Evidence map›Paper›PMID 31673247›Full record

ArticleCancer cell international2019

PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis.

Maria Palmieri, Margherita Baldassarri, Francesca Fava, Alessandra Fabbiani, Giuseppe Maria Campennì, Maria Antonietta Mencarelli, Rossella Tita, Stefania Marsili, Alessandra Renieri, Elisa Frullanti

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

10 authors at 4 institutions in 1 country.

Maria Palmieri1Medical Genetics Unit, Policlinico "Santa Maria alle Scotte", University of Siena, Viale Bracci, 2, 53100 Siena, Italy.
Margherita Baldassarri2Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Francesca Fava1Medical Genetics Unit, Policlinico "Santa Maria alle Scotte", University of Siena, Viale Bracci, 2, 53100 Siena, Italy.
Alessandra Fabbiani1Medical Genetics Unit, Policlinico "Santa Maria alle Scotte", University of Siena, Viale Bracci, 2, 53100 Siena, Italy.
Giuseppe Maria Campennì3European Institute of Oncology, Milan, Italy.
Maria Antonietta Mencarelli2Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Rossella Tita2Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Stefania Marsili4Oncology, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Alessandra Renieri1Medical Genetics Unit, Policlinico "Santa Maria alle Scotte", University of Siena, Viale Bracci, 2, 53100 Siena, Italy.ORCID 0000-0002-0846-9220
Elisa Frullanti1Medical Genetics Unit, Policlinico "Santa Maria alle Scotte", University of Siena, Viale Bracci, 2, 53100 Siena, Italy.
Azienda Ospedaliera Universitaria Senese · ITUniversity of Siena · ITEuropean Institute of Oncology · ITOspedale Santa Maria alle Scotte · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDaily experience tells us that breast cancer can be controlled using standard protocols up to the advent of a relapse. Now new frontiers in precision medicine like liquid biopsy of cell free DNA (cfDNA) give us the possibility to understand cancer evolution and pick up the key mutation on specific cancer driver gene. However, tight schedule of standardized protocol may impair the use of personalized experimental drugs in a timely therapeutic window. MAIN BODY: Here, using a combination of deep next generation sequencing and cfDNA liquid biopsy, we demonstrated that it is possible to monitor cancer relapse over time. We showed for the first time the exact correspondence from the increasing clonal expansion and clinical worsening of metastatic breast cancer.

conclusionThanks to liquid biopsy may be possible to introduce new experimental drugs in the correct therapeutic window which would lead in the near future to an effective treatment which otherwise remains challenging.

Indexed as

cfDNADeep-next generation sequencingLiquid biopsyPIK3CA-CDKN2ATargeted-therapy

Identifiers

PMID31673247
PMCPMC6819469
OpenAlexW2982572353

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.