Vanderbilt Clinical Trials

Eligibility

Eligible Ages

Over 18 Years

Eligible Genders

All

Accepts Healthy Volunteers

No

Criteria

Inclusion Criteria:

- Patients must have a new diagnosis of a germ cell tumor. confirmed pathologically or
serologically (diagnostic elevation of human chorionic gonadotropin
[HCG]/alpha-fetoprotein [AFP]). All primary sites, stages, histological subtypes of
germ cell tumor are eligible. Metachronous second primary germ cell tumors are
eligible

- If surgery is planned, male patients with clinical stage I testicular cancer must
have orchiectomy completed within 42 days prior to registration

- Patients must be registered within 42 days after diagnosis and prior to initiation
of a management plan or treatment for the disease

- Patients must have initial imaging, laboratory and other clinical evaluations (see
below) performed within 42 days prior to registration. Imaging reports, pathology
reports and performance status will be collected

- Patients must have beta-human chorionic gonadotropin (beta- HCG), alpha-fetoprotein
(AFP), and lactate dehydrogenase (LDH) assessments within 42 days prior to
registration

- NOTE: If the patient had an orchiectomy prior to registration, report tumor
marker values before and after surgery on the Baseline Tumor Marker form

- Patients must have risk of relapse assessment determined by the local investigator
prior to registration

- Patients must agree to submit required specimens for defined translational medicine
studies. These specimens are drawn at the same time as standard laboratory
evaluations (beta-HCG, AFP, and LDH); NOTE: Ideally, patients should be willing to
return to their center performing surveillance (registering site) for the duration
of the study to ensure that specimens are timed to standard clinical observations
(the registering site's surveillance schedule)

- Patients must be offered participation in specimen banking for future research. With
patient's consent, specimens must be submitted.

- Patients must be informed of the investigational nature of this study and must sign
and give written informed consent in accordance with institutional and federal
guidelines

- As a part of the Oncology Patient Enrollment Network (OPEN) registration process the
treating institution's identity is provided in order to ensure that the current
(within 365 days) date of institutional review board approval for this study has
been entered in the system