A Phase II Study of Topotecan in Children With Recurrent Wilms Tumor
Primary Purpose
Wilms Tumor
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Topotecan, Filgrastim (G-CSF), Pegfilgrastim
Sponsored by
About this trial
This is an interventional treatment trial for Wilms Tumor focused on measuring Wilms Tumor
Eligibility Criteria
Inclusion Criteria: Favorable histology Wilms tumor that has recurred or progressed after primary treatment and at least one standard salvage treatment regimen OR anaplastic histology Wilms tumor that has recurred or progressed after primary treatment Age< 21 years of age at the time of study entry Adequate bone marrow function Adequate liver function Adequate renal function Adequate performance status Exclusion Criteria: Subject is pregnant Subject is lactating Renal tumors other than Wilms tumors
Sites / Locations
- Children's Healthcare
- Dana Farber
- St. Jude Children's Research Hospital
- Baylor College of Medicine
- Tom Baker Cancer Center
- Alberta Children's Hospital
- Hospital of Sick Children
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
1
Arm Description
Outcomes
Primary Outcome Measures
Response rate (complete and partial response as per RECIST criteria).
Secondary Outcome Measures
Full Information
NCT ID
NCT00187031
First Posted
September 12, 2005
Last Updated
June 3, 2008
Sponsor
St. Jude Children's Research Hospital
Collaborators
GlaxoSmithKline, National Institutes of Health (NIH)
1. Study Identification
Unique Protocol Identification Number
NCT00187031
Brief Title
A Phase II Study of Topotecan in Children With Recurrent Wilms Tumor
Official Title
A Phase II Study of Topotecan in Children With Recurrent Wilms Tumor
Study Type
Interventional
2. Study Status
Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
November 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
St. Jude Children's Research Hospital
Collaborators
GlaxoSmithKline, National Institutes of Health (NIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In spite of the overall success of treating Wilms tumor, certain patients still have poor clinical outcomes. The sub-optimal outcomes for patients with anaplastic histology and recurrent Wilms tumor warrant the identification of new therapeutic agents. The objective of this trial is to estimate the response rate to two cycles of intravenous topotecan in children with recurrent Wilms tumor of favorable histology that is refractory to standard curative therapy.
Detailed Description
Topotecan administered intravenously over 30 minutes daily for 5 consecutive days for 2 consecutive weeks, with a two-day rest given in between the five-day treatment blocks. The topotecan dose started at 1.8 mg/m2/dosage and adjusted to attain a target systemic exposure of 80 plus or minus 10 ng-hr/ml.each cycle consists of 28 days and subsequent cycles can be administered upon hematological recovery. Patients with a CR, PR, or SD, can continue to receive up to a total of six cycles. Patients with PD are removed from the study.
Secondary Objectives include:
To describe the anti-tumor activity of topotecan in children with recurrent Wilms tumor of anaplastic histology.
To assess the relation between CYP3A4/5 genotype and the pharmacokinetics and pharmacodynamics of topotecan.
To assess the relation between ABCG2 genotype and the pharmacokinetics and pharmacodynamics of topotecan.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wilms Tumor
Keywords
Wilms Tumor
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
37 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Other
Intervention Type
Drug
Intervention Name(s)
Topotecan, Filgrastim (G-CSF), Pegfilgrastim
Intervention Description
See detailed description section for additional details.
Primary Outcome Measure Information:
Title
Response rate (complete and partial response as per RECIST criteria).
Time Frame
5 years
10. Eligibility
Sex
All
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Favorable histology Wilms tumor that has recurred or progressed after primary treatment and at least one standard salvage treatment regimen OR anaplastic histology Wilms tumor that has recurred or progressed after primary treatment
Age< 21 years of age at the time of study entry
Adequate bone marrow function
Adequate liver function
Adequate renal function
Adequate performance status
Exclusion Criteria:
Subject is pregnant
Subject is lactating
Renal tumors other than Wilms tumors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Monika Metzger, MD
Organizational Affiliation
St. Jude Children's Research Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30301
Country
United States
Facility Name
Dana Farber
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115-6084
Country
United States
Facility Name
St. Jude Children's Research Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38105
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Tom Baker Cancer Center
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4N2
Country
Canada
Facility Name
Alberta Children's Hospital
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2W 3N2
Country
Canada
Facility Name
Hospital of Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
17634492
Citation
Metzger ML, Stewart CF, Freeman BB 3rd, Billups CA, Hoffer FA, Wu J, Coppes MJ, Grant R, Chintagumpala M, Mullen EA, Alvarado C, Daw NC, Dome JS. Topotecan is active against Wilms' tumor: results of a multi-institutional phase II study. J Clin Oncol. 2007 Jul 20;25(21):3130-6. doi: 10.1200/JCO.2007.10.9298.
Results Reference
background
Links:
URL
http://www.stjude.org
Description
St. Jude Children's Research Hospital
Learn more about this trial
A Phase II Study of Topotecan in Children With Recurrent Wilms Tumor
We'll reach out to this number within 24 hrs