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TERT Promoter Mutations and Tumor Persistence/Recurrence in Papillary Thyroid Cancer / Journal of the Korean Cancer Association, 대한암학회지
Article de En | WPRIM | ID: wpr-61891
Bibliothèque responsable: WPRO
ABSTRACT
PURPOSE: A telomerase reverse transcriptase (TERT) promoter mutation was identified in thyroid cancer. This TERT promoter mutation is thought to be a prognostic molecular marker, because its association with tumor aggressiveness, persistence/recurrence, and disease-specific mortality in papillary thyroid carcinoma (PTC) has been reported. In this study, we attempted to determine whether the impact of the TERT promoter mutation on PTC persistence/recurrence is independent of clinicopathological parameters. MATERIALS AND METHODS: Using propensity score matching, 39 patients with PTC persistence or recurrence were matched with 35 patients without persistence or recurrence, with a similar age, sex, tumor size, multifocality, bilaterality, extrathyroidal extension, and lymph node metastasis. The TERT promoter and the BRAF V600E mutations were identified from PTC samples. RESULTS: The TERT promoter mutation was detected in 18% of PTC patients (13/74). No significant difference in the frequency of the TERT promoter mutation was observed between the persistence/recurrence group and the non-recurrence group. CONCLUSION: These results suggest that the prognostic implications of the TERT promoter mutation are dependent on clinicopathological parameters.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Récidive / Glande thyroide / Tumeurs de la thyroïde / Mortalité / Telomerase / Score de propension / Noeuds lymphatiques / Métastase tumorale Type d'étude: Prognostic_studies Limites du sujet: Humans langue: En Texte intégral: Cancer Research and Treatment Année: 2016 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Récidive / Glande thyroide / Tumeurs de la thyroïde / Mortalité / Telomerase / Score de propension / Noeuds lymphatiques / Métastase tumorale Type d'étude: Prognostic_studies Limites du sujet: Humans langue: En Texte intégral: Cancer Research and Treatment Année: 2016 Type: Article