Targeted Therapy Directed by Genetic Testing in Treating Pediatric Patients With Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphomas, or Histiocytic Disorders (The Pediatric MATCH Screening Trial)
NCT03155620 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1377
Last updated 2026-05-05
Summary
This phase II Pediatric MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in pediatric patients with solid tumors, non-Hodgkin lymphomas, or histiocytic disorders that have progressed following at least one line of standard systemic therapy and/or for which no standard treatment exists that has been shown to prolong survival. Genetic tests look at the unique genetic material (genes) of patients' tumor cells. Patients with genetic changes or abnormalities (mutations) may benefit more from treatment which targets their tumor's particular genetic mutation, and may help doctors plan better treatment for patients with solid tumors or non-Hodgkin lymphomas.
Conditions
- Advanced Malignant Solid Neoplasm
- Ann Arbor Stage III Non-Hodgkin Lymphoma
- Ann Arbor Stage IV Non-Hodgkin Lymphoma
- Histiocytic Sarcoma
- Juvenile Xanthogranuloma
- Langerhans Cell Histiocytosis
- Malignant Glioma
- Recurrent Childhood Rhabdomyosarcoma
- Recurrent Ependymoma
- Recurrent Ewing Sarcoma
- Recurrent Glioma
- Recurrent Hepatoblastoma
- Recurrent Langerhans Cell Histiocytosis
- Recurrent Malignant Germ Cell Tumor
- Recurrent Malignant Solid Neoplasm
- Recurrent Medulloblastoma
- Recurrent Neuroblastoma
- Recurrent Non-Hodgkin Lymphoma
- Recurrent Osteosarcoma
- Recurrent Peripheral Primitive Neuroectodermal Tumor
- Recurrent Primary Central Nervous System Neoplasm
- Recurrent Rhabdoid Tumor
- Recurrent Soft Tissue Sarcoma
- Refractory Ewing Sarcoma
- Refractory Glioma
- Refractory Hepatoblastoma
- Refractory Langerhans Cell Histiocytosis
- Refractory Malignant Germ Cell Tumor
- Refractory Malignant Solid Neoplasm
- Refractory Medulloblastoma
- Refractory Neuroblastoma
- Refractory Non-Hodgkin Lymphoma
- Refractory Osteosarcoma
- Refractory Peripheral Primitive Neuroectodermal Tumor
- Refractory Primary Central Nervous System Neoplasm
- Refractory Rhabdoid Tumor
- Refractory Rhabdomyosarcoma
- Rhabdoid Tumor
- Stage III Osteosarcoma AJCC v7
- Stage III Soft Tissue Sarcoma AJCC v7
- Stage IV Osteosarcoma AJCC v7
- Stage IV Soft Tissue Sarcoma AJCC v7
- Stage IVA Osteosarcoma AJCC v7
- Stage IVB Osteosarcoma AJCC v7
- Wilms Tumor
Interventions
- OTHER
-
Laboratory Biomarker Analysis
Undergo molecular analysis
- DRUG
-
Larotrectinib Sulfate
Given PO or via nasogastric- or gastric-tube
- PROCEDURE
-
Magnetic Resonance Imaging
Undergo MRI, PET/MRI, and/or CT/MRI
- PROCEDURE
-
Mutation Carrier Screening
Undergo tumor tissue mutation screening
- DRUG
-
Given PO
- DRUG
-
Given PO
- OTHER
-
Pharmacological Study
Correlative studies
- PROCEDURE
-
Positron Emission Tomography
Undergo PET, PET/CT, and/or PET/MRI
- PROCEDURE
-
Radionuclide Imaging
Undergo radionuclide imaging
- DRUG
-
Samotolisib
Given PO
- DRUG
-
Given PO
- DRUG
-
Selumetinib Sulfate
Given PO
- DRUG
-
Tazemetostat
Given PO
- DRUG
-
Tipifarnib
Given PO or via nasogastric or gastric tube
- DRUG
-
Ulixertinib
Receive PO
- DRUG
-
Vemurafenib
Given PO
- PROCEDURE
-
X-Ray Imaging
Undergo an x-ray
- DRUG
-
Ivosidenib
Given PO
- PROCEDURE
-
Biopsy Procedure
Undergo biopsy
- PROCEDURE
-
Biospecimen Collection
Undergo blood sample collection
- PROCEDURE
-
Bone Marrow Aspiration and Biopsy
Undergo a bone marrow and/or biopsy
- PROCEDURE
-
Bone Scan
Undergo a bone scan
- PROCEDURE
-
Computed Tomography
Undergo CT, PET/Ct, and/or CT/MRI
- DRUG
-
Ensartinib
Given PO
- DRUG
-
Erdafitinib
Given PO
Sponsors & Collaborators
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Donald W Parsons · Children's Oncology Group
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- SCREENING
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Months
- Max Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-07-31
- Primary Completion
- 2025-03-31
- Completion
- 2027-01-06
- FDA Drug
- Yes
Countries
- United States
- Australia
- Canada
- Puerto Rico
Study Locations
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