Evidence map›Paper›PMID 33640708›Full record

Trial reportLeukemia research2021

Efficacy of 10-day decitabine in acute myeloid leukemia.

Ian M Bouligny, Vivek Mehta, Scott Isom, Leslie R Ellis, Rupali R Bhave, Dianna S Howard, Susan Lyerly, Megan Manuel, Sarah Dralle, Bayard L Powell and 1 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Leukemia research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Ian M BoulignyComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Vivek MehtaComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Scott IsomComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Leslie R EllisComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Rupali R BhaveComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Dianna S HowardComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Susan LyerlyComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Megan ManuelComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Sarah DralleComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Bayard L PowellComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA.
Timothy S PardeeComprehensive Cancer Center of Wake Forest Baptist Health, Winston-Salem, NC 27157, USA. Electronic address: tspardee@wakehealth.edu.
Atrium Health Wake Forest Baptist · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Determining the Role of Metabolism in Resistance in Acute Myeloid LeukemiaR01CA197991 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARDEE, TIMOTHY SEBASTIAN · 2016 to 2020
$1.8M
NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA197991
6 · The paper itself

Abstract

The azanucleotide decitabine is used in the treatment of acute myeloid leukemia (AML). Studies have shown conflicting results with 10-day regimens used in previously untreated AML patients. Additionally, there is little data on 10-day decitabine regimens in the relapsed setting. This study investigated outcomes of 108 adult patients with AML in the upfront and relapsed setting treated with a 10-day decitabine regimen. In the upfront group, the overall response rate (ORR, CR + CRi) was 36.1% and the median overall survival (OS) was 6.6 months, while the relapsed/refractory group had an ORR of 25% with an OS of 4.8 months. When analyzed with respect to cytogenetics, the upfront group featured an ORR of 28.1% with an OS of 9.4 months in the intermediate cytogenetic cohort compared to a 40.5% ORR and an OS of 5.4 months in the unfavorable cytogenetic cohort. An analysis of the relapsed/refractory group demonstrated an ORR of 26.3% with an OS of 7.9 months for intermediate cytogenetics versus 25.0% with an OS of 1.8 months in the unfavorable cohort. While these response rates are similar to previously published data, the median OS appears shorter.

Indexed as

AdultAgedAged, 80 and overDecitabineDisease-Free SurvivalFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedSurvival RateTime FactorsDecitabineAcute myeloid leukemiaDecitabineReal world outcomesTreatment

Identifiers

PMID33640708
PMCPMC9006187
OpenAlexW3133019439

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.