Hashimoto’s thyroiditis predicts outcome in intrathyroidal papillary thyroid cancer

Author:

Marotta Vincenzo1,Sciammarella Concetta2,Chiofalo Maria Grazia3,Gambardella Claudio4,Bellevicine Claudio5,Grasso Marica6,Conzo Giovanni4,Docimo Giovanni4,Botti Gerardo7,Losito Simona7,Troncone Giancarlo5,De Palma Maurizio8,Giacomelli Laura9,Pezzullo Luciano3,Colao Annamaria1,Faggiano Antongiulio3

Affiliation:

1. Department of Clinical Medicine and SurgeryFederico II University, Naples, Italy

2. IOS & COLEMAN SrlNaples, Italy

3. Thyroid and Parathyroid Surgery UnitIstituto Nazionale per lo Studio e la Cura dei Tumori-IRCCS ‘Fondazione G. Pascale’, Naples, Italy

4. Department of AnesthesiologicSurgical and Emergency Sciences, Division of General and Oncologic Surgery, University of Campania Luigi Vanvitelli, Naples, Italy

5. Department of Public HealthUniversity of Naples ‘Federico II,’, Naples, Italy

6. San Giovanni di Dio e Ruggi D’AragonaUniversitary Hospital, Division of General Surgery, University of Salerno, Salerno, Italy

7. Department of PathologyIstituto Nazionale per lo Studio e la Cura dei Tumori-IRCCS ‘Fondazione G. Pascale’, Naples, Italy

8. Dipartimento Chirurgico Generale e PolispecialisticoChirurgia 2, AORN Cardarelli, Naples, Italy

9. Dipartimento di Scienze ChirurgicheUniversità di Roma Sapienza, Roma, Italy

Abstract

Hashimoto’s thyroiditis (HT) seems to have favourable prognostic impact on papillary thyroid cancer (PTC), but data were obtained analysing all disease stages. Given that HT-related microenvironment involves solely the thyroid, we aimed to assess the relationship between HT, as detected through pathological assessment, and outcome in intrathyroidal PTC. This was a multicentre, retrospective, observational study including 301 PTC with no evidence of extrathyroidal disease. Primary study endpoint was the rate of clinical remission. Auxiliary endpoint was recurrence-free survival (RFS). HT was detected in 42.5% of the cohort and was associated to female gender, smaller tumour size, lower rate of aggressive PTC variants and less frequent post-surgery radio-iodine administration. HT showed relationship with significantly higher rate of clinical remission (P < 0.001, OR 4, 95% CI 1.78–8.94). PTCs with concomitant HT had significantly longer RFS, as compared with non-HT tumours (P = 0.004). After adjustment for other parameters affecting disease outcome at univariate analysis (age at diagnosis, histology, tumour size and multifocality), prognostic effect of HT remained significant (P = 0.006, OR 3.28, 95% CI 1.39–7.72). To verify whether HT could optimise the identification of PTCs with unfavourable outcome, we assessed the accuracy of ‘non-HT status’ as negative prognostic marker, demonstrating poor capability of identifying patients not maintaining clinical remission until final follow-up (probability of no clinical remission in PTCs without HT: 21.05%, 95% CI 15.20–27.93). In conclusion, our data show that HT represents an independent prognostic parameter in intrathyroidal PTC, but cannot improve prognostic specificity.

Publisher

Bioscientifica

Subject

Cancer Research,Endocrinology,Oncology,Endocrinology, Diabetes and Metabolism

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