Evidence map›Paper›PMID 23955546›Full record

ArticleJournal of cancer research and clinical oncology2013

Predictive value of sphingosine kinase 1 expression in neoadjuvant treatment of breast cancer.

Eugen Ruckhäberle, Thomas Karn, Carsten Denkert, Sibylle Loibl, Beyhan Ataseven, Toralf Reimer, Sven Becker, Uwe Holtrich, Achim Rody, Silvia Darb-Esfahani and 2 more

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In one paragraph

Article in Journal of cancer research and clinical oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 23% 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.

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, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Anti-S1P Antibody as a Novel Therapeutic Strategy for VEGFR TKI-Resistant Renal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  7. Article
  8. Article
  9. Sphingosine kinase 1 isoform-specific interactions in breast cancer.Molecular endocrinology (Baltimore, Md.) · 2014
    Article
  10. Article
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

12 authors at 5 institutions in 1 country.

Eugen RuckhäberleDepartment of Obstetrics and Gynecology, Goethe University Frankfurt, Theodor-Stern Kai 7, 60590, Frankfurter, Germany.
Thomas Karn
Carsten Denkert
Sibylle Loibl
Beyhan Ataseven
Toralf Reimer
Sven Becker
Uwe Holtrich
Achim Rody
Silvia Darb-Esfahani
Valentina Nekljudova
Gunter von Minckwitz
Goethe University Frankfurt · DEGerman Breast group · DECharité - Universitätsmedizin Berlin · DEKlinikum Südstadt Rostock · DERotkreuzklinikum München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSphingolipids play important roles in apoptosis and cell proliferation. Sphingosine kinase 1 (SphK1) expression has a prognostic impact in primary breast cancer, but its predictive value is currently unknown.

methodsA total of 112 breast cancer specimens from a prospective neoadjuvant chemotherapy trial (GeparDuo) were studied. Using tissue microarrays of pre-treatment core cut biopsies, we determined the expression of SphK1 by immunohistochemistry. The upper quartile of the cohort according to an immune reactive score of SphK1 was used as cutoff for high expression.

resultsWe observed a larger number of samples with high SphK1 expression among ER-negative cancers (36.8 vs. 20.5 % among ER-positive cancers; Fisher test p = 0.073). Eighteen of the 112 patients demonstrated a pathological complete response. A significant predictive value for pathological complete response was observed for ER negativity (p = 0.003), young age (p = 0.037), and high tumor grade (p = 0.049). An increased pCR rate was observed in tumors with high SphK1 expression within the luminal subtype (26.7 vs. 5.8 %; Fisher test p = 0.040). No significant difference in survival was detected according to SphK1 expression.

conclusionsOur results suggest that SphK1 may be a predictive factor for pCR after neoadjuvant treatment in luminal type breast cancers and warrants further investigation.

Indexed as

Breast NeoplasmsChemotherapy, AdjuvantDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansKaplan-Meier EstimateMiddle AgedNeoadjuvant TherapyPhosphotransferases (Alcohol Group Acceptor)Proportional Hazards ModelsRandomized Controlled Trials as TopicReceptors, EstrogenSphingosine KinaseTreatment OutcomeERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPhosphotransferases (Alcohol Group Acceptor)Receptors, EstrogenSphingosine Kinase

Identifiers

PMID23955546
PMCPMC11824557
OpenAlexW2075629903

What OpenQuestion holds

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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.