Abstract

BackgroundAlthough the majority of solitary fibrous tumors of the pleura (SFTP) follow a benign course, 10–25% of patients suffer from recurrence or metastatic disease. Several scoring models have been proposed to predict the outcome. However, none of these included immunohistochemical (IHC) markers as possible prognosticators.MethodsIn this multicenter study, we collected clinical data and formalin-fixed and paraffin-embedded (FFPE) tissue blocks of patients with histologically proven SFTP which had been surgically resected between 2000 und 2015. After systematic and extensive IHC staining on tissue microarrays, the results were analyzed and compared to histomorphological and clinical data for their possible prognostic value.ResultsIn total, 78 patients (mean age 61 ± 11 years) were included. Of these, 9 patients (11%) had an adverse outcome including SFTP recurrence (n = 6) or SFTP-related death (n = 3). Mean overall survival was 172 ± 13 months. 1 and 10-year event-free survival rates were 99% and 93%. In the multivariable analysis only MIB-1 proliferation index (Ki-67) ≥10% (HR 12.3, CI 1.1–139.5, p = 0.043), ≥4 mitoses per 10 high power fields (HR 36.5, CI 1.2–1103.7, p = 0.039) and tumor size larger than 10 cm (HR 81.8, CI 1.7–4016.8, p = 0.027) were independently associated with adverse outcome.ConclusionA high proliferation rate by MIB-1 IHC was associated with impaired outcome. Upon this, we established a new score using mitosis, necrosis, size of the tumor and MIB-1, which performed better than the traditional scores in our data set. This prognostic score could help to better evaluate outcome of SFTP, but requires external validation.

Highlights

  • The majority of solitary fibrous tumors of the pleura (SFTP) follow a benign course, 10–25% of patients suffer from recurrence or metastatic disease

  • From the variables included in the criteria proposed by England et al, [16] only tumor size greater than 10 cm, nuclear pleomorphism and increased mitotic activity were significantly associated with an adverse outcome in univariable analysis

  • In the multivariable analysis, only two of these features remained significant. This finding was already confirmed by other studies demonstrating that only mitotic count and tumor size were associated with impaired outcome [20, 21]

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Summary

Introduction

The majority of solitary fibrous tumors of the pleura (SFTP) follow a benign course, 10–25% of patients suffer from recurrence or metastatic disease. Solitary fibrous tumors of the pleura (SFTP) are rare neoplasms of the chest cavity with an estimated incidence of 2.8 new cases/100,000 individuals/year [1, 2]. They are responsible for less than 5 % of all tumors arising from the pleura, but have been reported to occur in other anatomical locations [3,4,5]. A variety of other names were used, which made it difficult to classify them into one entity [7] They typically show alternate areas with varying hypercellularity.

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