Acute Lymphoblastic Leukemia With INPP5D-ABL1 Fusion Responds to Imatinib Treatment.
Adolescent
Antineoplastic Agents
/ therapeutic use
Down Syndrome
/ complications
Humans
Imatinib Mesylate
/ therapeutic use
Neoplasm Recurrence, Local
/ drug therapy
Oncogene Proteins, Fusion
/ genetics
Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
/ genetics
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
/ drug therapy
Proto-Oncogene Proteins c-abl
/ economics
Journal
Journal of pediatric hematology/oncology
ISSN: 1536-3678
Titre abrégé: J Pediatr Hematol Oncol
Pays: United States
ID NLM: 9505928
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
pubmed:
26
7
2018
medline:
11
4
2020
entrez:
26
7
2018
Statut:
ppublish
Résumé
We describe a patient with Down syndrome whose precursor B-cell acute lymphoblastic leukemia cells expressed INPP5D-ABL1 fusion gene that resulted in a reciprocal chromosome translocation t(2;9)(q27;q34). The fusion gene was present as a small subclone in the primary disease but was first identified at relapse when the subclone had expanded into a major clone. At relapse, the patient responded poorly to conventional induction chemotherapy but a transient morphologic remission was achieved after administration of imatinib monotherapy. This case demonstrates a pathway to relapse in a Down syndrome patients with acute lymphoblastic leukemia through a rare fusion event. It highlights the significance of minor subclonal events in therapy resistance and the opportunity provided for targeted therapy.
Identifiants
pubmed: 30045148
doi: 10.1097/MPH.0000000000001267
doi:
Substances chimiques
Antineoplastic Agents
0
Oncogene Proteins, Fusion
0
Imatinib Mesylate
8A1O1M485B
ABL1 protein, human
EC 2.7.10.2
Proto-Oncogene Proteins c-abl
EC 2.7.10.2
INPP5D protein, human
EC 3.1.3.86
Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases
EC 3.1.3.86
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM