Evidence map›Paper›PMID 21858416›Full record

ReviewStrahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]2011

[Hemangiosarcoma after breast-conserving therapy of breast cancer: report of four cases with molecular genetic diagnosis and literature review].

Carolin Nestle-Krämling, Edwin Bölke, Wilfried Budach, Matthias Peiper, Dieter Niederacher, Wolfgang Janni, Claus Ferdinand Eisenberger, Wolfram Trudo Knoefel, Axel Scherer, Stephan Ernst Baldus and 3 more

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. [Compliance of patients concerning recommended radiotherapy in breast cancer : Association with recurrence, age, and hormonal therapy].Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2012
    Trial
  4. Article
  5. [Second primary cancers after radiotherapy in breast cancer patients].Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2013
    Article
  6. Article
  7. Multiple malignancies in a single patient : a glimpse into 30 years of interdisciplinary oncology.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2013
    Article
  8. Postoperative periclavicular radiotherapy in breast cancer patients with 1-3 positive axillary lymph nodes. Outcome and morbidity.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2012
    Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Carolin Nestle-KrämlingFrauenklinik, Universitätsklinikum Düsseldorf, Germany.
Edwin Bölke
Wilfried Budach
Matthias Peiper
Dieter Niederacher
Wolfgang Janni
Claus Ferdinand Eisenberger
Wolfram Trudo Knoefel
Axel Scherer
Stephan Ernst Baldus
Guido Lammering
Peter Arne Gerber
Christiane Matuschek
Heinrich Heine University Düsseldorf · DEDüsseldorf University Hospital · DEKlinik und Poliklinik für Strahlentherapie und Radioonkologie · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemangiosarcomas of the breast represent a rare disease of the breast mainly occurring as secondary neoplasias with a latency of 5-10 years after primary treatment of breast cancer and are associated with an unfavourable prognosis. Radiation therapy, which is integrated within the concept of breast conserving therapy ranks as the main risk factor. PATIENTS AND

methodsIn this report we describe the clinical course of 4 patients including their molecular genetic pattern and give a summary of the actual literature.

resultsHemangiosarcomas occur as a secondary neoplasm with a latency of 5-10 years after primary treatment of breast cancer and have an unfavorable prognosis. A genetic predisposition is assumed, but we could not find a significant role of tumor suppressor genes BRCA1, BRCA2 or p53 in our patients.

conclusionDue to limited data available for these tumors, recommendations for therapy include radical tumor resection achieving wide free margins and inconsistent regimens of chemo- and/or immunetherapy modalities. In the majority these are based on systemic therapy regimens for other cutaneous sarcomas, such as Kaposi's sarcoma. Efforts should be taken for a nation-wide systematic registration of all cases of post-irradiation hemangiosarcomas.

Indexed as

Genes, SuppressorMastectomy, SegmentalPathology, MolecularAdultAgedBRCA2 ProteinBreast NeoplasmsChemotherapy, AdjuvantCombined Modality TherapyDiagnosis, DifferentialDNA Mutational AnalysisFatal OutcomeFemaleHemangiosarcomaHumansMiddle AgedBRAP protein, humanBRCA2 ProteinBRCA2 protein, humanTumor Suppressor Protein p53Ubiquitin-Protein Ligases

Identifiers

PMID21858416
OpenAlexW175321729

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.