Evidence map›Paper›PMID 35330128›Full record

ReviewLife (Basel, Switzerland)2022

How to Treat HR+/HER2- Metastatic Breast Cancer Patients after CDK4/6 Inhibitors: An Unfinished Story.

Viola Cogliati, Serena Capici, Francesca Fulvia Pepe, Pierluigi di Mauro, Francesca Riva, Federica Cicchiello, Claudia Maggioni, Nicoletta Cordani, Maria Grazia Cerrito, Marina Elena Cazzaniga

Abstract readReview
In one paragraph

Review in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Prognostic Biomarkers in Breast Cancer via Multi-Omics Clustering Analysis.International journal of molecular sciences · 2025
    Article
  3. Edaravone: A Novel Possible Drug for Cancer Treatment?International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Navigating next-generation HRTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2023
    Article
  10. Review
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.

Viola CogliatiPhase 1 Research Centre, ASST Monza, 20900 Monza, MB, Italy.
Serena CapiciPhase 1 Research Centre, ASST Monza, 20900 Monza, MB, Italy.
Francesca Fulvia PepePhase 1 Research Centre, ASST Monza, 20900 Monza, MB, Italy.
Pierluigi di MauroOncology Unit, ASST Monza, 20900 Monza, MB, Italy.
Francesca RivaOncology Unit, ASST Monza, 20900 Monza, MB, Italy.
Federica CicchielloOncology Unit, ASST Monza, 20900 Monza, MB, Italy.
Claudia MaggioniOncology Unit, ASST Monza, 20900 Monza, MB, Italy.
Nicoletta CordaniSchool of Medicine and Surgery, University of Milano Bicocca, 20900 Monza, MB, Italy.ORCID 0000-0002-3227-8280
Maria Grazia CerritoSchool of Medicine and Surgery, University of Milano Bicocca, 20900 Monza, MB, Italy.ORCID 0000-0002-3347-5817
Marina Elena CazzanigaPhase 1 Research Centre, ASST Monza, 20900 Monza, MB, Italy.ORCID 0000-0003-1756-6935

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CDK4/6 inhibitors in association with endocrine therapy represent the best therapeutic choice for either endocrine-sensitive or resistant hormone-receptor-positive advanced breast cancer patients. On the contrary, the optimal therapeutic strategy after the failure of CDK4/6 inhibitors-based treatment still remains an open question worldwide. In this review, we analyze the most studied mechanisms of resistance to CDK4/6 inhibitors treatment, as well as the most significant results of retrospective and prospective trials in the setting of progression after CDK4/6 inhibitors, to provide the reader a comprehensive overview from both a preclinical and especially a clinical perspective. In our opinion, an approach based on a deeper knowledge of resistance mechanisms to CDK4/6 inhibitors, but also on a careful analysis of what is done in clinical practice, can lead to a better definition of prospective randomized trials, to implement a personalized sequence approach, based on molecular analyses.

Indexed as

CDK4/6 inhibitorsmetastatic breast cancertherapy resistancetreatment sequencing

Identifiers

PMID35330128
PMCPMC8954717

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.