Abstract

Introduction. Acute myeloid leukemia (AML) is a clonal disease of the blood system that occurs as a result of mutations in the genome of hematopoietic progenitor cells. As a result of mutations, the linear differentiation of hematopoietic cells is replaced by the proliferation of malignant myeloid progenitors. Currently, the risk group for AML in children is determined mainly by the presence of specific gene and chromosomal abnormalities and an increased level of peripheral blood leukocytes. The features of the immunophenotype of blast cells can also influence the course of the disease.The aim of the work is to assess the relationship between the immunophenotypic parameters of blast cells and the probability of achieving remission in children with AML.Materials and methods. The study included 109 patients aged 3 months to 17 years who received treatment according to the AML BFM 87, AML BFM 2004, NII DOG AML 2007 и NII DOG AML 2012 protocol in the period from 1991 to 2020.Results. The study showed the relationship between the probability of achieving remission and the presence of markers CD33, CD19 and CD14 on tumor cells. Expression of lymphoid antigen CD19 on blasts was associated with a higher rate of remission (73.0 % vs 95.5 %, p = 0.027). The absence of the linearly associated myeloid marker CD33 negatively correlated with the remission rate (61.1 % vs 87.7 %, p = 0.007). In the presence of monocyte antigen CD14 on blasts, the probability of achieving remission was low (95 % vs 50 %, p = 0.013).Conclusion. Characteristics of the immunophenotype of tumor cells in AML in children are associated with the probability of achieving remission.

Highlights

  • Acute myeloid leukemia (AML) is a clonal disease of the blood system that occurs as a result of mutations in the genome of hematopoietic progenitor cells

  • The aim of the work is to assess the relationship between the immunophenotypic parameters of blast cells and the probability of achieving remission in children with AML

  • The study included 109 patients aged 3 months to 17 years who received treatment according to the AML BFM 87, AML BFM 2004, NII DOG AML 2007 и NII DOG AML 2012 protocol in the period from 1991 to 2020

Read more

Summary

ПРИ ОСТРОМ МИЕЛОИДНОМ ЛЕЙКОЗЕ У ДЕТЕЙ

Острый миелоидный лейкоз (ОМЛ) – клональное заболевание системы крови, которое возникает вследствие мутаций генетического аппарата гемопоэтических клеток-предшественников. Особенности иммунофенотипа бластных клеток могут также оказывать влияние на течение заболевания. Цель исследования – оценить взаимосвязь иммунофенотипических параметров бластных клеток с вероятностью достижения ремиссии при ОМЛ у детей. В ходе исследования была показана взаимосвязь между вероятностью достижения ремиссии и наличием на опухолевых клетках маркеров CD33, CD19 и CD14. Экспрессия на бластах лимфоидного антигена CD19 ассоциировалась с большей частотой достижения ремиссий (73,0 % vs 95,5 %, p = 0,027). При наличии на бластах моноцитарного антигена CD14 вероятность достижения ремиссии была низкой (95 % vs 50 %, р = 0,013). Особенности иммунофенотипа опухолевых клеток при ОМЛ у детей взаимосвязаны с вероятностью достижения ремиссии. Взаимосвязь иммунофенотипических особенностей бластных клеток с достижением ремиссии при остром миелоидном лейкозе у детей. Pirogov Russian National Research Medical University, Ministry of Health of Russia; 1а Ostrovitianov St., Moscow 117997, Russia; 3National Research Nuclear University MEPhI (Moscow Engineering Physics Institute); 31 Kashirskoe Shosse, Moscow 115409, Russia; 4Moscow state budgetary healthcare institution “Morozov Children’s City Clinical Hospital of the Moscow City Healthcare Department”; 1 / 9 4th Dobryninsky lane, Moscow 119049, Russia

Introduction
Всего Total
Итого Total
Маркер Marker
Findings
Присутствует Presence
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call