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Search / Trial NCT00045045

Positron Emission Tomography in Detecting Testicle Cancer

Launched by INSTITUTE OF CANCER RESEARCH, UNITED KINGDOM · Jan 26, 2003

Trial Information

Current as of June 12, 2025

Completed

Keywords

Stage I Malignant Testicular Germ Cell Tumor Testicular Choriocarcinoma Testicular Choriocarcinoma And Embryonal Carcinoma Testicular Choriocarcinoma And Seminoma Testicular Choriocarcinoma And Teratoma Testicular Choriocarcinoma And Yolk Sac Tumor Testicular Embryonal Carcinoma And Seminoma Testicular Embryonal Carcinoma And Teratoma With Seminoma Testicular Embryonal Carcinoma And Teratoma Testicular Embryonal Carcinoma And Yolk Sac Tumor With Seminoma Testicular Embryonal Carcinoma And Yolk Sac Tumor Testicular Embryonal Carcinoma Testicular Teratoma Testicular Yolk Sac Tumor And Teratoma With Seminoma Testicular Yolk Sac Tumor And Teratoma Testicular Yolk Sac Tumor

ClinConnect Summary

OBJECTIVES:

* Assess the ability of fludeoxyglucose F 18 positron emission tomography to predict relapse requiring adjuvant chemotherapy in patients with high-risk stage I non-seminomatous or mixed seminoma/non-seminomatous germ cell tumor of the testis who are on current management protocols.

OUTLINE: This is a multicenter study.

Patients receive fludeoxyglucose F 18 (FDG) IV followed 1 hour later by positron emission tomography (PET) imaging. Patients with metastatic disease identified by FDG PET imaging may receive adjuvant chemotherapy according to the standard clinical practice at e...

Gender

MALE

Eligibility criteria

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed non-seminomatous or mixed seminoma/non-seminomatous germ cell tumor of the testis with evidence of vascular (lymphatic or venous) invasion in primary specimen
  • Clinical stage I on the basis of clinical examination, chest x-ray, and CT scan of the chest, abdomen, and pelvis
  • Negative post-orchidectomy tumor markers (alpha-fetoprotein and beta human chorionic gonadotropin)
  • High-risk disease
  • PATIENT CHARACTERISTICS:
  • Age
  • Any age
  • Performance status
  • Not specified
  • Life expectancy
  • Not specified
  • Hematopoietic
  • Not specified
  • Hepatic
  • Not specified
  • Renal
  • Not specified
  • Other
  • No evidence of active inflammatory or infective diseases
  • No other disease or prior malignancy that would preclude study
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy
  • Not specified
  • Chemotherapy
  • Not specified
  • Endocrine therapy
  • Not specified
  • Radiotherapy
  • Not specified
  • Surgery
  • See Disease Characteristics
  • No more than 8 weeks since prior orchidectomy
  • Other
  • No prior positron emission tomography scans

About Institute Of Cancer Research, United Kingdom

The Institute of Cancer Research (ICR) in the United Kingdom is a leading cancer research organization dedicated to understanding the biology of cancer and developing innovative therapeutic strategies. Renowned for its pioneering contributions to cancer treatment and prevention, the ICR conducts cutting-edge clinical trials that translate laboratory discoveries into effective clinical applications. Collaborating with a network of academic, clinical, and industry partners, the ICR is committed to advancing cancer research and improving patient outcomes through rigorous scientific inquiry and a patient-centered approach.

Locations

Glasgow, Scotland, United Kingdom

Southampton, England, United Kingdom

Nottingham, England, United Kingdom

Exeter, England, United Kingdom

Sutton, England, United Kingdom

Ipswich, England, United Kingdom

London, England, United Kingdom

London, England, United Kingdom

Patients applied

0 patients applied

Trial Officials

Robert A. Huddart, MD

Study Chair

Royal Marsden NHS Foundation Trust

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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