Abstract
Blinatumomab is a bispecific T-cell engaging αCD19 antibody used in refractory or relapsed B-cell precursor acute lymphoblastic leukemia (ALL). Recently, lineage switch to a myeloid phenotype has been described following CD19 targeting treatment in three pediatric patients with mixed lineage leukemia (MLL) rearranged ALL. We report the case of a female who received blinatumomab for a first relapse of ALL without MLL alterations. She suffered from a second relapse early after hematopoietic stem cell transplantation and was treated with blinatumomab again. During this treatment, the leukemia lost CD19 expression as well as nearly all other B-cell markers, while still harboring the initial minimal residual disease marker, and switched to a myeloid phenotype.
Keywords:
ALL; MLL; blinatumomab; lineage switch.
© 2017 Wiley Periodicals, Inc.
MeSH terms
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Antibodies, Bispecific / adverse effects*
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Antigens, CD19 / metabolism*
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Antineoplastic Agents / adverse effects
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Cell Lineage*
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Child
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Female
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Gene Rearrangement
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Hematopoietic Stem Cell Transplantation / adverse effects*
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Histone-Lysine N-Methyltransferase / genetics
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Humans
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Leukemia, Myeloid, Acute / chemically induced*
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Leukemia, Myeloid, Acute / genetics
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Leukemia, Myeloid, Acute / metabolism
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Leukemia, Myeloid, Acute / pathology
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Myeloid-Lymphoid Leukemia Protein / genetics
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Neoplasm Recurrence, Local / drug therapy*
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Neoplasm Recurrence, Local / epidemiology
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Neoplasm, Residual / drug therapy
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / therapy
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Prognosis
Substances
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Antibodies, Bispecific
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Antigens, CD19
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Antineoplastic Agents
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KMT2A protein, human
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Myeloid-Lymphoid Leukemia Protein
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blinatumomab
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Histone-Lysine N-Methyltransferase