Molecular Characterization of Neuroblastic Tumor: Correlation With Clinical Outcome

ConditionNeuroblastoma
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is to find out the genetic and biochemical makeup of your neuroblastic tumor, which influences its aggressiveness and the suitable therapy. These research studies include surface marker analysis, cytogenetics, cancer genes,genome sequencing, tumor growth-related genes and tumor growth in test tubes. Your blood, marrow, and hematopoietic stem cell samples will also be tested for tumors or leukemia cells, and your serum tested for anti-tumor antibodies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Neuroblastic tumors diagnosed in accordance with the International Neuroblastoma Staging System

Clinically suspected neuroblastic tumors.

Patients who receive naxitamab as part of their standard of care

Disqualifiers

None

Trial population

Patients will be offered participation in this study by their attending oncologist in the Department of Pediatrics at Memorial Sloan Kettering Cancer Center.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Tumor and Marrow Markers

    Other intervention

    Tumor and Marrow Markers

Treatment groups

2,070 Participants
are divided into 1 treatment group
Group A: 11 intervention

Trial outcomes

Primary outcomes

1

To study the molecular-genetic makeup and metastasis of neuroblastic tumors.

Before surgery a maximum of 5 blood drawings (20-30 ml) will be performed per year (at least one month apart) per patient

Time frame
2 years

Secondary outcomes

1

To study the correlation of these biologic markers with clinical outcome.

Before surgery and a maximum of 5 blood drawings (20-30 ml) will be performed per year (at least one month apart) per patient

Time frame
2 years
2

To relate neuroblastic tumor and embryonic neuroectodermal cell circuitry.

Up to six fetal adrenal samples will be obtained (without patient identifiers) from gestational week 20, when neuroblasts are present and thought to be differentiating within the fetal adrenal gland.

Time frame
2 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Memorial Sloan Kettering Cancer Center

Lead sponsor

Southern Illinois University

Collaborator

Spanish National Cancer Center

Collaborator

St. Jude Children's Research Hospital

Collaborator

Washington University School of Medicine

Collaborator

University of Texas

Collaborator

Weill Medical College of Cornell University

Collaborator