Evidence map›Paper›PMID 25833957›Full record

Trial reportBlood2015

A randomized comparison of daunorubicin 90 mg/m2 vs 60 mg/m2 in AML induction: results from the UK NCRI AML17 trial in 1206 patients.

Alan K Burnett, Nigel H Russell, Robert K Hills, Jonathan Kell, Jamie Cavenagh, Lars Kjeldsen, Mary-Frances McMullin, Paul Cahalin, Mike Dennis, Lone Friis and 4 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

140 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  9. Venetoclax Combined With FLAG-IDA Induction and Consolidation in Newly Diagnosed and Relapsed or Refractory Acute Myeloid Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
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  12. Defining the Optimal Total Number of Chemotherapy Courses in Younger Patients With Acute Myeloid Leukemia: A Comparison of Three Versus Four Courses.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
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80 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Alan K BurnettDepartment of Haematology, Cardiff University School of Medicine, Cardiff, United Kingdom;
Nigel H RussellDepartment of Haematology, Nottingham University Hospital NHS Trust, Nottingham, United Kingdom;
Robert K HillsDepartment of Haematology, Cardiff University School of Medicine, Cardiff, United Kingdom;
Jonathan KellDepartment of Haematology, University Hospital of Wales Cardiff, United Kingdom;
Jamie CavenaghDepartment of Haematology, St Bartholomew's Hospital, West Smithfield, London United Kingdom;
Lars KjeldsenDepartment of Haematology, Rigshospitalet, Copenhagen, Denmark;
Mary-Frances McMullinDepartment of Haematology, Belfast City Hospital, Belfast, United Kingdom;
Paul CahalinBlackpool Victoria Hospital, Blackpool, United Kingdom;
Mike DennisDepartment of Haematology, Christie Hospital, Manchester, United Kingdom;
Lone FriisDepartment of Haematology, University of Odense, Odense, Denmark;
Ian F ThomasDepartment of Haematology, Cardiff University School of Medicine, Cardiff, United Kingdom;
Don MilliganDepartment of Haematology, Heartlands Hospital, Birmingham, United Kingdom; and.
Richard E ClarkDepartment of Haematology, Royal Liverpool University Hospital, Liverpool, United Kingdom.
UK NCRI AML Study Group

Funding

Cancer Research UK 9948
6 · The paper itself

Abstract

Modifying induction therapy in acute myeloid leukemia (AML) may improve the remission rate and reduce the risk of relapse, thereby improving survival. Escalation of the daunorubicin dose to 90 mg/m(2) has shown benefit for some patient subgroups when compared with a dose of 45 mg/m(2), and has been recommended as a standard of care. However, 60 mg/m(2) is widely used and has never been directly compared with 90 mg/m(2). As part of the UK National Cancer Research Institute (NCRI) AML17 trial, 1206 adults with untreated AML or high-risk myelodysplastic syndrome, mostly younger than 60 years of age, were randomized to a first-induction course of chemotherapy, which delivered either 90 mg/m(2) or 60 mg/m(2) on days 1, 3, and 5 combined with cytosine arabinoside. All patients then received a second course that included daunorubicin 50 mg/m(2) on days 1, 3, and 5. There was no overall difference in complete remission rate (73% vs 75%; odds ratio, 1.07 [0.83-1.39]; P = .6) or in any recognized subgroup. The 60-day mortality was increased in the 90 mg/m(2) arm (10% vs 5% (hazard ratio [HR] 1.98 [1.30-3.02]; P = .001), which resulted in no difference in overall 2-year survival (59% vs 60%; HR, 1.16 [0.95-1.43]; P = .15). In an exploratory subgroup analysis, there was no subgroup that showed significant benefit, although there was a significant interaction by FLT3 ITD mutation. This trial is registered at http://www.isrctn.com as #ISRCTN55675535.

Indexed as

AdolescentAdultAgedAntibiotics, AntineoplasticAntineoplastic Combined Chemotherapy ProtocolsCytarabineDaunorubicinDose-Response Relationship, DrugFemaleHumansInduction ChemotherapyKaplan-Meier EstimateLeukemia, Myeloid, AcuteMaleMiddle AgedYoung AdultAntibiotics, AntineoplasticCytarabineDaunorubicin

Identifiers

PMID25833957
PMCPMC4505010

What OpenQuestion holds

Textmetadata
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.