Tracking dynamic evolution of low‐ and intermediate‐risk differentiated thyroid cancer: Identification of individuals at risk of recurrence

Author:

Volpi Federico1ORCID,Alcalde Juan2ORCID,Larrache Javier3ORCID,Alegre Estíbaliz45ORCID,Argueta Allan6,Lozano María D.567ORCID,Colombo Carla18ORCID,Galofré Juan C.59ORCID

Affiliation:

1. Department of Endocrine and Metabolic Diseases IRCCS Istituto Auxologico Italiano Milan Italy

2. Department of Otorhinolaryngology‐Head and Neck Surgery, Clínica Universidad de Navarra University of Navarra Pamplona Spain

3. Department of Radiology, Clínica Universidad de Navarra University of Navarra Pamplona Spain

4. Service of Biochemistry Clínica Universidad de Navarra Pamplona Spain

5. Instituto de Investigación Sanitaria de Navarra (IdiSNA) Pamplona Spain

6. Department of Pathology, Clínica Universidad de Navarra University of Navarra Pamplona Spain

7. Centro de Investigación Biomedica en Red de Oncología (CIBERONC) Madrid Spain

8. Department of Pathophysiology and Transplantation University of Milan Milan Italy

9. Department of Endocrinology and Nutrition, Clínica Universidad de Navarra University of Navarra Pamplona Spain

Abstract

AbstractObjectiveThe generally good prognosis of low‐ and intermediate‐risk differentiated thyroid cancer (DTC) underscored the need to identify those few patients who relapse.DesignRecords of 299 low‐ or intermediate‐risk DTC patients (mean follow‐up 8.2 ± 6.2 years) were retrospectively reviewed. The sample was classified following the American Thyroid Association (ATA) dynamic risk stratification (DRS) system.Patients and MeasurementAfter classifying patients according to DRS at the first visit following initial therapy (FU1), structural recurrence occurred in 2/181 (1.1%), 5/81 (6.2%) and 13/26 (50.0%) with excellent, indeterminate and biochemical incomplete response to treatment, respectively. All relapses but one happened within 5 years from FU1. Univariate analysis comparing excellent, indeterminate and biochemical incomplete with structural incomplete responses at the end of the follow‐up, identified tumour size (p < .001), T status (<0.001), positive lymph nodes (N) (p < .01), multifocality (p < .004), need of additional radioactive iodine (RAI) (p < .0001) and first DRS status (p < .0003) as risk factors of recurrence. In the multivariate analysis, only RAI remained statistically significant (p < .02). Comparison between excellent and indeterminate with biochemical and structural incomplete responses, identified tumour size (p < .0004), T (p < .01), N (p < .0001), bilaterality (p < .03), first DRS status (p < .0001) and RAI (p < .001) as recurrence risk factors. T (p < .01) and first DRS (p < .0006) were confirmed in the multivariate analysis.ConclusionsPatients with DTC classified as low‐ or intermediate‐risk of recurrence with excellent response to treatment at FU1 rarely develop structural disease and this occurs almost exclusively in the first 5 years. Initial DRS status is an accurate tool for determining the risk of recurrence.

Publisher

Wiley

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