Abstract

Symptomatic gastrointestinal stromal tumours (GIST) are infrequent with an incidence of 12.7 per million inhabitants in the western population. We studied whether the incidence of GIST has further increased between 2003 and 2012 and assessed the frequency of mutations, risk groups, histological subtypes and immunohistochemistry results. From PALGA, the nationwide Dutch Pathology Registry, pathology excerpts from all patients with a GIST or GIST-like tumour between 2003 and 2012 were retrieved to calculate incidence rates. Full pathology reports were retrieved of resections in 2011 and 2012 to study the frequency of mutations, risk groups, histological subtypes and immunohistochemistry results. The incidence of GIST increased to 17.7 per million inhabitants in 2012 with a median age of 67 years. Mutational analysis was performed in 33.9% of patients with a resection between 2011 and 2012 (KIT mutation 67.5%, PDGFRA 16.3%, wild-type 11.4%). The percentage of high risk patients in the different risk classifications varied from 19.9% to 38.0% depending on the used classification. Only 35.9% of patients had diagnosis or revision of pathology diagnosis within three months in a designated GIST referral centre. No increase in proportion of central pathology reviews was found. Proportion of patients with mutational analysis increased over the years. The registered incidence of GIST, 17.7 per million inhabitants in 2012 in the Netherlands, is still rising. Despite incorporation in the ESMO GIST guidelines since 2008 for mutational testing and since 2010 for central review of pathology, both are performed in a minority of patients.

Highlights

  • The most common mesenchymal tumours of the gastrointestinal tract are the gastrointestinal stromal tumours (GISTs) [1].For the members of the PALGA group see below Electronic supplementary material The online version of this article contains supplementary material, which is available to authorized users.Clinical behaviour is predicted by primary localisation, tumour size, mitotic index and tumour rupture [2]

  • Because not all questions could be answered with the information in the excerpts, full pathology reports were retrieved for all patients with a primary resection for a GIST in 2011 or 2012

  • 2456 patients were included for incidence analysis and 489 patients were included for full pathology report analysis

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Summary

Introduction

The most common mesenchymal tumours of the gastrointestinal tract are the gastrointestinal stromal tumours (GISTs) [1]. Clinical behaviour is predicted by primary localisation, tumour size, mitotic index and tumour rupture [2]. The differential diagnosis contains gastrointestinal leiomyoma and leiomyosarcomas, desmoid-type fibromatosis and schwannoma [3]. The estimated incidence of GIST in the Netherlands was 12.7 per million inhabitants in 2003 [4]. Studies in other countries report incidences between 7.8 and 21.1/million [5,6,7,8,9,10]. Most studies were non-nationwide, doctor-driven cancer registry studies [11]

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