Prognostic scoring systems for myelodysplastic syndromes (MDS) in a population‐based setting: a report from the Swedish MDS register

Summary The myelodysplastic syndromes (MDS) have highly variable outcomes and prognostic scoring systems are important tools for risk assessment and to guide therapeutic decisions. However, few population‐based studies have compared the value of the different scoring systems. With data from the nati...

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Veröffentlicht in:British journal of haematology 2018-06, Vol.181 (5), p.614-627
Hauptverfasser: Moreno Berggren, Daniel, Folkvaljon, Yasin, Engvall, Marie, Sundberg, Johan, Lambe, Mats, Antunovic, Petar, Garelius, Hege, Lorenz, Fryderyk, Nilsson, Lars, Rasmussen, Bengt, Lehmann, Sören, Hellström‐Lindberg, Eva, Jädersten, Martin, Ejerblad, Elisabeth
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Sprache:eng
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Zusammenfassung:Summary The myelodysplastic syndromes (MDS) have highly variable outcomes and prognostic scoring systems are important tools for risk assessment and to guide therapeutic decisions. However, few population‐based studies have compared the value of the different scoring systems. With data from the nationwide Swedish population‐based MDS register we validated the International Prognostic Scoring System (IPSS), revised IPSS (IPSS‐R) and the World Health Organization (WHO) Classification‐based Prognostic Scoring System (WPSS). We also present population‐based data on incidence, clinical characteristics including detailed cytogenetics and outcome from the register. The study encompassed 1329 patients reported to the register between 2009 and 2013, 14% of these had therapy‐related MDS (t‐MDS). Based on the MDS register, the yearly crude incidence of MDS in Sweden was 2·9 per 100 000 inhabitants. IPSS‐R had a significantly better prognostic power than IPSS (P 
ISSN:0007-1048
1365-2141
1365-2141
DOI:10.1111/bjh.15243