Evidence map›Paper›PMID 39210220›Full record

ReviewMedical oncology (Northwood, London, England)2024

The treatment landscape of triple-negative breast cancer.

Yi Hu, Chen Wang, Huishi Liang, Jie Li, Qiong Yang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

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  14. Integrative analysis ofFrontiers in pharmacology · 2026
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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

5 authors.

Yi HuBeijing Key Laboratory of Gene Resource and Molecular Development, Beijing Normal University, Beijing, China.
Chen WangBeijing Key Laboratory of Gene Resource and Molecular Development, Beijing Normal University, Beijing, China.
Huishi LiangBeijing Key Laboratory of Gene Resource and Molecular Development, Beijing Normal University, Beijing, China.
Jie LiBeijing Key Laboratory of Gene Resource and Molecular Development, Beijing Normal University, Beijing, China. lj@bnu.edu.cn.
Qiong YangBeijing Key Laboratory of Gene Resource and Molecular Development, Beijing Normal University, Beijing, China. yangqiong@bnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) tumors are biologically aggressive breast cancer. On the molecular level, TNBC is a highly heterogeneous disease; more biotechnologies are gradually being used to advance the understanding of TNBC subtypes and help establish more targeted therapies. Multiple TNBC target-related agents are already approved by the Food and Drug Administration for clinical use, including PI3K/AKT/mTOR inhibitors, PRAP inhibitors, and antibody-drug conjugates. Some innovative approaches, like peptide strategies, also promise to treat TNBC. Currently, the interplay between TNBC tumors and their tumor microenvironment provides a promising prospect for improving the efficacy of immunotherapy. In this review, we summarize the prevalent TNBC subtype methodologies, discuss the evolving therapeutic strategies, and propose new therapeutic possibilities based on existing foundational theories, with the attempt to serve as a reference to further advance tailoring treatment of TNBC.

Indexed as

Triple Negative Breast NeoplasmsAntineoplastic AgentsFemaleHumansImmunotherapyMolecular Targeted TherapyTumor MicroenvironmentAntineoplastic AgentsImmunotherapyPersonalized treatmentTriple-negative breast cancer

Identifiers

What OpenQuestion holds

Textmetadata
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.