1.
Blood Adv
; 7(9): 1666-1670, 2023 05 09.
Artículo
en Inglés
| MEDLINE
| ID: mdl-36595452
Asunto(s)
Antineoplásicos , Inmunoconjugados , Leucemia , Leucemia-Linfoma Linfoblástico de Células Precursoras , Humanos , Antineoplásicos/farmacología , Antineoplásicos/uso terapéutico , Inmunoconjugados/farmacología , Inmunoconjugados/uso terapéutico , Leucemia/tratamiento farmacológico , Leucemia-Linfoma Linfoblástico de Células Precursoras/tratamiento farmacológico
2.
Pediatr Blood Cancer
; 70(4): e30180, 2023 04.
Artículo
en Inglés
| MEDLINE
| ID: mdl-36720638
RESUMEN
Acute myeloid leukemia (AML) patients have a wide array of cytogenetic and molecular aberrations, which can influence response to therapy. Monosomy 7 is a rare subset within pediatric AML (prevalence of <2%) that is highly associated with poor outcomes. Fusions involving the anaplastic tyrosine kinase (ALK) gene were exclusively identified in 14.3% of this high-risk cohort, while absent across all other AML. Given the dismal outcomes of monosomy 7, we evaluated the use of crizotinib, an FDA-approved tyrosine kinase inhibitor, used to treat patients with ALK fusions. Our findings suggest that crizotinib may serve as a novel therapy for these patients.