Entrectinib for the Treatment of Patients Less Than 3 Years of Age with NTRK1/2/3 or ROS1 Fused High Grade Glioma or Other Central Nervous System Tumor
This phase II trial tests how well entrectinib works to treat patients less than 3 years of age with NTRK 1/2/3 or ROS1 fused, high grade glioma or other central nervous system (CNS) tumor. Entrectinib may stop the growth of tumor cells and may kill them by blocking some of the enzymes needed for cell growth.
Inclusion Criteria
- SCREENING PHASE: Age from birth to age < 3 years at the time of diagnosis (date of surgical resection/biopsy)
- SCREENING PHASE: Participant with presumed newly diagnosed tumor in the supratentorial compartment
- SCREENING PHASE: Patient must have measurable disease based on RAPNO criteria
- SCREENING PHASE: ≤ 84 days since surgery (resection or biopsy)
- SCREENING PHASE: Available tumor tissue for central review
- SCREENING PHASE: Parent/guardian has the ability to understand and the willingness to sign a written informed consent document according to institutional guidelines
- COHORT 1: Patients must be < 3 years of age at the time of diagnosis (date of surgical resection/biopsy)
- COHORT 1: High-grade glioma (World Health Organization [WHO] grade III or IV) harboring NTRK1/2/3 or ROS1 gene fusions as determined by central pathology review
- COHORT 1: Patients must have measurable disease as defined by RAPNO criteria
- COHORT 1: Patients are eligible at the time of diagnosis, prior to any exposure to chemotherapy, targeted therapy, immunotherapy, cellular therapy or radiation
- COHORT 1: ≤ 28 days since study screening
- COHORT 1: Lansky score ≥ 50% and a minimum life expectancy of ≥ 12 weeks
- COHORT 1: Neurologic deficits must have been stable for at least 7 days prior to study enrollment
- COHORT 1: Hemoglobin ≥ 8 g/dL (without transfusion or erythropoietin use within 7 days prior to enrollment)
- COHORT 1: Platelet count ≥ 75,000/µL (without transfusion within 7-day period prior to enrollment)
- COHORT 1: Absolute neutrophil count >1,000/µL
- COHORT 1: Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x the upper limit of normal (ULN)
- COHORT 1: Bilirubin ≤ 1.5 x ULN
- COHORT 1: Adequate renal function as defined by the following age-based serum creatinine concentrations: * 0 to < 1 year: 0.5 mg/dL * 1 to < 2 years: 0.6 mg/dL * 2 to 3 years: 0.8 mg/dL
- COHORT 1: Adequate cardiac function as defined by electrocardiogram (ECG) with Fridericia's corrected QT interval (QTc) ≤ 450 msec and echocardiogram left ventricular ejection fraction (LVEF) > 50%
- COHORT 1: Screening and enrollment consents signed
- COHORT 1: Willingness and ability to comply with treatment plan, scheduled visits, laboratory tests and other study procedures
- COHORT 2: Patients must be < 3 years of age at the time of diagnosis (date of surgical resection/biopsy)
- COHORT 2: CNS tumor other than HGG harboring NTRK1/2/3 or ROS1 gene fusions as determined by central pathology review
- COHORT 2: Patients must have measurable disease as defined by RAPNO criteria
- COHORT 2: Patients are eligible at the time of diagnosis, prior to any exposure to chemotherapy, targeted therapy, immunotherapy, cellular therapy or radiation
- COHORT 2: ≤ 28 days since study screening
- COHORT 2: Lansky score ≥ 50% and a minimum life expectancy of ≥ 12 weeks
- COHORT 2: Neurologic deficits must have been stable for at least 7 days prior to study enrollment
- COHORT 2: Hemoglobin ≥ 8 g/dL (without transfusion or erythropoietin use within 7 days prior to enrollment)
- COHORT 2: Platelet count ≥ 75,000/µL (without transfusion within 7-day period prior to enrollment)
- COHORT 2: Absolute neutrophil count >1,000/µL
- COHORT 2: ALT and ALT ≤ 2.5x the upper limit of normal (ULN)
- COHORT 2: Bilirubin ≤ 1.5 x ULN
- COHORT 2: Adequate renal function as defined by the following age-based serum creatinine concentrations: * 0 to < 1 year: 0.5 mg/dL * 1 to < 2 years: 0.6 mg/dL * 2 to 3 years: 0.8 mg/dL
- COHORT 2: Adequate cardiac function as defined by ECG with QTc ≤ 450 msec and echocardiogram LVEF >50%
- COHORT 2: Screening and enrollment consents signed
- COHORT 2: Willingness and ability to comply with treatment plan, scheduled visits, laboratory tests and other study procedures
Exclusion Criteria
- SCREENING PHASE: Previous exposure to cytotoxic chemotherapy or radiotherapy
- COHORT 1 AND 2: Clinically significant medical disorder that could compromise the ability to tolerate study therapy or would interfere with the study procedures or results history
- COHORT 1 AND 2: History of recent (3 months) symptomatic congestive heart failure
- COHORT 1 AND 2: Known active, uncontrolled infection (bacterial, fungal, or viral)
- COHORT 1 AND 2: Receiving enzyme inducing antiepileptic drugs (EIAEDs)
- COHORT 1 AND 2: Any prior cancer therapy including chemotherapy (excluding bridging chemotherapy cycle), targeted therapy, immunotherapy, cellular therapy, or radiation
- COHORT 1 AND 2: Receiving another investigational agent concurrently
- COHORT 1 AND 2: Surgery within 2 weeks prior to treatment enrollment
- COHORT 1 AND 2: Patients with known hypersensitivity to excipients of the investigational medicinal product
- COHORT 1 AND 2: Active gastrointestinal disease or malabsorption disorder (e.g. Crohn’s disease, ulcerative colitis, short-gut syndrome) that would impair drug absorption
- COHORT 1 AND 2: Inability to take medication enterally
Additional locations may be listed on ClinicalTrials.gov for NCT06528691.
