Esthesioneuroblastoma is a rare cancer of the nasal cavity and sinuses that arises from the smell-sensing olfactory nerve lining at the roof of the nose, next to the brain. It is treated with surgery through the nose or skull base followed by radiotherapy, with chemotherapy added for high-grade or widespread tumours, and because it can return a decade or more later patients are followed for life.
Esthesioneuroblastoma arises from the olfactory neuroepithelium of the upper nasal vault and cribriform plate, and its position against the anterior skull base means it grows into the orbit and the frontal lobes as readily as into the sinuses. It presents with nasal obstruction, bleeding and loss of smell, and is staged by the Kadish system (A: nasal cavity; B: paranasal sinuses; C: beyond, including orbit and skull base; D: nodal or distant metastases, added later) and graded by Hyams (I to IV) on the degree of differentiation, rosettes, necrosis and mitotic activity; Hyams grade is the strongest predictor of survival, with low-grade tumours behaving indolently and high-grade tumours recurring early and spreading to neck nodes and distant sites. Immunohistochemistry (synaptophysin, chromogranin, S100 sustentacular cells) separates it from sinonasal undifferentiated carcinoma, NUT carcinoma, melanoma and lymphoma, which share the site. Most tumours express somatostatin receptor 2, which allows DOTATATE PET imaging and, in relapse, radioligand therapy; IDH2 mutations, typical of sinonasal undifferentiated carcinoma, occur in a subset of high-grade esthesioneuroblastomas.
Treatment is multimodal. Craniofacial resection through a combined transfacial and transcranial approach was the standard from the 1970s, and expanded endonasal endoscopic resection with skull base reconstruction now achieves equivalent margins with less morbidity in experienced hands; postoperative radiotherapy is recommended for almost all patients because it improves local control, and intensity-modulated or proton therapy spares the optic pathways and brain. Chemotherapy, usually cisplatin with etoposide, is given as induction for Kadish C and D or Hyams III to IV tumours, sometimes with radiotherapy for unresectable disease, and elective neck irradiation is considered for high-grade tumours because late nodal recurrence is common. Recurrence occurs in up to a third of patients, often years or decades later, so surveillance MRI continues indefinitely; relapses are treated with repeat surgery, re-irradiation or radioligand therapy with lutetium-177 dotatate where the tumour takes up the tracer, and platinum-etoposide or temozolomide for metastatic disease. Because of the tumour's rarity, care belongs in a skull base team, and prospective data are limited to registry series.
A rare tumour, a few percent of sinonasal cancers, affecting all ages with peaks in young adults and the middle-aged; slow-growing in its low-grade form, aggressive in its high-grade form, and prone to relapse many years after treatment.
Site decides cause and behaviour: HPV drives oropharyngeal cancer, EBV drives nasopharyngeal cancer, tobacco drives oral and laryngeal cancer; all drain into the neck node levels that surgeons and radiotherapists map.
Same organ: Acinic cell carcinoma of the salivary glands, Carcinoma ex pleomorphic adenoma, Multiple endocrine neoplasia type 1 (MEN1), Multiple endocrine neoplasia type 2 (MEN2A and MEN2B), Hyperparathyroidism-jaw tumour syndrome (CDC73-related parathyroid carcinoma), Oropharyngeal cancer (tonsil and base of tongue), Laryngeal and hypopharyngeal cancer, Oral cavity cancer (mouth and tongue), Head and neck squamous cell carcinoma, Nasopharyngeal carcinoma, Salivary gland cancers, Papillary thyroid cancer, Follicular thyroid cancer, Medullary thyroid cancer, Anaplastic thyroid cancer, Thyroid cancer, Nasal cavity and paranasal sinus cancers (including esthesioneuroblastoma), NUT carcinoma (midline carcinoma with NUTM1 rearrangement), Parathyroid carcinoma, Multiple endocrine neoplasia syndromes (MEN1, MEN2, MEN4), HPV-positive oropharyngeal cancer, HPV-negative head and neck squamous cell carcinoma (including HPV-negative oropharyngeal cancer), Recurrent or metastatic head and neck squamous cell carcinoma, Hypopharyngeal cancer, Adenoid cystic carcinoma, Salivary duct carcinoma, Mucoepidermoid carcinoma, Oral tongue and floor of mouth cancer, Buccal mucosa and gingivobuccal cancer (oral cancer in India), Lip cancer, Locoregionally advanced nasopharyngeal carcinoma (stage III to IVA), Recurrent and metastatic nasopharyngeal carcinoma, Sinonasal undifferentiated carcinoma (SNUC) and SWI/SNF-deficient sinonasal carcinoma
Nothing recorded yet.
