Approach to risk stratification for papillary thyroid carcinoma based on molecular profiling: institutional analysis

Author:

Staubitz Julia I1ORCID,Müller Celine2,Heymans Antonia2,Merten Christina2,Roos Bianca1,Poplawski Alicia3,Ludt Annekathrin3,Strobl Stephanie2,Springer Erik2,Schad Arno2,Roth Wilfried2,Musholt Thomas J1ORCID,Hartmann Nils2

Affiliation:

1. Section of Endocrine Surgery, Department of General, Visceral and Transplantation Surgery, University Medical Centre, Johannes Gutenberg University Mainz , Mainz , Germany

2. Institute of Pathology, University Medical Centre, Johannes Gutenberg-University Mainz , Mainz , Germany

3. Institute for Medical Biometry, Epidemiology and Informatics, University Medical Centre Mainz, Johannes Gutenberg University Mainz , Mainz , Germany

Abstract

Abstract Background Currently, treatment recommendations for papillary thyroid carcinoma are not based on the genetic background causing tumourigenesis. The aim of the present study was to correlate the mutational profile of papillary thyroid carcinoma with clinical parameters of tumour aggressiveness, to establish recommendations for risk-stratified surgical treatment. Method Papillary thyroid carcinoma tumour tissue of patients undergoing thyroid surgery at the University Medical Centre Mainz underwent analysis of BRAF, TERT promoter and RAS mutational status as well as potential RET and NTRK rearrangements. Mutation status was correlated with clinical course of disease. Results One hundred and seventy-one patients operated for papillary thyroid carcinoma were included. The median age was 48 years (range 8–85) and 69 per cent (118/171) of patients were females. One hundred and nine papillary thyroid carcinomas were BRAF-V600E mutant, 16 TERT promotor mutant and 12 RAS mutant; 12 papillary thyroid carcinomas harboured RET rearrangements and two papillary thyroid carcinomas showed NTRK rearrangements. TERT promoter mutant papillary thyroid carcinomas had a higher risk of distant metastasis (OR 51.3, 7.0 to 1048.2, P < 0.001) and radioiodine-refractory disease (OR 37.8, 9.9 to 169.5, P < 0.001). Concomitant BRAF and TERT promoter mutations increased the risk of radioiodine-refractory disease in papillary thyroid carcinoma (OR 21.7, 5.6 to 88.9, P < 0.001). RET rearrangements were associated with a higher count of tumour-affected lymph nodes (OR 7950.9, 233.7 to 270495.7, P < 0.001) but did not influence distant metastasis or radioiodine-refractory disease. Conclusions Papillary thyroid carcinoma with concomitant BRAF-V600E and TERT promoter mutations demonstrated an aggressive course of disease, suggesting the need for a more extensive surgical strategy. RET rearrangement-positive papillary thyroid carcinoma did not affect the clinical outcome, potentially obviating the need for prophylactic lymphadenectomy.

Funder

University Medical Centre of the Johannes Gutenberg University Mainz

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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