Long-Term Follow-Up of Elderly Patients with Acute Myeloid Leukemia Treated with Decitabine: A Real-World Study of the Apulian Hematological Network.
Michelina DargenioGiuseppe TarantiniNicola CascavillaEnzo PavonePellegrino MustoPatrizio MazzaLorella MelilloDomenico PastoreAttilio GuariniCaterina BuquicchioMaria Paola FinaVincenzo FedericoTeresa Maria SanteramoMarina Aurora UrbanoMariangela LeoVera CarluccioPaola CarluccioMario DeliaDaniela CarlinoCarolina VergineVito Pier GagliardiGiuseppina GrecoSilvia SibillaMariachiara AbbenanteGiovanni RossiGiuseppina SpinosaAnnamaria MazzoneLara AprileVincenza de FazioCrescenza PasciollaGiorgina SpecchiaNicola Di RenzoPublished in: Cancers (2022)
Decitabine, a DNA hypomethylating agent, was approved for use in adults with acute myeloid leukemia (AML) not eligible for standard chemotherapy and is now widely accepted as standard treatment. Although a number of clinical trials demonstrated its benefits in elderly AML patients, older adults and patients with frequent comorbidities are typically under-represented in such settings. Thus, the aim of the present study is to evaluate, in a real-world setting, the effectiveness and toxicity of decitabine administered as a single agent in unselected previously untreated elderly AML patients not eligible for intensive chemotherapy. In nine hematological departments of the Apulian Hematological Network (REP), we enrolled 199 patients (median age: 75.4 years; range: 61-91) with de novo ( n = 94) or secondary/therapy-related ( n = 105) AML treated with decitabine 20 mg/m 2 for five days every 4 weeks. Hazard ratios (HR) and their 95% confidence intervals (CI) were estimated using multivariate Cox regression. The average number of cycles administered per patient was 6.3 (SD: 6.0; median: 5 cycles). Complete response was achieved by 31 patients (15.6%) and partial response by 57 (28.6%), for a total of 88 responders overall (44.2%). After a median follow-up of 33.6 months, median OS was 8.7 months (95% CI: 7.4-10.3), and the 6-month, 1-year, and 3-year OS rates were 62.7%, 37.0%, and 7.1%, respectively. Mortality was increased in AML patients with ≥3 comorbidities (HR = 2.45; 95% CI: 1.18-5.08) vs. no comorbidities and in those with adverse karyotype (HR = 1.58; 95% CI: 1.05-2.38) vs. favourable or intermediate profile. Infection was the main registered adverse event (46.0%). In conclusion, this REP real-life study demonstrates, after a follow-up of almost 3 years, how decitabine administered to AML patients not suitable for intensive chemotherapy is effective and well tolerated, even in a population of truly elderly patients with frequent comorbidities.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- clinical trial
- prognostic factors
- allogeneic hematopoietic stem cell transplantation
- emergency department
- randomized controlled trial
- systematic review
- patient reported outcomes
- squamous cell carcinoma
- type diabetes
- mesenchymal stem cells
- risk factors
- oxidative stress
- bone marrow
- cardiovascular events
- patient reported
- radiation therapy
- electronic health record
- drug induced
- combination therapy
- adverse drug
- network analysis