Prognostic Factors of Disease-Free Survival after Thyroidectomy in 170 Young Patients with a RET Germline Mutation: A Multicenter Study of the Groupe Français d'Etude des Tumeurs Endocrines

Author:

Rohmer V.12,Vidal-Trecan G.3,Bourdelot A.1,Niccoli P.4,Murat A.5,Wemeau J. L.6,Borson-Chazot F.7,Schvartz C.8,Tabarin A.9,Chabre O.10,Chabrier G.11,Caron P.12,Rodien P.12,Schlumberger M.13,Baudin E.13,

Affiliation:

1. Centre hospitalier universitaire Angers (V.R., A.B., P.R.), Endocrinologie, Faculté de médecine, Université Angers, Angers 49933, France;

2. Unité INSERM 694 (V.R., P.R.), Université d'Angers, F 49000 Angers, France;

3. Centre hospitalier Cochin Saint Vincent de Paul (G.V.-T.), Assistance Publique – Hôpitaux de Paris, Département de santé publique, Faculté de médecine; Equipe d'accueil 4069, Université Paris Descartes, Ecole des Hautes Etudes en Santé Publique, 75014 Paris, France;

4. Centre hospitalier universitaire de Marseille (P.N.), Endocrinologie, Marseille F 13000 France;

5. Centre hospitalier universitaire de Nantes (A.M.), Endocrinologie, Nantes F 44000 France;

6. Centre hospitalier universitaire de Lille (J.L.W.), Endocrinologie, Lille F 59000, France;

7. Hospices Civils de Lyon et Université Lyon1 (F.B.-C.), Fédération d'Endocrinologie du Pôle Est, Lyon F 69003, France;

8. Centre de lutte contre le cancer (C.S.), Reims F 51000, France;

9. Centre hospitalier universitaire de Bordeaux (A.T.), Endocrinologie, Hôpital Haut Lévêque, Pessac F 33604, France;

10. Centre hospitalier universitaire de Grenoble (O.C.), Endocrinologie, Grenoble, F38043, Unité INSERM 878, France;

11. Centre Hospitalier Universitaire de Strasbourg (G.C.), Endocrinologie, Strasbourg F 67000, France;

12. Centre Hospitalier Universitaire de Toulouse (P.C.), Endocrinologie, Toulouse F 31000, France;

13. Institut Gustave Roussy, département de médecine nucléaire et oncologie endocrinienne (M.S., E.B.), Université Paris Sud-XI, Villejuif, F 94800, France

Abstract

Background: In hereditary medullary thyroid carcinoma (HMTC), prophylactic surgery is the only curative option, which should be properly defined both in time and extent. Objectives: To identify and characterize prognostic factors associated with disease-free survival (DFS) in children from HMTC families. Design: We conducted a retrospective analysis of a multi-center cohort of 170 patients below age 21 at surgery. Demographic, clinical, genetic, biological data [basal and pentagastrine-stimulated calcitonin (CT and CT/Pg, respectively)], and tumor node metastasis (TNM) status were collected. DFS was assessed based on basal CT levels. Kaplan–Meier curves, Cox regression, and logistic regression models were used to determine factors associated with DFS and TNM staging. Results: No patients with a preoperative basal CT <31 ng/ml had persistent or recurrent disease. Medullary thyroid carcinoma defined by a diameter ≥10 mm [hazard ratio (HR): 6.0; 95% confidence interval (95% CI): 1.8–19.8] and N1 status (HR: 20.8; 95% CI: 3.9–109.8) were independently associated with DFS. Class D genotype [odds ratio (OR): 48.5, 95% CI: 10.6–225.1], preoperative basal CT >30 ng/liter (OR: 43.4, 95% CI: 5.2–359.8), and age >10 (OR: 5.5, 95% CI: 1.4–21.8) were associated with medullary thyroid carcinoma ≥10 mm. No patient with a preoperative basal CT <31 ng/ml had a N1 status. Class D genotype (OR: 48.6, 95% CI: 8.6–274.1), and age >10 (OR: 4.6, 95% CI: 1.1–19.0) were associated with N1 status. Conclusion: In HMTC patients, DFS is best predicted by TNM staging and preoperative basal CT level below 30 pg/ml. Basal CT, class D genotype, and age constitute key determinants to decide preoperatively timely surgery.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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