Evidence map›Paper›PMID 32633764›Full record

ArticleJAMA network open2020

Association of Sperm-Associated Antigen 5 and Treatment Response in Patients With Estrogen Receptor-Positive Breast Cancer.

Tarek M A Abdel-Fatah, Graham R Ball, Pulari U Thangavelu, Lynne E Reid, Amy E McCart Reed, Jodi M Saunus, Pascal H G Duijf, Peter T Simpson, Sunil R Lakhani, Lorinc Pongor and 7 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 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
0.2field-weighted citation impact, top 52% 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, 2 citations in OpenAlex.

  1. Article
  2. Clinicopathologic significance of nuclear HER4 and phospho-YAP(STherapeutic advances in medical oncology · 2020
    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

17 authors at 8 institutions in 4 countries.

Tarek M A Abdel-FatahDepartment of Clinical Oncology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Graham R BallJohn van Geest Cancer Research Centre, Nottingham Trent University School of Science and Technology, Nottingham United Kingdom.
Pulari U ThangaveluDiamantina Institute, Translational Research Institute, The University of Queensland, Brisbane, Australia.
Lynne E ReidUQ Centre for Clinical Research, Faculty of Research, The University of Queensland, Herston, Australia.
Amy E McCart ReedUQ Centre for Clinical Research, Faculty of Research, The University of Queensland, Herston, Australia.
Jodi M SaunusUQ Centre for Clinical Research, Faculty of Research, The University of Queensland, Herston, Australia.
Pascal H G DuijfDiamantina Institute, Translational Research Institute, The University of Queensland, Brisbane, Australia.
Peter T SimpsonUQ Centre for Clinical Research, Faculty of Research, The University of Queensland, Herston, Australia.
Sunil R LakhaniUQ Centre for Clinical Research, Faculty of Research, The University of Queensland, Herston, Australia.
Lorinc PongorLendület Cancer Biomarker Research Group, Second Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Balázs GyorffyLendület Cancer Biomarker Research Group, Second Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Paul M MoseleyDepartment of Clinical Oncology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
Andrew R GreenNottingham Breast Cancer Research Center, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham Biodiscovery Institute, University Park, Nottingham, United Kingdom.
Alan G PockleyJohn van Geest Cancer Research Centre, Nottingham Trent University School of Science and Technology, Nottingham United Kingdom.
Carlos CaldasDepartment of Oncology and Cancer Research, UK Cambridge Institute, Li Ka Shing Centre, University of Cambridge, Cambridge, United Kingdom.
Ian O EllisNottingham Breast Cancer Research Center, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham Biodiscovery Institute, University Park, Nottingham, United Kingdom.
Stephen Y T ChanDepartment of Clinical Oncology, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
University of Queensland · AUNottingham Trent University · GBNottingham University Hospitals NHS Trust · GBSemmelweis University · HUUniversity of Nottingham · GBMenoufia University · EGTranslational Research Institute · AUUniversity of Cambridge · GB

Funding

Cancer Research UK 16942
6 · The paper itself

Abstract

Importance: There is no proven test that can guide the optimal treatment, either endocrine therapy or chemotherapy, for estrogen receptor-positive breast cancer. Objective: To investigate the associations of sperm-associated antigen 5 (SPAG5) transcript and SPAG5 protein expressions with treatment response in systemic therapy for estrogen receptor-positive breast cancer. Design, Settings, and Participants: This retrospective cohort study included patients with estrogen receptor-positive breast cancer who received 5 years of adjuvant endocrine therapy with or without neoadjuvant anthracycline-based combination chemotherapy (NACT) derived from 11 cohorts from December 1, 1986, to November 28, 2019. The associations of SPAG5 transcript and SPAG5 protein expression with pathological complete response to NACT were evaluated, as was the association of SPAG5 mRNA expression with response to neoadjuvant endocrine therapy. The associations of distal relapse-free survival with SPAG5 transcript or SPAG5 protein expressions were analyzed. Data were analyzed from September 9, 2015, to November 28, 2019. Main Outcomes and Measures: The primary outcomes were breast cancer-specific survival, distal relapse-free survival, pathological complete response, and clinical response. Outcomes were examined using Kaplan-Meier, multivariable logistic, and Cox regression models. Results: This study included 12 720 women aged 24 to 78 years (mean [SD] age, 58.46 [12.45] years) with estrogen receptor-positive breast cancer, including 1073 women with SPAG5 transcript expression and 361 women with SPAG5 protein expression of locally advanced disease stage IIA through IIIC. Women with SPAG5 transcript and SPAG5 protein expressions achieved higher pathological complete response compared with those without SPAG5 transcript or SPAG5 protein expressions (transcript: odds ratio, 2.45 [95% CI, 1.71-3.51]; P < .001; protein: odds ratio, 7.32 [95% CI, 3.33-16.22]; P < .001). Adding adjuvant anthracycline chemotherapy to adjuvant endocrine therapy for SPAG5 mRNA expression in estrogen receptor-positive breast cancer was associated with prolonged 5-year distal relapse-free survival in patients without lymph node involvement (hazard ratio, 0.34 [95% CI, 0.14-0.87]; P = .03) and patients with lymph node involvement (hazard ratio, 0.35 [95% CI, 0.18-0.68]; P = .002) compared with receiving 5-year endocrine therapy alone. Mean (SD) SPAG5 transcript was found to be downregulated after 2 weeks of neoadjuvant endocrine therapy compared with pretreatment levels in 68 of 92 patients (74%) (0.23 [0.18] vs 0.34 [0.24]; P < .001). Conclusions and Relevance: These findings suggest that SPAG5 transcript and SPAG5 protein expressions could be used to guide the optimal therapies for estrogen receptor-positive breast cancer. Retrospective and prospective clinical trials are warranted.

Indexed as

Breast NeoplasmsCell Cycle ProteinsAnthracyclinesAntineoplastic AgentsBiomarkers, PharmacologicalChemotherapy, AdjuvantDrug MonitoringDrug Resistance, NeoplasmEstrogen Receptor AntagonistsEstrogen Receptor ModulatorsFemaleGene Expression ProfilingHumansMiddle AgedNeoplasm StagingProgression-Free SurvivalAnthracyclinesAntineoplastic AgentsBiomarkers, PharmacologicalCell Cycle ProteinsEstrogen Receptor AntagonistsEstrogen Receptor ModulatorsReceptors, EstrogenSPAG5 protein, human

Identifiers

PMID32633764
PMCPMC7341179
OpenAlexW3039592470

What OpenQuestion holds

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LicenceCC BY
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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.