Evidence map›Paper›PMID 27206449›Full record

ReviewDer Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete2016

[Melanoma brain metastases : Treatment options].

R Rauschenberg, G Tabatabai, E G C Troost, M Garzarolli, S Beissert, F Meier

Open access · hybridAbstract readReview
PubMed Publisher
In one paragraph

Review in Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. [Acute emergencies in oncology].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2018
    Review
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

6 authors at 5 institutions in 1 country.

R RauschenbergHauttumorzentrum am Universitäts Krebs-Centrum Dresden (UCC), Klinik und Poliklinik für Dermatologie, Universitätsklinikum Carl-Gustav-Carus Dresden, Technische Universität Dresden, Fetscherstr. 74, 01307, Dresden, Deutschland.
G TabatabaiInterdisziplinäre Sektion Neuroonkologie, Zentrum für Neurologie und Klinik für Neurochirurgie, Hertie-Institut für Klinische Hirnforschung, Universitätsklinik Tübingen, Eberhard Karls Universität Tübingen, Tübingen, Deutschland.
E G C TroostDepartment of Radiation Oncology, University Hospital and Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Deutschland.
M GarzarolliHauttumorzentrum am Universitäts Krebs-Centrum Dresden (UCC), Klinik und Poliklinik für Dermatologie, Universitätsklinikum Carl-Gustav-Carus Dresden, Technische Universität Dresden, Fetscherstr. 74, 01307, Dresden, Deutschland.
S BeissertHauttumorzentrum am Universitäts Krebs-Centrum Dresden (UCC), Klinik und Poliklinik für Dermatologie, Universitätsklinikum Carl-Gustav-Carus Dresden, Technische Universität Dresden, Fetscherstr. 74, 01307, Dresden, Deutschland.
F MeierHauttumorzentrum am Universitäts Krebs-Centrum Dresden (UCC), Klinik und Poliklinik für Dermatologie, Universitätsklinikum Carl-Gustav-Carus Dresden, Technische Universität Dresden, Fetscherstr. 74, 01307, Dresden, Deutschland. Friedegund.Meier@uniklinikum-dresden.de.
Klinik und Poliklinik für Psychotherapie und Psychosomatik · DEHelmholtz-Zentrum Dresden-Rossendorf · DEHertie Institute for Clinical Brain Research · DETechnische Universität Dresden · DEUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of patients with metastatic melanoma will develop brain metastases, which are the most common cause of death. Until recently, local therapies (e. g., neurosurgery, radiotherapy) were the only options for brain metastases; however, effective systemic treatment options are now available. Upon suspicion of brain metastases, diagnostic staging with brain MRI and a neurological investigation are indicated. Prognostic factors such as number of cerebral metastases and symptoms, serum lactate dehydrogenase and S‑100 levels, extracerebral metastases, and ECOG status are considered during therapeutic planning. Treatment planning and therapeutic interventions should be based on an interdisciplinary and multimodal approach. Established treatments for singular brain metastases are neurosurgical resection and stereotactic radiotherapy, which can prolong survival. In patients with asymptomatic BRAF V600E-mutant brain metastases, the BRAF inhibitors dabrafenib, vemurafenib, and immunotherapy with ipilimumab are used. In the case of multiple symptomatic brain metastases, palliative whole-brain radiotherapy is used for treatment, although it has failed to show an overall survival benefit. Increased intracranial pressure and epileptic seizures are addressed with corticosteroids and anticonvulsants. Current clinical studies for melanoma patients with brain metastases are investigating new treatment options such as PD-1 antibodies, combined ipilimumab and nivolumab, combined BRAF inhibitors and MEK inhibitors, and stereotactic radiation in combination with immunotherapy or targeted therapy.

Indexed as

Antineoplastic AgentsBrain NeoplasmsChemoradiotherapyCranial IrradiationEvidence-Based MedicineHumansMelanomaMolecular Targeted TherapyRadiosurgeryTreatment OutcomeAntineoplastic AgentsBRAF inhibitorsImmunotherapyRadiotherapySurgerySystemic therapy

Identifiers

PMID27206449
OpenAlexW2402331048

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.