Germ Cell Tumor and Testicular Tumor DNA Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

This study is being done to create a registry to help us learn more about germ cell tumors (GCT) and other testicular tumors. The registry will include people with these tumors and also relatives and unrelated people without these tumors. This study will help us learn more about the prevention, diagnosis, treatment and outcome of these tumors. Studying relatives of patients and people unrelated to patients with GCT and other testicular tumors will help us understand why some people get these tumors and why some people don't.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Must be ≥ 18 years of age AND

Must be an English-speaker AND

Must have a diagnosis or suspicion of germ cell tumor and/or a testicular mass

Must be ≥ 18 years of age AND

Disqualifiers

None

Trial population

At MSKCC, the following outpatient clinics will be used to recruit GCT and testicular tumor cases and controls: Urology (Department of Surgery), Gynecologic Oncology (Department of Surgery) Clinical Genetics, Genitourinary Oncology (Department of Medicine), and Gynecologic Medical Oncology (Department of Medicine).

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Questionnaires

    Behavioral
  • sample of blood or saliva

    Other intervention

    A sample of blood or saliva will be obtained for DNA extraction. Approximately 2-4 tubes of blood will be collected or one tablespoon of saliva. If a participant has already provided a DNA sample for another MSKCC IRB approved protocol, they may not need to provide an additional sample.

Treatment groups

1,000 Participants
are divided into 3 treatment groups
Group A: A: suspicion of germ cell tumor and/or a testicular mass2 interventions
Group B: B: family members of Group A2 interventions
Group C: C: healthy controls unrelated to Group A or B2 interventions

Trial outcomes

Primary outcomes

1

creation of a Germ Cell Tumor and testicular tumor registry

We will collect clinical data including diagnosis date, pathology, family history, and risk factors in patients with GCT-TT.

Time frame
5 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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