DARWIN EU® Prevalence of rare blood cancers in Europe

31/01/2023
20/08/2026
EU PAS number:
EUPAS50800
Study
Finalised
Study type

Study topic

Disease /health condition

Study type

Non-interventional study

Scope of the study

Disease epidemiology

Data collection methods

Secondary use of data
Non-interventional study

Non-interventional study design

Cohort
Other

Non-interventional study design, other

Population-based
Study drug and medical condition

Medical condition to be studied

Follicular lymphoma
Diffuse large B-cell lymphoma
Plasma cell myeloma
Chronic lymphocytic leukaemia
Acute myeloid leukaemia
Acute lymphocytic leukaemia
Population studied

Short description of the study population

The study included all individuals reported in the five European databases, including IPCI, SIDIAP, CPRD, IQVIA LPD Belgium, and IQVIA DA Germany, to determine the prevalence of haematological cancers.

Age groups

  • Preterm newborn infants (0 – 27 days)
  • Term newborn infants (0 – 27 days)
  • Infants and toddlers (28 days – 23 months)
  • Children (2 to < 12 years)
  • Adolescents (12 to < 18 years)
  • Adults (18 to < 46 years)
  • Adults (46 to < 65 years)
  • Adults (65 to < 75 years)
  • Adults (75 to < 85 years)
  • Adults (85 years and over)

Special population of interest

Other

Special population of interest, other

Patients with haematological cancers

Estimated number of subjects

10000000
Study design details

Study design

Population-based cohort

Main study objective

To estimate the prevalence of rare blood cancers (follicular lymphoma, diffuse Large B-Cell Lymphoma, Multiple Myeloma, Chronic Lymphocytic Leukaemia, Acute Myeloid Leukaemia, Acute Lymphocytic Leukaemia)

Outcomes

Follicular lymphoma, diffuse Large B-Cell Lymphoma, Multiple Myeloma, Chronic Lymphocytic Leukaemia, Acute Myeloid Leukaemia, Acute Lymphocytic.

Data analysis plan

5-year partial prevalence will be estimated for each outcome of interest.

Summary results

CONCLUSION
Across the included databases, ALL and AML were the blood cancers with the lowest prevalence, with a 5 year partial point prevalence at less than 1 per 10,000. DLBCL and FL were slightly more common, with estimated prevalence of less than 2 per 10,000 and less than 3 per 10,000, respectively. Lastly, 5-year partial point prevalence as of 1st January 2020 of CLL and MM was also below 5 per 10,000. Differences in analytic settings, in particular whether using partial or complete prevalence, had a meaningful impact on estimates of prevalence. Prevalence also varied substantially across age groups.