Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet

Luca Malcovati(University of Pavia), Eva Hellström‐Lindberg(Karolinska University Hospital), David Bowen(St James's University Hospital), Lionel Adès(Université Sorbonne Paris Nord), Jaroslav Čermák(Institute of Haematology and Blood Transfusion), Consuelo del Cañizo(Complejo Hospitalario de Salamanca), Matteo Giovanni Della Porta(Istituti di Ricovero e Cura a Carattere Scientifico), Pierre Fenaux(Université Sorbonne Paris Nord), Norbert Gattermann(Heinrich Heine University Düsseldorf), Ulrich Germing(Heinrich Heine University Düsseldorf), Joop H. Jansen(Radboud University Nijmegen), Moshe Mittelman(Tel Aviv University), Ghulam Mufti(King's College Hospital), Uwe Platzbecker(University Hospital Carl Gustav Carus), Guillermo Sanz(Hospital Universitari i Politècnic La Fe), Dominik Selleslag(AZ Sint-Jan), Mette Skov-Holm(Aarhus University Hospital), Reinhard Stauder(Innsbruck Medical University), Argiris Symeonidis(University of Patras), Arjan A. van de Loosdrecht, Théo de Witte(Radboud University Nijmegen), Mario Cazzola(University of Pavia)
Blood
August 27, 2013
Cited by 665Open Access
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Abstract

Within the myelodysplastic syndrome (MDS) work package of the European LeukemiaNet, an Expert Panel was selected according to the framework elements of the National Institutes of Health Consensus Development Program. A systematic review of the literature was performed that included indexed original papers, indexed reviews and educational papers, and abstracts of conference proceedings. Guidelines were developed on the basis of a list of patient- and therapy-oriented questions, and recommendations were formulated and ranked according to the supporting level of evidence. MDSs should be classified according to the 2008 World Health Organization criteria. An accurate risk assessment requires the evaluation of not only disease-related factors but also of those related to extrahematologic comorbidity. The assessment of individual risk enables the identification of fit patients with a poor prognosis who are candidates for up-front intensive treatments, primarily allogeneic stem cell transplantation. A high proportion of MDS patients are not eligible for potentially curative treatment because of advanced age and/or clinically relevant comorbidities and poor performance status. In these patients, the therapeutic intervention is aimed at preventing cytopenia-related morbidity and preserving quality of life. A number of new agents are being developed for which the available evidence is not sufficient to recommend routine use. The inclusion of patients into prospective clinical trials is strongly recommended.


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