A Study of a New Way to Treat Children and Young Adults With a Brain Tumor Called NGGCT

Launched by CHILDREN'S ONCOLOGY GROUP · Dec 22, 2020

Keywords

ClinConnect Summary

This clinical trial is exploring a new way to treat children and young adults with a type of brain tumor called non-germinomatous germ cell tumor (NGGCT). The study aims to find the best combination of chemotherapy and radiation therapy for patients whose tumors have not spread. The researchers will first give participants chemotherapy to see how well their tumors respond. Based on the results, some patients may receive targeted radiation therapy to specific areas of the brain and spine, while others might get a higher dose of chemotherapy followed by radiation. The goal is to improve treatment effectiveness and reduce side effects.

To be eligible for the trial, participants need to be between 3 and 30 years old and newly diagnosed with localized NGGCT. They will also need to meet certain health criteria, such as having specific tumor markers in their blood or cerebrospinal fluid. Throughout the trial, participants will receive close monitoring and care, and their quality of life will be assessed. It's important for families to know that this study is actively recruiting, and all patients or their guardians must provide written consent to participate.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patients must be \>= 3 years and \< 30 years at the time of study enrollment
• • Patients must be newly diagnosed with localized primary CNS NGGCT of the suprasellar and/or pineal region by pathology and/or serum or cerebrospinal fluid (CSF) elevation of AFP above institutional normal or \> 10 ng/mL or human chorionic gonadotropin (hCG) beta \> 100 mIU/mL as confirmed by Rapid Central Marker Screening Review on APEC14B1-CNS. Suprasellar, pineal and bifocal tumors are included. (CSF tumor markers and cytology must be within 31 days prior to enrollment and start of protocol therapy \[repeat if necessary\]. Serum tumor markers, AFP and hCGbeta must be within 7 days prior to enrollment and start of protocol therapy \[repeat if necessary\]). Basal ganglia or other primary sites are excluded
• • Patients with any of the following pathological elements are eligible: endodermal sinus (yolk sac), embryonal carcinoma, choriocarcinoma, malignant/immature teratoma and mixed germ cell tumor (GCT) (i.e., may include some pure germinoma) if malignant elements listed above are present. Patients with only mature teratoma are excluded. Patients with pure germinoma admixed with mature teratoma are excluded (would be eligible for pure germinoma protocols)
• • Patients must have a cranial MRI with and without gadolinium at diagnosis/prior to enrollment. If surgical resection is performed, patients must have pre-operative and post operative brain MRI with and without gadolinium. The post operative brain MRI should be obtained within 72 hours of surgery. If patient has a biopsy only, post-operative brain MRI is recommended but not required (within 31 days prior to study enrollment and start of protocol therapy )
• • Patients must have a spine MRI with gadolinium obtained at diagnosis/prior to enrollment. Spine MRI with and without gadolinium is recommended (within 31 days prior to study enrollment and start of protocol therapy)
• • Lumbar CSF must be obtained prior to study enrollment unless medically contraindicated. If a patient undergoes surgery and lumbar CSF cytology cannot be obtained at the time of surgery, then it should be performed at least 10 days following surgery and prior to study enrollment. False positive cytology can occur within 10 days of surgery
• • Patients must have RAPID CENTRAL TUMOR MARKER REVIEW CSF tumor markers obtained prior to enrollment unless medically contraindicated. Ventricular CSF obtained at the time of CSF diversion procedure (if performed) is acceptable for tumor markers but lumbar CSF is preferred. In case CSF diversion and biopsy/surgery are combined, CSF tumor markers should be collected first
• • Peripheral absolute neutrophil count (ANC) \>= 1000/uL (within 7 days prior to enrollment)
• • Platelet count \>= 100,000/uL (transfusion independent) (within 7 days prior to enrollment)
• • Hemoglobin \>= 8.0 g/dL (may receive red blood cell \[RBC\] transfusions) (within 7 days prior to enrollment)
• * Creatinine clearance or radioisotope glomerular filtration rate (GFR) \>= 70 mL/min/1.73 m\^2 or a serum creatinine based on age/gender as follows (within 7 days prior to enrollment):
• • Age: Maximum serum creatinine (mg/dL)
• • 3 to \< 6 years: 0.8 (male), 0.8 (female)
• • 6 to \< 10 years: 1 (male), 1 (female)
• • 10 to \< 13 years: 1.2 (male), 1.2 (female)
• • 13 to \< 16 years: 1.5 (male), 1.4 (female)
• • \>= 16 years: male (1.7), 1.4 (female)
• • Total bilirubin =\< 1.5 x upper limit of normal (ULN) for age (within 7 days prior to enrollment)
• • Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase \[ALT\]) =\< 135 U/L (within 7 days prior to enrollment)
• • Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L
• * Central nervous system function defined as:
• • Patients with seizure disorder may be enrolled if on anticonvulsants and well controlled
• • Patients must not be in status epilepticus, coma or assisted ventilation prior to study enrollment
• • Protocol therapy must begin within 31 calendar days of definitive surgery or clinical diagnosis, whichever is later. If a biopsy only was performed, the biopsy date will be considered the date of definitive surgery. For patients who have a biopsy or incomplete resection at diagnosis followed by additional surgery, the date of the last resection will be considered the date of definitive surgery.
• • All patients and/or their parents or legal guardians must sign a written informed consent
• • All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met
• * NEUROCOGNITIVE FUNCTION AND QUALITY OF LIFE ASSESSMENT:
• • English-, Spanish-, or French- speaking
• • Note: Patients who speak a language other than English, Spanish, or French will be allowed to participate in ACNS2021 but will not complete the neurocognitive and quality of life assessments
• • No known history of neurodevelopmental disorder prior to diagnosis of NGGCT (e.g., Down syndrome, fragile X, William syndrome, intellectual disability). Patients with NF1 will be allowed to participate
• • Additional eligibility criteria for the COG Standardized Neuropsychological Battery only: must be at a site that has a psychologist to administer the battery
• • Note: If not eligible for the COG Standardized Battery, patients should still complete the Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2), Pediatric Quality of Life Inventory (PedsQL), Adaptive Behavior Assessment System Third Edition (ABAS-3), and Behavior Assessment System for Children, Third Edition (BASC-3) questionnaires
• Exclusion Criteria:
• • Patients with tumors located outside the ventricles (i.e., basal ganglia, thalamus)
• • Patients with only mature teratoma and non-elevated markers upon tumor sampling at diagnosis
• • Patients who have received any prior tumor-directed therapy for their diagnosis of NGGCT other than surgical intervention and corticosteroids
• • Patients with metastatic disease (i.e., MRI evaluation, lumbar CSF cytology or intraoperative evidence of dissemination)
• • Female patients who are pregnant, since fetal toxicities and teratogenic effects have been noted for several of the study drugs
• • Note: Serum and urine pregnancy tests may be falsely positive due to HCGbeta-secreting germ cell tumors. Ensure the patient is not pregnant by institutional standards
• • Lactating females who plan to breastfeed their infants
• • Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of their study participation