Evidence map›Paper›PMID 24783217›Full record

ArticleBioMed research international2014

Can ki-67 play a role in prediction of breast cancer patients' response to neoadjuvant chemotherapy?

Juhasz-Böss Ingolf, Mavrova Russalina, Moga Simona, Radosa Julia, Schmidt Gilda, Rainer M Bohle, Hasenfus Andrea, Solomayer Erich, Herr Daniel

Abstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Review
  7. Observational
  8. Article
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  11. Oncotarget · 2018
    Article
  12. Article
  13. Article
  14. Tumor Heterogeneity in Breast Cancer.Frontiers in medicine · 2017
    Review
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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

9 authors.

Juhasz-Böss IngolfDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Mavrova RussalinaDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Moga SimonaDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Radosa JuliaDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Schmidt GildaDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Rainer M BohleDepartment of Pathology, Homburg University Medical Centre, 66421 Homburg, Germany.
Hasenfus AndreaDepartment of Pathology, Homburg University Medical Centre, 66421 Homburg, Germany.
Solomayer ErichDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.
Herr DanielDepartment of Obstetrics and Gynecology, Homburg University Medical Centre, 66421 Homburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently the choice of breast cancer therapy is based on prognostic factors. The proliferation marker Ki-67 is used increasingly to determine the method of therapy. The current study analyses the predictive value of Ki-67 in foreseeing breast cancer patients' responses to neoadjuvant chemotherapy.

methodsThis study includes patients with invasive breast cancer treated between 2008 and 2013. The clinical response was assessed by correlating Ki-67 to histological examination, mammography, and ultrasonography findings.

resultsThe average Ki-67 value in our patients collectively (n = 77) is 34.9 ± 24.6%. The average Ki-67 value is the highest with 37.4 ± 24.0% in patients with a pCR. The Ki-67 values do not differ significantly among the 3 groups: pCR versus partial pathological response versus stable disease/progress (P = 0.896). However, Ki-67 values of patients with luminal, Her2 enriched, and basal-like cancers differed significantly from each other. Furthermore, within the group of luminal tumors Ki-67 values of patients with versus without pCR also differed significantly.

conclusionOur data shows that the Ki-67 value predicts the response to neoadjuvant chemotherapy as a function of the molecular subtype, reflecting the daily routine concerning Ki-67 and its impressing potential and limitation as a predictive marker for neoadjuvant chemotherapy response.

Indexed as

Neoadjuvant TherapyAdultBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHumansKi-67 AntigenMiddle AgedRetrospective StudiesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesKi-67 Antigen

Identifiers

PMID24783217
PMCPMC3982412

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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.