Evidence map›Paper›PMID 32517735›Full record

ReviewBreast cancer research : BCR2020

Triple-negative breast cancer molecular subtyping and treatment progress.

Li Yin, Jiang-Jie Duan, Xiu-Wu Bian, Shi-Cang Yu

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Breast cancer research : BCR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06309459 (Carbonic Anhydrase IX Enzyme in Triple Negative Breast Carcinoma), which is not on this map. Cited by 1,328 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,328citing papers in PubMed, 4 pooled it
99.7field-weighted citation impact, top 1% of its field
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.

NCT06309459 completednot on this map

Carbonic Anhydrase IX Enzyme in Triple Negative Breast Carcinoma: Relationship With Prognostic Factors and Response to Neoadjuvant Chemotherapy

TypeobservationalSponsorKahramanmaras Sutcu Imam UniversityRan2018 to 2023Enrolled40ConditionsTriple Negative Breast Cancer, Carbonic Anhydrase IXArmsCarbonic anhydrase staining levels
3 · Its place in the literature

Who cites it

1,328 citing papers in PubMed, 4 syntheses or guidelines pooled it, 2,436 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Prospective pilot study with [European journal of nuclear medicine and molecular imaging · 2026
    Trial
  11. Trial
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

1,268 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 1 country.

Li YinDepartment of Stem Cell and Regenerative Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), ChongQing, 400038, China.
Jiang-Jie DuanDepartment of Stem Cell and Regenerative Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), ChongQing, 400038, China.
Xiu-Wu BianInstitute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University (Army Medical University), ChongQing, 400038, China.
Shi-Cang YuDepartment of Stem Cell and Regenerative Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), ChongQing, 400038, China. yushicang@163.com.
Southwest Hospital · CNArmy Medical University · CN

Funding

National Key Research and Development Program of China 2016YFA0202104National Natural Science Foundation of China 81602730
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC), a specific subtype of breast cancer that does not express estrogen receptor (ER), progesterone receptor (PR), or human epidermal growth factor receptor 2 (HER-2), has clinical features that include high invasiveness, high metastatic potential, proneness to relapse, and poor prognosis. Because TNBC tumors lack ER, PR, and HER2 expression, they are not sensitive to endocrine therapy or HER2 treatment, and standardized TNBC treatment regimens are still lacking. Therefore, development of new TNBC treatment strategies has become an urgent clinical need. By summarizing existing treatment regimens, therapeutic drugs, and their efficacy for different TNBC subtypes and reviewing some new preclinical studies and targeted treatment regimens for TNBC, this paper aims to provide new ideas for TNBC treatment.

Indexed as

AnimalsAntineoplastic AgentsErb-b2 Receptor Tyrosine KinasesFemaleHumansMolecular Targeted TherapyReceptors, EstrogenReceptors, ProgesteroneTriple Negative Breast NeoplasmsAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneMolecular subtypeTherapeutic regimenTherapeutic targetTriple-negative breast cancer

Identifiers

PMID32517735
PMCPMC7285581
OpenAlexW3033869790

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.