Phase II Study Temozolomide for Retinoblastoma Metastatic to the Central Nervous System for Patients From Guatemala

Not Recruiting

Trial ID: NCT01857752

Purpose

Primary Objectives: 1. To investigate the response rate (complete response plus partial response) of temozolomide for 8 weeks (2 cycles), in patients with retinoblastoma metastatic to the central nervous system (mass only) in two strata: - A. Initial diagnosis (mass) - B. At relapse (mass) 2. To determine hematologic toxicity: absolute neutrophil count (ANC), platelets and hemoglobin count. Secondary Objectives: 1. To determine the response in other metastatic sites (non target) (orbit, bone marrow, bone, lung, liver and others) 2. To determine the remission rate and time to relapse on temozolomide. 3. To document the response of leptomeningeal metastasis (cerebrospinal fluid) to temozolomide

Official Title

Phase II Study Temozolomide for Retinoblastoma Metastatic to the Central Nervous System for Patients From Guatemala

Eligibility


Inclusion Criteria:

   1. This study must be evaluated and confirmed by the local ethics committees and
   institutional review board of the participating institution, in accordance to the
   declaration of Helsinki. Informed consent must be administered and the parent or
   guardian must sign the document, authorized by the Ethics Committee and human subjects
   (therapy can not start if the documents are not signed).

   2. Patients less than 21 years of age with diagnosis of retinoblastoma with metastasis to
   the CNS (central nervous system) must be confirmed by an ophthalmologist and/or a
   pathologist; in conjunction with the pediatric oncologist.

   3. Metastasis to the CNS is defined as a mass in the chiasm or other site in the CNS,
   confirmed by MRI and/or

   CT:

      1. At diagnosis

      2. At relapse after conventional therapy.

   It is acceptable to have other sites of metastatic disease: lymphatic, bone, bone
   marrow or others.

   4. All sites of metastasis must be measured in 3 planes, in millimeters and described in
   POND (Pediatric Oncology Network Database*)

   5. Quality of life must be 3 by Lansky and 50% by Karnofksy

   6. Hemogram: Hemoglobin of 7, ANC of 750, platelets of 75K.

   7. Chemistry: direct bilirubin less than 3.0, indirect bilirubin less than 4.0, AST less
   5x normal and ALT 5x normal, creatinine less than 1.5.

   8. Treatment must start not more than 15 days from diagnosis of metastatic
   retinoblastoma.

   9. Every patient with relapse or progression into the CNS must be documented with CT scan
   or MRI of the brain. Other sites of relapse may be evaluated, including bone marrow.

10. Patients who are newly diagnosed should have not received any other chemotherapeutic
   therapy (with the exception of dexamethasone) 1 week before starting, or radiotherapy,
   4 weeks before starting.

11. All patients to be included in this study must be presented to the principal
   investigator using Horizon Live Web-conferencing through the Cure4Kids website.
   Eligibility and target CNS sites will be determined, as well as non-target sites.

Exclusion Criteria:

   1. Patients with metastatic to CNS with only CSF involvement are NOT ELIGIBLE.

   2. Relapse patients should have NOT received chemotherapy for 4 weeks, and no patient
   should have received nitroureas (melphalan, CCNU or mustard). No patient should have
   received radiation therapy in the previous 42 days. These patients are NOT eligible.

   3. Diagnosis of AIDS or HIV positive.

   4. Patients with disease NOT in the CNS are NOT eligible

Intervention(s):

drug: Temozolomide

Not Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305