Evidence map›Paper›PMID 31970440›Full record

ReviewCancer immunology, immunotherapy : CII2020

New targets for therapy: antigen identification in adults with B-cell acute lymphoblastic leukaemia.

Stephanie Jordaens, Leah Cooksey, Laurie Freire Boullosa, Viggo Van Tendeloo, Evelien Smits, Ken I Mills, Kim H Orchard, Barbara-Ann Guinn

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 4 institutions in 2 countries.

Stephanie JordaensDepartment of Biomedical Sciences, University of Hull, Cottingham Road, Hardy Building, Room 111, Hull, HU7 6RX, UK.ORCID http://orcid.org/0000-0001-6730-367X
Leah CookseyDepartment of Biomedical Sciences, University of Hull, Cottingham Road, Hardy Building, Room 111, Hull, HU7 6RX, UK.
Laurie Freire BoullosaCentre for Oncological Research, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0001-6788-6211
Viggo Van TendelooLaboratory of Experimental Hematology, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0003-3217-9917
Evelien SmitsCentre for Oncological Research, University of Antwerp, Antwerp, Belgium.ORCID http://orcid.org/0000-0001-9255-3435
Ken I MillsCentre for Cancer Research and Cell Biology, Queens University Belfast, Lisburn Road, Belfast, UK.ORCID http://orcid.org/0000-0002-6362-4481
Kim H OrchardDepartment of Haematology, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton, UK.ORCID http://orcid.org/0000-0003-2276-3925
Barbara-Ann GuinnDepartment of Biomedical Sciences, University of Hull, Cottingham Road, Hardy Building, Room 111, Hull, HU7 6RX, UK. B.Guinn@hull.ac.uk.ORCID http://orcid.org/0000-0003-0639-4541
University of Antwerp · BEUniversity of Hull · GBQueen's University Belfast · GBUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukaemia (ALL) in adults is a rare and difficult-to-treat cancer that is characterised by excess lymphoblasts in the bone marrow. Although many patients achieve remission with chemotherapy, relapse rates are high and the associated impact on survival devastating. Most patients receive chemotherapy and for those whose overall fitness supports it, the most effective treatment to date is allogeneic stem cell transplant that can improve overall survival rates in part due to a 'graft-versus-leukaemia' effect. However, due to the rarity of this disease, and the availability of mature B-cell antigens on the cell surface, few new cancer antigens have been identified in adult B-ALL that could act as targets to remove residual disease in first remission or provide alternative targets for escape variants if and when current immunotherapy strategies fail. We have used RT-PCR analysis, literature searches, antibody-specific profiling and gene expression microarray analysis to identify and prioritise antigens as novel targets for the treatment of adult B-ALL.

Indexed as

AdultAntigens, NeoplasmAntineoplastic Agents, ImmunologicalB-LymphocytesDatasets as TopicGene Expression ProfilingHumansImmunotherapyMolecular Targeted TherapyOligonucleotide Array Sequence AnalysisPrecursor B-Cell Lymphoblastic Leukemia-LymphomaRemission InductionReverse Transcriptase Polymerase Chain ReactionTreatment OutcomeTumor EscapeAntigens, NeoplasmAntineoplastic Agents, ImmunologicalB-cell acute lymphoblastic leukaemiaBMXImmunotherapyPIVAC19SurvivinTumour antigens

Identifiers

PMID31970440
PMCPMC7183504
OpenAlexW3001860969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.