| Literature DB >> 27335276 |
Michael Pfeilstöcker1, Heinz Tuechler2, Guillermo Sanz3, Julie Schanz4, Guillermo Garcia-Manero5, Francesc Solé6, John M Bennett7, David Bowen8, Pierre Fenaux9, Francois Dreyfus10, Hagop Kantarjian5, Andrea Kuendgen11, Luca Malcovati12, Mario Cazzola12, Jaroslav Cermak13, Christa Fonatsch14, Michelle M Le Beau15, Marilyn L Slovak16, Alessandro Levis17, Michael Luebbert18, Jaroslaw Maciejewski19, Sigrid Machherndl-Spandl20, Silvia M M Magalhaes21, Yasushi Miyazaki22, Mikkael A Sekeres19, Wolfgang R Sperr23, Reinhard Stauder24, Sudhir Tauro25, Peter Valent26, Teresa Vallespi27, Arjan A van de Loosdrecht28, Ulrich Germing11, Detlef Haase4, Peter L Greenberg29.
Abstract
In myelodysplastic syndromes (MDSs), the evolution of risk for disease progression or death has not been systematically investigated despite being crucial for correct interpretation of prognostic risk scores. In a multicenter retrospective study, we described changes in risk over time, the consequences for basal prognostic scores, and their potential clinical implications. Major MDS prognostic risk scoring systems and their constituent individual predictors were analyzed in 7212 primary untreated MDS patients from the International Working Group for Prognosis in MDS database. Changes in risk of mortality and of leukemic transformation over time from diagnosis were described. Hazards regarding mortality and acute myeloid leukemia transformation diminished over time from diagnosis in higher-risk MDS patients, whereas they remained stable in lower-risk patients. After approximately 3.5 years, hazards in the separate risk groups became similar and were essentially equivalent after 5 years. This fact led to loss of prognostic power of different scoring systems considered, which was more pronounced for survival. Inclusion of age resulted in increased initial prognostic power for survival and less attenuation in hazards. If needed for practicability in clinical management, the differing development of risks suggested a reasonable division into lower- and higher-risk MDS based on the IPSS-R at a cutoff of 3.5 points. Our data regarding time-dependent performance of prognostic scores reflect the disparate change of risks in MDS subpopulations. Lower-risk patients at diagnosis remain lower risk whereas initially high-risk patients demonstrate decreasing risk over time. This change of risk should be considered in clinical decision making.Entities:
Mesh:
Year: 2016 PMID: 27335276 PMCID: PMC5161006 DOI: 10.1182/blood-2016-02-700054
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113