Evidence map›Paper›PMID 26452060›Full record

Trial reportPloS one2015

Significance of PIK3CA Mutations in Patients with Early Breast Cancer Treated with Adjuvant Chemotherapy: A Hellenic Cooperative Oncology Group (HeCOG) Study.

George Papaxoinis, Vassiliki Kotoula, Zoi Alexopoulou, Konstantine T Kalogeras, Flora Zagouri, Eleni Timotheadou, Helen Gogas, George Pentheroudakis, Christos Christodoulou, Angelos Koutras and 14 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04033965 (Tumor Mutational Patterns and Infiltrating Lymphocyte Density in Young and Old Patients With Breast Cancer), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 15% 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.

NCT04033965 completednot on this map

Tumor Mutational Patterns and Infiltrating Lymphocyte Density in Young and Old Patients With Breast Cancer

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan1997 to 2010Enrolled345ConditionsBreast CancerArmsCorellation of Mutations, TILs and Age in Breast Cancer
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  14. Review
  15. Observational
  16. Article
  17. Article
  18. Mutation distributions and clinical correlations of PIK3CA gene mutations in breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  19. Article
  20. Disease evolution and heterogeneity in bilateral breast cancer.American journal of cancer research · 2016
    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

24 authors at 12 institutions in 1 country.

George PapaxoinisOncology Section, Second Department of Internal Medicine, "Hippokration" Hospital, Athens, Greece.
Vassiliki KotoulaDepartment of Pathology, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece; Laboratory of Molecular Oncology, Hellenic Foundation for Cancer Research, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Zoi AlexopoulouHealth Data Specialists Ltd, Dept of Biostatistics, Athens, Greece.
Konstantine T KalogerasLaboratory of Molecular Oncology, Hellenic Foundation for Cancer Research, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece; Translational Research Section, Hellenic Cooperative Oncology Group, Data Office, Athens, Greece.
Flora ZagouriDepartment of Clinical Therapeutics, "Alexandra" Hospital, University of Athens School of Medicine, Athens, Greece.
Eleni TimotheadouDepartment of Medical Oncology, "Papageorgiou" Hospital, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Helen GogasFirst Department of Medicine, "Laiko" General Hospital, University of Athens School of Medicine, Athens, Greece.
George PentheroudakisDepartment of Medical Oncology, Ioannina University Hospital, Ioannina, Greece.
Christos ChristodoulouSecond Department of Medical Oncology, "Metropolitan" Hospital, Piraeus, Greece.
Angelos KoutrasDivision of Oncology, Department of Medicine, University Hospital, University of Patras Medical School, Patras, Greece.
Dimitrios BafaloukosFirst Department of Medical Oncology, "Metropolitan" Hospital, Piraeus, Greece.
Gerasimos AravantinosSecond Department of Medical Oncology, "Agii Anargiri" Cancer Hospital, Athens, Greece.
Pavlos PapakostasOncology Unit, "Hippokration" Hospital, Athens, Greece.
Elpida CharalambousLaboratory of Molecular Oncology, Hellenic Foundation for Cancer Research, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Kyriaki PapadopoulouDepartment of Pathology, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Ioannis VarthalitisOncology Department, General Hospital of Chania, Crete, Greece.
Ioannis EfstratiouDepartment of Pathology, "Papageorgiou" Hospital, Thessaloniki, Greece.
Thomas ZaramboukasDepartment of Pathology, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Helen PatseaDepartment of Pathology, IASSO General Hospital, Athens, Greece.
Chrisoula D ScopaDepartment of Pathology, University Hospital, University of Patras Medical School, Patras, Greece.
Maria SkondraOncology Section, Second Department of Internal Medicine, "Hippokration" Hospital, Athens, Greece.
Paris KosmidisSecond Department of Medical Oncology, Hygeia Hospital, Athens, Greece.
Dimitrios PectasidesOncology Section, Second Department of Internal Medicine, "Hippokration" Hospital, Athens, Greece.
George FountzilasLaboratory of Molecular Oncology, Hellenic Foundation for Cancer Research, Aristotle University of Thessaloniki, Faculty of Medicine, Thessaloniki, Greece.
Aristotle University of Thessaloniki · GRHippocration General Hospital · GRMetropolitan Hospital · GRPapageorgiou General Hospital · GRUniversity of Patras · GRAlexandra Hospital · GRChania General Hospital ”St. George” · GRHospital Agioi Anargyroi · GRHygeia Hospital · GRIASO General Hospital · GRNational and Kapodistrian University of Athens · GRUniversity Hospital of Ioannina · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe PI3K-AKT pathway is frequently activated in breast cancer. PIK3CA mutations are most frequently found in the helical (exon 9) and kinase (exon 20) domains of this protein. The aim of the present study was to examine the role of different types of PIK3CA mutations in combination with molecular biomarkers related to PI3K-AKT signaling in patients with early breast cancer.

methodsTumor tissue samples from 1008 early breast cancer patients treated with adjuvant chemotherapy in two similar randomized trials of HeCOG were examined. Tumors were subtyped with immunohistochemistry (IHC) and FISH for ER, PgR, Ki67, HER2 and androgen receptor (AR). PIK3CA mutations were analyzed by Sanger sequencing (exon 20) and qPCR (exon 9) (Sanger/qPCR mutations). In 610 cases, next generation sequencing (NGS) PIK3CA mutation data were also available. PIK3CA mutations and PTEN protein expression (IHC) were analyzed in luminal tumors (ER and/or PgR positive), molecular apocrine carcinomas (MAC; ER/PgR negative / AR positive) and hormone receptor (ER/PgR/AR) negative tumors.

resultsPIK3CA mutations were detected in 235/1008 tumors (23%) with Sanger/qPCR and in 149/610 tumors (24%) with NGS. Concordance between the two methods was good with a Kappa coefficient of 0.76 (95% CI 0.69-0.82). Lobular histology, low tumor grade and luminal A tumors were associated with helical domain mutations (PIK3CAhel), while luminal B with kinase domain mutations (PIK3CAkin). The overall incidence of PIK3CA mutations was higher in luminal as compared to MAC and hormone receptor negative tumors (p = 0.004). Disease-free and overall survival did not significantly differ with respect to PIK3CA mutation presence and type. However, a statistically significant interaction between PIK3CA mutation status and PTEN low protein expression with regard to prognosis was identified.

conclusionsThe present study did not show any prognostic significance of specific PIK3CA mutations in a large group of predominantly lymph-node positive breast cancer women treated with adjuvant chemotherapy. Further analyses in larger cohorts are warranted to investigate possible differential effect of distinct PIK3CA mutations in small subgroups of patients.

Indexed as

MutationAdultAgedBiomarkers, TumorBreast NeoplasmsChemotherapy, AdjuvantClass I Phosphatidylinositol 3-KinasesFemaleHumansMiddle AgedMutation RateNeoplasm StagingPhosphatidylinositol 3-KinasesPrognosisSignal TransductionYoung AdultBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasesPIK3CA protein, human

Identifiers

PMID26452060
PMCPMC4599795
OpenAlexW2197545912

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Registered trials

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.