The prognostic value of ASXL1 mutation in primary myelofibrosis. Literature review and clinical case description
- 作者: Melikyan A.1, Subortseva I.1, Gilyazitdinova E.1, Koloshejnova T.1, Egorova E.1, Pustovaya E.1, Sudarikov A.1, Abdullaev A.1, Gorgidze L.1, Chebotarev D.1
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隶属关系:
- National Research Center for Hematology
- 期: 卷 92, 编号 7 (2020)
- 页面: 95-99
- 栏目: Clinical notes
- URL: https://journals.rcsi.science/0040-3660/article/view/43132
- DOI: https://doi.org/10.26442/00403660.2020.07.000788
- ID: 43132
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Primary myelofibrosis is a myeloproliferative neoplasm that occurs de novo, characterized by clonal proliferation of stem cells, abnormal expression of cytokines, bone marrow fibrosis, hepatosplenomegaly – as a result of extramedullary hematopoiesis, symptoms of tumor intoxication, cachexemia, peripheral blood leukoerythroblastosis, leukemic progression and low survival. Primary myelofibrosis is a chronic incurable disease. The aims of therapy: preventing progression, increasing overall survival, improving quality of life. The choice of therapeutic tactics is limited. Allogenic hematopoietic stem cell transplantation is the only method that gives a chance for a cure. The role of mutations in a number of genes in the early identification of candidates for allogeneic hematopoietic stem cell transplantation is being actively studied. The article describes the clinical case of the detection of ASXL1 gene mutations in a patient with prefibrous primary myelofibrosis. The diagnosis was established on the basis of WHO criteria 2016. The examination revealed a mutation of ASXL1. Interferon alfa therapy is carried out, against the background of which clinico-hematological remission has been achieved. Despite the identified mutation, the patient is not a candidate for allogeneic hematopoietic stem cell transplantation. Given the unfavorable prognostic value of the ASXL1 mutation, the patient is subject to active dynamic observation and aggressive therapeutic tactics when signs of disease progression appear.
作者简介
A. Melikyan
National Research Center for Hematology
编辑信件的主要联系方式.
Email: anoblood@mail.ru
ORCID iD: 0000-0002-2119-3775
д.м.н., зав. отд-нием стандартизации методов лечения
俄罗斯联邦, MoscowI. Subortseva
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0001-9045-8653
к.м.н., c.н.с., врач-онколог отд-ния стандартизации методов лечения
俄罗斯联邦, MoscowE. Gilyazitdinova
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0002-3883-185X
врач-гематолог отд-ния стандартизации методов лечения
俄罗斯联邦, MoscowT. Koloshejnova
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0003-4580-040X
к.м.н., зам. зав. отд-нием стандартизации методов лечения
俄罗斯联邦, MoscowE. Egorova
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0002-6770-1544
к.м.н., врач-гематолог отд-ния стандартизации методов лечения
俄罗斯联邦, MoscowE. Pustovaya
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0002-1099-8092
к.м.н., врач-гематолог отд-ния стандартизации методов лечения
俄罗斯联邦, MoscowA. Sudarikov
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0001-9463-9187
д.б.н., проф., рук. лаб. молекулярной гематологии
俄罗斯联邦, MoscowA. Abdullaev
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0003-2530-808X
к.м.н., н.с. лаб. молекулярной гематологии
俄罗斯联邦, MoscowL. Gorgidze
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0001-5235-2356
к.б.н., с.н.с. отд-ния реанимации и интенсивной терапии с экспресс-лабораторией
俄罗斯联邦, MoscowD. Chebotarev
National Research Center for Hematology
Email: anoblood@mail.ru
ORCID iD: 0000-0003-2146-0818
врач-патологоанатом патологоанатомического отд-ния
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