Recommendations for diagnostics and therapy of gastrointestinal stromal tumors (GIST) in 2010 Recommendations

Main Article Content

Piotr Rutkowski
Jan Kulig
Maciej Krzakowski
Czesław Osuch
Janusz A. Siedlecki
Anna Nasierowska-Guttmejer
Jacek Sygut
Janusz Limon
Arkadiusz Jeziorski
Urszula Grzesiakowska
Konrad Ptaszyński
Janusz Słuszniak
Wojciech Polkowski
Elżbieta Starosławska
Marcin Polkowski
Marek Bębenek
Maciej Matłok
Katarzyna Urbańczyk
Włodzimierz Olszewski
Stanisław Głuszek
Zbigniew I. Nowecki

Abstract

Gastrointestinal stromal tumors (GIST) are the most common mesenchymal tumors of gastrointestinal tract. Advances in the understanding of the molecular mechanisms of GIST pathogenesis have resulted for last years in the emerging of GIST as a distinct sarcoma entity. The paper describes guidelines for diagnostics and therapy of these tumors based on scientific basis and experts’ experience, which are commonly accepted and worth to recommend. Overexpression of KIT receptor, as a consequence of mutation of protooncogene KIT, is highly specific for GIST and enable for detection by immunohistochemistry staining (CD117) in tumor specimens. It is the most important criterion in microscopic diagnostics and indications for treatment with small-molecule tyrosine kinas inhibitors. Sending material for molecular analysis is strongly recommended (for KIT and PDGFRA genotyping). Radical surgery is still the mainstay treatment for primary, localized, resectable GISTs, although high percentages of the patients after potentially curative operations develop recurrent or metastatic disease. In inoperable/metastatic lesions the treatment of choice is tyrosine kinase inhibitor – imatynib mesylate – the first effective systemic therapy in advanced CD117(+) GIST. Recommended initial dose should be 400 mg daily (800 mg for exon 9 KIT mutants). Monitoring of the therapy should be based on serial computed tomography imaging of abdominal cavity with the assessment of changes of tumor size and density. In case of disease progression the increase of imatynib dose to 800 mg daily is recommended and if further progression exists – sunitinib in the initial dose 50 mg daily should be introduced. Clinical trials evaluating the role of surgery in combination of imatynib and the efficacy of other molecular targeted drugs in resistant cases are ongoing. Existing data indicate beneficial role of adjuvant imatynib therapy in terms of relapse-free survival, especially in group of patients with significant risk of relapse.. Presented recommendations for diagnostics and therapy of GIST should be practically implemented by physicians involved in management of GIST patients in Poland. The including GIST cases in national Clinical Registry (http://gist.coi.waw.pl) and standard treatment of patients in multidisciplinary team with expertise in GIST therapy, as well as enrollment of new cases to prospective clinical trials, are recommended.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Article Details

How to Cite
1.
Rutkowski P, Kulig J, Krzakowski M, Osuch C, Siedlecki JA, Nasierowska-Guttmejer A, Sygut J, Limon J, Jeziorski A, Grzesiakowska U, Ptaszyński K, Słuszniak J, Polkowski W, Starosławska E, Polkowski M, Bębenek M, Matłok M, Urbańczyk K, Olszewski W, Głuszek S, Nowecki ZI. Recommendations for diagnostics and therapy of gastrointestinal stromal tumors (GIST) in 2010. OncoReview [Internet]. 2011Feb.28 [cited 2024Jul.23];1(1(1):8-20. Available from: https://journalsmededu.pl/index.php/OncoReview/article/view/151
Section
Articles

