Neuroblastoma with Dr. Meera Kotagal
With Dr. Dr. Meera Kotagal · hosted by Dr. Em Gootee · StayCurrentMD
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Neuroblastoma 26 items
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Educational content from recorded physician discussions — not medical advice. Talk to your (or your child's) care team about your situation.
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What the experts said
Neuroblastoma makes up about 8 to 10% of all pediatric cancers and about 15% of cancer-related deaths.
For patients with relapsed high risk neuroblastoma, the survival rate is 0%.
90% of neuroblastomas have elevated HVA and VMA (catecholamine metabolites).
Neuroblastomas are not typically thought of as causing elevated blood pressure despite producing catecholamines.
Image-defined risk factors (IDRFs) are best understood as things that touch important structures: vessels, brachial plexus, or trachea.
Intermediate risk neuroblastoma patients receive neoadjuvant chemotherapy with 2, 4, 6, or 8 cycles depending on chromosomal factors, followed by surgical resection.
The key surgical principle for neuroblastoma resection is to stay on the vessels and work from normal to abnormal anatomy.
Image-defined risk factors (IDRFs) are associated with increased risk of surgical complications.
When percutaneous core biopsies are performed by experienced practitioners who obtain multiple cores, the adequacy of these biopsies significantly improves and they are not inferior to open surgical biopsies.
At Cincinnati Children's, radiologists obtain 25 cores from different parts of neuroblastoma tumors during percutaneous biopsy.
For neuroblastoma, unlike most tumors, the goal is to get as much tumor as possible but complete resection of every ounce of tumor is not expected.
Tumor extending into neural foramina or other difficult locations should not be aggressively pursued; the goal is maximal safe resection without causing harm.
The observation protocol for infants with neuroblastoma has been expanded from primary adrenal tumors to L1 tumors in children under 6 months.
The Curie score is used to assess the extent of metastasis in neuroblastoma patients based on MIBG scans, with the body divided into 10 regions each scored 0-3, for a maximum score of 30.
The International Neuroblastoma Staging System (INSS) takes into account the results of surgery to remove the tumor and cannot help doctors determine a stage before any treatment has started.
The International Neuroblastoma Risk Group (INRG) is a preoperative staging system designed to assess how difficult patients may be to resect and allow comparison of patients preoperatively.
NMYC amplification status, ploidy, and 11Q aberrations are factors considered for neuroblastoma staging.
For low stage neuroblastoma with good survival rates, the goal is to reduce therapy and avoid late effects, as 2/3 of cancer patients will have some long-term morbidity from chemotherapy.
Neuroblastoma resections differ from other tumors because the tumor is divided into tiny pieces during removal.
A Children's Oncology Group study of 87 patients less than 6 months of age with small adrenal masses and no metastatic disease showed 97% four-year event-free survival with observation.