Abstract:
:Homoharringtonine combined aclarubicin and cytarabine (HAA) has been demonstrated to achieve a high remission rate and provide a survival advantage in acute myeloid leukemia (AML). To investigate whether HAA is an ideal induction regimen for t(8;21)AML, we retrospectively analyzed the data of 140 patients from the last 8 years in our center. When achieving complete remission (CR), the post-remission treatment was administered as a minimal residual disease-directed risk-stratification treatment protocol. The RUNX1/RUNX1T1 transcript level was assessed by RT-qPCR. The last follow-up was conducted in October 2015. In total, thirty patients received an HAA regimen as the induction treatment. The CR rate after one cycle of the HAA regimen was 93.3% (28/30). One patient achieved partial remission, and one had no response. No patients died during induction treatment. The median fold decrease of the RUNX1/RUNX1T1 transcript level was 200 (1-358000), and 16.7% (5/30) patients achieved >3 log decrease after one cycle of the HAA regimen. The estimated 4-year disease-free survival and overall survival were 89.9% and 90.8%, respectively. We concluded that the HAA regimen is highly effective as the first course of induction therapy for t(8;21) AML, and this needs to be confirmed in a large population in the future.
journal_name
Leuk Resjournal_title
Leukemia researchauthors
Zhu HH,Jiang H,Jiang Q,Jia JS,Qin YZ,Huang XJdoi
10.1016/j.leukres.2016.02.012subject
Has Abstractpub_date
2016-05-01 00:00:00pages
40-4eissn
0145-2126issn
1873-5835pii
S0145-2126(16)30027-3journal_volume
44pub_type
杂志文章abstract::Useful prognostic markers for patients with diffuse large B cell lymphoma (DLBCL) have been reported. To identify which biomarker best predicts the prognosis of patients with DLBCL, we performed a retrospective study that included 319 DLBCL patients who had received rituximab, cyclophosphamide, doxorubicin, vincristin...
journal_title:Leukemia research
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journal_title:Leukemia research
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/0145-2126(91)90165-p
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doi:10.1016/s0145-2126(01)00175-8
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journal_title:Leukemia research
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/s0145-2126(01)00181-3
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2004.11.015
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/s0145-2126(96)00062-8
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/0145-2126(86)90091-3
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2005.07.015
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pub_type: 杂志文章
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更新日期:2019-04-01 00:00:00
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2005.02.007
更新日期:2005-09-01 00:00:00
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/0145-2126(89)90166-5
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pub_type: 杂志文章
doi:10.1016/0145-2126(91)90189-z
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pub_type: 杂志文章
doi:10.1016/j.leukres.2008.10.009
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pub_type: 杂志文章,多中心研究
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journal_title:Leukemia research
pub_type: 杂志文章
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journal_title:Leukemia research
pub_type: 杂志文章
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/0145-2126(85)90100-6
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/0145-2126(85)90006-2
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2006.02.028
更新日期:2006-12-01 00:00:00
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2004.06.003
更新日期:2005-02-01 00:00:00
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journal_title:Leukemia research
pub_type: 杂志文章
doi:10.1016/j.leukres.2013.04.018
更新日期:2013-08-01 00:00:00
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journal_title:Leukemia research
pub_type: 杂志文章
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pub_type: 杂志文章
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