Monitoring of minimal residual disease in the perspective of treatment of acute lymphoblastic leukemias in children

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Abstract

Treatment and diagnosis of acute lymphoblastic leukemias (ALL) in children have achieved much progress in the past years. Highly effective protocols for treatment of ALL have been developed, permitting to obtain remission in more than 90% of patients. Study of the level of minimal residual disease (MRD) permits to refer a patient to a certain group of risk, requiring a particular scheme of therapy and also to choose the optimal terms for bone marrow transplantation (BMT). Bone marrow (BM) samples of MRD-positive patients are very important for clarification of the mechanisms of tumour resistance to therapy. Introduction of new generation methods (high throughput sequencing, proteomics, bioinformatics) will permit to determine additional genetic and protein markers associated with higher levels of MRD, which in its turn might lead to creation of new effective markers and target therapeutic preparations.

About the authors

Elena S. Zakharova

Dmitry Rogachev Federal Research Centre of Paediatric Haematology, Oncology and Immunology, Ministry of Health of the Russian Federation; Institute of Gene Biology, Russian Academy of Medical Sciences; N.I.Pirogov Russian National Research Medical University, Research Institute of Translational Medicine

Author for correspondence.
Email: eszakh@gmail.com
Russian Federation

Nikolay V. Gnuchev

Institute of Gene Biology, Russian Academy of Medical Sciences

Email: gnuchev@igb.ac.ru
Russian Federation

Georgiy P. Georgiev

Institute of Gene Biology, Russian Academy of Medical Sciences

Email: georgiev@igb.ac.ru
Russian Federation

Sergey S. Larin

Dmitry Rogachev Federal Research Centre of Paediatric Haematology, Oncology and Immunology, Ministry of Health of the Russian Federation; Institute of Gene Biology, Russian Academy of Medical Sciences

Email: sergei_larin@mail.ru
Russian Federation

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Copyright (c) 2016 Zakharova E.S., Gnuchev N.V., Georgiev G.P., Larin S.S.

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