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World J Gastroenterol. Dec 14, 2012; 18(46): 6720-6728
Published online Dec 14, 2012. doi: 10.3748/wjg.v18.i46.6720
Modern treatment of gastric gastrointestinal stromal tumors
Kevin K Roggin, Mitchell C Posner
Kevin K Roggin, Mitchell C Posner, Department of Surgery, Pritzker School of Medicine, University of Chicago, IL 60637, United States
Author contributions: Roggin KK performed literature review and analyzed studies, and wrote the manuscript; Posner MC assisted with the analysis and edited the manuscript.
Correspondence to: Kevin K Roggin, MD, FACS, Associate Professor, Department of Surgery, Pritzker School of Medicine, University of Chicago, 5841 South Maryland Ave, MC 5094 G-216, Chicago, IL 60637, United States. kroggin@surgery.bsd.uchicago.edu
Telephone: +1-773-7954595 Fax: +1-773-7026120
Received: April 11, 2012
Revised: June 26, 2012
Accepted: June 28, 2012
Published online: December 14, 2012
Abstract

Gastrointestinal stromal tumors (GIST) are rare mesenchymal smooth muscle sarcomas that can arise anywhere within the gastrointestinal tract. Sporadic mutations within the tyrosine kinase receptors of the interstitial cells of Cajal have been identified as the key molecular step in GIST carcinogenesis. Although many patients are asymptomatic, the most common associated symptoms include: abdominal pain, dyspepsia, gastric outlet obstruction, and anorexia. Rarely, GIST can perforate causing life-threatening hemoperitoneum. Most are ultimately diagnosed on cross-sectional imaging studies (i.e., computed tomography and/or magnetic resonance imaging in combination with upper endoscopy. Endoscopic ultrasonographic localization of these tumors within the smooth muscle layer and acquisition of neoplastic spindle cells harboring mutations in the c-KIT gene is pathognomonic. Curative treatment requires a complete gross resection of the tumor. Both open and minimally invasive operations have been shown to reduce recurrence rates and improve long-term survival. While there is considerable debate over whether GIST can be benign neoplasms, we believe that all GIST have malignant potential, but vary in their propensity to recur after resection and metastasize to distant organ sites. Prognostic factors include location, size (i.e., > 5 cm), grade (> 5-10 mitoses per 50 high power fields and specific mutational events that are still being defined. Adjuvant therapy with tyrosine kinase inhibitors, such as imatinib mesylate, has been shown to reduce the risk of recurrence after one year of therapy. Treatment of locally-advanced or borderline resectable gastric GIST with neoadjuvant imatinib has been shown to induce regression in a minority of patients and stabilization in the majority of cases. This treatment strategy potentially reduces the need for more extensive surgical resections and increases the number of patients eligible for curative therapy. The modern surgical treatment of gastric GIST combines the novel use of targeted therapy and aggressive minimally invasive surgical procedures to provide effective treatment for this lethal, but rare gastrointestinal malignancy.

Keywords: Gastrointestinal stromal tumors, Laparoscopic resections of gastrointestinal stromal tumors, Imatinib mesylate, Gastrectomy