BRAF V600E Mutation-Assisted Risk Stratification of Solitary Intrathyroidal Papillary Thyroid Cancer for Precision Treatment

Author:

Huang Yueye12,Qu Shen2,Zhu Guangwu1,Wang Fei1,Liu Rengyun1,Shen Xiaopei1,Viola David3,Elisei Rossella3,Puxeddu Efisio4,Fugazzola Laura5,Colombo Carla5,Jarzab Barbara6,Czarniecka Agnieszka6,Lam Alfred K7,Mian Caterina8,Vianello Federica9,Yip Linwah10,Riesco-Eizaguirre Garcilaso111213,Santisteban Pilar1213,O’Neill Christine J14,Sywak Mark S14,Clifton-Bligh Roderick14,Bendlova Bela15,Sýkorová Vlasta15,Xing Mingzhao1

Affiliation:

1. Laboratory for Cellular and Molecular Thyroid Research, Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD

2. Department of Endocrinology and Metabolism and the Shanghai Research Center of Thyroid Diseases, The Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai, China

3. Endocrine Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

4. Department of Internal Medicine, University of Perugia, Perugia, Italy

5. Division of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano, and Department of Pathophysiology and Transplantation, University of Milan, Milan Italy

6. Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice, Poland

7. Cancer Molecular Pathology of School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia

8. Department of Medicine, Endocrinology Unit, University of Padua, Padua, Italy

9. Veneto Institute of Oncology, IRCCS, Padua, Italy

10. University of Pittsburgh School of Medicine, Pittsburgh, PA

11. Department of Endocrinology and Nutrition Hospital Universitario La Paz and Hospital, Universitario de Mostoles, 28029 Madrid, Spain

12. Biomedical Research Institute “Alberto Sols,” Consejo Superior de Investigaciones Cientificas and Universidad Autonoma de Madrid, 28029 Madrid, Spain

13. Ciberonc, Health Institute Carlos III, 28029 Madrid, Spain

14. Endocrine Surgical Unit, The University of Sydney, Sydney, Australia

15. Department of Molecular Endocrinology Institute of Endocrinology, Prague, Czech Republic

Abstract

Abstract Background Precise risk stratification-based treatment of solitary intrathyroidal papillary thyroid cancer (SI-PTC) that is larger than 1.0 cm and 4.0 cm or less is undefined. Methods A genetic-clinical risk study was performed on BRAF V600E in 955 patients (768 women and 187 men) with SI-PTC, with median age of 46 years and median clinical follow–up time of 64 months at 11 medical centers in six countries. The chi-square test or, for analyses with small numbers, Fisher’s exact test was performed to compare recurrence rates. Recurrence-free probability was estimated by Kaplan-Meier (KM) analysis, and the independent effect of BRAF mutation on the recurrence was analyzed by Cox regression and Cox proportional hazard analyses. All statistical tests were two-sided. Results Recurrence of SI-PTC larger than 1.0 cm and 4.0 cm or less was 9.5% (21/221) vs 3.4% (11/319) in BRAF mutation vs wild-type BRAF patients, with a hazard ratio (HR) of 3.03 (95% confidence interval [CI] = 1.46 to 6.30) and a patient age- and sex-adjusted hazard ratio of 3.10 (95% CI = 1.49 to 6.45, P = .002). Recurrence rates of SI-PTC larger than 2.0 cm and 4.0 cm or less were 16.5% (13/79) vs 3.6% (5/139) in mutation vs wild-type patients (HR = 5.44, 95% CI = 1.93 to 15.34; and adjusted HR = 5.58, 95% CI = 1.96 to 15.85, P = .001). Recurrence rates of SI-PTC larger than 3.0 cm and 4 cm or less were 30.0% (6/20) vs 1.9% (1/54) in mutation vs wild-type patients (HR = 18.40, 95% CI = 2.21 to 152.98; and adjusted HR = 14.73, 95% CI = 1.74 to 124.80, P = .01). Recurrences of mutation-positive SI-PTC were comparable with those of counterpart invasive solitary PTC, around 20% to 30%, in tumors larger than 2.0 cm to 3.0 cm. BRAF mutation was associated with a statistically significant decrease in recurrence-free patient survival on KM analysis, particularly in SI-PTC larger than 2.0 cm and 4.0 cm or less. Similar results were obtained in conventional SI-PTC. The negative predictive values of BRAF mutation for recurrence were 97.8% (95% CI = 96.3% to 98.8%) for general SI-PTC and 98.2% (95% CI = 96.3% to 99.3%) for conventional SI-PTC. Conclusions BRAF V600E identifies a subgroup of SI-PTC larger than 1.0 cm and 4.0 cm or less, particularly tumors larger than 2.0 cm and 4.0 cm or less, that has high risk for recurrence comparable with that of invasive solitary PTC, making more aggressive treatment reasonable.

Funder

National Institutes of Health

National Institute on Aging

Polish National Center of Research and Development

Menzies Health Institute, Queensland and Queensland Smart State fellowship

MINECO and FEDER

ISCIII

AECC Foundation

Fondazione Cassa di Risparmio di Perugia

Associazione Italiana per la Ricerca sul Cancro

Beadle Family Foundation

Institute of Endocrinology-EU

New South Wales Cancer Institute

Cancer Council of New South Wales

Ministero della Istruzione Universitaria e Ricerca Scientifica

Istituto Toscano Tumori

Ministero della Salute

Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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