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The solid variant of papillary thyroid carcinoma: a multi-institutional retrospective study.
Xu, Bin; Viswanathan, Kartik; Zhang, Lingxin; Edmund, Liz N; Ganly, Olivia; Tuttle, R Michael; Lubin, Daniel; Ghossein, Ronald A.
Afiliação
  • Xu B; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Viswanathan K; Department of Pathology and Laboratory Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
  • Zhang L; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada.
  • Edmund LN; Department of Pathobiology and Laboratory Medicine, University of Toronto, Toronto, ON, Canada.
  • Ganly O; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Tuttle RM; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Lubin D; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Ghossein RA; Department of Pathology and Laboratory Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Histopathology ; 81(2): 171-182, 2022 Aug.
Article em En | MEDLINE | ID: mdl-35474588
ABSTRACT

AIMS:

The definition of papillary thyroid carcinoma, solid variant (PTC-SV) varies from >50% to 100% of solid/trabecular/insular growth (STI). We aimed to identify prognostic factors and to establish an appropriate STI cutoff for PTC-SV in this multi-institutional study of 156 PTCs with STI.

RESULTS:

Nodal metastases were seen in 18% and were associated with a higher percentage of papillary and STI. When substratified by infiltration/encapsulation status, the STI percentage did not impact the risk of nodal metastasis. pN1 stage was seen in 51% of infiltrative tumours and 1% of encapsulated lesions. Overall, PTC with STI had an excellent prognosis. The 10-year disease-free survival (DFS) was 87% in the entire cohort, 94% in encapsulated lesions, and 76% in infiltrative tumours. The STI percentage did not impact DFS. Fifty-four patients had noninvasive encapsulated lesions with 2-100% STI. None developed recurrence. Encapsulated lesions were enriched with RAS mutations (54%), whereas infiltrative lesions lacked RAS mutations (4%). The BRAF V600E mutation was an infrequent event, being seen in 11% of the entire cohort.

CONCLUSION:

In PTC with STI, the determining factor for nodal metastasis and DFS is the encapsulation/infiltration status rather than the STI percentage. Encapsulated noninvasive tumours with STI follow an indolent course with a very low risk of nodal metastasis and recurrence. Overall, PTC with STI has an excellent prognosis, with a 10-year disease-specific survival (DSS) and DFS of 96% and 87%, respectively. Therefore, the classification of SV-PTC as an aggressive PTC subtype may be reconsidered.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article