RecruitingPhase 2NCT06255210

Efficacy and Safety of Induction Chemotherapy for Olfactory Neuroblastoma (ESICON)

Efficacy and Safety of Induction Chemotherapy for Olfactory Neuroblastoma: a Prospective Umbrella Clinical Study


Sponsor

Hongmeng Yu

Enrollment

25 participants

Start Date

Mar 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn about the induction chemotherapy efficacy in olfactory neuroblastoma. The main question it aims to answer is: wether olfactory neuroblastoma patients with different pathology subtypes apply to different induction chemotherapy schemes. Participants will be treated with different chemotherapy schemes, to evaluate the tumor remission rate and long term survival.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial studies the effectiveness of induction chemotherapy (chemo given before the main treatment) in patients with olfactory neuroblastoma — a rare cancer that starts in nerve cells in the nasal cavity near the brain. The goal is to determine whether adding early chemotherapy to the treatment plan improves outcomes for people with more advanced cases of this rare cancer. **You may be eligible if...** - You are 18 or older with a confirmed diagnosis of olfactory neuroblastoma - Your tumor is stage T2, T3, or T4 (moderately to significantly advanced) - Your cancer has not spread to distant organs - You have signed informed consent **You may NOT be eligible if...** - You have an uncontrolled medical condition that could interfere with treatment - You have a severe neurological or psychiatric illness (including dementia or seizures) - You have an active, uncontrolled infection - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGemcitabine+Cisplatin(GP); Cyclophosphamide+Etoposide+Cisplatin(CEP)

When the Ki67% index of the tumor is ≥ 25%, patients were treated with the GP regimen for induction chemotherapy; When the Ki67% index of the tumor is \< 25%, patients were treated with the CEP regimen for induction chemotherapy.


Locations(1)

Eye & ENT Hospital of Fudan University

Shanghai, Shanghai Municipality, China

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NCT06255210


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