Locations matching your search criteria
United States
Tennessee
Memphis
PRIMARY OBJECTIVE:
I. To determine the overall response rate of entrectinib when used as first line therapy in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused high-grade glioma (HGG). (Cohort 1)
SECONDARY OBJECTIVES:
I. To estimate the 2-year and 5-year progression free survival (PFS) and overall survival (OS) in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused HGG treated with entrectinib as first line therapy. (Cohort 1)
II. To estimate the duration of response (DOR) in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused HGG treated with entrectinib as first line therapy. (Cohort 1)
III. To evaluate the fraction of patients with NTRK1/2/3- or ROS1-fused HGG treated who have second surgeries and a gross-total resection after treatment with entrectinib is achieved, overall and by country and hospital. (Cohort 1)
IV. To describe the overall response rate of entrectinib when used as first line therapy in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused central nervous system (CNS) tumors other than HGG. (Cohort 2)
V. To estimate the 2-year and 5-year PFS and OS in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused CNS tumors other than HGG treated with entrectinib as first line therapy. (Cohort 2)
VI. To estimate the duration of response (DOR) in patients who are younger than 3 years of age with NTRK1/2/3- or ROS1-fused CNS tumors other than HGG treated with entrectinib as first line therapy. (Cohort 2)
VII. To evaluate the fraction of patients with NTRK1/2/3- or ROS1-fused CNS tumors other than HGG who have second surgeries and a gross-total resection after treatment with entrectinib is achieved, overall and by country and hospital. (Cohort 2)
VIII. To describe toxicities experienced by patients younger than 3 years of age treated with entrectinib.
IX. To evaluate number of patients that are screened for the study and eligible versus enrolled and treated with entrectinib.
X. To measure the time intervals (days) from time of initial diagnostic surgery to screening and enrollment in this study.
EXPLORATORY OBJECTIVES:
I. To explore correlation between different fusions and fusion partners, and treatment response, 2-year PFS, 2-year OS, 5-year PFS, and 5-year OS.
II. To explore correlation between histology, expression profiles, and deoxyribonucleic acid (DNA) methylome profiles, and treatment response, 2-year PFS, 2-year OS, 5-year PFS, and 5-year OS.
III. To characterize and monitor neurocognitive function in patients younger than 3 years of age treated with entrectinib.
IV. To compare bi-perpendicular dimeter (Response Assessment in Pediatric Neuro-Oncology Tumor Response Criteria [RAPNO]) with volumetric assessment for response assessment.
V. To explore the pharmacokinetics of entrectinib and the M5 metabolite in patients younger than 3 years of age treated with entrectinib.
OUTLINE:
Patients receive entrectinib enterally once daily (QD) on days 1-28 of each cycle. Treatment repeats every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients requiring bridging therapy prior to starting entrectinib may receive cyclophosphamide intravenously (IV) over 1 hour on day 1, etoposide IV over 1 hour on day 1 and 2, carboplatin IV over 1 hour on day 2, filgrastim subcutaneously (SC) or IV or pegfilgrastim SC on day 3. Patients undergo magnetic resonance imaging (MRI), echocardiography, and blood sample collection throughout the study.
After completion of study treatment, patients are followed up at months 27, 30, 33, 36, 42, 48, 54, and 60.
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationSaint Jude Children's Research Hospital
Principal InvestigatorDaniel Crowther Moreira Ridsdale
- Primary IDGLOBOTRK
- Secondary IDsNCI-2024-02977
- ClinicalTrials.gov IDNCT06528691