Role of visceral pleural invasion and tumor sizing at CT of resected NSCLC in clinical-radiological and pathological T agreement

Author:

Colombi Davide1ORCID,Petrini Marcello1,Rapacioli Fausto1,Bodini Flavio C.1,Chiesa Sara2,Franco Cosimo2,Citterio Chiara3,Cavanna Luigi3,Zangrandi Adriano4,Sverzellati Nicola5,Michieletti Emanuele1

Affiliation:

1. Department of Radiological Functions, Radiology Unit, “Guglielmo da Saliceto” Hospital, Piacenza, Italy

2. Emergency Department, Pneumology Unit, “Guglielmo da Saliceto” Hospital, Piacenza, Italy

3. Department of Oncology-Hematology, Oncology Unit, “Guglielmo da Saliceto” Hospital, Piacenza, Italy

4. Department of Oncology-Hematology, Pathology Unit, “Guglielmo da Saliceto” Hospital, Piacenza, Italy

5. Department of Medicine and Surgery (DiMeC), Radiological Sciences, University of Parma, Parma, Italy

Abstract

Objective: To describe in non-small cell lung cancer (NSCLC) the impact of visceral pleural invasion (VPI) and of tumor sizing assessed at computed tomography (CT) on the agreement between clinical-radiological and pathological T staging and its prognostic value. Methods: Patients affected by NSCLC treated by surgery in the period from January 2017 to September 2020 were retrospectively evaluated. Exclusion criteria were: (1) baseline CT not performed in our hospital; (2) failure of software segmentation at CT of the primary lesion. Clinical-radiological T (cT) was assessed at baseline CT, evaluating in particular T size by semi-automatic tool and VPI (cVPI) visually. Pathological T (pT) and VPI (pVPI) were recorded by pathological report and obtained after formalin-fixation and eventual elastic stain on surgical specimen. The agreement between cT and pT was evaluated by calculating the weighted kappa by Cohen (κw); the association between progression free survival (PFS) with both cT and pT was assessed by the Cox regression analysis. Results: The study included 84 NSCLC in 82 patients (median age 71 years, IQR 63-76 years; females 22/82, 27%). The agreement between cT and pT was poor (κw 0.302, 95%CI 0.158-0.447). The main causes of disagreement were CT oversizing (21%) and false positive cVPI (29%). A significant association was found between PFS and pT2-T3 (HR 2.75, 95%CI 1.21-6.25, p=0.015) but not with cT2-T3 (not retained in the model). Conclusions: False positive cVPI and oversizing at CT are causes of disagreement between cT and pT in around one-third of resected NSCLC. PFS was significantly associated with pT but not with cT.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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