RecruitingPhase 2NCT05278715

Modified CV Regimen in Optic Pathway Glioma

Clinical Study of Modified Carboplatin/vincristine Chemotherapy Regimen for Visual Function Protection in Children with Optic Pathway Gliomas


Sponsor

Beijing Sanbo Brain Hospital

Enrollment

75 participants

Start Date

Apr 13, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Optic pathway glioma (OPG) can result in visual deterioration. Symptomatic patients often report deficits in visual acuity (VA), visual field, visual-evoked potentials (VEPs), strabismus, proptosis, disc swelling, and other visual/neurological problems. VA itself remains one of the most important outcome measures for OPG patients, with various studies showing strong ties of VA level to overall quality of life and well-being . Maintenance of favorable VA and vision outcomes is of paramount importance in the management of OPG. In terms of management of OPG, surgery and radiotherapy are used on a more limited basis because of location of the tumors and risk of secondary tumors, respectively. Tumor stabilization often prioritized, and chemotherapy is considered ideal for tumor stabilization in OPG, but vision is not always retained and may worsen in some cases, partially due to low radiographic efficacy and long time interval to response of the current chemotherapy regimen. In the prior study, the investigators modified the traditional carboplatin combined with vincristine regimen by increasing the dose of carboplatin and combining with an anti-angiogenic drug. Of the 15 OPG patients, objective response rate was 80% and the time to response was only 3.3 months. 8 (53%) patients experienced an improvement in visual acuity during therapy and 6 (40%) were stable, which was higher than the historical studies. This study was launched to further verify the clinical efficacy of the modified regimen and its effect on visual acuity improvement.


Eligibility

Min Age: 3 MonthsMax Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This study tests a modified chemotherapy regimen (using carboplatin and vincristine) for children and young adults with optic pathway glioma — a type of slow-growing brain tumor affecting the nerves connected to the eyes. The goal is to evaluate whether this adjusted treatment can slow tumor growth and protect vision. **You may be eligible if...** - You are between 3 months and 21 years old - You have been diagnosed with optic pathway glioma, confirmed by biopsy or by characteristic MRI and clinical features - You have measurable tumor remaining after surgery, or the tumor was less than 95% removed - You have symptoms such as vision loss, eye bulging, or increased pressure in the brain **You may NOT be eligible if...** - MRI is not available for your follow-up - Your tumor has a specific genetic change called H3K27 mutation - You are currently on another experimental treatment - You have a serious heart condition or a bleeding disorder - 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

DRUGCarboplatin

Dose of carboplatin is adjusted for age (over 1 year old, full dose, 220 mg/m\^2; 6 months of age or less, 66 percent of the full dose; 7 to 12 months of age, 80 percent).

DRUGVincristine

Dose of vincristine is adjusted for age (over 1 year old, full dose, 1.5 mg/m\^2; 6 months of age or less, 66 percent of the full dose; 7 to 12 months of age, 80 percent). Maximum dose is 2 mg.

DRUGRecombinant human endostatin

Recombinant human endostatin (rh-ES) is administrated at a dose of 15mg daily, for 14 consecutive days every 3 weeks.


Locations(1)

Capital Medical University Sanbo Brain Hospital

Beijing, China

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NCT05278715