Risk Favorable Histology Wilms Tumor

Children's Oncology Group·interventional·Posted Jul 14, 2006·Updated Jun 3, 2026

In Brief

A Phase 3 clinical trial evaluating 3-Dimensional Conformal Radiation Therapy, Biospecimen Collection, and 9 other interventions for Stage I Kidney Wilms Tumor and 2 related conditions. Completed, enrolled 808 participants across 240 sites in 7 countries.

Signals

Enrolling slower than its timeline implies

Detailed Summary

This phase III trial is studying vincristine, dactinomycin, and doxorubicin with or without radiation therapy or observation only to see how well they work in treating patients undergoing surgery for newly diagnosed stage I, stage II, or stage III Wilms' tumor. Drugs used in chemotherapy, such as vincristine, dactinomycin, and doxorubicin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing, or by stopping them from spreading. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors.Giving these treatments after surgery may kill any tumor cells that remain after surgery. Sometimes, after surgery, the tumor may not need additional treatment until it progresses. In this case, observation may be sufficient.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, Israel, New Zealand, Puerto Rico, Switzerland, United States

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 14, 2006
Enrollment StartNov 6, 2006
Primary CompletionDec 31, 2014
Study CompletionMar 31, 2026
TodayJul 2, 2026
Enrollment to primary: 8.2 yearsPosted 20.0 years ago

Arms & Interventions

Stratum I (very low-risk disease)experimental

Patients undergo nephrectomy only. If they meet criteria, they are then observed periodically for 5 years. Patients with recurrent disease undergo surgery (immediate or delayed) and receive chemotherapy as in stratum III. Patients with no metachronous renal disease receive radiotherapy. Patients with metachronous disease undergo renal-sparing surgery and chemotherapy as in stratum III, but no radiotherapy. Treatment continues for up to 25 weeks. Additionally, patients undergo chest X-ray, CT or MRI, ultrasound, echocardiography, and blood sample collection throughout the study.

Radiation: 3-Dimensional Conformal Radiation TherapyProcedure: Biospecimen CollectionProcedure: Chest RadiographyProcedure: Computed TomographyBiological: DactinomycinDrug: Doxorubicin HydrochlorideProcedure: Echocardiography TestProcedure: Magnetic Resonance ImagingProcedure: Therapeutic Conventional SurgeryProcedure: Ultrasound ImagingDrug: Vincristine Sulfate
Stratum II (standard-risk, stage I or II)experimental

Patients undergo nephrectomy. Between 9 and 14 days post-nephrectomy, patients receive vincristine IV beginning on day 1, every week for 10 weeks then every 3 weeks for a total of 15 doses. Patients receive dactinomycin IV beginning day 1, alternating every 3 weeks with doxorubicin hydrochloride IV for a total of 5 doses of dactinomycin and 4 doses of doxorubicin. Treatment continues for up to 25 weeks. Additionally, patients undergo chest X-ray, CT or MRI, ultrasound, echocardiography, and blood sample collection throughout the study.

Radiation: 3-Dimensional Conformal Radiation TherapyProcedure: Biospecimen CollectionProcedure: Chest RadiographyProcedure: Computed TomographyBiological: DactinomycinDrug: Doxorubicin HydrochlorideProcedure: Echocardiography TestProcedure: Magnetic Resonance ImagingProcedure: Therapeutic Conventional SurgeryProcedure: Ultrasound ImagingDrug: Vincristine Sulfate
Stratum III (standard-risk, stage III)experimental

Patients undergo nephrectomy, if feasible, or biopsy. For patients who undergo biopsy only, definitive surgery is undertaken at week 7 or 13. Between 9 and 14 days post-nephrectomy, patients receive vincristine IV beginning on day 1 every week for 10 weeks then every 3 weeks for a total of 15 doses. Patients receive dactinomycin IV beginning day 1, alternating every 3 weeks with doxorubicin hydrochloride IV for a total of 5 doses of dactinomycin and 4 dose of doxorubicin hydrochloride. Patients undergo radiotherapy over 5-7 days after nephrectomy. Treatment continues for up to 25 weeks. Additionally, patients undergo chest X-ray, CT or MRI, ultrasound, echocardiography, and blood sample collection throughout the study.

Radiation: 3-Dimensional Conformal Radiation TherapyProcedure: Biospecimen CollectionProcedure: Chest RadiographyProcedure: Computed TomographyBiological: DactinomycinDrug: Doxorubicin HydrochlorideProcedure: Echocardiography TestProcedure: Magnetic Resonance ImagingProcedure: Therapeutic Conventional SurgeryProcedure: Ultrasound ImagingDrug: Vincristine Sulfate

Interventions

3-Dimensional Conformal Radiation Therapyradiation

Patients undergo radiotherapy

Biospecimen Collectionprocedure

Undergo blood sample collection

Chest Radiographyprocedure

Undergo chest X-ray

Computed Tomographyprocedure

Undergo CT

Dactinomycinbiological

Given IV

Doxorubicin Hydrochloridedrug

Given IV

Echocardiography Testprocedure

Undergo echocardiography

Magnetic Resonance Imagingprocedure

Undergo MRI

Therapeutic Conventional Surgeryprocedure

Undergo surgery

Ultrasound Imagingprocedure

Undergo ultrasound

Vincristine Sulfatedrug

Given IV