Evidence map›Paper›PMID 28676659›Full record

ArticleScientific reports2017

Mutations in BRCA2 and taxane resistance in prostate cancer.

Cathleen Nientiedt, Martina Heller, Volker Endris, Anna-Lena Volckmar, Stefanie Zschäbitz, María A Tapia-Laliena, Anette Duensing, Dirk Jäger, Peter Schirmacher, Holger Sültmann and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Lesion Absorbed Dose-Response Relationship in Patients with Metastatic Castration-Resistant Prostate Cancer Undergoing [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Characteristics of BRCA2 Mutated Prostate Cancer at Presentation.International journal of molecular sciences · 2022
    Article
  9. Article
  10. Article
  11. Outcome ofCancers · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. International journal of molecular sciences · 2020
    Review
  16. Review
  17. Article
  18. Review
  19. Journal of Cancer · 2019
    Review
  20. The Novel Pathogenic Mutation c.849dupT inJournal of breast cancer · 2018
    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

14 authors at 3 institutions in 2 countries.

Cathleen NientiedtMolecular Urooncology, Department of Urology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 517, D-69120, Heidelberg, Germany.
Martina HellerMolecular Urooncology, Department of Urology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 517, D-69120, Heidelberg, Germany.
Volker EndrisDepartment of Pathology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 224, D-69120, Heidelberg, Germany.
Anna-Lena VolckmarDepartment of Pathology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 224, D-69120, Heidelberg, Germany.
Stefanie ZschäbitzDepartment of Medical Oncology, University of Heidelberg School of Medicine, National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 460, D-69120, Heidelberg, Germany.
María A Tapia-LalienaMolecular Urooncology, Department of Urology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 517, D-69120, Heidelberg, Germany.
Anette DuensingCancer Therapeutics Program, University of Pittsburgh Cancer Institute, Hillman Cancer Center, 5117 Centre Avenue, Pittsburgh, PA, 15213, USA.ORCID 0000-0002-0168-4067
Dirk JägerDepartment of Medical Oncology, University of Heidelberg School of Medicine, National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 460, D-69120, Heidelberg, Germany.
Peter SchirmacherDepartment of Pathology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 224, D-69120, Heidelberg, Germany.
Holger SültmannCancer Genome Research, National Center for Tumor Diseases, German Cancer Research Center and German Cancer Consortium (DKTK), Im Neuenheimer Feld 460, D-69120, Heidelberg, Germany.
Albrecht StenzingerDepartment of Pathology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 224, D-69120, Heidelberg, Germany.
Markus HohenfellnerDepartment of Urology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 110, D-69120, Heidelberg, Germany.
Carsten GrüllichDepartment of Medical Oncology, University of Heidelberg School of Medicine, National Center for Tumor Diseases (NCT), Im Neuenheimer Feld 460, D-69120, Heidelberg, Germany.
Stefan DuensingMolecular Urooncology, Department of Urology, University of Heidelberg School of Medicine, Im Neuenheimer Feld 517, D-69120, Heidelberg, Germany. stefan.duensing@med.uni-heidelberg.de.
Heidelberg University · DEGerman Cancer Research Center · DEUPMC Hillman Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in BRCA1 or BRCA2 define a subset of prostate cancer patients. Herein, we address the question whether BRCA1/2 mutations have a predictive impact on chemotherapy with docetaxel, a widely used drug in patients with metastatic castration resistant prostate cancer (mCRPC). Fifty-three men treated with docetaxel for mCRPC were tested for somatic BRCA1/2 mutations of the primary tumor. In a subgroup of patients, BRCA1/2 protein expression was tested as a potential surrogate marker for BRCA1/2 inactivation. Eight of 53 patients (15.1%) harbored a deleterious BRCA2 mutation. No BRCA1 mutation was found. Patients with a BRCA2 mutation showed a response rate of 25% to docetaxel in comparison to 71.1% in men with wildtype BRCA2 (p = 0.019). While the time to develop castration resistance was similar in both subgroups, the overall survival was significantly shorter in patients harboring a BRCA2 mutation. No correlation between the BRCA1/2 protein expression and the response to docetaxel was found. While the presence of a BRCA2 mutation does not preclude a response to docetaxel, there is overall a significant correlation between BRCA2 inactivation and a poor response rate. Our results suggest that a close oncological monitoring of patients with BRCA2 mutations for taxane resistance is warranted.

Indexed as

Biomarkers, TumorGenes, BRCA2MutationAntineoplastic AgentsBridged-Ring CompoundsCell Line, TumorCombined Modality TherapyDrug Resistance, NeoplasmGene ExpressionGenes, BRCA1Genetic Predisposition to DiseaseHumansImmunohistochemistryMaleMutation RateNeoplasm GradingAntineoplastic AgentsBiomarkers, TumorBridged-Ring CompoundstaxaneTaxoids

Identifiers

PMID28676659
PMCPMC5496866
OpenAlexW2727056237

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.