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A Phase II Study of Iressa in Patients With Chemo Refractory Germ Cell Tumors Expressing EGFR (IUCRO-0021)

Primary Purpose

Refractory Germ Cell Tumors Expressing EGRF

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
ZD1839 Iressa
Sponsored by
Indiana University School of Medicine
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Germ Cell Tumors Expressing EGRF focused on measuring Refractory Germ Cell Tumors, Germ Cell Tumors

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histologic or serologic proof of metastatic germ cell neoplasm(gonadal or extragonadal primary) with disease not amenable to cure with either surgery or chemotherapy. Patients w/ seminoma and non-seminoma are eligible, as are women w/ ovarian germ cell tumors. Evidence of recurrent or metastatic carcinoma Must have received initial cisplatin combination therapy & demonstrated progression following the administration of at least one "salvage" regimen for advanced germ cell neoplasms. Patients are eligible after first line platinum bsed chemotherapy if their disease has relapsed and they have primary mediastinal non seminomatous germ cell tumor, late relapse or progressed w/in 4 wks of last platinum dose. immunohistochemical documentation of EGFR expression documented. adequate organ function: ANC >/=150,plt >100K, total bili </= upper limit of normal(ULN). Pts w/ liver mets up to 3x ULN.Transaminases up to 1.5 x ULN if alk phos is </=ULN or alk phos may be up to 4x ULN if transaminases are </= ULN. Pts w/ liver mets may have alk phos up to 5x ULN. Serum crt </= 2.0. ECOG performance status 0-2. Exclusion Criteria: Must be 3 weeks post major surgery, radiotherapy, or chemotherapy and hae recovered from all toxicity. Active unresolved infection and/or are receiving concurrent treatment with parenteral antibiotics are ineligible. Patients requiring steroids for symptomatic brain metastasis are not eligible. Pregnant or lactating patients are not eligible. Class III/IV heart disease

Sites / Locations

  • Indiana University Cancer Center

Outcomes

Primary Outcome Measures

To determine the response rate of ZD1839

Secondary Outcome Measures

To determine duration of response, time to progression and overall survival

Full Information

First Posted
September 8, 2005
Last Updated
September 18, 2014
Sponsor
Indiana University School of Medicine
Collaborators
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT00198159
Brief Title
A Phase II Study of Iressa in Patients With Chemo Refractory Germ Cell Tumors Expressing EGFR
Acronym
IUCRO-0021
Official Title
A Phase II Study of ZD1839 (Iressa)in Chemotherapy Refractory Germ Cell Tumors Expressing Epidermal Growth Factor Receptor (EGFR)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Terminated
Study Start Date
September 2002 (undefined)
Primary Completion Date
February 2006 (Actual)
Study Completion Date
March 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Indiana University School of Medicine
Collaborators
AstraZeneca

4. Oversight

5. Study Description

Brief Summary
This study will evaluate the use of ZD1839 in the treatment of subjects with refractory germ cell tumors. Subjects will take ZD1839 for one year in the absence of excessive toxicity or decision to withdraw.
Detailed Description
The primary objective is to determine the response rate of ZD1839 in patients with refractory germ cell tumors expressing EGFR. The secondary objectives are to determine the duration of response, time to progression and overall survival in patients with refractory germ cell tumors expressing EGFR and treated with ZD1839; to evaluate the tolerability of ZD1839 in patients with refractory germ cell tumors and to correlate tumor response to degree of EGFR expression by immunohistochemistry.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Germ Cell Tumors Expressing EGRF
Keywords
Refractory Germ Cell Tumors, Germ Cell Tumors

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
21 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
ZD1839 Iressa
Primary Outcome Measure Information:
Title
To determine the response rate of ZD1839
Secondary Outcome Measure Information:
Title
To determine duration of response, time to progression and overall survival

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic or serologic proof of metastatic germ cell neoplasm(gonadal or extragonadal primary) with disease not amenable to cure with either surgery or chemotherapy. Patients w/ seminoma and non-seminoma are eligible, as are women w/ ovarian germ cell tumors. Evidence of recurrent or metastatic carcinoma Must have received initial cisplatin combination therapy & demonstrated progression following the administration of at least one "salvage" regimen for advanced germ cell neoplasms. Patients are eligible after first line platinum bsed chemotherapy if their disease has relapsed and they have primary mediastinal non seminomatous germ cell tumor, late relapse or progressed w/in 4 wks of last platinum dose. immunohistochemical documentation of EGFR expression documented. adequate organ function: ANC >/=150,plt >100K, total bili </= upper limit of normal(ULN). Pts w/ liver mets up to 3x ULN.Transaminases up to 1.5 x ULN if alk phos is </=ULN or alk phos may be up to 4x ULN if transaminases are </= ULN. Pts w/ liver mets may have alk phos up to 5x ULN. Serum crt </= 2.0. ECOG performance status 0-2. Exclusion Criteria: Must be 3 weeks post major surgery, radiotherapy, or chemotherapy and hae recovered from all toxicity. Active unresolved infection and/or are receiving concurrent treatment with parenteral antibiotics are ineligible. Patients requiring steroids for symptomatic brain metastasis are not eligible. Pregnant or lactating patients are not eligible. Class III/IV heart disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lawrence Einhorn, M
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indiana University Cancer Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Phase II Study of Iressa in Patients With Chemo Refractory Germ Cell Tumors Expressing EGFR

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