Gastrointestinal stromal tumor surgery: Difference between revisions

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{{Gastrointestinal stromal tumor}}
{{Gastrointestinal stromal tumor}}
==Overview==
==Overview==
 
The predominant therapy for gastrointestinal stromal tumor is surgical resection. Adjunctive chemotherapy/tyrosine Kinase Inhibitor therapy may be required.
==Surgical Therapy==
==Surgical Therapy==



Revision as of 15:34, 3 September 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Parminder Dhingra, M.D. [2]

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Overview

The predominant therapy for gastrointestinal stromal tumor is surgical resection. Adjunctive chemotherapy/tyrosine Kinase Inhibitor therapy may be required.

Surgical Therapy

Surgery is typically the initial therapy for the following types of patients:

  • Those with primary GIST who do not have evidence of metastasis
  • Those with tumors that are technically resectable if the risks of morbidity are acceptable

In the surgical treatment of GIST, the goal is complete gross resection with an intact pseudocapsule and negative microscopic margins. Because lymph node metastasis is rare with GIST, lymphadenectomy of clinically uninvolved nodes is not necessary.

  • Most small GISTs (<5 and especially <2 cm) with a low rate of mitosis (<5 dividing cells per 50 high-power fields) are benign and,after surgery, do not require adjuvant therapy.
  • Larger GISTs (>5 cm), and especially when the cell division rate is high (>6 mitoses/50 HPF), may disseminate and/or recur.
  • Until recently, GISTs were notorious for being resistant to chemotherapy, with a success rate of <5%. Recently, the c-kit tyrosine kinase inhibitor imatinib, a drug initially marketed for chronic myelogenous leukemia, was found to be useful in treating GISTs, leading to a 40-70% response rate in metastatic or inoperable cases.[1]

References

  1. "Gastrointestinal Stromal Tumors Treatment".


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