Evidence map›Paper›PMID 38170436›Full record

ArticleAdvances in therapy2024

TIROSEC: Molecular, Clinical and Histopathological Profile of Papillary Thyroid Carcinoma in a Colombian Cohort.

Sergio D Cruz-Romero, Sebastián González, José Y Juez, David S Becerra, Ana M Baldión, José A Hakim, Deyanira González-Devia, Sandra Perdomo, Paula A Rodríguez-Urrego

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Article in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-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

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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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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

9 authors at 4 institutions in 2 countries.

Sergio D Cruz-RomeroPathology Department, Univeristy Hospital Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Sebastián GonzálezPathology Department, Univeristy Hospital Fundación Santa Fe de Bogotá, Bogotá, Colombia.
José Y JuezSchool of Engineer, Los Andes University, Bogotá, Colombia.
David S BecerraFaculty of Medicine, Nacional University, Bogotá, Colombia.
Ana M BaldiónPathology Department, Univeristy Hospital Fundación Santa Fe de Bogotá, Bogotá, Colombia.
José A HakimHead and Neck Surgery, University Hospital Fundación Santa Fe de Bogotá, Bogotá, Colombia.
Deyanira González-DeviaEndocrine Division, University Hospital Fundación Santa Fe. Bogotá, Bogotá, Colombia.
Sandra PerdomoNutrition, Genetics, and Metabolism Research Group, El Bosque University, Bogotá, Colombia.
Paula A Rodríguez-UrregoPathology Department, Univeristy Hospital Fundación Santa Fe de Bogotá, Bogotá, Colombia. paula.rodriguez@fsfb.org.co.
Fundación Santa Fe de Bogotá · COUniversidad de Los Andes · COUniversidad El Bosque · COUniversidad Nacional de Colombia · CO

Funding

World Health Organization 001
6 · The paper itself

Abstract

introductionIn Colombia, thyroid cancer ranks among the highest incidences, yet our population lacks studies on its molecular profile. This study aims to characterize clinical, histopathologic and molecular data in a Colombian cohort with papillary thyroid carcinoma (PTC).

methodsA retrospective review of clinical history, clinicopathologic characteristics, treatment and 5-10-year follow-up for all patients was done. DNA and RNA were extracted from formalin-fixed paraffin-embedded (FFPE) tissue using the Quick-DNA & RNA FFPE Min iPrep kit (Zymo Research). Next-generation sequencing (NGS) analysis was performed with SOPHiA Solid Tumor Solutions kit (SOPHiA GENETICS). Tumor mutation genomic analysis used SOPHiA DDM™ platform, with descriptive analysis reporting frequencies, means and associations via chi-square analysis.

resultsAmong 231 sequenced patients, mean age at diagnosis was 46 (± 12.35) years, with higher frequency in women (81.82%). Two cases were reclassified as non-invasive follicular thyroid neoplasm (NIFT-P); an NRAS mutation was found in one of them. Predominant histologic subtype was classic PTC (57.64%) followed by tall cell (28.82%). Of the 229 sequenced carcinomas, mutations were identified in 186 cases, including BRAF, IDH1, RAS and PIK3CA. Notable copy number variations (CNVs) were PDGFRA, CDK4 and KIT, with RET being the most frequent gene fusion, including CCDC6-RET in two classic subtype cases.

conclusionThis is the first study in Colombia (TIROSEC) to our knowledge that integrates molecular and histopathologic profiles enriching our local comprehension and knowledge of PTC. The identification of target mutations such as BRAF, RET and NTRK fusions holds the potential to guide targeted therapies for tumor recurrence and predict aggressive behavior.

Indexed as

Carcinoma, PapillaryThyroid NeoplasmsAdultColombiaDNADNA Copy Number VariationsFemaleHumansMiddle AgedMutationNeoplasm Recurrence, LocalProto-Oncogene Proteins B-rafRNAThyroid Cancer, PapillaryDNAProto-Oncogene Proteins B-rafRNAInsertion-deletion mutationMolecular sequence dataNeoplasmsPapillary thyroid cancer pathologyPoint mutation

Identifiers

PMID38170436
OpenAlexW4390571115

What OpenQuestion holds

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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.