Combination Chemotherapy and Surgery in Treating Young Patients With Wilms Tumor
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Purpose
RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Giving combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving it after surgery may kill any tumor cells that remain after surgery.
PURPOSE: This phase III clinical trial is studying how well combination chemotherapy and surgery work in treating young patients with Wilms tumor.
| Condition | Intervention | Phase |
|---|---|---|
|
Kidney Cancer Nonneoplastic Condition |
Biological: dactinomycin Drug: carboplatin Drug: cyclophosphamide Drug: doxorubicin hydrochloride Drug: etoposide phosphate Drug: vincristine sulfate Procedure: adjuvant therapy Procedure: neoadjuvant therapy Procedure: therapeutic conventional surgery |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Treatment for Patients With Bilateral, Multicentric, or Bilaterally-Predisposed Unilateral Wilms Tumor |
- 4-year event-free survival [ Designated as safety issue: No ]
- Prevention of complete removal of at least one kidney in 50% of patients with bilateral Wilms tumor (BWT) [ Designated as safety issue: No ]
- Efficacy of chemotherapy in preserving renal units and preventing Wilms tumor development in patients with diffuse hyperplastic perilobular nephrogenic rests [ Designated as safety issue: No ]
- Facilitation of partial nephrectomy in lieu of total nephrectomy in 25% of patients with unilateral Wilms tumor [ Designated as safety issue: No ]
- Percentage of patients with BWT undergoing definitive surgical treatment by week 12 [ Designated as safety issue: No ]
| Estimated Enrollment: | 260 |
| Study Start Date: | July 2009 |
| Estimated Primary Completion Date: | March 2015 (Final data collection date for primary outcome measure) |
Show Detailed Description
Eligibility| Ages Eligible for Study: | up to 29 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Diagnosis of 1 of the following:
- Synchronous or metachronous bilateral Wilms tumor (BWT)*
Unilateral Wilms tumor (WT) AND aniridia, Beckwith-Wiedemann syndrome, idiopathic hemihypertrophy, Simpson-Golabi-Behmel syndrome, Denys-Drash syndrome, or other associated genitourinary anomalies associated with bilateral Wilms tumor, such as hypospadias and undescended testis
- To be eligible, these patients must not undergo any nephrectomy at diagnosis
- Note: horseshoe kidney is not associated with bilateral Wilms tumor and these patients should go on the appropriate unilateral Wilms tumor study)
Multicentric WT (any age)
- To be eligible, these patients must not undergo any nephrectomy at diagnosis
Multicentric WT or unilateral WT with contralateral nephrogenic rest(s) (any size) in a patient < 1 year of age
- To be eligible, these patients must not undergo any nephrectomy at diagnosis
- Diffuse hyperplastic perilobar nephroblastomatosis (unilateral or bilateral) defined by central radiological review
WT arising in a solitary kidney
- Patients with metachronous WT are not eligible NOTE: *It is often difficult to distinguish WT from nephrogenic rests based on imaging studies and percutaneous biopsies. The AREN0534 study uses the guideline that WT with a single lesion 1 cm or greater in the contralateral kidney or multiple lesions (of any size) in the contralateral kidney should be treated on the synchronous bilateral WT stratum. Patients with an isolated lesion less than 1 cm in the contralateral kidney should be treated on the appropriate study for unilateral WT OR on the unilateral WT/contralateral nephrogenic rest stratum of this study if they have not undergone nephrectomy and are under one year of age.
- Patients with BWT who underwent total or partial nephrectomy at diagnosis are eligible
- Previously enrolled in COG-AREN03B2
- Loss of heterozygosity (LOH) results—which are used in the unilateral WT studies—are not a requirement for enrollment on AREN0534
- Patients must begin protocol therapy by Day 14 following surgery or diagnosis by initial CT/MRI, unless medically contraindicated
PATIENT CHARACTERISTICS:
- Karnofsky performance status (PS) 50-100% (for patients > 16 years of age) or Lansky PS 50-100% (for patients ≤ 16 years of age)
- Total bilirubin ≤ 1.5 times upper limit of normal (ULN) for age
- AST or ALT < 2.5 times ULN for age
Shortening fraction ≥ 27% by ECHO OR ejection fraction ≥ 50% by radionuclide angiogram
- Cardiac function does not need to be assessed in patients who will not receive doxorubicin as part of their initial therapy on this study (i.e., patients who start on Regimen EE-4A)
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No prior systemic chemotherapy or radiotherapy
- No concurrent aprepitant
Contacts and Locations
Show 136 Study Locations| Study Chair: | Peter F. Ehrlich, MD, MSC | C.S. Mott Children's Hospital at University of Michigan Medical Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | Gregory H. Reaman, Children's Oncology Group - Group Chair Office |
| ClinicalTrials.gov Identifier: | NCT00945009 History of Changes |
| Other Study ID Numbers: | CDR0000649716, COG-AREN0534 |
| Study First Received: | July 22, 2009 |
| Last Updated: | November 21, 2012 |
| Health Authority: | Unspecified |
Keywords provided by National Cancer Institute (NCI):
|
stage I Wilms tumor stage II Wilms tumor stage III Wilms tumor stage IV Wilms tumor |
stage V Wilms tumor rhabdoid tumor of the kidney diffuse hyperplastic perilobar nephroblastomatosis |
Additional relevant MeSH terms:
|
Carcinoma, Renal Cell Kidney Neoplasms Wilms Tumor Adenocarcinoma Carcinoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Urologic Neoplasms Urogenital Neoplasms Neoplasms by Site Kidney Diseases Urologic Diseases Neoplasms, Complex and Mixed Neoplastic Syndromes, Hereditary |
Genetic Diseases, Inborn Dactinomycin Doxorubicin Etoposide phosphate Cyclophosphamide Etoposide Vincristine Carboplatin Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Protein Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on May 22, 2013