Evidence map›Paper›PMID 21220611›Full record

ReviewJournal of clinical oncology : official journal of the American Society of Clinical Oncology2011

Biology, risk stratification, and therapy of pediatric acute leukemias: an update.

Ching-Hon Pui, William L Carroll, Soheil Meshinchi, Robert J Arceci

Erratum issued 2 registry-linked trialsAbstract readReview
In one paragraph

Review in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 400 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
400citing 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.

NCT02451774 phase2 / phase3unknown statusnot on this mapstarted 2015, after this paper: background citation

Safety and efficacy of pentoxifylline versus placebo administered as apoptosis inductor during remission induction phase of pediatric patients with acute lymphoblastic leukemia

TypeinterventionalSponsorRamón Óscar González-Ramella, Ph.DRan2015 to 2020Enrolled44ConditionsAcute Lymphoblastic LeukemiaArmsPentoxifylline Plus Chemotherapy, Placebo Plus Chemotherapy
NCT04224571 phase2completednot on this mapstarted 2018, after this paper: background citation

Chinese Children Cancer Group Relapsed Acute Lymphoblastic Leukemia 2017 Study

TypeinterventionalSponsorChinese University of Hong KongRan2018 to 2023Enrolled208ConditionsAcute Lymphoblastic Leukemia, in RelapseArmsBortezomib Injection, rituximab injection
3 · Its place in the literature

Who cites it

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

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340 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors.

Ching-Hon PuiSt Jude Children's Research Hospital, 262 Danny Thomas Pl, Memphis, TN 38105, USA. ching-hon.pui@stjude.org
William L Carroll
Soheil Meshinchi
Robert J Arceci

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS CA21765NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

purposeWe review recent advances in the biologic understanding and treatment of childhood acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML), identify therapeutically challenging subgroups, and suggest future directions of research.

methodsA review of English literature on childhood acute leukemias from the past 5 years was performed.

resultsContemporary treatments have resulted in 5-year event-free survival rates of approximately 80% for childhood ALL and almost 60% for pediatric AML. The advent of high-resolution genome-wide analyses has provided new insights into leukemogenesis and identified many novel subtypes of leukemia. Virtually all ALL and the vast majority of AML cases can be classified according to specific genetic abnormalities. Cooperative mutations involved in cell differentiation, cell cycle regulation, tumor suppression, drug responsiveness, and apoptosis have also been identified in many cases. The development of new formulations of existing drugs, molecularly targeted therapy, and immunotherapies promises to further advance the cure rates and improve quality of life of patients.

conclusionThe application of new high-throughput sequencing techniques to define the complete DNA sequence of leukemia and host normal cells and the development of new agents targeted to leukemogenic pathways promise to further improve outcome in the coming decade.

Indexed as

ChildGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLeukemia, Myeloid, AcuteMutationPrecursor Cell Lymphoblastic Leukemia-LymphomaRecurrenceTranscription, Genetic

Identifiers

PMID21220611
PMCPMC3071256

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.