Evidence map›Paper›PMID 26693224›Full record

ArticleInternational journal of endocrinology2015

BRAF Mutations in an Italian Regional Population: Implications for the Therapy of Thyroid Cancer.

Eleonora Monti, Michela Bovero, Lorenzo Mortara, Giorgia Pera, Simonetta Zupo, Elena Gugiatti, Mariella Dono, Barbara Massa, Gian Luca Ansaldo, Giusti Massimo

Open access · goldAbstract read
In one paragraph

Article in International journal of endocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 30% 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Deep Small RNA Sequencing ofFrontiers in genetics · 2019
    Article
  7. Article
  8. 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

10 authors at 1 institution in 1 country.

Eleonora MontiDepartment of Internal Medicine, Endocrinology Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Michela BoveroDepartment of Internal Medicine, Endocrinology Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Lorenzo MortaraDepartment of Internal Medicine, Endocrinology Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Giorgia PeraDepartment of Internal Medicine, Endocrinology Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Simonetta ZupoDepartment of Pathology, Molecular Diagnostic Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Elena GugiattiDepartment of Pathology, Molecular Diagnostic Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Mariella DonoDepartment of Pathology, Molecular Diagnostic Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Barbara MassaDepartment of Pathology, Molecular Diagnostic Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Gian Luca AnsaldoDepartment of Surgery, Endocrinology Surgery Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Giusti MassimoDepartment of Internal Medicine, Endocrinology Unit, IRCCS IST Azienda Ospedaliera Universitaria "San Martino", Largo R. Benzi, No. 10, 16132 Genoa, Italy.
Ospedale Policlinico San Martino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background. Molecular diagnostics has offered new techniques for searching for mutations in thyroid indeterminate lesions. The study's aim was to evaluate the BRAF mutations' incidence in an Italian regional population. Subjects and Methods. 70 Caucasian patients born in Liguria with indeterminate or suspicious cytological diagnoses. Results. A BRAF gene mutation was successfully analyzed in 56/70 patients. The mutation was BRAF V600E in 12/56 cases (21%) and BRAF K601E in 2/56 (4%). Of the BRAF mutated samples on cytological diagnosis (14/56 cases), 2/14 cases (14%) were benign on final histology and 12/14 (86%) were malignant. All BRAF-mutated cases on cytology that were found to be benign on histological examination carried the K601E mutation. Of the nonmutated BRAF cases (42/56, 75%) which were later found to be malignant on definitive histology, 5 cases were follicular carcinomas (36%), 3 cases were incidentally found to be papillary microcarcinomas (22%), 2 were cases papillary carcinomas (14%), 1 was case follicular variant of papillary carcinoma (7%), 1 was case medullary carcinoma (7%), 1 case was Hurtle cell tumor (7%), and 1 case was combined cell carcinoma and papillary oncocytic carcinoma (7%). Conclusions. The presence of the BRAF V600E mutation may suggest a more aggressive surgical approach. BRAF K601E mutation did not correlate with malignancy indexes.

Identifiers

PMID26693224
PMCPMC4674605
OpenAlexW2180687240

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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.