Evidence map›Paper›PMID 29282361›Full record

ArticleThe pharmacogenomics journal2019

Influence of BCL2L11 polymorphism on osteonecrosis during treatment of childhood acute lymphoblastic leukemia.

Maria Plesa, Vincent Gagné, Sanja Glisovic, Melissa Younan, Bahram Sharif-Askari, Caroline Laverdière, Nathalie Alos, Jean-Marie Leclerc, Stephen E Sallan, Donna Neuberg and 4 more

Abstract read
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In one paragraph

Article in The pharmacogenomics journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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

14 authors at 4 institutions in 2 countries.

Maria PlesaCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Vincent GagnéCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Sanja GlisovicCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Melissa YounanCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Bahram Sharif-AskariCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Caroline LaverdièreCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Nathalie AlosCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Jean-Marie LeclercCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Stephen E SallanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Donna NeubergDepartment of Biostatistics & Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jeffery L KutokDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Lewis B SilvermanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Daniel SinnettCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Maja KrajinovicCharles-Bruneau Cancer Center, CHU Sainte-Justine Research Center, Montreal, QC, Canada. maja.krajinovic@umontreal.ca.
Centre Hospitalier Universitaire Sainte-Justine · CADana-Farber Cancer Institute · USUniversité de Montréal · CABrigham and Women's Hospital · US

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Osteonecrosis (ON) is corticosteroid-related complication, reported in children with acute lymphoblastic leukemia (ALL). We have previously found that polymorphisms in BCL2L11 gene coding for pro-apoptotic Bim protein influence reduction of overall survival (OS) in a corticosteroid (CS) dose-dependent manner in childhood ALL patients. The same set of SNPs was here investigated for an association with CS-related ON assessed retrospectively in 304 children with ALL from Quebec (QcALL cohort) who received Dana-Farber Cancer Institute (DFCI) ALL treatment protocols. Two-year cumulative incidence of symptomatic ON was 10.6%. Two BCL2L11 polymorphisms, the 891T>G (rs2241843) in all QcALL patients and 29201C>T (rs724710) in high-risk group were significantly associated with ON, P = 0.009 and P = 0.003, respectively. The association remained significant in multivariate model (HR

Indexed as

Bcl-2-Like Protein 11ChildCohort StudiesDexamethasoneFemaleHumansIncidenceMaleOsteonecrosisPolymorphism, Single NucleotidePrecursor Cell Lymphoblastic Leukemia-LymphomaRetrospective StudiesBCL2L11 protein, humanBcl-2-Like Protein 11Dexamethasone

Identifiers

PMID29282361
OpenAlexW2776888942

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.