Study of Recombinant Human Endostatin Combined With CV Regimen in the Treatment of Pediatric Low-grade Gliomas

NCT04659421 | Completed Phase 2

• 1 other identifier: SBNK-YJ-2020-016-02
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

Low-grade gliomas (LGGs) are the most common intracranial tumors in children, accounting for about 40% of intracranial tumors in children. The biological characteristics and clinical prognosis of LGGs vary greatly, and they can present different biological characteristics such as restricted growth, invasive growth, and malignant transformation during their development. The prognosis of LGGs is related to the degree of tumor resection, histological type, and whether it has spread. For LGGs, surgical resection is the main treatment method. However, many tumors located in the visual pathway, brainstem, hypothalamus and other midline parts, it is impossible to completely remove. Radiotherapy can effectively control tumor progression to a certain extent, but radiotherapy can cause obvious and serious delayed damage, such as cognitive impairment, endocrine disorders, cerebrovascular events, and second tumors. Chemotherapy can effectively treat LGGs in children, and can postpone or avoid radiotherapy. It is the preferred treatment for children with LGGs after surgery. Carboplatin combined with vincristine, the CV regimen, is currently the main chemotherapy regimen for the treatment of children with LGGs. Anti-angiogenesis is a new type of treatment. Bevacizumab, a humanized monoclonal antibody that targets vascular endothelial growth factor (VEGF). Among children with relapsed, refractory or progressing LGGs, the effective rate of Bev combined with irinotecan was 44%, and the 6-month and 2-year progression-free survival rates were 85% and 48%, respectively. However, almost all of them were treated with Bev progressed again. Tumor growth is more aggressive after Bev treatment fails. Recombinant human endostatin (rh-ES) is an endogenous broad-spectrum angiogenesis inhibitor that has been shown to significantly improve therapeutic efficacy when combining with conventional chemotherapy agents in non-small-cell lung cancer, breast cancer and melanoma.Previous retrospective studies of the research team found that rh-ES combined with CV can treat LGGs in children effectively, shorten the onset time, help quickly alleviate the symptoms of brainstem damage, and improve the quality of life. This study intends to use prospective clinical studies to further confirm the efficacy and safety of the anti-angiogenic drug rh-ES combined with traditional CV regimens in the treatment of children with LGGs.

Conditions

Low-grade Glioma; Pediatric Brain Tumor

Outcome Measures

Primary Outcomes (1)

• objective response rate

  the percentage of patients who achieved confirmed complete response or partial response according to the Response Assessment in Neuro-Oncology (RANO) criteria

  up to 5years

Secondary Outcomes (5)

• median time to response

  up to 5years

• Progression-free survival

  up to 5years

• Overall survival

  up to 5years

• The correlation between KPS change and efficacy

  up to 5years

• Frequency and severity of treatment-related adverse events as assessed by CTCAE v5.0

  up to 5years

Study Arms (1)

Low-grade gliomas

EXPERIMENTAL

Treated with Recombinant human endostatin, Carboplatin, and Vincristine

Drug: combined therapy with rh-ES and CV

Interventions

combined therapy with rh-ES and CV DRUG

All the patients receive combined therapy with recombinant human endostatin and traditional weekly CV regimen. Carboplatin is administered at a dose of 220 mg/m2. Vincristine is administered at a dose of 1.5 mg/m2 (maximum dose 2 mg). Recombinant human endostatin (rh-ES) is administrated at a dose of 15mg daily, for 14 consecutive days every 3 weeks.

Low-grade gliomas

Eligibility Criteria

• Age: 3 Months - 18 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64)

You may qualify if:

• Age ≥ 3months and ≤18years;
• Histopathologically confirmed low-grade glioma (WHO grade I and II), including astrocytoma, pilocytic astrocytoma, pleomorphic xanthoastrocytoma, subependymal giant cell astrocytoma, infantile desmoplastic astrocytoma, low-grade oligodendroglioma, oligoastrocytoma, ganglioglioma, and infantile desmoplastic ganglioglioma. Chiasmatic-hypothalamic tumors intrinsic to the optic pathway were eligible without pathologic confirmation.
• There is a clear evaluable lesion with less than 95% resection or residual tumor of more than 1.5 cm\^2；
• KPS score ≥50 (age\> 12 years old) or Lansky score ≥ 50 (age ≤ 12 years old)；
• Estimated survival of at least 12 weeks;
• Have not been received radiotherapy or chemotherapy before；
• Participants must have adequate organ function as defined by the following criteria (within 7 days before treatment):
• Hematology (No transfusion within 14 days):
• Hemoglobin(HB)≥90g/L; Absolute neutrophil count (ANC)≥1.5×10\^9/L; Platelet (PLT)≥80×10\^9/L.
• Chemistry:
• Serum bilirubin ≤ 1.5×upper limit of normal (ULN) ALT and AST≤2.5ULN； Serum creatinine ≤1.5ULN or creatinine clearance rate(CCr)≥60ml/min； ECG: heart rate in the normal range (55-100beats/min), normal or slightly prolonged QT interval (QTc\<480ms), normal or low T wave, normal or non-specific ST segment changes；
• The patient or his legal guardian signs an informed consent form.

You may not qualify if:

• MRI examination is not available;
• Diffuse intrinsic pontine glioma or diffuse midline glioma with H3K27 mutation, even though the histopathology is grade I/II;
• Non-glial low-grade rare intracranial tumors;
• 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 with HIV or Treponema pallidum infection;
• Severe heart disease; ECG shows T wave inversion or elevation or ST segment specific changes;
• There were clinically significant bleeding symptoms or clear bleeding tendency in the first 3 months before enrollment, such as gastrointestinal bleeding, hemorrhagic gastric ulcer, gastrointestinal perforation, baseline fecal occult blood ++ and above, intracranial or intracranial hemorrhage, or vasculitis;
• Arteriovenous thrombosis events occurred within 6 months before enrollment, such as cerebrovascular accidents (including temporary ischemic attack, cerebral hemorrhage, cerebral infarction), deep vein thrombosis and pulmonary embolism, etc.;
• Having bleeding disorder and are being treated with thrombolytic or anticoagulant drugs.
• Patients who are pregnant or breastfeeding.

Sponsors & Collaborators

• Beijing Sanbo Brain Hospital: lead

Study Sites (1)

Capital Medical University Sanbo Brain Hospital

Beijing, China

Location

MeSH Terms

Interventions

Psychotherapy, Multiple

Intervention Hierarchy (Ancestors)

Psychotherapy; Behavioral Disciplines and Activities

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Chief physician

Study Record Dates

• First Submitted: November 24, 2020
• First Posted: December 9, 2020
• Study Start: November 3, 2020
• Primary Completion: July 1, 2023
• Study Completion: July 20, 2023
• Last Updated: July 24, 2023

Record last verified: 2023-07

Locations

CN (1)