4.5 Article

Combined use of interferon alpha-1b, interleukin-2, and thalidomide to reverse the AML1-ETO fusion gene in acute myeloid leukemia

期刊

ANNALS OF HEMATOLOGY
卷 100, 期 10, 页码 2593-2601

出版社

SPRINGER
DOI: 10.1007/s00277-021-04621-w

关键词

Myeloid leukemia; Interferon; Interleukin-2; Thalidomide; AML1-ETO fusion gene

资金

  1. Science and Technology Research Project of Henan Provincial Department of Science and Technology [202102310365]

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The ITI regimen effectively reduces AML1-ETO fusion gene levels in patients with AML who are in hematologic remission but are fusion gene-positive. Patients showed improved response to higher dose administration and good tolerance to the treatment.
This study aims to explore the effect of the ITI (interferon alpha-1b, thalidomide, and interleukin-2) regimen on the AML1-ETO fusion gene in patients with t(8;21) acute myeloid leukemia (AML) who were in hematologic remission but positive for the AML1-ETO fusion gene. From September 2014 to November 2020; 20 patients with AML (15 from The Affiliated Cancer Hospital of Zhengzhou University, 4 from The First Affiliated Hospital; and College of Clinical Medicine of Henan University of Science and Technology, and 1 from Anyang District Hospital) with hematological remission but AML1-ETO fusion gene positivity were treated with different doses of the ITI regimen to monitor changes in AML1-ETO fusion gene levels. Twenty patients were treated with a routine dose of the ITI regimen, including 13 males and 7 females. The median patient age was 38 (14-70 years). The fusion gene was negative in 10 patients after 1 (0.5 similar to 8.6) month, significantly decreased in 4 patients after 2.8 (1 similar to 6) months, increased in 4 patients, and unchanged in 2 patients. The 4 patients with elevated levels of the fusion gene were treated with an increased dose of the ITI regimen, and all four patients became negative, for a total effective rate of 90%. The ITI regimen reduces AML1-ETO fusion gene levels in patients with AML who are in hematologic remission but are fusion gene-positive. Improvement was observed in patients' response to a higher dose administration, and patients tolerated the treatment well.

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