References

1. Miettinen M., Lasota J.: Gastrointestinal stromal tumors – definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis. Virchows Arch. 2001; 438: 1-12.
2. Fletcher C.D.M., Berman J.J., Corless C. et al.: Diagnosis of gastrointestinal stromal tumors: a consensus approach. Human Pathology 2002; 33: 459-465.
3. Kindblom L.G., Remotti H.E., Aldenborg F., Meis-Kinblom J.M.: Gastrointestinal pacemaker cell tumor (GIPACT): gastrointestinal stromal tumors show phenotypic characteristic of the interstitial cell of Cajal. Am. J. Pathol. 1998; 152: 1259-69.
4. Casali P.G., Jost L., Reichardt P., Schlemmer M., Blay J.Y.: Gastrointestinal stromal tumors: ESMO clinical Recommendations for diagnosis, treatment and follow-up. Ann. Oncol. 2009; 20(Suppl 4): 64-7.
5. Demetri G.D., von Mehren M., Blanke C.D. et al.: Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors. N. Engl. J. Med. 2002; 347: 472-480.
6. Nilsson B., Bumming P., Meis-Kindblom J.M., Oden A., Dortok A., Gustavsson B., Sablinska K., Kindblom L.G.: Gastrointestinal stromal tumors: the incidence, prevalence, clinical course, and prognostication in preimatinib mesylate era. Cancer 2005; 103: 821-829.
7. Ruka W., Rutkowski P., Nowecki Z. et al.: Przeżycia chorych na rozsiany i nieoperacyjny GIST leczonych imatinibem – analiza etapowa Klinicznego Rejestru GIST. Nowotwory – Journal of Oncology 2005, 55: 195-199.
8. Miettinen M., Lasota J.: Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis. Arch. Pathol. Lab. Med. 2006; 130(10): 1466-1478.
9. Urbańczyk K., Limon J., Korobowicz E., Chosia M., Sygut J., Karcz D., Iwanik K., Osuch J., Lasota J., Stachura J.: Gastrointestinal stromal tumors: a multicenter experience. Pol. J. Pathol. 2005; 56: 51-61.
10. Nowecki Z.I., Rutkowski P., Lindner B., Michej W., Ruka W.: Nowotwory podścieliskowe przewodu pokarmowego (GIST, gastrointestinal stromal tumor) umiejscowione w jelicie cienkim i rozpoznawane przedoperacyjnie jako nowotwory narządu rodnego. Gin. Pol. 2005; 76: 855-862.
11. Debiec-Rychter M., Dumez H., Judson I. et al.: Use of c-KIT/PDGFRA mutational analysis to predict the clinical response to imatinib in patients with advanced gastrointestinal stromal tumours entered on phase I and II studies of the EORTC Soft Tissue and Bone Sarcoma Group. Eur. J. Cancer 2004; 40: 689-95.
12. Heinrich M.C., Corless C.L., Demetri G.D. et al.: Kinase mutations and imatinib response in patients with metastatic gastrointestinal stromal tumor. J. Clin. Oncol. 2003; 21: 4342-49.
13. Wozniak A., Floris G., Debiec-Rychter M., Sciot R., Schoffski P.: Implications of mutational analysis fort he management of patients with gastrointestinal stromal tumors and the application of targeted therapies. Cancer Invest 2010. https://doi.org/10.3109/07357907.2010.494322.
14. Debiec-Rychter M., Sciot R., Le Cesne A. et al.: KIT mutations and dose selection for imatinib in patients with advanced gastrointestinal stromal tumours. Eur. J. Cancer 2006; 42: 1093-103.
15. DeMatteo R.P., Lewis J.J., Leung D. et al.: Two hundred gastrointestinal stromal tumors. Recurrence patterns and prognostic factors for survival. Ann. Surg. 2000; 231: 51-58.
16. Trent J.C., Benjamin R.S.: New developments in gastrointestinal stromal tumor. Curr. Opin. Oncol. 2006; 18: 386-395.
17. Rutkowski P., Nowecki Z.I., Michej W., Dębiec-Rychter M., Woźniak A., Limon J., Siedlecki J.A., Grzesiakowska U., Kąkol M., Osuch C., Polkowski M., Głuszek S., Żurawski Z., Ruka W.: Risk criteria and prognostic factors for predicting recurrences after resection of primary gastrointestinal stromal tumors (GISTs). Ann. Surg. Oncol. 2007; 14: 2018-27.
18. Hohenberger P., Eisenberg B.: Role of surgery combined with kinase inhibition in management of gastrointestinal stromal tumor (GIST). Ann. Surg. Oncol. 2010. https://doi.org/10.1245/s10434-010-1053-9.
19. DeMatteo R., Ballman K.V., Antonescu C.R. et al.: Adjuvant imatinib mesylate after resection of localised, primary gastrointestinal stromal tumour: a randomised, double-blind, placebo-controlled trial. Lancet 2009; 373: 1079-104.
20. Verweij J., Casali P.G., Zalcberg J. et al.: Progression-free survival in gastrointestinal stromal tumours with high-dose imatinib: randomised trial. Lancet 2004; 364: 1127-34.
