Evidence map›Paper›PMID 25738144›Full record

ReviewAnnals of translational medicine2015

Impact of BRAF mutation status in the prognosis of cutaneous melanoma: an area of ongoing research.

Parisha Bhatia, Paul Friedlander, Elmageed A Zakaria, Emad Kandil

Erratum issuedAbstract readReview
In one paragraph

Review in Annals of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 61 citations in OpenAlex.

  1. Adjuvant bevacizumab for melanoma patients at high risk of recurrence: survival analysis of the AVAST-M trial.Annals of oncology : official journal of the European Society for Medical Oncology · 2018
    Trial
  2. Article
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  8. South Asian journal of cancer · 2023
    Article
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  15. Article
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  18. Mitochondrial Sirtuins in Skin and Skin Cancers.Photochemistry and photobiology · 2020
    Review
  19. Article
  20. Coexistence of BRAF V600E and TERT Promoter Mutations in Low-grade Serous Carcinoma of Ovary Recurring as Carcinosarcoma in a Lymph Node: Report of a Case.International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Parisha Bhatia1 Department of Surgery, 2 Department of Otolaryngology, Tulane University School Of Medicine, New Orleans, LA 70112, USA.
Paul Friedlander1 Department of Surgery, 2 Department of Otolaryngology, Tulane University School Of Medicine, New Orleans, LA 70112, USA.
Elmageed A Zakaria1 Department of Surgery, 2 Department of Otolaryngology, Tulane University School Of Medicine, New Orleans, LA 70112, USA.
Emad Kandil1 Department of Surgery, 2 Department of Otolaryngology, Tulane University School Of Medicine, New Orleans, LA 70112, USA.
Tulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review is intended to provide an updated role of molecular genetics and various targeted therapies that have been developed to treat advanced stages of melanoma. Because of the declining success in melanoma therapy, the curative treatment for advanced stage melanoma has been a challenge for clinicians. Several mutations such as N-RAS, p53, BRAF including mutant-BRAF that lead to activation of kinase pathway, are implicated in the development of malignant melanoma. However, the current literature depicts that the prognostic role of BRAF mutation in disease progression is still controversial. While its higher level in advanced stage disease is associated with decreased overall survival (OS), some studies show that it failed to confer as an independent prognostic predictor of the disease. This has also led researchers to accomplish newer therapeutic strategies that lead to improved disease-response and grant survival benefits. Vemurafenib, a BRAF inhibitor agent, is one of the few available targeted therapies that is FDA approved and provides promising results in metastatic disease. However, its resistance at an early stage is of great concern. Recent implementation of combinational therapies including "targeted therapy", immunotherapy, and biological agents has appealed many researchers to define the adjunctive role of available therapies and their limitations in advanced stage and metastatic melanoma. This commends the need for future multi-institutional studies to confirm the clinical validity of different therapeutic strategies on a large scale population.

Indexed as

disease progressionimmunotherapyMalignant melanomamutationsvemurafenib

Identifiers

PMID25738144
PMCPMC4322160
OpenAlexW156085488

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.