Unsolved Issues in Thymic Epithelial Tumour Stage Classification: The Role of Tumour Dimension

Author:

Sassorossi Carolina12,Bertoglio Pietro34ORCID,Lococo Filippo12ORCID,Santoro Gloria5,Meacci Elisa12ORCID,Nachira Dania12ORCID,Congedo Maria Teresa12ORCID,Brandolini Jury3,Petroncini Matteo3,Nocera Adriana12ORCID,Charles-Davies Diepriye6,Solli Piergiorgio3,Margaritora Stefano12,Chiappetta Marco12ORCID

Affiliation:

1. UOC di Chirurgia Toracica, Università Cattolica del Sacro Cuore, 00168 Rome, Italy

2. UOC di Chirurgia Toracica, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy

3. Divisione di Chirurgia Toracica IRCCS Azienda Ospedaliera Universitaria Bologna, 40138 Bologna, Italy

4. Chirurgia Toracica, Alma Mater Studiorum, Università di Bologna, 40126 Bologna, Italy

5. UOC di Chirurgia Generale, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy

6. Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Agostino Gemelli, 00168 Roma, Italy

Abstract

According to the different classifications now in use, thymic tumours are staged by the extent of local invasiveness, and tumour size is not included as a major determinant for the T category. The aim of this double-site retrospective study is to analyse the correlation between tumour dimension and overall survival (OS) in patients who underwent surgical treatment. From January 2000 to December 2020, patients with thymic epithelial tumours who underwent surgical resection were included in this study. Data from a total of 332 patients were analysed. Five- and ten-year overall survival (5–10 YOS) was 89.26% and 87.08%, respectively, while five- and ten-year disease-free survival (DFS) was 88.12% and 84.2%, respectively. Univariate analysis showed a significant correlation between male sex (p-value 0.02), older age (p-value < 0.01), absence of myasthenia gravis (p-value < 0.01), increase in pTNM (pathological Tumor Node Metastasis) (p-value 0.03) and increase in the number of infiltrated organs (p-value 0.02) with an increase in tumour dimension. Tumour dimension alone was not effective in the prediction of DFS and OS, both when considered as a continuous variable and when considered with a cut-off of 3 and 5 cm. However, with multivariate analysis, it was effective in predicting OS in the aforementioned conditions (p-value < 0.01). Moreover, multivariate analysis was also used in the thymoma and Masaoka I subgroups. In our experience, the role of tumour dimension as a descriptor of the T parameter of the TNM (Tumor Node Metastasis) staging system seemed to be useful in improving this system.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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