iTestis: Development of a detailed database for collection of clinical data in patients with testicular cancer
Not Applicable
Recruiting
- Conditions
- testicular cancerCancer - Testicular
- Registration Number
- ACTRN12618000735257
- Lead Sponsor
- Walter and Eliza Hall Institute for Medical Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 300
Inclusion Criteria
Histologically or cytologically confirmed GCT (non-seminoma or seminoma); or exceptionally raised tumour markers (AFP greater then or equal to 1000ng/mL and/or HCG greater than or equal to 5000 IU/L) without histological or cytological confirmation in the rare case where biopsy may not be feasible.
Primary arising in testis, retro-peritoneum, or mediastinum.
Exclusion Criteria
None
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of patients diagnosed with Germ Cell Tumour (GCT) in Australia that are recurrence-free after treatment. This outcome is being assessed from each patient's medical record,[End of 4 year data collection period. Data will be collected at up to 6 timepoints:<br>Diagnosis<br>Surgery<br>Surveillance<br>Chemotherapy<br>Radiotherapy<br>Recurrence]
- Secondary Outcome Measures
Name Time Method Overall survival of patients diagnosed with Germ Cell Tumour (GCT) in Australia after treatment. This outcome is being assessed from each patient's medical record,[End of 4 year data collection period. Data will be collected at up to 6 timepoints:<br>Diagnosis<br>Surgery<br>Surveillance<br>Chemotherapy<br>Radiotherapy<br>Recurrence]