Abstract
Larotrectinib can be effective in patients with ETV6-NTRK3–positive B-cell lymphoblastic leukemia, inducing prolonged molecular remission.
Single-agent tyrosine kinase inhibitor treatment could be a valuable treatment option in subgroups of kinase fusion–positive ALL patients.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Combined Modality Therapy
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Disease Models, Animal
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Hematopoietic Stem Cell Transplantation
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Humans
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Mice
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Molecular Targeted Therapy
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Oncogene Proteins, Fusion / antagonists & inhibitors
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Oncogene Proteins, Fusion / genetics
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / genetics*
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / pathology
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Protein Kinase Inhibitors / pharmacology
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Protein Kinase Inhibitors / therapeutic use*
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Proteins / antagonists & inhibitors*
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Proteins / genetics*
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Pyrazoles / pharmacology
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Pyrazoles / therapeutic use*
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Pyrimidines / pharmacology
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Pyrimidines / therapeutic use*
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Recurrence
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Retreatment
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Treatment Outcome
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Xenograft Model Antitumor Assays
Substances
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ETV6-NTRK3 fusion protein, human
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Oncogene Proteins, Fusion
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Protein Kinase Inhibitors
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Proteins
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Pyrazoles
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Pyrimidines
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TFG protein, human
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larotrectinib