Abstract 1774

Poster Board I-800

Background

Population-based data on myelodysplastic syndromes (MDS) are scarce. Since its inception in 1982, the Düsseldorf MDS Registry has captured 3598 patients with MDS, of whom 21 % live in the town district of Düsseldorf. Between 1996-2005 we are confident that all MDS patients residing in the town district of Düsseldorf were entered and followed in the registry through regular follow-ups. As yearly age- and sex-specific population counts are also available for Düsseldorf, the Registry provides a unique opportunity to estimate MDS disease frequency. Here we aim to quantify the incidence and prevalence of MDS disease subtypes.

Methods

Patients were identified from the MDS Registry. Age- and sex-specific yearly population counts were obtained from the Statistical Office of North-Rhine Westphalia. The number of residents in Düsseldorf minimally increased during the study period from 1996 to 2005 (mean: 571,000 residents). The number of patients with a first-time MDS diagnosis in a given calendar year (incident cases) was divided by the total Düsseldorf population in that year to estimate incidence. Prevalence was estimated by dividing the number of existing plus incident MDS patients in a given year by the total population of Düsseldorf that year. Incidence (per 100,000 person-years (PY) and prevalence per 100,000 persons are presented with corresponding 95% confidence intervals (CI) calculated using the delta and Wilson methods, respectively. Low-risk MDS was defined as WHO subtypes RA, RCMD or MDS with del(5q). High-risk included subtypes RAEB-I and RAEB-II.

Results

344 MDS patients were included in our analyses (279 incident patients). Incidence and prevalence of low-risk MDS was 2.87 (95%CI 2.46–3.35) per 100,000PY and 12.4 (95%CI 11.5–13.4) per 100,000 persons, respectively, with no difference between men and women (Table). High-risk disease was less common. The incidence of high-risk disease in men appeared to be higher (1.22 (95%CI 0.87–1.72) per 100,000PY) than in women (0.63 (95%CI 0.40–0.99) per 100,000PY). Prevalence of high-risk disease among men was statistically significantly higher in men compared to women (2.93 (95%CI 2.35 – 3.65) per 100,000 persons) and 1.56 (95%CI 1.17 – 2.08) per 100,000 persons), respectively (Table).

Conclusion

In this population-based study we found that MDS more common in men than in women. The majority of MDS cases had low-risk disease. Incidence and prevalence of high risk disease (but not low risk) is higher in men compared to women.

Financial disclosures: This study was supported by Amgen Inc.

Table 1

Incidence and prevalence of myelodysplastic syndromes (MDS) by disease subtype in Düsseldorf 1996 - 2005

MDS subtypeIncidencePrevalence
NIncidence rate1 (95% CI)N2Prevalence3 (95% CI)
Overall4 279 4.88 (4.34–5.49) 344 17.8 (16.7–18.9) 
    Male 155 5.74 (4.90–6.72) 191 19.1 (17.5–20.8) 
    Female 124 4.12 (3.45–4.91) 153 16.6 (15.2–18.2) 
     
Disease risk group     
Low-risk disease5 164 2.87 (2.46–3.35) 201 12.4 (11.5–13.4) 
    Male 83 3.07 (2.48–3.81) 101 12.5 (11.3–13.9) 
    Female 81 2.69 (2.16–3.34) 100 12.3 (11.1–13.6) 
     
High-risk disease6 52 0.91 (0.69–1.19) 64 2.21 (1.85–2.63) 
Male 33 1.22 (0.87–1.72) 41 2.9 (2.35–3.65) 
Female 19 0.63 (0.40–0.99) 23 1.56 (1.17–2.08) 
     
WHO classification4     
RA/RARS 37 0.65 (0.47–0.89) 50 3.92 (3.44–4.47) 
5q- 0.09 (0.04–0.21) 0.42 (0.28–0.63) 
RCMD/RCMDRS 122 2.14 (1.79–2.55) 143 8.07 (7.37–8.84) 
RAEB I 21 0.37 (0.24–0.56) 28 1.16 (0.91–1.47) 
RAEB II 31 0.54 (0.38–0.77) 36 1.05 (0.82–1.35) 
CMML I 30 0.53 (0.37–0.75) 40 1.96 (1.63–2.36) 
CMML II 0.12 (0.06–0.26) 0.26 (0.16–0.43) 
RAEB-T 26 0.46 (0.31–0.67) 31 0.93 (0.71–1.21) 
MDS subtypeIncidencePrevalence
NIncidence rate1 (95% CI)N2Prevalence3 (95% CI)
Overall4 279 4.88 (4.34–5.49) 344 17.8 (16.7–18.9) 
    Male 155 5.74 (4.90–6.72) 191 19.1 (17.5–20.8) 
    Female 124 4.12 (3.45–4.91) 153 16.6 (15.2–18.2) 
     
Disease risk group     
Low-risk disease5 164 2.87 (2.46–3.35) 201 12.4 (11.5–13.4) 
    Male 83 3.07 (2.48–3.81) 101 12.5 (11.3–13.9) 
    Female 81 2.69 (2.16–3.34) 100 12.3 (11.1–13.6) 
     
High-risk disease6 52 0.91 (0.69–1.19) 64 2.21 (1.85–2.63) 
Male 33 1.22 (0.87–1.72) 41 2.9 (2.35–3.65) 
Female 19 0.63 (0.40–0.99) 23 1.56 (1.17–2.08) 
     
WHO classification4     
RA/RARS 37 0.65 (0.47–0.89) 50 3.92 (3.44–4.47) 
5q- 0.09 (0.04–0.21) 0.42 (0.28–0.63) 
RCMD/RCMDRS 122 2.14 (1.79–2.55) 143 8.07 (7.37–8.84) 
RAEB I 21 0.37 (0.24–0.56) 28 1.16 (0.91–1.47) 
RAEB II 31 0.54 (0.38–0.77) 36 1.05 (0.82–1.35) 
CMML I 30 0.53 (0.37–0.75) 40 1.96 (1.63–2.36) 
CMML II 0.12 (0.06–0.26) 0.26 (0.16–0.43) 
RAEB-T 26 0.46 (0.31–0.67) 31 0.93 (0.71–1.21) 

1) Incidence per 100,000 person-years

2) Prevalent patients alive during >1 calendar year counted once each year

3) Prevalence per 100,000 persons

4) Including CMML and RAEB-T

5) WHO subtypes RA,RARS,RCMD,RCMDRS and del (5q)

6) WHO subtypes RAEB-I, RAEB-II

Disclosures

Neukirchen:Amgen Inc.: Research Funding. Schoonen:Amgen Inc.: Research Funding. Aul:Amgen Inc.: Research Funding. Haas:Amgen Inc.: Research Funding. Gattermann:Amgen Inc., Celgene, Novartis: Honoraria, Research Funding. Germing:Amgen Inc., Celgene, Novartis: Honoraria, Research Funding.

Author notes

*

Asterisk with author names denotes non-ASH members.

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