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Can we consider discontinuation of hypomethylating agents in patients with myelodysplastic syndrome : a retrospective study from The Korean Society of Hematology AML/MDS Working Party

Authors
Kim, Da JungLee, Ho SupMoon, Joon-HoSohn, Sang KyunKim, Hyeoung JoonCheong, June-WonJo, Deog-YeonKim, HawkLee, HyewonBangs, Soo-MeeLee, Won SikPark, YongLee, Mark HongLee, Jae HoonBae, Sung HwaKim, Min Kyoung
Issue Date
3-10월-2017
Publisher
IMPACT JOURNALS LLC
Keywords
myelodysplastic syndrome; discontinuation; survival; decitabine; azacitidine
Citation
ONCOTARGET, v.8, no.45, pp.79414 - 79424
Indexed
SCIE
SCOPUS
Journal Title
ONCOTARGET
Volume
8
Number
45
Start Page
79414
End Page
79424
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81944
DOI
10.18632/oncotarget.18258
ISSN
1949-2553
Abstract
It is often difficult to continue treatment with hypomethylating agent(HMA) in clinical practice because of problems such as toxicities, poor economics, etc. We compared clinical outcomes of those patients who continued HMA and those who discontinued HMA because of other causes, and evaluated factors associated with survival in those patients who discontinued HMA. Patients were divided into two groups: treatment failure, those who stopped treatment due to disease progression; and discontinuation, those who discontinued treatment because of other causes. The median progression free survival(PFS) was 9.2 months (range 7.7 - 10.7 months) vs 28.9 months (range 22.6-35.2) in the treatment failure and discontinuation groups, respectively (P < 0.001). In a multivariate analysis, a lower risk by WPSS was an independent predictive factor for a longer PFS, and a lower risk by WPSS and median number of HMA cycles greater than seven were independent predictive factors for longer overall survival(OS) only in the discontinuation group. Patients who discontinued HMA without disease progression showed a prolonged survival than those who failed HMA treatment. Especially, a lower risk by WPSS and longer duration of HMA treatment may be predictive factors for a longer PFS and OS in patients who discontinued HMA.
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