Evidence map›Paper›PMID 23760400›Full record

ArticleLeukemia2014

Declining rates of treatment-related mortality in patients with newly diagnosed AML given 'intense' induction regimens: a report from SWOG and MD Anderson.

M Othus, H Kantarjian, S Petersdorf, F Ravandi, J Godwin, J Cortes, S Pierce, H Erba, S Faderl, F R Appelbaum and 1 more

Open access · greenAbstract read
In one paragraph

Article in Leukemia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 1% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 171 citations in OpenAlex.

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  9. Fate of patients with newly diagnosed acute myeloid leukemia who fail primary induction therapy.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
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15 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

M OthusPublic Health Sciences Division's Biostatistics and Biomathematics Group, Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA.
H KantarjianMD Anderson Cancer Center, Houston, TX, USA.
S PetersdorfPublic Health Sciences Division's Biostatistics and Biomathematics Group, Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA.
F RavandiMD Anderson Cancer Center, Houston, TX, USA.
J GodwinHematology and Oncology Division, Southern Illinois University, Springfield, IL, USA.
J CortesMD Anderson Cancer Center, Houston, TX, USA.
S PierceMD Anderson Cancer Center, Houston, TX, USA.
H ErbaHematologic Malignancy Program, University of Alabama, Birmingham, AL, USA.
S FaderlMD Anderson Cancer Center, Houston, TX, USA.
F R AppelbaumPublic Health Sciences Division's Biostatistics and Biomathematics Group, Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA.
E EsteyPublic Health Sciences Division's Biostatistics and Biomathematics Group, Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA.
The University of Texas MD Anderson Cancer Center · USUniversity of Washington · USFred Hutch Cancer Center · USSouthern Illinois University School of Medicine · USUniversity of Alabama at Birmingham · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Michael L. LeBlanc · 2014 to 2026
$115.2M
SOUTHWEST ONCOLOGY GROUP--STATISTICAL CENTERU10CA038926 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEBLANC, MICHAEL L. · 1985 to 2013
$69.8M
NCTN Deep South Research ConsortiumU10CA180855 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BJORNSTI, MARY-ANN, FALKSON, CARLA I · 2014 to 2018
$2.6M
NCI NIH HHS P30 CA016672NCI NIH HHS U10 CA038926NCI NIH HHS U10 CA180819NCI NIH HHS U10 CA180855
6 · The paper itself

Abstract

Less-intense remission induction regimens for adults with newly diagnosed acute myeloid leukemia (AML) aim to reduce treatment-related mortality (TRM), here defined as death within 4 weeks after starting induction therapy. This assumes that TRM rates are similar to the 15-20% observed 20 years ago. Herein we test this assumption. We examined TRM rates in 1409 patients treated on SWOG (Southwest Oncology Group) trials and 1942 patients treated at MD Anderson (MDA) from 1991 to 2009. Eighty-eight percent of SWOG patients received '3+7' or regimens of similar intensity while 92% of the MDA patients received ara-C at 1.5-2.0 g/m(2) daily × 3-5 days+other cytotoxic agents. We examined the relationship between time and TRM rates after accounting for other covariates. TRM rates between 1991 and 2009 decreased from 18-3% in SWOG and 16-4% at MDA. Multivariate analyses showed a significant decrease in TRM over time (P=0.001). The decrease in TRM was not limited to younger patients, those with a better performance status or a lower white blood cell count. Though our observations are limited to patients treated with intensive therapy at SWOG institutions and MDA, the decrease in TRM with time emphasizes the problem with historical controls and could be considered when selecting AML induction therapy.

Indexed as

AdolescentAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMiddle AgedRetrospective StudiesTreatment OutcomeYoung Adult

Identifiers

PMID23760400
PMCPMC4457325
OpenAlexW1977917277

What OpenQuestion 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 OpenQuestion graph.