Ponatinib as a Valid Alternative Strategy in Patients with Blast Crisis-Chronic Myeloid Leukemia Not Eligible for Allogeneic Stem Cells Transplantation and/or Conventional Chemotherapy: Report of a Case.
Cristina BucelliDaniele CattaneoValeria FerlaManuela ZappaCaterina de BenedittisSimona SoveriniAlessandra IurloPublished in: Case reports in hematology (2017)
Currently, imatinib and dasatinib are the only tyrosine-kinase inhibitors approved in the US and Europe for the treatment of blast crisis of chronic myeloid leukemia (BC-CML) at diagnosis, while ponatinib is the only inhibitor used in patients bearing T315I mutation. Here we report the case of a 61-year-old man diagnosed with B-cell lymphoid BC-CML, initially treated with imatinib 800 mg day and then with dasatinib 140 mg day because of intolerance. A complete cytogenetic response (CCyR) was achieved at three months; however, three months later a relapse was observed, and the T315I mutation was detected. Ponatinib 45 mg once daily was then started together with a short course of chemotherapy. Bone marrow evaluation after six months of therapy showed the regaining of CCyR, together with the achievement of a deep molecular response. However, one year from ponatinib start the patient experienced a new disease relapse; he was effectively treated with ponatinib and chemotherapy once again, but in the meanwhile an ischemic stroke was detected. This case report confirms the high efficacy of ponatinib monotherapy in BC-CML patients, representing a valid option for non-allogeneic stem cells transplantation eligible cases and the only one available for those carrying the T315I mutation.
Keyphrases
- chronic myeloid leukemia
- stem cells
- bone marrow
- end stage renal disease
- case report
- newly diagnosed
- stem cell transplantation
- ejection fraction
- public health
- chronic kidney disease
- prognostic factors
- peritoneal dialysis
- cell therapy
- atrial fibrillation
- mesenchymal stem cells
- randomized controlled trial
- squamous cell carcinoma
- radiation therapy
- high dose
- combination therapy
- open label
- study protocol
- double blind
- drug administration