Evidence map›Paper›PMID 23563239›Full record

ReviewLeukemia2013

Novel therapies for children with acute myeloid leukaemia.

A S Moore, P R Kearns, S Knapper, A D J Pearson, C M Zwaan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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

25 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Oncotarget · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Low miR-192 expression predicts poor prognosis in pediatric acute myeloid leukemia.Cancer biomarkers : section A of Disease markers · 2018
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Collaborative Efforts Driving Progress in Pediatric Acute Myeloid Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Review
  20. Hypertension and Life-Threatening Bleeding in Children with Relapsed Acute Myeloblastic Leukemia Treated with FLT3 Inhibitors.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2015
    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

5 authors.

A S MooreQueensland Children's Medical Research Institute, The University of Queensland, Brisbane, Australia. andrew.moore@uq.edu.au
P R Kearns
S Knapper
A D J Pearson
C M Zwaan

Funding

Cancer Research UK 15958Cancer Research UK C1178/A10294
6 · The paper itself

Abstract

Significant improvements in survival for children with acute myeloid leukaemia (AML) have been made over the past three decades, with overall survival rates now approximately 60-70%. However, these gains can be largely attributed to more intensive use of conventional cytotoxics made possible by advances in supportive care, and although over 90% of children achieve remission with frontline therapy, approximately one third in current protocols relapse. Furthermore, late effects of therapy cause significant morbidity for many survivors. Novel therapies are therefore desperately needed. Early-phase paediatric trials of several new agents such as clofarabine, sorafenib and gemtuzumab ozogamicin have shown encouraging results in recent years. Due to the relatively low incidence of AML in childhood, the success of paediatric early-phase clinical trials is largely dependent upon collaborative clinical trial design by international cooperative study groups. Successfully incorporating novel therapies into frontline therapy remains a challenge, but the potential for significant improvement in the duration and quality of survival for children with AML is high.

Indexed as

Adenine NucleotidesAminoglycosidesAntibodies, Monoclonal, HumanizedAntineoplastic AgentsArabinonucleosidesChildClofarabineGemtuzumabHumansImmunotoxinsLeukemia, Monocytic, AcuteNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsSorafenibAdenine NucleotidesAminoglycosidesAntibodies, Monoclonal, HumanizedAntineoplastic AgentsArabinonucleosidesClofarabineGemtuzumabImmunotoxinsNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsSorafenib

Identifiers

PMID23563239

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.