Evidence map›Paper›PMID 32947780›Full record

ReviewCancers2020

Beyond Chemotherapies: Recent Strategies in Breast Cancer Treatment.

Arthur Foulon, Pierrick Theret, Lise Rodat-Despoix, Philippe Kischel

Abstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

4 authors.

Arthur FoulonLaboratoire de Physiologie Cellulaire et Moléculaire (UR-UPJV 4667), UFR des Sciences, Université de Picardie Jules Verne, 33 Rue St Leu, 80039 Amiens, France.
Pierrick TheretService de Gynécologie Obstétrique, CHU Amiens Picardie, 80039 Amiens, France.
Lise Rodat-DespoixLaboratoire de Physiologie Cellulaire et Moléculaire (UR-UPJV 4667), UFR des Sciences, Université de Picardie Jules Verne, 33 Rue St Leu, 80039 Amiens, France.ORCID 0000-0002-2456-6039
Philippe KischelLaboratoire de Physiologie Cellulaire et Moléculaire (UR-UPJV 4667), UFR des Sciences, Université de Picardie Jules Verne, 33 Rue St Leu, 80039 Amiens, France.ORCID 0000-0001-7201-2797

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2018, about 2.1 million women have been diagnosed with breast cancer worldwide. Treatments include-among others-surgery, chemotherapy, radiotherapy, or endocrine therapy. The current policy of care tends rather at therapeutic de-escalation, and systemic treatment such as chemotherapies alone are not systematically considered as the best option anymore. With recent advances in the understanding of cancer biology, and as a complement to anatomic staging, some biological factors (assessed notably via gene-expression signatures) are taken into account to evaluate the benefit of a chemotherapy regimen. The first aim of this review will be to summarize when chemotherapies can be avoided or used only combined with other treatments. The second aim will focus on molecules that can be used instead of chemotherapeutic drugs or used in combination with chemotherapeutic drugs to improve treatment outcomes. These therapeutic molecules have emerged from the collaboration between fundamental and clinical research, and include molecules, such as tyrosine kinase inhibitors, CDK4/6 inhibitors, and monoclonal antibodies (such as anti-PD-L1). In the fight against cancer, new tools aiding decision making are of the utmost importance: gene-expression signatures have proven to be valuable in the clinic, notably, to know when chemotherapies can be avoided. When substitution treatments are also available, a big step can be made toward personalized medicine for the patient's benefit.

Indexed as

anti-PD-L1breast cancerCDK4/6 inhibitorsgene-expression signaturemetastasistyrosine kinase inhibitors

Identifiers

PMID32947780
PMCPMC7565588

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.