Abstract

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract. The majority of GISTs harbor gain of function mutations in either KIT or PDGFRα. Determination of the GIST molecular subtype upon diagnosis is important because this information informs therapeutic decisions in both the adjuvant and metastatic setting. The management of GIST was revolutionized by the introduction of imatinib, a KIT inhibitor, which has become the standard first line treatment for metastatic GIST. However, despite a clinical benefit rate of 80%, the majority of patients with GIST experience disease progression after 2–3 years of imatinib therapy. Second and third line options include sunitinib and regorafenib, respectively, and yield low response rates and limited clinical benefit. There have been recent FDA approvals for GIST including ripretinib in the fourth-line setting and avapritinib for PDGFRA exon 18-mutant GIST. This article aims to review the optimal treatment approach for the management of patients with advanced GIST. It examines the standard treatment options available but also explores the novel treatment approaches in the setting of imatinib refractory GIST.

Highlights

  • Gastrointestinal stromal tumor (GIST) is the most common soft tissue sarcoma subtype

  • GIST originates from the interstitial cells of cajal (ICCs), and it can arise from any part of the gastrointestinal tract, most commonly in the stomach (55.6%), followed by the small bowel (31.8%), colorectum (6%), other locations (5.5%) and the esophagus (0.7%) [1]

  • This review aims to discuss the management of advanced GIST focusing on the standard-of-care therapeutic options and novel therapeutics in clinical investigation

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Summary

Introduction

Gastrointestinal stromal tumor (GIST) is the most common soft tissue sarcoma subtype. The incidence of GIST is between 10 and 15 cases per million worldwide and ~ 5000 in the USA [1, 2]. The median age at diagnosis is 66–69 years, with equal distribution of men and women [1, 2]. GIST originates from the interstitial cells of cajal (ICCs), and it can arise from any part of the gastrointestinal tract, most commonly in the stomach (55.6%), followed by the small bowel (31.8%), colorectum (6%), other locations (5.5%) and the esophagus (0.7%) [1]. The diagnosis of GIST relies on the combination of the clinical scenario, the tumor’s anatomic location, the immunohistochemistry (IHC) patterns, as well as molecular features. The majority of GIST are immunohistochemically positive for KIT (CD117) and DOG-1

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