Anthracycline-based consolidation may determine outcome of post-consolidation immunotherapy in AML.
Johan AureliusLars MöllgårdRoberta KiffinFrida Ewald SanderStaffan NilssonFredrik Bergh ThorénKristoffer HellstrandAnna MartnerPublished in: Leukemia & lymphoma (2019)
Consolidation chemotherapy in acute myeloid leukemia (AML) aims at eradicating residual leukemic cells and mostly comprises high-dose cytarabine with or without the addition of anthracyclines, including daunorubicin. Immunogenic cell death (ICD) may contribute to the efficacy of anthracyclines in solid cancer, but the impact of ICD in AML is only partly explored. We assessed aspects of ICD, as reflected by calreticulin expression, in primary human AML blasts and observed induction of surface calreticulin upon exposure to daunorubicin but not to cytarabine. We next assessed immune phenotypes in AML patients in complete remission (CR), following consolidation chemotherapy with or without anthracyclines. These patients subsequently received immunotherapy with histamine dihydrochloride (HDC) and IL-2. Patients who had received anthracyclines for consolidation showed enhanced frequencies of CD8+ TEM cells in blood along with improved survival. We propose that the choice of consolidation therapy prior to AML immunotherapy may determine clinical outcome.
Keyphrases
- acute myeloid leukemia
- high dose
- end stage renal disease
- allogeneic hematopoietic stem cell transplantation
- cell death
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- induced apoptosis
- chronic kidney disease
- cell cycle arrest
- endothelial cells
- prognostic factors
- poor prognosis
- oxidative stress
- stem cells
- patient reported outcomes
- early breast cancer
- locally advanced
- bone marrow
- disease activity
- pi k akt
- free survival
- cell therapy
- childhood cancer