Nothing recorded yet.
Also on OnCo: Symptoms and red flags · Early detection roadmap.
Endoscopic biopsy with immunohistochemistry, MRI and CT of the sinuses and skull base, neck imaging, DOTATATE PET where available.
Endoscopic endonasal or craniofacial resection with skull base reconstruction by a skull base team, followed by postoperative radiotherapy (intensity-modulated or proton) for nearly all patients.
Induction cisplatin and etoposide, then surgery and radiotherapy or definitive chemoradiotherapy; elective neck irradiation considered.
Repeat surgery or re-irradiation for local relapse; lutetium-177 dotatate for somatostatin-receptor-positive disease; platinum-etoposide or temozolomide; trials.
MRI surveillance indefinitely because of late relapse; management of anosmia, cerebrospinal fluid leak and visual effects.
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Craniofacial or endoscopic resection followed by radiotherapy is the standard for esthesioneuroblastoma, with chemotherapy reserved for high-grade or advanced disease.
The stage on an esthesioneuroblastoma page or pathology report is almost always a Kadish stage, and treatment intensity follows it.
Query for this cancer: (TITLE:"Esthesioneuroblastoma" OR ABSTRACT:"Esthesioneuroblastoma" OR TITLE:"olfactory neuroblastoma" OR ABSTRACT:"olfactory neuroblastoma" OR TITLE:"Olfactory neuroblastoma" OR ABSTRACT:"Olfactory neuroblastoma" OR TITLE:"ONB" OR ABSTRACT:"ONB" OR TITLE:"Esthesioneuroepithelioma" OR ABSTRACT:"Esthesioneuroepithelioma" OR TITLE:"Neuroblastoma of the olfactory epithelium" OR ABSTRACT:"Neuroblastoma of the olfactory epithelium") AND (treatment OR therapy OR trial OR survival OR diagnosis). Results are unfiltered search hits about Esthesioneuroblastoma (olfactory neuroblastoma), not a curated reading list.
The targets of this cancer's medicines and the ones linked to it directly.
Cases by country, the UK and NHS pathway and other country lenses, the expert centres with trials on record, and the centres named on this cancer's subtypes.
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Bleeding that does not stop by itself, bleeding from more than one site, or new bruising in several places or one large area.
Sudden severe bone pain, or back pain with weakness or numbness in the legs (possible spinal cord compression).
Take on an empty stomach or at bedtime to reduce nausea; PJP prophylaxis during concurrent chemoradiation.
Dose reduce or avoid for CrCl below 60 (carboplatin is the alternative).
Reduce to 75% for CrCl 15-50.
The leukaemia risk after chemotherapy was described in the era of mustards and etoposide, and it did not stay there. Platinum drugs carry it, PARP inhibitors raise it about two and a half times against placebo, and lenalidomide with oral melphalan raises it nearly fivefold against melphalan alone. The absolute numbers are small, but the choice of partner drug is sometimes a real decision.
See all on the product pages:CisplatinEtoposideLutetium-177 dotatatePlatinum + etoposide (EP / CE)Temozolomide·Printable cards in the navigator
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