Abstract
We report a 10-year-old male with relapsing Ph-like acute lymphoblastic leukemia (ALL) bearing ATF7IP/PDGFRB translocation. He was refractory to conventional therapy, and was finally treated with single-agent second-generation TKI dasatinib. The therapeutic response was prompt, with the disappearance of minimum residual disease (MRD) based on genomic PCR analysis within 3 months, and he has maintained complete molecular remission for 12 months. This case report describes an early-phase response to TKI monotherapy on Ph-like ALL, and technical tips for MRD monitoring on long-term follow-up.
Keywords:
MRD; PDGFRB fusion; Ph-like ALL; TKI; genomic PCR.
© 2014 Wiley Periodicals, Inc.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Child
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Dasatinib
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Humans
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Male
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Neoplasm, Residual
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics
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Protein Kinase Inhibitors / therapeutic use*
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Protein-Tyrosine Kinases / antagonists & inhibitors*
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Pyrimidines / therapeutic use*
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Receptor, Platelet-Derived Growth Factor beta / genetics*
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Repressor Proteins
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Thiazoles / therapeutic use*
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Transcription Factors / genetics*
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Translocation, Genetic*
Substances
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ATF7IP protein, human
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Protein Kinase Inhibitors
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Pyrimidines
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Repressor Proteins
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Thiazoles
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Transcription Factors
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Protein-Tyrosine Kinases
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Receptor, Platelet-Derived Growth Factor beta
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Dasatinib