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==Overview==
Children oncology group (COG) risk stratification system determines the protocol of management used for neuroblastoma patients. Low risk neuroblastoma patients are usually managed with either observation or surgical resection of the tumor. Intermidiate risk neuroblastoma patients are usually managed with neoadjuvant chemotherapy in advance of a definitive surgical resection. Whereas high risk neuroblastoma patients are usually managed with a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.
Children oncology group (COG) risk stratification system determines the protocol of management used for neuroblastoma patients. Low risk neuroblastoma patients are usually managed with either observation or surgical resection of the tumor. Intermidiate risk neuroblastoma patients are usually managed with neoadjuvant chemotherapy in advance of a definitive surgical resection. Whereas high risk neuroblastoma patients are usually managed with a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.


 
==Medical Therapy==
Low risk neuroblastoma patients are managed with either observation or surgical resection of the tumor.
===Risk Stratification===
Intermediate risk neuroblastoma patients are managed with neoadjuvant chemotherapy in advance of a definitive surgical resection.
* Children oncology group (COG) risk stratification system determines the protocol of management used for neuroblastoma patients.
High risk neuroblastoma patients are managed with a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.
* Low risk neuroblastoma patients are usually managed by either observation or surgical resection of the tumor.
 
* Intermediate risk neuroblastoma patients are usually managed by neoadjuvant chemotherapy in advance of a definitive surgical resection.
Children's Oncology Group Risk Stratification
* High risk neuroblastoma patients are usually managed by a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.
A regimen of chemotherapy, surgery, SCT, radiation therapy, and anti-GD2 antibody ch14.18, with interleukin-2/GM-CSF and isotretinoin
* The algorithm below summarizes the management approach for neuroblastoma patients:
 
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===Management of Low Risk Neuroblastoma Patients===
* Surgical intervention alone may be curative as a single therapeutic modality for the management of low risk neuroblastoma patients.
*  Indications for chemotherapy among low risk neuroblastoma patients include:
:* Stage 1 or stage 2 tumors associated with MYCN amplification
:* Age older than 18 months presenting with a stage 2B tumor and an unfavorable histology
:* Symptomatic patients due to spinal cord compression, respiratory compromise, and hepatic infiltration
* The majority of low risk neuroblastoma cases among infants younger than 6 months of age may spontaneously regress. Such patients may safely be observed without obtaining a definitive histologic diagnosis or performing any surgical intervention.

Revision as of 20:38, 9 October 2015

Overview

Children oncology group (COG) risk stratification system determines the protocol of management used for neuroblastoma patients. Low risk neuroblastoma patients are usually managed with either observation or surgical resection of the tumor. Intermidiate risk neuroblastoma patients are usually managed with neoadjuvant chemotherapy in advance of a definitive surgical resection. Whereas high risk neuroblastoma patients are usually managed with a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.

Medical Therapy

Risk Stratification

  • Children oncology group (COG) risk stratification system determines the protocol of management used for neuroblastoma patients.
  • Low risk neuroblastoma patients are usually managed by either observation or surgical resection of the tumor.
  • Intermediate risk neuroblastoma patients are usually managed by neoadjuvant chemotherapy in advance of a definitive surgical resection.
  • High risk neuroblastoma patients are usually managed by a combination of surgery, chemotherapy, radiation therapy, hematopoietic stem cell transplantation, and immunotherapy.
  • The algorithm below summarizes the management approach for neuroblastoma patients:


 
 
 
 
 
Children's oncology group risk stratification
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Low risk patients
 
Intermediate risk patients
 
High risk patients
 
 
 
 
  • Surgery followed by chemotherapy
  • Chemotherapy with or without surgery
  • Observation without biopsy
 
  • Chemotherapy with or without surgery
  • Surgery and observation
  • Radiation therapy
 
  • A combination of chemotherapy, surgery, stem cell transplantation, radiation therapy, immunotherapy, and isotretinoin
 
 
 


Management of Low Risk Neuroblastoma Patients

  • Surgical intervention alone may be curative as a single therapeutic modality for the management of low risk neuroblastoma patients.
  • Indications for chemotherapy among low risk neuroblastoma patients include:
  • Stage 1 or stage 2 tumors associated with MYCN amplification
  • Age older than 18 months presenting with a stage 2B tumor and an unfavorable histology
  • Symptomatic patients due to spinal cord compression, respiratory compromise, and hepatic infiltration
  • The majority of low risk neuroblastoma cases among infants younger than 6 months of age may spontaneously regress. Such patients may safely be observed without obtaining a definitive histologic diagnosis or performing any surgical intervention.