Axitinib in Ponatinib-Resistant B-Cell Acute Lymphoblastic Leukemia Harboring a T315L Mutation.
Valentina GiudiceAndrea Ghelli Luserna di RoràBianca SerioRoberto GuarigliaMaria Benedetta GianniniAnna FerrariFrancesco LanzaCarmine SelleriGiovanni MartinelliPublished in: International journal of molecular sciences (2020)
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.
Keyphrases
- chronic myeloid leukemia
- acute lymphoblastic leukemia
- metastatic renal cell carcinoma
- tyrosine kinase
- clinical trial
- copy number
- allogeneic hematopoietic stem cell transplantation
- protein kinase
- case report
- physical activity
- young adults
- cancer therapy
- brain injury
- mesenchymal stem cells
- binding protein
- drug delivery
- phase ii
- blood brain barrier
- study protocol
- amino acid