21. Blanke C.D., Demetri G.D., von Mehren M. et al.: Long-term results from a randomized phase II trial of standard- versus higher-dose imatinib mesylate for patients with unresectable or metastatic gastrointestinal stromal tumors expressing KIT. J. Clin. Oncol. 2008; 26: 620-25.
22. Blanke C.D., Rankin C., Demetri G.D. et al.: Phase III randomized, intergroup trial assessing imatinib mesylate at two dose levels in patients with unresectable or metastatic gastrointestinal stromal tumors expressing the kit receptor tyrosine kinase: S0033. J. Clin. Oncol. 2008; 26: 626-32.
23. Rutkowski P., Nowecki Z.I., Dębiec-Rychter M. et al.: Predictive factors for long term effects of imatinib therapy in patients with inoperable/metastatic CD117(+) gastrointestinal stromal tumors (GISTs). J. Can. Res. Clin. Oncol. 2007; 133: 589-97.
24. Gastrointestinal Stromal Tumor Meta-Analysis Group (MetaGIST). Comparison of two doses of imatinib for the treatment of unresectable or metastatic gastrointestinal stromal tumors: a meta-analysis of 1640 patients. J. Clin. Oncol. 2010; 28: 1247-53.
25. Therasse P., Arbuck S.G., Eisenhauer E.A. et al.: New guidelines to evaluate the response to treatment in solid tumors. J. Natl. Cancer Inst. 2000; 92: 205-16.
26. Choi H., Charnsangavej C., de Castro Faria S., Tamm E.P., Benjamin R.S., Johnson M.M., Macapinlac H.A., Podoloff D.A.: CT evaluation of the response of gastrointestinal stromal tumors after imatinib mesylate treatment: a quantitative analysis correlated with FDG PET findings. Am. J. Roentgenol. 2004; 183: 1619-28.
27. Zalcberg J.R., Verweij J., Casali P.G. et al.: Outcome of patients with advanced gastro-intestinal stromal tumours crossing over to a daily imatinib dose of 800 mg after progression on 400 mg. Eur. J. Cancer 2005; 41: 1751-1757.
28. Van Glabbeke M., Verweij J., Casali P.G. et al.: Initial and late resistance to imatinib in advanced gastrointestinal stromal tumors are predicted by different prognostic factors: a European Organisation for Research and Treatment of Cancer-Italian Sarcoma Group-Australasian Gastrointestinal Trials Group study. J. Clin. Oncol. 2005; 23: 5795-804.
29. Heinrich M.C., Corless C.L., Blanke D.C., Demetri G.D. et al.: Molecular correlates of imatinib resistance in gastrointestinal stromal tumors. J. Clin. Oncol. 2006; 29: 4764-74.
30. Demetri G.D., van Oosterom A.T., Garrett C.R. et al.: Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomized controlled trial. Lancet 2006; 368: 1329-38.
31. Reichardt P., Kang Y.K., Ruka W. et al.: Subpopulation analyses in a worldwide treatment-use trial of sunitinib (SU) in GIST patients (pts) with resistance or intolerance to prior imatinib (IM) therapy. J. Clin. Oncol. 2007; 25 (18S): Abs 10022.
32. Heinrich M.C., Maki R.G., Corless C.L. et al.: Primary and secondary kinase genotypes correlate with the biological and clinical activity of sunitynib in imatinib-resistant gastrointestinal stromal tumor. J. Clin. Oncol. 2008; 26: 5352-59.
33. George S., Blay J.Y., Casali P.G. et al.: Clinical evaluation of continuous daily dosing of sunitinib malate in patients with advanced gastrointestinal stromal tumour after imatinib failure. Eur. J. Cancer 2009; 45: 1959-68.
34. Rutkowski P., Nowecki Z.I., Nyckowski P., Dziewirski W., Grzesiakowska U., Nasierowska-Guttmejer A., Krawczyk M., Ruka W.: Surgical treatment of patients with initially inoperable and/or metastatic gastrointestinal stromal tumors (GIST) during therapy with imatinib mesylate. J. Surg. Oncol. 2006; 4: 304-11.
35. Raut C.P., Posner M., Desai J., Morgan J.A., George S., Zahrieh D., Fletcher C.D., Demetri G.D., Bertagnolli M.M.: Surgical management of advanced gastrointestinal stromal tumors after treatment with targeted systemic therapy using kinase inhibitors. J. Clin. Oncol. 2006; 24: 2325-31.
36. Mussi C., Ronellenfitsch U., Jakob J., Tamborini E., Reichardt P., Casali P.G., Fiore M., Hohenberger P., Gronchi A.: Post-imatinib surgery in advanced/metastatic GIST: is it worthwhile in all patients? Ann. Oncol. 2010; 21: 403-8.
37. Reichardt P., Blay J.Y., von Mehren M.: Towards global consensus in the treatment of gastrointestinal stromal tumor. Expert Rev. Anticancer Ther. 2010; 10: 221-32.