Related Experiment Video
Updated: Jan 8, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Recurrence factors in familial papillary thyroid carcinoma
Antonio Ríos1,2, Iñaki Amunategui3, José Ruiz Pardo4
1Unit of Endocrine Surgery, Department of General and Digestive Surgery Murcia Biosanitary Research Institute (IMIB-Arrixaca), Murcia Department of Health, University Hospital Virgen de la Arrixaca, Murcia, Spain - arzrios@um.es.
Familial papillary thyroid carcinoma (FPTC) shows a high recurrence rate. Key risk factors include family history, multifocality, vascular invasion, TNM staging, and ATA risk assessment.
Area of Science:
- Endocrinology
- Oncology
- Genetics
Background:
- Familial papillary thyroid carcinoma (FPTC) is a distinct subtype with poorer prognosis than sporadic PTC.
- Understanding FPTC recurrence is crucial for improved patient outcomes.
Purpose of the Study:
- To analyze recurrence rates in familial PTC (FPTC) patients treated with curative intent.
- To identify independent prognostic factors associated with FPTC recurrence.
Main Methods:
- Multicenter national study involving patients with confirmed FPTC.
- Utilized Cox regression and survival analysis for recurrence risk factor identification.
- Included TNM staging and American Thyroid Association (ATA) risk assessment.
Main Results:
- 252 FPTC cases analyzed with a mean follow-up of 90 months.
- Recurrence observed in 26.9% of patients.
- Independent recurrence predictors: number of FPTC cases in family, multifocality, vascular invasion, TNM stage, and ATA risk score.
Conclusions:
- FPTC exhibits a significant recurrence rate.
- Recurrence is strongly associated with family history, tumor characteristics (multifocality, vascular invasion), TNM staging, and ATA risk stratification.
Related Concept Videos
Cancers Originate from Somatic Mutations in a Single Cell
Cancer Prevention
Some...
The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Mitogens and the Cell Cycle
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Replicative Cell Senescence

