Trial Search Results

131I-MIBG Alone VS. 131I-MIBG With Vincristine and Irinotecan VS131I-MIBG With Vorinostat

This study will compare three treatment regimens containing metaiodobenzylguanidine (MIBG) and compare their effects on tumor response and associated side effects, to determine if one therapy is better than the other for people diagnosed with relapsed or persistent neuroblastoma.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

New Approaches to Neuroblastoma Therapy Consortium

Stanford Investigator(s):


  • Radiation: 131I-MIBG
  • Drug: Vincristine
  • Drug: Irinotecan
  • Drug: Vorinostat


Phase 2


Inclusion Criteria:

   - Patients must be > 24 months and < 30 years of age when registered on study.

   - Patients must have relapsed neuroblastoma, refractory neuroblastoma that had less than
   a partial response to standard treatment or persistent neuroblastoma that had at least
   a partial response to frontline therapy frontline therapy with > 3 residual lesions on
   end-induction MIBG scan.

   - Patients must have evidence of MIBG uptake into tumor at ≥ one site within 4 weeks
   prior to entry on study and subsequent to any intervening therapy.

   - Patients must have adequate heart, kidney, liver and bone marrow function. Patients
   who have bone marrow disease must still have adequate bone marrow function to enter
   the study.

   - Patients must have a dose of unpurged peripheral blood stem cells is 2.0 x 106 viable
   CD34+ cells/kg available.

Exclusion Criteria:

   - They have had previous I-131 MIBG therapy

   - They have other medical problems that could get much worse with this treatment.

   - They are pregnant or breast feeding.

   - They have a history of a venous or arterial thrombosis that was not associated to a
   central line.

   - They have active infections such as hepatitis or fungal infections.

   - They have active diarrhea.

   - They have had an allogeneic stem cell transplant (received stem cell from someone

   - They can't cooperate with the special precautions that are needed for this trial.

Ages Eligible for Study

2 Years - 30 Years

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Ped Hem/Onc CRAs
Not Recruiting