Disease Duration, Not Age Alone, Drives Cancer Risk in Blood Disorder Patients
A Swedish study of 15,000+ patients reveals that transformation risk to leukemia varies sharply by blood disorder type and disease progression timeline—challenging decades of assumptions that age is the primary driver. The findings could reshape treatment monitoring strategies and clinical trial design for myeloproliferative neoplasm patients.
Originaltitel: Risk of Transformation to Acute Myeloid Leukaemia and Myelodysplastic Syndromes in Patients With Myeloproliferative Neoplasms Over Attained Age and Time Since Diagnosis: A Nationwide Cohort Study
ABSTRACT Background Individuals with polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF) face transformation risks to acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). While older age is linked to increased risk, it remains unclear whether risk increases with age or with disease duration. Objectives To examine how age and disease duration affect AML and MDS transformation in MPN. Methods We used Swedish nationwide register data to model transformation rates as continuous functions of age and disease duration for each subtype and outcome. Cumulative incidences were estimated accounting for competing risk of death. Results This study included 7156 patients with PV, 6810 with ET, and 1080 with PMF diagnosed in 2001–2021. In PV and ET, AML rates increased with disease duration. In PMF, AML rates were highest soon after diagnosis and declined over time. The 10‐year cumulative incidence of AML at diagnosis age 70 was 3.5% in PV, 4.7% in ET, and 18.2% in PMF; for MDS, it was 1.7%, 3.1%, and 10.7%, respectively. Conclusion AML and MDS transformation risks vary by MPN subtype and depend on age and disease duration, with disease duration elevating AML risk in PV and ET; incorporating both factors is essential for individualized risk assessment.