Evidence map›Paper›PMID 40656600›Full record

ReviewTherapeutic advances in medical oncology2025

Understanding and overcoming CDK4/6 inhibitor resistance in HR+/HER2- metastatic breast cancer: clinical and molecular perspectives.

Jessé Lopes da Silva, Leandro Jonata de Carvalho Oliveira, Cristiano Augusto Andrade de Resende, Tomas Reinert, Lucas Zanetti de Albuquerque, Luís Felipe Leite da Silva, Max Senna Mano

Abstract readReview
In one paragraph

Review in Therapeutic advances in medical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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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

7 authors.

Jessé Lopes da SilvaDivision of Clinical Research and Technological Development, Brazilian National Cancer Institute, 37 Andre Cavalcanti Street, 5th Floor, Annex Building, Rio de Janeiro 20231050, Brazil.ORCID https://orcid.org/0000-0002-0790-9917
Leandro Jonata de Carvalho OliveiraOncoclínicas&Co, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-6344-3544
Cristiano Augusto Andrade de ResendeOncoclínicas&Co, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-9358-7693
Tomas ReinertGrupo Brasileiro de Estudos em Câncer de Mama, Porto Alegre, Brazil.ORCID https://orcid.org/0000-0003-4715-1415
Lucas Zanetti de AlbuquerqueDivision of Clinical Research and Technological Development, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0003-4945-1788
Luís Felipe Leite da SilvaDepartment of Medical Sciences, Federal Fluminense University, Rio de Janeiro, Brazil.ORCID https://orcid.org/0009-0006-8347-1212
Max Senna ManoHospital Israelita Albert Einstein, São Paulo, Brasil.ORCID https://orcid.org/0000-0001-5666-5261

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This narrative review explores the mechanisms underlying resistance to cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) in hormone receptor (HR)-positive metastatic breast cancer (MBC), a critical challenge in contemporary oncology. Despite the proven efficacy of CDK4/6i in improving clinical outcomes, both intrinsic and acquired resistance remain substantial challenges. We discuss clinical data that underscore pivotal molecular alterations associated with resistance, including mutations in the

Indexed as

breast cancerCDK4/6 inhibitorcyclin-dependent kinase inhibitorluminal breast cancermechanism of resistance

Identifiers

PMID40656600
PMCPMC12254669

What OpenQuestion holds

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LicenceCC BY-NC
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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.