Abstract | INTRODUCTION: METHODS: The BCR-ABL1-like phenotype was diagnosed on the basis of an increased expression of ABL1 and CRLF2 genes. RESULTS: We combined a nilotinib-based therapy targeting the overexpressed ABL1 gene with a proteasome inhibitor and Peg-asparaginase, achieving a spectacular response: the percentage of lymphoblasts in the bone marrow was reduced from 70% to 5%, which enabled a second HCT to be performed. Moreover, the relatively low toxicity of the treatment led to a good quality of life and no need for prolonged hospitalization. CONCLUSION: To our knowledge, this is the first successful use of nilotinib in BCR-ABL1-like phenotype ALL. This case should encourage routine clinical use of molecular data to individualize therapies targeting the overexpressed pathways responsible for leukemic cell proliferation, as a means to overcome chemoresistance.
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Authors | Agnieszka Piekarska, Alicja Sadowska-Klasa, Marta Libura, Karolina Karabin, Andrzej Hellmann |
Journal | Oncology research and treatment
(Oncol Res Treat)
Vol. 41
Issue 9
Pg. 550-553
( 2018)
ISSN: 2296-5262 [Electronic] Switzerland |
PMID | 30121665
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2018 S. Karger GmbH, Freiburg. |
Chemical References |
- Antibodies, Bispecific
- CRLF2 protein, human
- Pyrimidines
- Receptors, Cytokine
- Polyethylene Glycols
- blinatumomab
- Bortezomib
- pegaspargase
- ABL1 protein, human
- Proto-Oncogene Proteins c-abl
- Asparaginase
- nilotinib
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Topics |
- Adult
- Antibodies, Bispecific
(pharmacology, therapeutic use)
- Antineoplastic Combined Chemotherapy Protocols
(pharmacology, therapeutic use)
- Asparaginase
(pharmacology, therapeutic use)
- Bortezomib
(pharmacology, therapeutic use)
- Drug Resistance, Neoplasm
- Female
- Hematopoietic Stem Cell Transplantation
- Humans
- Neoplasm Recurrence, Local
- Phenotype
- Polyethylene Glycols
(pharmacology, therapeutic use)
- Precursor Cell Lymphoblastic Leukemia-Lymphoma
(pathology, therapy)
- Proto-Oncogene Proteins c-abl
(metabolism)
- Pyrimidines
(pharmacology, therapeutic use)
- Receptors, Cytokine
(metabolism)
- Salvage Therapy
(methods)
- Treatment Outcome
- Young Adult
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