Evidence map›Paper›PMID 32064003›Full record

ArticleTherapeutic advances in medical oncology2020

Combined targeting EGFR and SRC as a potential novel therapeutic approach for the treatment of triple negative breast cancer.

Alexandra Canonici, Alacoque L Browne, Mohamed F K Ibrahim, Kevin P Fanning, Sandra Roche, Neil T Conlon, Fiona O'Neill, Justine Meiller, Mattia Cremona, Clare Morgan and 5 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 33 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

15 authors at 4 institutions in 2 countries.

Alexandra CanoniciNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Alacoque L BrowneNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Mohamed F K IbrahimNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Kevin P FanningNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Sandra RocheNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Neil T ConlonNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Fiona O'NeillNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Justine MeillerNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Mattia CremonaMedical Oncology Group, Department of Molecular Medicine, Beaumont Hospital, Royal College of Surgeons in Ireland, Dublin, Ireland.
Clare MorganMedical Oncology Group, Department of Molecular Medicine, Beaumont Hospital, Royal College of Surgeons in Ireland, Dublin, Ireland.
Bryan T HennessyMedical Oncology Group, Department of Molecular Medicine, Beaumont Hospital, Royal College of Surgeons in Ireland, Dublin, Ireland.
Alex J EustaceNational Institute for Cellular Biotechnology, Dublin City University, Whitehall, Glasnevin, Dublin 9, Ireland.ORCID https://orcid.org/0000-0002-4092-1360
Flavio SolcaBoehringer Ingelheim RCV GmbH & Co KG, Vienna, Austria.
Norma O'DonovanNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
John CrownNational Institute for Cellular Biotechnology, Dublin City University, Dublin, Ireland.
Dublin City University · IERoyal College of Surgeons in Ireland · IEBoehringer Ingelheim (Austria) · ATSt. Vincent's University Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple negative breast cancer (TNBC) is an aggressive subtype of breast cancer with limited therapeutic options. Epidermal growth factor receptor (EGFR) has been shown to be over-expressed in TNBC and represents a rational treatment target.

methodsWe examined single agent and combination effects for afatinib and dasatinib in TNBC. We then determined IC

resultsA total of 14 TNBC cell lines responded to afatinib with IC

conclusionsWe demonstrate that afatinib combined with dasatinib has potential clinical activity in TNBC but warrants further preclinical investigation.

Indexed as

afatinibBcl2dasatinibEGFRTNBC

Identifiers

PMID32064003
PMCPMC6987485
OpenAlexW3003174025

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.