Immunotherapy with HDC/IL-2 may be clinically efficacious in acute myeloid leukemia of normal karyotype.
Malin S NilssonAlexander HallnerMats BruneStaffan NilssonFredrik Bergh ThorénAnna MartnerKristoffer HellstrandPublished in: Human vaccines & immunotherapeutics (2019)
Immunotherapy with histamine dihydrochloride and low-dose interleukin-2 (HDC/IL-2) reduces the risk of relapse in the post-chemotherapy phase of acute myeloid leukemia (AML). Here we report the results of exploratory analyses of the clinical efficacy of HDC/IL-2 in AML with focus on the impact of karyotype aberrations in leukemic cells. Post-hoc analyses of phase III trial data suggested that HDC/IL-2 is primarily beneficial for patients with AML of normal karyotype. These results may be helpful in the selection of patients who are suitable for therapy and in the design of future immunotherapy protocols aiming at further defining the mechanism of relapse prevention by HDC/IL-2.
Keyphrases
- acute myeloid leukemia
- phase iii
- low dose
- clinical trial
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- ejection fraction
- squamous cell carcinoma
- open label
- induced apoptosis
- stem cells
- chronic kidney disease
- randomized controlled trial
- study protocol
- peritoneal dialysis
- newly diagnosed
- radiation therapy
- free survival
- high dose
- prognostic factors
- big data
- signaling pathway
- machine learning
- endoplasmic reticulum stress
- current status
- cell cycle arrest
- artificial intelligence