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Search / Trial NCT01857453

Interest of a Dose Decrease for Radiotherapy Associated With Chemotherapy for Treatment of Standard Risk Adult Medulloblastomas

Launched by CENTRAL HOSPITAL, NANCY, FRANCE · May 16, 2013

Trial Information

Current as of May 27, 2025

Unknown status

Keywords

Adult Patients Medulloblatoma Standard Risk Group Chemotherapy Radiotherapy Quality Of Life

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Pathologic diagnosis of medulloblastoma expect large cells type
  • Patients between 18 and 70 years
  • Résidual tumor les than 1.5 square centimeter (greater diameter)
  • No sus tentorial or spinal location
  • Absence of tumoral cells in the cerebrospinal fluid taken before, during or 14 days after surgery
  • Absence of MYC amplification
  • AID, B and C hepatitis positive serologies
  • Negative βHCG dosage and effective contraception for potentially pregnant women
  • Writed consent obtain
  • Exclusion Criteria:
  • Age \< 18 or \> 70 years
  • Previous diagnosis of medulloblastoma
  • Previous treatment with chemotherapy
  • Previous cranial or spinal radiation therapy
  • Carboplatinum or etoposide contraindication
  • Previous cancer in the five years before the inclusion except basocellular carcinoma of the skin and in situ cancer of the uterine cervix
  • Severe renal renal insufficiency with a creatinine clearance \< 60 ml/min
  • Liver insufficiency with a contraindication of carboplatinum or etoposide based chemotherapy or elevated transaminases \> 3N.
  • Insufficient haematopoetic reserve (thrombocytes \< 100 000/mm3 ou neutrophil polynuclear \< 1500/mm3)
  • Previous organ transplantation or immunosuppression
  • Pregnant women or women without contraception
  • Incapacity of respecting the recommanded follow up
  • Participation in another therapeutic clinical trial
  • Patient under custody
  • Not social security regime membership

About Central Hospital, Nancy, France

Central Hospital, located in Nancy, France, is a leading healthcare institution dedicated to advancing medical research and improving patient outcomes. As a prominent clinical trial sponsor, the hospital is committed to conducting innovative studies across various therapeutic areas, fostering collaboration among multidisciplinary teams of healthcare professionals and researchers. With a strong emphasis on ethical standards and patient safety, Central Hospital leverages its state-of-the-art facilities and expertise to contribute to the development of cutting-edge treatments and enhance the overall quality of care within the community and beyond.

Locations

Strasbourg, , France

Villejuif, , France

Colmar, , France

Paris, , France

Toulouse, , France

Lille, , France

Marseille, , France

Montpellier, , France

Nimes, , France

Caen, , France

Nancy, , France

Rennes, , France

Nice, , France

Bordeaux, , France

Amiens, , France

Dijon, , France

Lyon, , France

Nantes, , France

Paris, , France

Reims, , France

Patients applied

0 patients applied

Trial Officials

Luc TAILLANDIER

Principal Investigator

CHU NANCY - France

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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