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โ† Trials
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Modified CV Regimen in Optic Pathway Glioma

RecruitingPhase 2Ages 3 Months - 21 YearsAllBeijing Sanbo Brain Hospital
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In plain words

What the trial is, and whether it could suit you

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 radiogra

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Age โ‰ฅ 3months and โ‰ค21years; * Patients with optic pathway gliomas diagnosed by histopathology or characteristic brain MRI and clinical features; * Measurable lesions, surgical resection degree \< 95% or postoperative residual tumor โ‰ฅ1.5cm\^2; * KPS score โ‰ฅ50 (age \>12 years) or Lansky score โ‰ฅ50 (age โ‰ค12 years); * Clinical symptoms such as decreased visual acuity, visual field defect, optic disc edema, exophthalmia, increased intracranial pressure, diencephalic syndrome, etc; * No dysfunction of major organs. Exclusion Criteria: * MRI examination is not available. * Failing to comply with the visual examination. * H3K27 mutations, even histopathological grade 1/2. * Receiving any other investigational agent. * History of allergic reactions attributed to compounds of similar chemical or biologic composition to the drugs used in this study. * Patients who have received organ transplants. * Patients infected with HIV or treponema pallidum. * Suffering from serious cardiovascular disease;T wave inversion or elevation or ST segment changes. * Patients who had coagulation disorder and were being treated with thrombolytic or anticoagulant drugs. Patients with significant clinical bleeding symptoms or clear bleeding tendency occurred within 3 months before enrollment, such as gastrointestinal bleeding, hemorrhagic gastric ulcer, gastrointestinal perforation, baseline fecal occult blood ++ or above, intratumoral or intracranial bleeding, or vasculitis, etc. Arteriovenous thrombosis events (such as cerebrovascular accident (including transient ischemic attack, cerebral hemorrhage and cerebral infarction), deep vein thrombosis and pulmonary embolism) occurred within 6 months before enrollment. * Pregnant or breastfeeding. * Other conditions considered inappropriate by the researcher for inclusion.
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What it tests

  • Carboplatin
  • Vincristine
  • Recombinant human endostatin
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Where

1 site
Capital Medical University Sanbo Brain Hospital
Beijing, China
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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