The combination of a tyrosine kinase inhibitor and blinatumomab in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia or Philadelphia chromosome-like acute lymphoblastic leukemia.
Xiaoxia WuShenqi LuXinhui ZhangZhen YangAining SunDepei WuHuifen ZhouMiao MiaoPublished in: Cancer medicine (2024)
Tyrosine kinase inhibitors (TKIs) have revolutionized Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) treatment. The combination of blinatumomab and a TKI in the frontline setting has shown the safety and efficacy of the chemotherapy-free treatment approach in patients with Ph + ALL. This retrospective analysis included 19 patients with Ph + ALL and Ph-like ALL treated with the combination of blinatumomab and a TKI. Of the 14 newly diagnosed patients, the overall response, complete remission (CR), and molecular response (CMR) rates after one cycle of blinatumomab were 100% (10/10), 90% (9/10), and 57% (8/14), respectively. Of the five relapsed patients, the CR and CMR rates were 50% (2/4) and 40% (2/5). Blinatumomab in combination with TKIs is safe and effective and hence this combination therapy could be a viable therapeutic option in front-line treatment of patients with Ph + ALL.
Keyphrases
- acute lymphoblastic leukemia
- newly diagnosed
- combination therapy
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- ejection fraction
- chronic kidney disease
- prognostic factors
- peritoneal dialysis
- squamous cell carcinoma
- rheumatoid arthritis
- tyrosine kinase
- replacement therapy
- diffuse large b cell lymphoma
- smoking cessation
- genome wide
- locally advanced
- multiple myeloma
- disease activity
- rectal cancer