Evidence map›Paper›PMID 39371618›Full record

ReviewTherapeutic advances in medical oncology2024

Advances in the mechanism of CDK4/6 inhibitor resistance in HR+/HER2- breast cancer.

Sijia Wu, Junnan Xu, Yiwen Ma, Guilian Liang, Jiaxing Wang, Tao Sun

Abstract readReview
In one paragraph

Review in Therapeutic advances in medical oncology, 2024. 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. Review
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  4. Article
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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

6 authors.

Sijia WuBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning, China.ORCID https://orcid.org/0009-0003-8569-328X
Junnan XuBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning, China.
Yiwen MaBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning, China.
Guilian LiangBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning, China.
Jiaxing WangBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning, China.
Tao SunBreast Medicine Section One, Liaoning Cancer Hospital, Shenyang, Liaoning 110000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among women, breast cancer is the most prevalent form of a malignant tumour. Among the subtypes of breast cancer, hormone receptor (HR) positive and human epidermal growth factor receptor (HER2) negative kinds make up the biggest proportion. The advent of cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitors, which are dependent on cell cycle proteins, has greatly enhanced the prognosis of patients with advanced HR+/HER2- breast cancer. This is a specific treatment that stops the growth of cancer cells by preventing them from dividing. Nevertheless, the drug resistance of the disease unavoidably impacts the effectiveness of treatment and the prognosis of patients. This report provides a thorough analysis of the current research advancements about the resistance mechanism of CDK4/6 inhibitors in HR+/HER2- breast cancer. It presents an in-depth discussion from numerous viewpoints, such as aberrant cell cycle regulation and changes in signalling pathways. In response to the drug resistance problem, subsequent treatment strategies are also being explored, including switching to other CDK4/6 inhibitor drugs, a combination of novel endocrine therapeutic agents, an optimal combination of targeted therapies and switching to chemotherapy. An in-depth study of the resistance mechanism can assist in identifying creative tactics that can overcome or postpone drug resistance, alleviate the problem of restricted treatment strategies following drug resistance and enhance the prognosis of patients.

Indexed as

breast cancerCDK4/6 inhibitorsdrug resistanceendocrine therapyhormone receptor-positivetargeted therapy

Identifiers

PMID39371618
PMCPMC11450575

What OpenQuestion holds

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Registered trials

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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.