Onkologie. 2007:1(2):61-65

Gastrointestinal stromal tumor: A new entity in oncology

Jozef Šufliarsky
Národný onkologický ústav, Bratislava

Gastrointestinal stromal tumours (GISTs) are the most common mesenchymal tumours of the digestive tract. The advent of targeted molecular therapy in the oncology setting has helped to transform the care of patients with these malignancies. Five years ago surgery has been the only effective treatment. Understanding of molecular pathophysiology of GIST led to the clinical development of imatinib for treating patients with this disease. Although imatinib is effective in most patients with advanced GIST, early or late resistance of tumours to imatinib is an increasing clinical problem. Number of new drugs have been tested for activity against imatinib-resistant disease. Notably, a phase III trial of sunitinib in patients with intolerance or progression on imatinib demonstrated significant improvements in progression-free and overall survival versus placebo.

Keywords: gastrointestinal stromal tumor, imatinib mesylate, sunitinib

Published: October 23, 2007  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Šufliarsky J. Gastrointestinal stromal tumor: A new entity in oncology. Onkologie. 2007;1(2):61-65.
Download citation

References

  1. Thomsen L, et al. Intersticial cells of Cajal generate a rhytmic pacemaker current. Nat Med 1998; 4: 848-851. Go to original source... Go to PubMed...
  2. Duensing A, et al. Mechanisms of oncogenic KIT signal transduction in primary gastrointestinal stromal tumors (GISTs). Oncogene 2004; 23: 3999-4006. Go to original source... Go to PubMed...
  3. Rossi F, et al. Oncogenic Kit signaling and therapeutic intervention in a mouse model of gastrointestinal stromal tumor. Proc Natl Acad Sci USA 2006; 103: 12843-8. Go to original source... Go to PubMed...
  4. Pidhorecky I, et al. Gastrointestinal stromal tumors: current diagnosis, biologic behavior, and management. Ann Surg Oncol 2000; 7: 705-712. Go to original source... Go to PubMed...
  5. DeMatteo RP, et al. Clinical management of gastrointestinal stromal tumors: before and after STI-571. Hum Pathol 2002; 33: 466-77. Go to original source... Go to PubMed...
  6. Fletcher CDM, et al. Diagnosis of gastrointestinal stromal tumors: a consensus approach. Hum Pathol 2002; 33: 459-65. Go to original source... Go to PubMed...
  7. Ng EH, et al. Prognostic factors influencing survival in gastrointestinal leiomyosarcomas: implications for surgical management and staging. Ann Surg 1992; 215: 68-77. Go to original source... Go to PubMed...
  8. Joensuu H, et al. Effect of the tyrosine kinase inhibitor STI571 in a patient with a metastatic gastrointestinal stromal tumor. N Engl J Med 2001; 344: 1052-6. Go to original source... Go to PubMed...
  9. van Oosterom AT, et al. Safety and efficacy of imatinib (STI571) in metastatic gastrointestinal stromal tumours: a phase I study. Lancet 2001; 358: 1421-3. Go to original source... Go to PubMed...
  10. von Mehren M, et al. High incidence of durable responses induced by imatinib mesylate (Gleevec) in patients with unresectable and metastatic gastrointestinal stromal tumors. Proc Am Soc Clin Oncol 2002; 21: 403a (abstract 1 608).
  11. Verweij, et al. Progression-free survival in gastrointestinal stromal tumors with high-dose imatinib: randomised trial. Lancet 2004; 364, 1127-34. Go to original source... Go to PubMed...
  12. Heinrich MC, et al. Molecular correlates of imatinib resistance in gastrointestinal stromal tumors. J Clin Oncol 2006; 24: 4764-74. Go to original source... Go to PubMed...
  13. Debiec-Rychter M, et al. Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants. Gastroenterology 2005; 128: 270-9. Go to original source... Go to PubMed...
  14. Wardelmann E, et al. Acquired resistance to imatinib in gastrointestinal stromal tumors caused by multiple KIT mutations. Lancet Oncol 2005; 6: 249-51. Go to original source... Go to PubMed...
  15. Fletcher JA, et al. KIT mutations in GIST. Curr Opin Genet Dev 2007; 17: 1-5. Go to original source... Go to PubMed...
  16. Bauer S, et al. Heat shock protein 90 inhibition in imatinib-resistant gastrointestinal stromal tumor. Cancer Res 2006; 66: 9153-61. Go to original source... Go to PubMed...
  17. Sambol EB, et al. Flavopiridol targets c-KIT transcription and induces apoptosis in gastrointestinal stromal tumor cells. Cances Res 2006; 66: 5858-66. Go to original source... Go to PubMed...
  18. Glabbeke MV, et al. Predicting toxicities for patients with advanced gastrointestinal stromal tumors treated with imatinib: A study of the European Organisation for Research and Treatment of Cancer, the Italian Sarcoma Group, and the Australasian GastroIntestinal Trials Group (EORTC-ISG-AGITG). Eur J Cancer 2006; 42, 2277-85. Go to original source... Go to PubMed...
  19. Lassau N, et al. Gastrointestinal stromal tumors treated with imatinib: monitoring response with contrast-enhanced sonography. Am J Roentgenol 2006; 187: 1267-73. Go to original source... Go to PubMed...
  20. Tarn C, et al. Therapeutic effect of imatinib in gastrointestinal stromal tumors: AKT signaling dependent and independent mechanisms. Cancer Res 2006; 66: 5477-86. Go to original source... Go to PubMed...
  21. Van den Abbeele, AD, et al. 18F-FDG-PET predicts response to imatinib mesylate (Gleevec) in patients with advanced gastrointestinal stromal tumors (GIST). Proc Am Soc Clin Oncol 2002; 21: 403a (abstract 1 610).




Oncology

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.