Observational studyThe Journal of international medical research2026
Real-world disease characteristics and frontline treatments used in chronic lymphocytic leukaemia in Bulgaria: An observational cohort study (DESCRIBE).
Observational study in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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16 authors.
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Abstract
ObjectiveBruton tyrosine kinase inhibitors and B-cell lymphoma 2 inhibitors are currently the new standard active agents in chronic lymphocytic leukaemia. This observational study describes the real-world use of frontline treatment in Bulgarian patients with active chronic lymphocytic leukaemia and characterises the patient population receiving these treatments.MethodsDESCRIBE was a physician-chart review study conducted at eight haematology centres across Bulgaria. Adult patients with confirmed active chronic lymphocytic leukaemia requiring frontline treatment initiation after January 2022 were considered for enrolment.ResultsA total of 90 patients were included in the study. The mean age (standard deviation) was 62.8 (11.2) years, and 58% were male. The median (range) duration of disease was 6 (0-198) months at the time of frontline treatment initiation and 19.2 (1.2-206.4) months at enrolment. Comorbidities were reported in 58 (64%) patients, with cardiovascular diseases being the most common (57%). Cytogenetic testing rates were lower, particularly for del(11q), tumour protein p53 gene and immunoglobulin heavy chain variable region gene mutation status, which were assessed in only 44%, 21% and 37% of patients, respectively. At the time of frontline treatment initiation, most patients presented with Rai stage II (44%) or Binet stage B (63%). Targeted therapy was used in 77% of cases (46% Bruton tyrosine kinase inhibitors and 31% B-cell lymphoma 2 inhibitors), while chemoimmunotherapy was used in the remaining 23%. Patients with high-risk chronic lymphocytic leukaemia were more likely to receive second-generation Bruton tyrosine kinase inhibitors (odds ratio = 5.59,
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