Evidence map›Paper›PMID 37671897›Full record

ArticleEndocrine-related cancer2023

ThyroidPrint®: clinical utility for indeterminate thyroid cytology.

Roberto Olmos, José Miguel Domínguez, Sergio Vargas-Salas, Lorena Mosso, Carlos E Fardella, Gilberto González, René Baudrand, Francisco Guarda, Felipe Valenzuela, Eugenio Arteaga and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Endocrine-related cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. The actual and future role of molecular tests in thyroid pathology.Virchows Archiv : an international journal of pathology · 2026
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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

32 authors at 1 institution in 1 country.

Roberto OlmosDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
José Miguel DomínguezDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Sergio Vargas-SalasDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Lorena MossoDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Carlos E FardellaDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Gilberto GonzálezDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
René BaudrandDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Francisco GuardaDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Felipe ValenzuelaDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Eugenio ArteagaDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Pablo FlorenzanoDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Flavia NiloDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Nicole LustigDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Alejandra MartínezDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
José M LópezDepartment of Endocrinology, School of Medicine Pontificia Universidad Católica de Chile.
Francisco CruzDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile.
Soledad LoyolaDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile.
Augusto LeonDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Nicolás DroppelmannDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Pablo MonteroDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Francisco DomínguezDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Mauricio CamusDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Antonieta SolarDepartment of Anatomic Pathology, School of Medicine Pontificia Universidad Católica de Chile.
Pablo ZoroquiainDepartment of Anatomic Pathology, School of Medicine Pontificia Universidad Católica de Chile.
Juan Carlos RoaDepartment of Anatomic Pathology, School of Medicine Pontificia Universidad Católica de Chile.
Estefanía MuñozDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Elsa BruceDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Rossio GajardoDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Giovanna MirandaDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Francisco RiquelmeDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Natalia MenaDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.
Hernán E GonzálezDepartment of Surgical Oncology, School of Medicine Pontificia Universidad Católica de Chile.ORCID 0000-0001-6301-4547
Pontificia Universidad Católica de Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular testing contributes to improving the diagnosis of indeterminate thyroid nodules (ITNs). ThyroidPrint® is a ten-gene classifier aimed to rule out malignancy in ITN. Post-validation studies are necessary to determine the real-world clinical benefit of ThyroidPrint® in patients with ITN. A single-center, prospective, noninterventional clinical utility study was performed, analyzing the impact of ThyroidPrint® in the physicians' clinical decisions for ITN. Demographics, nodule characteristics, benign call rates (BCRs), and surgical outcomes were measured. Histopathological data were collected from surgical biopsies of resected nodules. Of 1272 fine-needle aspirations, 109 (8.6%) were Bethesda III and 135 (10.6%) were Bethesda IV. Molecular testing was performed in 155 of 244 ITN (63.5%), of which 104 were classified as benign (BCR of 67.1%). After a median follow-up of 15 months, 103 of 104 (99.0%) patients with a benign ThyroidPrint® remained under surveillance and one patient underwent surgery which was a follicular adenoma. Surgery was performed in all 51 patients with a suspicious for malignancy as per ThyroidPrint® result and in 56 patients who did not undergo testing, with a rate of malignancy of 70.6% and 32.1%, respectively. A higher BCR was observed in follicular lesion of undetermined significance (87%) compared to atypia of undetermined significance (58%) (P < 0.05). False-positive cases included four benign follicular nodules and six follicular and four oncocytic adenomas. Our results show that, physicians chose active surveillance instead of diagnostic surgery in all patients with a benign ThyroidPrint® result, reducing the need for diagnostic surgery in 67% of patients with preoperative diagnosis of ITN.

Indexed as

Thyroid NeoplasmsThyroid NoduleBiopsy, Fine-NeedleGene Expression ProfilingHumansProspective StudiesRetrospective Studiesclinical utilitygenetic classifierindeterminate thyroid cytology

Identifiers

PMID37671897
PMCPMC10563504
OpenAlexW4386467356

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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.