A Thyroid Genetic Classifier Correctly Predicts Benign Nodules with Indeterminate Cytology: Two Independent, Multicenter, Prospective Validation Trials
Author
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Zafereo, Mark
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McIver, Bryan
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Vargas Salas, Sergio
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Domínguez, Jose
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Steward, David L.
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Holsinger, F. Christopher
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Kandil, Emad
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Williams, Michelle
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Loyola, Soledad
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Solar, Antonieta
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Roa, Juan
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Leon, Augusto
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Droppelman, Nicolas
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Lobos, Maite
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Arias, Tatiana
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Kong, Christina S.
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Busaidy, Naifa
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Grubbs, Elizabeth G.
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Graham, Paul
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Stewart, John
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Tang, Alice
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Wang, Jiang
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Orloff, Lisa
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Henriquez, Marcela
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Lagos, Marcela
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Osorio, Miren
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Schachter, Dina
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Franco, Carmen
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Medina, Francisco
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Wohllk Gonzalez, Nelson
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Diaz, Rene
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Veliz Lopez, Jesus
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Horvath, Eleonora
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Tala, Hernan
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Pineda Bravo, Pedro
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Arroyo Albala, Patricia
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Vásquez, Felix
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Traipe, Eufrosina
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Marin, Luis
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Miranda, Giovanna
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Bruce, Elsa
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Bracamonte, Milagros
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Mena, Natalia
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Gonzalez, Hernan E.
Admission date
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2020-05-28T22:33:59Z
Available date
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2020-05-28T22:33:59Z
Publication date
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2020
Cita de ítem
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Thyroid Volumen: 30 Número: 5 Páginas: 704-712 MAY 1 2020
es_ES
Identifier
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10.1089/thy.2019.0490
Identifier
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https://repositorio.uchile.cl/handle/2250/175075
Abstract
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Background: Although most thyroid nodules with indeterminate cytology are benign, in most of the world, surgery remains as the most frequent diagnostic approach. We have previously reported a 10-gene thyroid genetic classifier, which accurately predicts benign thyroid nodules. The assay is a prototype diagnostic kit suitable for reference laboratory testing and could potentially avoid unnecessary diagnostic surgery in patients with indeterminate thyroid cytology.
Methods: Classifier performance was tested in two independent, ethnically diverse, prospective multicenter trials (TGCT-1/Chile and TGCT-2/USA). A total of 4061 fine-needle aspirations were collected from 15 institutions, of which 897 (22%) were called indeterminate. The clinical site was blind to the classifier score and the clinical laboratory blind to the pathology report. A matched surgical pathology and valid classifier score was available for 270 samples.
Results: Cohorts showed significant differences, including (i) clinical site patient source (academic, 43% and 97% for TGCT-1 and -2, respectively); (ii) ethnic diversity, with a greater proportion of the Hispanic population (40% vs. 3%) for TGCT-1 and a greater proportion of African American (11% vs. 0%) and Asian (10% vs. 1%) populations for TGCT-2; and (iii) tumor size (mean of 1.7 and 2.5 cm for TGCT-1 and -2, respectively). Overall, there were no differences in the histopathological profile between cohorts. Forty-one of 155 and 45 of 115 nodules were malignant (cancer prevalence of 26% and 39% for TGCT-1 and -2, respectively). The classifier predicted 37 of 41 and 41 of 45 malignant nodules, yielding a sensitivity of 90% [95% confidence interval; CI 77-97] and 91% [95% CI 79-98] for TGCT-1 and -2, respectively. One hundred one of 114 and 61 of 70 nodules were correctly predicted as benign, yielding a specificity of 89% [95% CI 82-94] and 87% [95% CI 77-94], respectively. The negative predictive values for TGCT-1 and TGCT-2 were 96% and 94%, respectively, whereas the positive predictive values were 74% and 82%, respectively. The overall accuracy for both cohorts was 89%.
Conclusions: Clinical validation of the classifier demonstrates equivalent performance in two independent and ethnically diverse cohorts, accurately predicting benign thyroid nodules that can undergo surveillance as an alternative to diagnostic surgery.
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Patrocinador
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Biomedical Research Consortium-Chile
13CTI-21526P2
Chilean Economic Development Agency
14IEAT-28672
17ITE2-82143
GeneproDX Chile SpA