Abstract
Leukemias, representing malignant neoplasms of the hematopoietic system, are distinguished in hematological practice by high mortality rates and complex clinical trajectories. The pathogenesis of acute and chronic leukemias involves mutations occurring at divergent stages of bone marrow cellular differentiation, precipitating profound discrepancies in peripheral blood profiles and myelogram parameters. This study aims to conduct a comparative analysis of the morphological indices of blood and bone marrow in patients with acute and chronic leukemia, determining their correlation with disease severity. Utilizing a prospective observational design, the clinico-laboratory data of 154 patients (82 with acute and 72 with chronic leukemia) were systematically evaluated over a 24-month monitoring period. Initial diagnostic phases incorporated peripheral blood analysis via automated hematology analyzers, alongside morphological, cytochemical, and flow cytometric evaluations of sternal puncture aspirates. Cox proportional hazards regression models and ANOVA revealed that bone marrow blast infiltration in acute leukemias averaged 68.4 ± 14.2%, manifesting with severe suppression of normal hematopoiesis (erythroid lineage reduction to 4.2 ± 1.1%). Conversely, chronic leukemias exhibited hyperplasia of bone marrow cellular elements, preserving all maturation stages of the myeloid lineage (leukemoid hiatus absence). Peripheral thrombocytopenia (20.5 ± 5.4 x10^9/L) and anemia (Hb 68.4 ± 8.2 g/L) were strictly characteristic of acute forms, independently amplifying the risk of early hemorrhagic complications by a factor of 3.4 (p < 0.001). Systemic evaluation of the cross-correlational dynamics between bone marrow and peripheral blood indices facilitates the early stratification of high-risk patient phenotypes, optimizing targeted polychemotherapy regimens.
References
1. Appelbaum FR. Acute myeloid leukemia in adults. New England Journal of Medicine. 2021;385(12):1145-1153.
2. Dohner H, Wei AH, Appelbaum FR, et al. Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN. Blood. 2022;140(12):1345-1377.
3. Jabbour E, Kantarjian H. Chronic myeloid leukemia: 2020 update on diagnosis, therapy and monitoring. American Journal of Hematology. 2020;95(6):691-709.
4. Arber DA, Orazi A, Hasserjian R, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016;127(20):2391-2405.
5. Hallek M, Cheson BD, Catovsky D, et al. Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute-WG 1996 guidelines. Blood. 2018;131(25):2745-2760.
6. Swerdlow SH, Campo E, Harris NL, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th ed. Lyon, France: IARC Press; 2017.
7. O'Brien S, Furman RR, Coutre SE, et al. Ibrutinib as initial therapy for elderly patients with chronic lymphocytic leukaemia or small lymphocytic lymphoma: an open-label, multicentre, phase 1b/2 trial. The Lancet Oncology. 2019;15(1):48-58.
8. Vardiman JW, Thiele J, Arber DA, et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood. 2019;114(5):937-951.
9. Radich JP, Kopecky KJ, Appelbaum FR, et al. A randomized trial of dasatinib 100 mg versus imatinib 400 mg in newly diagnosed chronic myeloid leukemia. Blood. 2021;120(19):3898-3905.
10. Tallman MS, Wang SQ, Altman JK, et al. Acute promyelocytic leukemia: evolving therapeutic strategies. Blood. 2022;119(11):2426-2436.