Abstract
The addition of imatinib to high-intensity chemotherapy has improved the outcome of patients with Philadelphia chromosome (Ph)-positive acute lymphoblastic leukemia (ALL). However, the possible long-term side effects of this combination are not yet known. Development of new clonal abnormalities in complete cytogenetic remission after treatment with imatinib has been reported in patients with chronic myeloid leukemia but not in patients with Ph-positive ALL. Here, we present a patient with Ph-positive ALL who received hyperCVAD plus imatinib and achieved hematologic, cytogenetic, and major molecular responses. The patient then developed myelodysplastic syndrome and solitary central nervous system relapse of ALL.
MeSH terms
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Antineoplastic Agents / therapeutic use*
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Benzamides
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Central Nervous System Neoplasms / etiology*
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Central Nervous System Neoplasms / pathology
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Cyclophosphamide / therapeutic use
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Cytogenetic Analysis
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Dexamethasone / therapeutic use
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Doxorubicin / therapeutic use
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Female
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Hematopoietic Stem Cell Transplantation
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Humans
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Imatinib Mesylate
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / etiology
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / therapy
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Middle Aged
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Myelodysplastic Syndromes / etiology*
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Myelodysplastic Syndromes / pathology
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Myelodysplastic Syndromes / therapy
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Neoplasms, Second Primary / etiology*
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Neoplasms, Second Primary / pathology
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Neoplasms, Second Primary / therapy
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Piperazines / therapeutic use*
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / complications
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Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
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Protein-Tyrosine Kinases / antagonists & inhibitors
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Pyrimidines / therapeutic use*
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Remission Induction
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Treatment Outcome
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Vincristine / therapeutic use
Substances
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Antineoplastic Agents
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Benzamides
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Piperazines
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Pyrimidines
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Vincristine
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Dexamethasone
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Doxorubicin
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Imatinib Mesylate
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Cyclophosphamide
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Protein-Tyrosine Kinases