Evidence map›Paper›PMID 29689598›Full record

ArticleMolecular oncology2018

Correlation between circulating cell-free PIK3CA tumor DNA levels and treatment response in patients with PIK3CA-mutated metastatic breast cancer.

Annette R Kodahl, Sidse Ehmsen, Niels Pallisgaard, Anne M B Jylling, Jeanette D Jensen, Anne-Vibeke Laenkholm, Ann S Knoop, Henrik J Ditzel

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 71 citations in OpenAlex.

  1. Pooled it
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  4. Detection ofBiomolecules · 2021
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  14. A Basic Review on Estrogen Receptor Signaling Pathways in Breast Cancer.International journal of molecular sciences · 2023
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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

8 authors at 5 institutions in 1 country.

Annette R KodahlDepartment of Oncology, Odense University Hospital, Denmark.
Sidse EhmsenDepartment of Cancer and Inflammation, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark.ORCID 0000-0002-4807-6325
Niels PallisgaardDepartment of Clinical Biochemistry, Køge Hospital, Denmark.
Anne M B JyllingDepartment of Pathology, Odense University Hospital, Denmark.
Jeanette D JensenDepartment of Oncology, Odense University Hospital, Denmark.
Anne-Vibeke LaenkholmDepartment of Surgical Pathology, Zealand University Hospital, Slagelse, Denmark.
Ann S KnoopDepartment of Oncology, Rigshospitalet, Copenhagen, Denmark.
Henrik J DitzelDepartment of Oncology, Odense University Hospital, Denmark.ORCID 0000-0003-3927-5135
Odense University Hospital · DKUniversity of Southern Denmark · DKRigshospitalet · DKZealand University Hospital · DKZealand University Hospital Køge · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid biopsies focusing on the analysis of cell-free circulating tumor DNA (ctDNA) may have important clinical implications for personalized medicine, including early detection of cancer, therapeutic guidance, and monitoring of recurrence. Mutations in the oncogene, PIK3CA, are frequently observed in breast cancer and have been suggested as a predictive biomarker for PI3K-selective inhibitor treatment. In this study, we analyzed the presence of PIK3CA mutations in formalin-fixed, paraffin-embedded, metastatic tissue and corresponding ctDNA from serum of patients with advanced breast cancer using a highly sensitive, optimized droplet digital PCR (ddPCR) assay. We found 83% of patients with PIK3CA mutation in the metastatic tumor tissue also had detectable PIK3CA mutations in serum ctDNA. Patients lacking the PIK3CA mutation in corresponding serum ctDNA all had nonvisceral metastatic disease. Four patients with detectable PIK3CA-mutated ctDNA were followed with an additional serum sample during oncological treatment. In all cases, changes in PIK3CA ctDNA level correlated with treatment response. Our results showed high concordance between detection of PIK3CA mutations in tumor tissue and in corresponding serum ctDNA and suggest that serum samples from patients with advanced breast cancer and ddPCR may be used for PIK3CA mutation status assessment to complement imaging techniques as an early marker of treatment response.

Indexed as

Biomarkers, TumorBreast NeoplasmsCirculating Tumor DNAClass I Phosphatidylinositol 3-KinasesDNA Mutational AnalysisFemaleHumansNeoplasm MetastasisPoint MutationTreatment OutcomeBiomarkers, TumorCirculating Tumor DNAClass I Phosphatidylinositol 3-KinasesPIK3CA protein, humanddPCRliquid biopsymetastatic breast cancerPIK3CA

Identifiers

PMID29689598
PMCPMC5983134
OpenAlexW2799525990

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.