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Bleomycin, Etoposide, and Cisplatin in Treating Patients With Metastatic Germ Cell Cancer of the Testicles

Primary Purpose

Drug/Agent Toxicity by Tissue/Organ, Testicular Germ Cell Tumor

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
bleomycin sulfate
cisplatin
etoposide
management of therapy complications
Sponsored by
Queen Mary University of London
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Drug/Agent Toxicity by Tissue/Organ focused on measuring drug/agent toxicity by tissue/organ, stage III malignant testicular germ cell tumor

Eligibility Criteria

18 Years - 50 Years (Adult)MaleDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Diagnosis of metastatic germ cell cancer of the testes Good-prognosis disease Eligible for treatment with bleomycin, etoposide, and cisplatin PATIENT CHARACTERISTICS: Creatinine clearance ≥ 60 mL/min No other prior or concurrent malignancy except basal cell skin cancer No other major systemic illness No impaired respiratory function, including any of the following: Shortness of breath on minimal exertion Hypoxia at rest Carbon monoxide transfer, total lung capacity, and FEV_1 > 60% of predicted PRIOR CONCURRENT THERAPY: No prior chemotherapy or radiotherapy

Sites / Locations

  • Basildon University Hospital
  • Addenbrooke's Hospital
  • Essex County Hospital
  • Ipswich Hospital
  • Leeds Cancer Centre at St. James's University Hospital
  • Saint Bartholomew's Hospital
  • University College of London Hospitals
  • Norfolk and Norwich University Hospital
  • Royal Marsden - Surrey
  • Southend University Hospital NHS Foundation Trust

Outcomes

Primary Outcome Measures

Pulmonary toxicity

Secondary Outcome Measures

Response to treatment
Progression-free survival
Overall survival

Full Information

First Posted
May 10, 2006
Last Updated
August 9, 2013
Sponsor
Queen Mary University of London
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1. Study Identification

Unique Protocol Identification Number
NCT00324298
Brief Title
Bleomycin, Etoposide, and Cisplatin in Treating Patients With Metastatic Germ Cell Cancer of the Testicles
Official Title
A Randomized Phase III Toxicity Study of Day 2, 3, 8, 15 Short (30 Minute) Versus Day 1, 2, 3 Long (72 Hours) Infusion Bleomycin for Patients With IGCCCG Good Prognosis Germ Cell Tumors, TE3
Study Type
Interventional

2. Study Status

Record Verification Date
January 2007
Overall Recruitment Status
Completed
Study Start Date
July 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Queen Mary University of London

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy, such as bleomycin, etoposide, and cisplatin, 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. It is not yet known which schedule of bleomycin is more effective when given together with etoposide and cisplatin in treating metastatic germ cell cancer of the testicles. PURPOSE: This randomized phase III trial is studying two different schedules of bleomycin to compare how well they work when given together with etoposide and cisplatin in treating patients with metastatic germ cell cancer of the testicles.
Detailed Description
OBJECTIVES: Primary Determine if long-infusion schedule of bleomycin is less toxic to the lungs than short-infusion schedule of bleomycin in patients who are undergoing combination chemotherapy comprising bleomycin, etoposide, and cisplatin for good-prognosis, metastatic germ cell cancer of the testes. Determine if early lung function tests are a predictor for late toxicity. Determine if any indication of enhanced response to the long-infusion schedule justifies a large-scale phase III evaluation. Validate the O'Sullivan et al prognostic scoring system for bleomycin toxicity. Secondary Determine response to treatment. Determine progression-free survival and overall survival of patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to age (≤ 30 years vs > 30 years), current smoker or has smoked within the past 1 year (yes vs no), and creatinine clearance (≤ 80 mL/min vs > 80 mL/min). Patients are randomized to 1 of 2 treatment arms. Arm I (short-infusion schedule of bleomycin): Patients receive etoposide IV over 2 hours on days 1-3, cisplatin IV over 4 hours on days 1 and 2, and bleomycin IV over 30 minutes on days 2, 8, and 15. Arm II (long-infusion schedule of bleomycin): Patients receive etoposide and cisplatin as in arm I. Patients also receive bleomycin IV continuously over 72 hours on days 1-3. In both arms, treatment repeats every 3 weeks for up to 3 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed at 4 weeks and then every 3 months for 24 months. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 210 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Drug/Agent Toxicity by Tissue/Organ, Testicular Germ Cell Tumor
Keywords
drug/agent toxicity by tissue/organ, stage III malignant testicular germ cell tumor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
bleomycin sulfate
Intervention Type
Drug
Intervention Name(s)
cisplatin
Intervention Type
Drug
Intervention Name(s)
etoposide
Intervention Type
Procedure
Intervention Name(s)
management of therapy complications
Primary Outcome Measure Information:
Title
Pulmonary toxicity
Secondary Outcome Measure Information:
Title
Response to treatment
Title
Progression-free survival
Title
Overall survival

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of metastatic germ cell cancer of the testes Good-prognosis disease Eligible for treatment with bleomycin, etoposide, and cisplatin PATIENT CHARACTERISTICS: Creatinine clearance ≥ 60 mL/min No other prior or concurrent malignancy except basal cell skin cancer No other major systemic illness No impaired respiratory function, including any of the following: Shortness of breath on minimal exertion Hypoxia at rest Carbon monoxide transfer, total lung capacity, and FEV_1 > 60% of predicted PRIOR CONCURRENT THERAPY: No prior chemotherapy or radiotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Shamash, MD, FRCP
Organizational Affiliation
St. Bartholomew's Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Basildon University Hospital
City
Basildon
State/Province
England
ZIP/Postal Code
SS16 5NL
Country
United Kingdom
Facility Name
Addenbrooke's Hospital
City
Cambridge
State/Province
England
ZIP/Postal Code
CB2 2QQ
Country
United Kingdom
Facility Name
Essex County Hospital
City
Colchester
State/Province
England
ZIP/Postal Code
C03 3NB
Country
United Kingdom
Facility Name
Ipswich Hospital
City
Ipswich
State/Province
England
ZIP/Postal Code
IP4 5PD
Country
United Kingdom
Facility Name
Leeds Cancer Centre at St. James's University Hospital
City
Leeds
State/Province
England
ZIP/Postal Code
LS9 7TF
Country
United Kingdom
Facility Name
Saint Bartholomew's Hospital
City
London
State/Province
England
ZIP/Postal Code
EC1A 7BE
Country
United Kingdom
Facility Name
University College of London Hospitals
City
London
State/Province
England
ZIP/Postal Code
WIT 3AA
Country
United Kingdom
Facility Name
Norfolk and Norwich University Hospital
City
Norwich
State/Province
England
ZIP/Postal Code
NR4 7UY
Country
United Kingdom
Facility Name
Royal Marsden - Surrey
City
Sutton
State/Province
England
ZIP/Postal Code
SM2 5PT
Country
United Kingdom
Facility Name
Southend University Hospital NHS Foundation Trust
City
Westcliff-On-Sea
State/Province
England
ZIP/Postal Code
SS0 0RY
Country
United Kingdom

12. IPD Sharing Statement

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Bleomycin, Etoposide, and Cisplatin in Treating Patients With Metastatic Germ Cell Cancer of the Testicles

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