| Literature DB >> 33419251 |
Valentina Giudice1,2,3, Andrea Ghelli Luserna di Rorà4, Bianca Serio3, Roberto Guariglia3, Maria Benedetta Giannini5, Anna Ferrari4, Giorgia Simonetti4, Carmine Selleri1,3, Giovanni Martinelli6.
Abstract
Adult acute lymphoblastic leukemia (ALL) with BCR-ABL1 rearrangement (Philadelphia chromosome, Ph) is a hematological aggressive disease with a fatal outcome in more than 50% of cases. Tyrosine kinase inhibitors (TKIs) targeting the activity of BCR-ABL1 protein have improved the prognosis; however, relapses are frequent because of acquired somatic mutations in the BCR-ABL1 kinase domain causing resistance to first, second and third generation TKIs. Axitinib has shown in vitro and ex vivo activity in blocking ABL1; however, clinical trials exploring its efficacy in ALL are missing. Here, we presented a 77-year-old male with a diagnosis of Ph positive ALL resistant to ponatinib and carrying a rare threonine to leucine (T315L) mutation on BCR-ABL1 gene. The patient was treated with axitinib at 5 mg/twice daily as salvage therapy showing an immediate although transient benefit with an overall survival of 9.3 months. Further dose-finding and randomized clinical trials are required to assess the real efficacy of axitinib for adult Ph positive ALL resistant to third generation TKIs.Entities:
Keywords: TKI inhibitor; acute lymphoblastic leukemia; axitinib; ponatinib
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Year: 2020 PMID: 33419251 PMCID: PMC7765866 DOI: 10.3390/ijms21249724
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923