Study Objectives: To collect and describe demographics, disease-management, and treatment outcomes of Myelodysplastic Syndromes (MDS) patients who are newly diagnosed and classified according to the World Health Organization (WHO) criteria. To perform observational studies concerning relevant scientific research questions in MDS using clinical data and biological samples, and to present relevant research outcomes in the fields of diagnosis and prognostication, health related quality of life issues, health economics, and risk stratification for newly developed classes of drugs. To disseminate results of the studies to all stakeholders involved.
Methodology: Data on patients with MDS will be collected prospectively at diagnosis and at 6-months intervals after diagnosis. The data will be gathered by seventeen (or more) countries that are represented within the LeukemiaNet MDS Working Party and will be combined in one central European Database. Data analyses will be conducted by the Data Management Centre at the University of York in various sub studies, at specific time points as decided or requested by the steering committee, but at least once a year included in the European Registry and at the end of the follow-up period. Number of Patients \& Centres Over 149 hematology centres in eighteen (or more) different countries (Austria, Croatia, Czech Republic, Denmark, France, Germany, Greece, Israel, Italy, The Netherlands, Romania, Spain, Sweden, Switzerland and United Kingdom) will participate as referral centres in this Registry. The recruitment target is a minimum of 3000 cases lower-risk MDS and 1000 higher-risk cases. Population: The study population will consist of newly diagnosed patients with all subtypes of MDS classified according to the WHO criteria, including therapy-related MDS and MDS-F, AML with 20-\<30 percent marrow blasts (former RAEB-t), and CMML and other forms of mixed MDS/MPD. Study Duration: The enrolment time is scheduled to continue until at least December 2022 but extension of the recruitment period is possible. Patients will be followed until withdrawal (for any reason) or termination of the EUMDS Registry.
Study Type
OBSERVATIONAL
Enrollment
4,000
Only registration of clinical practice
University of Innsbruck Fachartz fur Innere Medizin, Dept of Hematology
Innsbruck, Austria
RECRUITINGClinical Hospital Merkur
Zagreb, Croatia
RECRUITINGInstitute of Haematology and Blood Transfusion U nemocnice
Prague, Czechia
RECRUITINGAarhus University Hospital
Aarhus, Denmark
RECRUITINGHopital Avicenne Universite Paris, Dept of Hematology
Paris, France
RECRUITINGMedizinische Klinik und Poliklinik fur Haematologie, Onkologie und Klinische Immunologie
Düsseldorf, Germany
RECRUITINGUniversity of Patras Medical School, Haematology Division, Dept of Internal Medicine
Pátrai, Greece
RECRUITINGTel-Aviv Sourasky Medical Center, Dept. of Medicine A
Tel Aviv, Israel
RECRUITINGUniversity of Pavia Medical SChool, Dept of Hematology
Pavia, Italy
RECRUITINGRadboud University Nijmegen Medical Centre, dept of Hematology
Nijmegen, Netherlands
RECRUITING...and 8 more locations
Demographics
The primary objective of this study is collect and describe demographics, clinical and lab manifestations, epidemiological data, genetic characteristics, HRQoL, disease-management, and treatment outcomes of MDS patients who are newly diagnosed and classified according to the WHO-2008 and WHO-2016 criteria
Time frame: 14.5 years of follow-up (FU)
Correlations
To investigate the relationship between: * Clinical characteristics at inclusion and during follow-up * Treatments received, including transfusions, and * Responses to treatment * Overall survival * Disease progression * General and disease specific HRQoL, and Karnofsky Performance Status * Health Economics
Time frame: 14.5 years of FU
New prognostic scoring systems
To derive and validate new prognostic scoring systems
Time frame: 14.5 years of FU
Scientific research in MDS
To perform observational studies concerning relevant scientific research questions in MDS using clinical data and biological samples and to present relevant research outcomes in the fields of diagnosis \& prognostication, HRQoL issues, health economics, risk stratification for newly developed classes of drugs.
Time frame: 14.5 years of FU
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