| Authors |
Hilberink, Jacobien R ; van Zeventer, Isabelle A ; Chitu, Dana A ; Pabst, T ; Klein, Saskia K ; Stussi, G ; Griškevičius, Laimonas ; Valk, P. J.M ; Cloos, J ; van de Loosdrecht, A. A ; Breems, D ; van Lammeren-Venema, D ; Boersma, R ; Jongen-Lavrencic, M ; Fehr, Martin ; Hoogendoorn, Mels ; Manz, Markus G ; Söhne, M ; van Marwijk Kooy, R ; Deeren, D ; van der Poel, M. W.M ; Legdeur, M. C ; Tick, L ; Chalandon, Y ; Ammatuna, E ; Blum, Sabine ; Löwenberg, Bob ; Ossenkoppele, G. J ; Chitu, D. A ; Klein, S. K ; Löwenberg, B ; Huls, Gerwin ; Fehr, M ; Manz, M. G ; Blum, S |
| Abstract [eng] |
Treatment choice according to the individual conditions remains challenging, particularly in older patients with acute myeloid leukemia (AML) and high risk myelodysplastic syndrome (MDS). The impact of performance status, comorbidities, and physical functioning on survival is not well defined for patients treated with hypomethylating agents. Here we describe the impact of performance status (14% ECOG performance status 2), comorbidity (40% HCT-comorbidity index ≥ 2), and physical functioning (41% short physical performance battery 76 years was significantly associated with reduced OS (HR 1.58; p = 0.043) and female sex was associated with superior OS (HR 0.62; p = 0.06). We further compared the genetic profiles of these subgroups. This revealed comparable mutational profiles in patients younger and older than 76 years, but, interestingly, revealed significantly more prevalent mutated ASXL1, STAG2, and U2AF1 in male compared to female patients. In this cohort of older patients treated with decitabine age and sex, but not comorbidities, physical functioning or cytogenetic risk were associated with overall survival. |
