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Temozolomide,Thiotepa and Carboplatin With Autologous Stem Cell Rescue Followed by 13-Cis-Retinoic Acid in Patients With Recurrent/Refractory Malignant Brain Tumors
This study is currently recruiting participants.
Verified by New York University School of Medicine, May 2008
First Received: September 10, 2007   Last Updated: May 21, 2008   History of Changes
Sponsor: New York University School of Medicine
Collaborators: Children's Hospitals and Clinics of Minnesota
Schneider Children's Hospital
Information provided by: New York University School of Medicine
ClinicalTrials.gov Identifier: NCT00528437
  Purpose

The purpose of this study is to:

Find out how safe and effective (by monitoring the good and/or bad effects) treatment with high dose temozolomide, thiotepa and carboplatin with stem cell rescue followed by 13-cisretinoic acid has on children and adolescents with recurrent/refractory brain tumors

Find out how the body uses 13-cisretinoic acid by studying the your blood levels and proteins in the blood that break down the 13-cisretinoic acid

Determine how well 13-cisretinoic acid penetrates into the spinal fluid.


Condition Intervention Phase
Brain Tumors
Drug: temozolomide, thiotepa, carboplatin, 13-cis-retinoic acid
Phase II

Study Type: Interventional
Study Design: Treatment, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: NYU 05-40 PBMTC ONC-032P:High Dose Temozolomide,Thiotepa and Carboplatin With Autologous Stem Cell Rescue (ASCR) Followed by Continuation Therapy With 13-Cis-Retinoic Acid in Patients With Recurrent/Refractory Malignant Brain Tumors

Resource links provided by NLM:


Further study details as provided by New York University School of Medicine:

Primary Outcome Measures:
  • Assess the event-free and overall survival of patients with recurrent or refractory medulloblastoma,primitive neuroectodermal tumors treated with temozolomide, thiotepa and carboplatin with ASCR followed by continuation therapy with 13-cis-retinoic acid.

Secondary Outcome Measures:
  • To evaluate the toxicity of of 13-cis-retinoic acid following high dose temozolomide, thiotepa and carboplatin with ASCR.

Estimated Enrollment: 36
Study Start Date: October 2005
Detailed Description:

Researchers have used high doses of combination chemotherapy followed by a stem cell rescue to treat recurrent brain tumors with moderate success. High dose chemotherapy with stem cell rescue has resulted in long term survival of about 25% in patients with several different types of recurrent brain tumors. Stem cells are cells in the bone marrow that produce blood cells. The stem cells are collected from the blood of the patient before the high dose chemotherapy. Patients are given high doses of chemotherapy to kill every brain tumor cell, but in the process the cells of the bone marrow are also killed. The previously collected stem cells are then infused into the patient to rescue the bone marrow and allow for healthy blood cells to re-populate and grow in the bone marrow. Initial studies used the drug etoposide along with carboplatin and thiotepa for the high dose chemotherapy. Patients had severe side effects, especially severe mouth-sores, thought mainly due to the etoposide, and some patients died from these side effects.

Recent studies have shown that a new drug, temozolomide, is active against some types of brain tumors. When it was given as a single drug to children with solid tumors, the side effects were considered to be tolerable. Temozolomide is given by mouth. In this study, researchers want to give high dose chemotherapy that includes the drugs temozolomide in place of etoposide, along with thiotepa and carboplatin. Patients will then be given their own stem cells back to rescue the bone marrow from the chemotherapy. A preliminary trial using this new drug combination was performed and has shown that patients tolerate this drug combination, even at the very high doses that will be used in this protocol.

Another drug that is being used in pediatric cancer treatment is called 13-cis-retinoic acid. This drug is closely related to vitamin A. It is taken by mouth. Cancer cells are immature cells that have not "grown up" into adult cells that do work in the body. 13-cis-retinoic acid is thought to act on some types of cancer cells to make them mature into cells that function in the body. It has also been shown in the laboratory to cause some brain tumor cells to undergo apoptosis. It has been used in other types of pediatric cancers and research is just beginning to use it for treatment of recurrent brain tumors. In this study researchers want to give you 13-cis-retinoic acid for 6 months after you recover from the high dose chemotherapy with stem cell rescue.

  Eligibility

Ages Eligible for Study:   6 Months to 21 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Patients with recurrent or refractory medulloblastoma/PNET, CNS germ cell tumors, ependymomas, AT/RT, high grade glioma and other malignant brain tumors. Brainstem gliomas are eligible if residual disease is < 1.5cc and if the patient is off decadron.
  2. Patients must have recurrent or refractory disease following at least one prior course of therapy and must have minimal residual disease defined as < 1.5 cm2 of enhancement. Patients with + CSF cytology, linear or fine nodular leptomeningeal disease are eligible.
  3. Adequate hematologic, renal, liver, and cardiac function as demonstrated by laboratory values performed within 21 days, inclusive, prior to administration of temozolomide.
  4. Patients must have an adequate number of autologous stem cells available defined as a minimum of 2 x 106 CD 34+ cells/kg and preferably at least 5 x 106 CD 34+ cells/kg.

Exclusion Criteria:

  1. Previous myeloablative therapy
  2. Frequent vomiting or medical condition that could interfere with oral medication intake (e.g., partial bowel obstruction)
  3. Previous or concurrent malignancies at other sites with the exception of surgically cured carcinoma in-situ of the cervix and basal or squamous cell carcinoma of the skin. Patients with prior malignancies which have not required anti-tumor treatment within the preceding 24 months are eligible.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00528437

Contacts
Contact: Sharon L Gardner, M.D. 212-263-8400 sharon.gardner@nyumc.org
Contact: Monique duPlessis 212-263-9929 monique.duplessis@nyumc.org

Locations
United States, New York
NYU Hassenfeld Center Recruiting
New York, New York, United States, 10016
Contact: Sharon L Gardner, M.D.     212-263-8400     sharon.gardner@nyumc.org    
Contact: Monique du Plessis     212-263-9929     monique.duplessis@nyumc.org    
Principal Investigator: Sharon L Gardner, M.D.            
Sponsors and Collaborators
New York University School of Medicine
Children's Hospitals and Clinics of Minnesota
Schneider Children's Hospital
Investigators
Principal Investigator: Sharon L Gardner, M.D. New York University Medical Center
  More Information

No publications provided

Responsible Party: New York University School of Medicine ( David Fishman, M.D. )
Study ID Numbers: NYU 05-40 H12853, PBMTC ONC-032P
Study First Received: September 10, 2007
Last Updated: May 21, 2008
ClinicalTrials.gov Identifier: NCT00528437     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by New York University School of Medicine:
Recurrent or refractory medulloblastoma/PNET
CNS germ cell tumors
Ependymomas
AT/RT
High grade glioma
Other malignant brain tumors

Additional relevant MeSH terms:
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Antineoplastic Agents
Physiological Effects of Drugs
Central Nervous System Neoplasms
Brain Diseases
Keratolytic Agents
Neoplasms by Site
Therapeutic Uses
Isotretinoin
Dermatologic Agents
Alkylating Agents
Nervous System Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Carboplatin
Temozolomide
Immunosuppressive Agents
Pharmacologic Actions
Thiotepa
Brain Neoplasms
Neoplasms
Myeloablative Agonists
Tretinoin
Antineoplastic Agents, Alkylating

ClinicalTrials.gov processed this record on November 27, 2009