Evidence map›Paper›PMID 25906750›Full record

SynthesisOncotarget2015

FKBPL: a marker of good prognosis in breast cancer.

Laura Nelson, Hayley D McKeen, Andrea Marshall, Laoighse Mulrane, Jane Starczynski, Sarah J Storr, Fiona Lanigan, Christopher Byrne, Ken Arthur, Shauna Hegarty and 20 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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  9. Review
  10. Article
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

30 authors.

Laura NelsonSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Hayley D McKeenSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Andrea MarshallWarwick Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Laoighse MulraneConway Institute, University College Dublin, Dublin, Ireland.
Jane StarczynskiOntario Institute for Cancer Research, Toronto, Canada.
Sarah J StorrDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Fiona LaniganConway Institute, University College Dublin, Dublin, Ireland.
Christopher ByrneRoyal College of Surgeons Ireland, Dublin, Ireland.
Ken ArthurNorthern Ireland Molecular Pathology Laboratory, CCRCB, Queens University Belfast, Belfast, United Kingdom.
Shauna HegartyDepartment of Pathology, Royal Group of Hospitals, Grosvenor Road, Belfast, United Kingdom.
Ahlam Abdunnabi AliSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Fiona FurlongSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Helen O McCarthySchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Ian O EllisDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Andrew R GreenDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Emad RakhaDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
Leonie YoungRoyal College of Surgeons Ireland, Dublin, Ireland.
Ian KunklerEdinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
Jeremy ThomasEdinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
Wilma JackEdinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
David CameronEdinburgh Breast Unit, The University of Edinburgh, Edinburgh, United Kingdom.
Karin JirströmDepartment of Clinical Sciences, Lund University, Sweden.
Anita YakkundiSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Lana McClementsSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.
Stewart G MartinDivision of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham, United Kingdom.
William M GallagherConway Institute, University College Dublin, Dublin, Ireland.
Janet DunnWarwick Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
John BartlettOntario Institute for Cancer Research, Toronto, Canada.
Darran O'ConnorConway Institute, University College Dublin, Dublin, Ireland.
Tracy RobsonSchool of Pharmacy, Queen's University Belfast, Belfast, United Kingdom.

Funding

Medical Research Council G1001473Medical Research Council G1001473/1
6 · The paper itself

Abstract

FK506-binding protein-like (FKBPL) has established roles as an anti-tumor protein, with a therapeutic peptide based on this protein, ALM201, shortly entering phase I/II clinical trials. Here, we evaluated FKBPL's prognostic ability in primary breast cancer tissue, represented on tissue microarrays (TMA) from 3277 women recruited into five independent retrospective studies, using immunohistochemistry (IHC). In a meta-analysis, FKBPL levels were a significant predictor of BCSS; low FKBPL levels indicated poorer breast cancer specific survival (BCSS) (hazard ratio (HR) = 1.30, 95% confidence interval (CI) 1.14-1.49, p < 0.001). The prognostic impact of FKBPL remained significant after adjusting for other known prognostic factors (HR = 1.25, 95% CI 1.07-1.45, p = 0.004). For the sub-groups of 2365 estrogen receptor (ER) positive patients and 1649 tamoxifen treated patients, FKBPL was significantly associated with BCSS (HR = 1.34, 95% CI 1.13-1.58, p < 0.001, and HR = 1.25, 95% CI 1.04-1.49, p = 0.02, respectively). A univariate analysis revealed that FKBPL was also a significant predictor of relapse free interval (RFI) within the ER positive patient group, but it was only borderline significant within the smaller tamoxifen treated patient group (HR = 1.32 95% CI 1.05-1.65, p = 0.02 and HR = 1.23 95% CI 0.99-1.54, p = 0.06, respectively). The data suggests a role for FKBPL as a prognostic factor for BCSS, with the potential to be routinely evaluated within the clinic.

Indexed as

Breast NeoplasmsCohort StudiesFemaleHumansImmunophilinsPrecision MedicinePrognosisSurvival AnalysisTacrolimus Binding ProteinsFKBPL protein, humanImmunophilinsTacrolimus Binding Proteinsbiomarkerbreast cancerFKBPLpersonalized medicine

Identifiers

PMID25906750
PMCPMC4494933

What OpenQuestion holds

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Registered trials

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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.