Nivolumab in Combination With Temozolomide and Radiotherapy in Children and Adolescents With Newly Diagnosed High-grade Glioma

STATUS

Recruiting
participants needed

40
sponsor

Gustave Roussy, Cancer Campus, Grand Paris

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Updated on 19 February 2024

See if I qualify

blood transfusion

platelet count

renal function

serum pregnancy test

screening procedures

neutrophil count

nivolumab

proteinuria

histological diagnosis

major surgery

temozolomide

kidney function test

malignant glioma

astrocytoma

ganglioglioma

coagulopathy

bleeding diathesis

stereotactic biopsy

glioma

gliomatosis cerebri

anaplastic ganglioglioma

diffuse glioma

Summary

Multicenter, open label, prospective study including successively a phase I trial and then a phase II trial Phase I : Open label, non-randomized, safety run study in nine patients. In case of safety issue a -1 dose level will be tested.

Phase II : Open label, non randomized, efficacy study of nivolumab in addition to radiotherapy and temozolomide. This phase will start when the RP2D has been defined after the last patients evaluable for DLT achieved the first 6 weeks of treatment (the radio-chemotherapy period) with a DLT rate below 30% during the the phase I study.

Details

Condition	High Grade Glioma
Age	3-18 years
Treatment	Radiotherapy, Temozolomide, Nivolumab
Clinical Study Identifier	NCT04267146
Sponsor	Gustave Roussy, Cancer Campus, Grand Paris
Last Modified on	19 February 2024

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Eligibility		Yes	No	Not Sure
Inclusion Criteria
	Written informed consent from parents/legal representative, patient, and age-appropriate assent before any study-specific screening procedures are conducted according to local, regional or national guidelines
	Age at inclusion: >/= 3 to <18 years of age
	Patients should be able and willing to comply with study visits and procedures as per protocol
	Patients must be affiliated to a social security system or beneficiary of the same according to local requirements
	Sexually actice females of childbearing potential must have a negative serum pregnancy test within 24 hours prior to initiation of treatment. Sexually active women of childbearing potential must agree to use acceptable and appropriate contraception during the study and for at least 5 months after the last study treatment administration. Sexually active males patients (and their female partner) must agree to use condom during the study and for at least 7 months after the last study treatment administration
	Newly diagnosed non-brainstem WHO grade III and IV HGG and neuroglial tumors; gliomatosis cerebri or diffuse glioma, metastatic malignant glial tumors, multifocal gliomas and bithalamic gliomas are eligible for the study. Diffuse midline gliomas with H3K27M mutation are not eligible. Anaplastic ganglioglioma and anaplastic pleomorphic astrocytoma will be eligible
	Local histological diagnosis after either stereotactic biopsy or surgical procedure has been confirmed centrally by a designated reference pathologist
	Able to commence trial treatment within 6 weeks following the last major surgery
	Adequate Bone Marrow Function : Hemoglobin >/= 10 g/dL (transfusion independent), Neutrophil count >/= 1.0 x 10^9/L
	Platelet count >/= 1.0 x 10^9/L (transfusion independent)
	\. Absence of Coagulation Disorder
	\. Adequate Liver Function : AST </= 2.5x institutional ULN for age, ALT </=
	5x institutional ULN for age, Total Bilirubin </= 1.5x institutional ULN for
	age
	\. Adequate Renal Function : Serum creatinine must be </= 1.5x ULN for age
	absence of clinically significant proteinuria as defined by a screening early
	morning urine (first sample) dipstick urinalysis of </= 2
Exclusion Criteria
	Any disease or condition that contraindicates the use of the study medication/treatment (for TMZ, see the approved product labelling) or places the patient at an unacceptable risk of experiencing treatment related complications
	Patients should not be on high-dose steroids (ie > 1mg/kg) before study entry; doses should be stable for at least two weeks or decreasing
	Low probability of protocol compliance
	Radiological evidence of surgically related intracranial bleeding (excluding asymptomatic, resolving hemorrhagic changes associated with recent surgery and the presence of punctuate hemorrhage in the tumor)
	Subjects with concommitant second malignanices are excluded unless a complete remission is achieved as it is empirically determined based on the malignancy and treatment provided prior to study entry and no additional therapy is required or anticipated to be required during the study period
	Previous cranial irradiation
	Any known auto-immune disease, previous or ongoing
	Known chronic inflammatory digestive disease, previous or ongoing
	Chronic asthma receiving corticotherapy, even only with inhalation
	Vaccinated with live attenuated vaccines within 4 weeks of the first dose of study drug
	Pregnant or breastfeeding women
	Known hypersensitivity to any component of the products (study drug or ingredients)
	Clinically significant, uncontrolled heart disease (including history of any cardiac arrhythmias, e.g., ventricular, supraventricular, nodal arrhythmias, or conduction abnormality within 12 months of screening)
	Patients who are currently receiving another investigational drug or anticancer agent
	Patient who have an uncontrolled infection
	Patient with known human immunodeficiency virus (HIV) / AIDS infection or acute / chronic Hepatitis B or C

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Nivolumab in Combination With Temozolomide and Radiotherapy in Children and Adolescents With Newly Diagnosed High-grade Glioma