A relatively uncommon neuroblastoma that is found in the neck.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 30, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 30, 2026
Documentation on cervical neuroblastoma is limited primarily due to its rarity, which affects fewer than a few hundred individuals worldwide. This rarity leads to fewer systematic studies and clinical trials, making it challenging to gather comprehensive clinical data. The absence of established genetic factors further complicates the documentation and understanding of this condition.
To navigate cervical neuroblastoma, consider seeking a pediatric oncologist with experience in neuroblastoma or rare cancers. Genetic counseling may be beneficial, even though specific genetic factors are not yet established. Resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Additionally, participating in clinical trials may offer access to cutting-edge treatments and contribute to ongoing research efforts.
There are several orphan drugs associated with cervical neuroblastoma, including FDA-approved treatments like dinutuximab, eflornithine, and naxitamab-gqgk. Additionally, there are multiple drugs in development aimed at treating this condition. Currently, there are 8 active clinical trials that may offer potential treatment options. For more information, you can visit the ClinicalTrials.gov search page at https://clinicaltrials.gov/search?cond=cervical%20neuroblastoma.
Actionable guidance for navigating care for cervical neuroblastoma
To navigate cervical neuroblastoma, consider seeking a pediatric oncologist with experience in neuroblastoma or rare cancers. Genetic counseling may be beneficial, even though specific genetic factors are not yet established. Resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Additionally, participating in clinical trials may offer access to cutting-edge treatments and contribute to ongoing research efforts.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 30, 2026
Consider asking your healthcare providers these condition-specific questions
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.