Journal article
Outcome of azacitidine therapy in acute myeloid leukemia is not improved by concurrent vorinostat therapy but is predicted by a diagnostic molecular signature
- Abstract:
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Purpose: Azacitidine (AZA) is a novel therapeutic option in older patients with acute myeloid leukemia (AML), but its rational utilization is compromised by the fact that neither the determinants of clinical response nor its mechanism of action are defined. Co-administration of histone deacetylase inhibitors, such as vorinostat (VOR), is reported to improve the clinical activity of AZA, but this has not been prospectively studied in patients with AML. Experimental De... Expand abstract
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
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(Preview, Accepted manuscript, pdf, 973.5KB, Terms of use)
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- Publisher copy:
- 10.1158/1078-0432.ccr-17-1423
Authors
Funding
+ National Institute for Health Research
More from this funder
Funding agency for:
Quek, L
Metzner, M
Kennedy, A
Grant:
Biomedical Research Centre Funding scheme
Biomedical Research Centre Funding scheme
Biomedical Research Centre Funding scheme
+ Medical Research Council
More from this funder
Funding agency for:
Quek, L
Metzner, M
Kennedy, A
Grant:
Biomedical Research Centre Funding scheme
Biomedical Research Centre Funding scheme
Biomedical Research Centre Funding scheme
Bibliographic Details
- Publisher:
- American Association for Cancer Research
- Journal:
- Clinical Cancer Research More from this journal
- Volume:
- 23
- Issue:
- 21
- Pages:
- 6430-6440
- Publication date:
- 2017-08-01
- Acceptance date:
- 2017-07-26
- DOI:
- EISSN:
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1557-3265
- ISSN:
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1078-0432
- Pmid:
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28765326
Item Description
- Language:
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English
- Keywords:
-
- Pubs id:
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pubs:710779
- UUID:
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uuid:2037f1f0-35f3-408b-bc2e-7800594ab946
- Local pid:
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pubs:710779
- Source identifiers:
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710779
- Deposit date:
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2018-09-20
Terms of use
- Copyright holder:
- American Association for Cancer Research
- Copyright date:
- 2017
- Notes:
- © 2017 American Association for Cancer Research. This is the accepted manuscript version of the article. The final version is available online from American Association for Cancer Research at: https://doi.org/10.1158/1078-0432.CCR-17-1423
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