Prognostic Impact of Serum Calcitonin and Carcinoembryonic Antigen Doubling-Times in Patients with Medullary Thyroid Carcinoma
Jacques Barbet,
Loïc Campion,
Françoise Kraeber-Bodéré,
Jean-François Chatal and the GTE Study Group
Institut National de la Santé et de la Recherche Médicale, Unité 601 (J.B., F.K.-B., J.-F.C.), F-44000 Nantes, France; Université de Nantes (J.B., F.K.-B., J.-F.C.), F-44000 Nantes, France; and René Gauducheau Cancer Center (L.C.), F-44805 Nantes-St. Herblain, France
Address all correspondence and requests for reprints to: Jacques Barbet, Département de Recherche en Cancérologie, Institut National de la Santé et de la Recherche Médicale, Unité 601, Institut de Biologie, 9 quai Moncousu, 44093 Nantes cedex 1, France. E-mail: Jacques.Barbet{at}nantes.inserm.fr.
Context: After unsuccessful surgery, medullary thyroid carcinoma(MTC) may be fatal or remain stable for decades, and precisesurvival predictors are needed.
Objective: This study assesses the prognostic value of calcitoninand carcinoembryonic antigen (CEA) doubling-times (DT).
Design: This is a retrospective study on 65 MTC patients from2.929.5 yr after surgery.
Setting: Data registered in the database of the French NeuroendocrineTumor Group were analyzed anonymously.
Patients: All patients had abnormal calcitonin levels aftertotal thyroidectomy and bilateral lymph node dissection.
Intervention: Calcitonin and CEA serum levels were measuredduring routine disease follow-up.
Main Outcome Measure: To assess DT as prognostic factors, apatient population was extracted from the database.
Results: When calcitonin DT was less than 6 months, 5- and 10-yrsurvivals were three of 12 (25%) and one of 12 (8%), respectively;when between 6 months and 2 yr, 5- and 10-yr survivals were11 of 12 (92%) and three of eight (37%), whereas all 41 patientswith calcitonin DT greater than 2 yr were alive at the end ofthe study. Tumor-Node-Metastasis (TNM) stage, European Organizationfor Research and Treatment of Cancer (EORTC) score, and calcitoninDT were significant predictors of survival by univariate analysis,but only calcitonin DT remained an independent predictor ofsurvival by multivariate analysis (P = 0.002) with a proportionof variance explained (PVE) of 37.4%. Calcitonin DT was a betterpredictor than CEA (PVE 63.3% and 47.0%, respectively). CalcitoninDT calculated using only the first four measurements was alsoan independent predictor of survival (P < 0.000001; PVE 40.4%).
Conclusion: Calcitonin DT may be superior to initial clinicalstaging and among the most powerful prognostic indicators inMTC.
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