Neuroblastoma Protocol 2008: Therapy for Children With Advanced Stage High Risk Neuroblastoma

Stopped early · Phase 2

Conditions studied: Neuroblastoma

In brief

A Phase II study of temsirolimus in combination with standard chemotherapy (irinotecan; cyclophosphamide, doxorubicin and etoposide (CAE); cisplatin and etoposide (HiPE) and topotecan (TPT) followed by and additional six courses of induction chemotherapy and then intensification with autologous hematopoietic stem cell transplantation. The first five courses of induction chemotherapy will also evaluate the feasibility of combining weekly temsirolimus with these standard chemotherapy combinations. This will be followed by 16 months of oral maintenance therapy with eight months of 13-cis-retinoic acid and then eight months of oral topotecan.

Key facts

Study ID

NCT00808899

Run by

St. Jude Children's Research Hospital

People needed

4

Starts

2008-12-01

Expected to finish

2009-07-01

Last updated by the study team

2017-05-30

Who can join

Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients <18 years old with newly diagnosed, advanced stage, high-risk neuroblastoma defined as one of the following:
• Children < 1 yo with International Neuroblastoma Staging System (INSS) stage 2a, 2b, 3, 4 or 4S disease and MYCN amplification (>10 copies, or greater than four-fold increase in MYCN signal as compared to reference signal)
• INSS 2a or 2b disease and MYCN amplification, regardless of age or additional biologic features
• INSS stage 3 and:
• MYCN amplification (>10 copies, or greater than four-fold increase in MYCN signal as compared to reference signal, regardless of age or additional biologic features
• Age > 18 mo (> 547 days) with unfavorable pathology, regardless of MYCN status
• INSS stage 4 and:
• MYCN amplification, regardless of age or additional biologic features
• Age > 18 months (> 547 days) regardless of biologic features
• Age 12 - 18 months (365 - 547 days) with any of the following three unfavorable biologic features (MYCN amplification, unfavorable pathology and/or DNA index =1) or any biologic feature that is indeterminant/unknown
• Children less than or equal to 365 days initially diagnosed with: INSS stage 1, 2, 4S who progressed to a stage 4 without interval chemotherapy.
• Histologic proof of neuroblastoma or positive bone marrow for tumor cells with increased urine catecholamines.
• Adequate renal and hepatic function (serum creatinine <3 x upper limit of normal for age, (AST) aspartate aminotransferase < 3 x upper limit of normal).
• No prior therapy, unless an emergency situation requires local tumor treatment (discuss with PI)
• Written, informed consent according to institutional guidelines

You may not qualify if…

• Any evidence, as judged by the investigator, of severe or uncontrolled systemic disease (e.g., unstable or uncompensated respiratory, cardiac, hepatic, or renal disease).
• Pregnant or breast feeding (women of child-bearing potential).
• Children with INSS 4 disease, age <12 months with all 3 favorable biologic features (non-amplified MYCN, favorable pathology and DNA index >1).

Where it is running

• St. Jude Children's Research Hospital — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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