Evidence map›Paper›PMID 25376477›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2015

Discordancy in BRAF mutations among primary and metastatic melanoma lesions: clinical implications for targeted therapy.

Joshua R Bradish, Justin D Richey, Kristin M Post, Kari Meehan, Joyashree D Sen, Amanda J Malek, Terrence M Katona, Simon Warren, Theodore F Logan, Leslie A Fecher and 1 more

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. BRAF Heterogeneity in Melanoma.Current treatment options in oncology · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Adjuvant Therapy for Melanoma.Current treatment options in oncology · 2019
    Review
  14. Cancers · 2019
    Article
  15. Detection of driver mutations in BRAF can aid in diagnosis and early treatment of dedifferentiated metastatic melanoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019
    Article
  16. Updates in adjuvant systemic therapy for melanoma.Journal of surgical oncology · 2019
    Review
  17. Molecular testing for BRAF mutations to inform melanoma treatment decisions: a move toward precision medicine.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
    Review
  18. Review
  19. Molecular genetic and immunotherapeutic targets in metastatic melanoma.Virchows Archiv : an international journal of pathology · 2017
    Review
  20. 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

11 authors at 2 institutions in 1 country.

Joshua R BradishDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Justin D RicheyDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Kristin M PostDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Kari MeehanDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Joyashree D SenDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Amanda J MalekDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Terrence M Katona1] Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA [2] Department of Pathology, Richard L Roudebush Veteran's Affairs Medical Center, Indianapolis, IN, USA.
Simon WarrenDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Theodore F LoganDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Leslie A FecherDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Liang ChengDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic targeted molecular therapy, in the form of a selective BRAF inhibitor with or without a MEK inhibitor, is a standard treatment for patients with BRAF V600 mutation-positive melanoma with unresectable stage III and IV disease. Patients with BRAF mutation-negative primary tumors may manifest BRAF mutation-positive metastatic disease. It is unclear whether all metastatic lesions carry the same BRAF mutation status found in the primary tumor and if discordancy exists, in what frequency it occurs. Primary and matched metastatic lesions in 25 melanoma patients were tested for the BRAF V600E/Ec, V600K, V600D, and V600R mutations using a BRAF RGQ PCR kit (Qiagen). Four patients (16%) had discrepancies between their primary and metastatic melanoma BRAF status. Of these patients, 2 (8%) had BRAF mutation-positive primary melanomas with BRAF mutation-negative metastatic lesions and 2 (8%) patient had BRAF mutation-negative melanoma with a BRAF mutation-positive metastatic lesion. In summary, discordancy of BRAF mutation status is not an infrequent finding between primary and metastatic melanoma. It may be prudent in previously negative patients to determine BRAF mutation status of new metastatic tumors for proper allocation of BRAF inhibitor therapy. Discordant BRAF status may have a role in the varying patterns of response and inevitable resistance seen with BRAF inhibitor therapies.

Indexed as

MutationAdultAgedAged, 80 and overFemaleHumansMaleMelanomaMiddle AgedMolecular Targeted TherapyProto-Oncogene Proteins B-rafSkin NeoplasmsYoung AdultBRAF protein, humanProto-Oncogene Proteins B-raf

Identifiers

PMID25376477
OpenAlexW2054310049

What OpenQuestion holds

Textmetadata
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.