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Search / Trial NCT00002472

Cisplatin and Etoposide Prior to Radiation Therapy in Treating Patients With CNS Tumors

Launched by MAYO CLINIC · Jan 26, 2003

Trial Information

Current as of March 23, 2025

Completed

Keywords

Childhood Central Nervous System Germ Cell Tumor Extragonadal Germ Cell Tumor Adult Central Nervous System Germ Cell Tumor Childhood Teratoma Childhood Central Nervous System Choriocarcinoma Childhood Central Nervous System Embryonal Tumor Childhood Central Nervous System Germinoma Childhood Central Nervous System Mixed Germ Cell Tumor Childhood Central Nervous System Teratoma Childhood Central Nervous System Yolk Sac Tumor

ClinConnect Summary

OBJECTIVES:

* Determine the response rate of patients with newly diagnosed CNS germ cell tumors treated with cisplatin and etoposide.
* Determine the survival of patients with CNS germ cell tumors treated with cisplatin and etoposide followed by cranial radiotherapy.
* Determine endocrine and cognitive function in these patients before and after receiving this regimen.

OUTLINE: Patients are stratified by histology (germinoma vs nongerminoma).

Patients receive cisplatin IV over 4 hours followed by etoposide IV over 30-60 minutes on days 1-5. Treatment continues every 3 weeks for 4 courses...

Gender

ALL

Eligibility criteria

  • DISEASE CHARACTERISTICS:
  • * Histologically proven CNS germ cell tumor of 1 of the following subtypes:
  • CNS germinoma
  • Immature teratoma
  • Embryonal cell carcinoma
  • Yolk sac tumor
  • Endodermal sinus tumor
  • Choriocarcinoma OR
  • Pineal or suprasellar mass associated with elevated CSF alpha fetoprotein or beta-human chorionic gonadotropin allowed
  • Patients 18 years and over with localized pure germinomas ineligible
  • Evaluable CT or MRI of brain and/or spinal cord required
  • PATIENT CHARACTERISTICS:
  • Age:
  • 3 and over
  • Hematopoietic:
  • * Age 18 and over:
  • WBC at least 4,000/mm\^3
  • Platelet count at least 100,000/mm\^3
  • * Under age 18:
  • Absolute neutrophil count at least 1,000/mm\^3
  • Platelet count at least 100,000/mm\^3
  • Hepatic:
  • Not specified
  • Renal:
  • Creatinine no greater than 0.3 mg/dL above upper limit of normal for age
  • Other:
  • No uncontrolled infection
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy:
  • Not specified
  • Chemotherapy:
  • No prior chemotherapy for CNS germ cell tumor
  • Endocrine therapy:
  • Concurrent corticosteroids allowed except as antiemetics
  • Radiotherapy:
  • No prior cranial or spinal radiotherapy
  • Surgery:
  • Not specified

Trial Officials

Jan C. Buckner, MD

Study Chair

Mayo Clinic

About Mayo Clinic

Mayo Clinic is a renowned nonprofit medical practice and research institution dedicated to providing comprehensive healthcare and advancing medical knowledge through innovative research and education. With a commitment to patient-centered care, Mayo Clinic conducts numerous clinical trials aimed at exploring new therapies and improving treatment outcomes across various disciplines. Leveraging a multidisciplinary approach, the institution collaborates with leading experts and cutting-edge technology to ensure rigorous scientific standards and ethical practices in all its research endeavors. Through its trials, Mayo Clinic seeks to translate breakthroughs in science into tangible benefits for patients, fostering advancements in medicine that enhance health and quality of life.

Locations

Scottsdale, Arizona, United States

Jacksonville, Florida, United States

Rochester, Minnesota, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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