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Blood, 16 April 2009, Vol. 113, No. 16, pp. 3666-3672. Prepublished online as a Blood First Edition Paper on November 19, 2008; DOI 10.1182/blood-2008-09-179341.
Submitted September 19, 2008
Department of Medicine, Division of Hematology, Karolinska University Hospital, Solna and Karolinska Institutet, Stockholm, Sweden * Corresponding author; email: asa.derolf{at}karolinska.se.
We evaluated survival patterns for all registered acute myeloid leukemia (AML) patients diagnosed in Sweden 1973-2005 (n=9,729; median age 69 years). Patients were categorized into six age groups and four calendar periods (1973-1980, 1981-1988, 1989-1996, and 1997-2005). Relative survival ratios (RSRs) were computed as measures of patient survival. One-year survival improved over time in all age groups while five- and ten-year survival improved in all age groups except for patients 80+ years. The five-year RSRs in the last calendar period were 0.65, 0.58, 0.36, 0.15, 0.05, and 0.01 for the age groups 0-18, 19-40, 41-60, 61-70, 71-80, and 80+ years, respectively. Intensified chemotherapy, a continuous improvement in supportive care, and allogeneic stem cell transplantation are probably the most important factors contributing to this finding. In contrast, there was no improvement in survival in AML patients with a prior diagnosis of a myelodysplastic syndrome during 1993-2005 (n=219). In conclusion, AML survival has improved during the last decades. However, the majority of AML patients die from their disease and age remains an important predictor of prognosis. New effective agents with a more favorable toxicity profile are needed to improve survival, particularly in the elderly.
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