Yonsei Med J.  2009 Jun;50(3):437-440. 10.3349/ymj.2009.50.3.437.

Long-Surviving Patients with Recurrent GIST after Receiving Cytoreductive Surgery with Imatinib Therapy

Affiliations
  • 1Department of Surgery, Yonsei University College of Medicine, Seoul, Korea. choish@yuhs.ac
  • 2Department of Radiology, Yonsei University College of Medicine, Seoul, Korea.
  • 3Department of Pathology, Yonsei University College of Medicine, Seoul, Korea.

Abstract

In the treatment of recurrent or metastatic gastrointestinal stromal tumors (GIST), good prognoses may not be expected by surgery alone. Recently, imatinib has been applied for the treatment of GISTs, resulting in improved patient survival. However, long-term success is limited due to the development of resistance. Herein, we report two cases of long-surviving patients with recurrent GIST after receiving cytoreductive surgery with imatinib therapy. A 49 year-old man was diagnosed to a duodenal GIST with single hepatic metastasis, and an antrectomy including the duodenal lesion with intraoperative radiofrequency ablation were performed in April, 2002. After four months, a new metastatic hepatic lesion was identified. Percutaneous radiofrequency ablation was done, and imatinib therapy was started. A 56 year-old man underwent laparoscopic segmental resection of the distal ileum and partial excision of parietal peritoneum in March, 2001 to treat a malignant GIST of the distal ileum that was attached to parietal peritoneum. After six months, recurrence of GIST with peritoneal seeding and hepatic metastasis was found, and he underwent cytoreductive surgery including right hemicolectomy and wedge resection of liver. After surgery, there was no residual tumor grossly and imatinib therapy was started. In both cases, they were doing well with no evidence of recurrence for 5 years with imatinib therapy. Therefore, in patients with a recurrent GIST, improved survival can be expected with imatinib therapy after cytoreductive surgery.

Keyword

Gastrointestinal stromal tumors; recurrence; cytoreductive surgery; Imatinib

MeSH Terms

Gastrointestinal Stromal Tumors/*drug therapy/*surgery
Humans
Male
Middle Aged
Piperazines/*therapeutic use
Protein Kinase Inhibitors/*therapeutic use
Pyrimidines/*therapeutic use
Treatment Outcome

Figure

  • Fig. 1 Post-contrast CT. About a 1.3 cm round focal lesion with low attenuation density (arrow) showing a target-like appearance of mild contrast enhancement with centrally non-enhancing necrotic area in the right lobe of the liver suggests a single hepatic metastasis.

  • Fig. 2 The histologic picture of duodenal tumor shows the bundles of spindle cells (hematoxylin and eosin staining).

  • Fig. 3 Four-month follow-up CT shows a newly developed metastasis (arrow) in the posterior segment of right lobe of the liver.

  • Fig. 4 Post-contrast CT. About 3 cm low attenuation density lesion (arrowheads) in left lobe of the liver suggests a metastatic malignancy.

  • Fig. 5 The mesenteric tumors are composed of spindle cells (hematoxylin and eosin staining).

  • Fig. 6 Immunohistochemically, the cytoplasm of tumor cells tests diffusely positive for c-kit.


Cited by  1 articles

Successful Resection of Locally Advanced Gastrointestinal Stromal Tumor of the Ampulla of Vater after Treatment with Imatinib
Jeung Eun Park, Seok-Ho Dong, Kun Hyung Cho, Jae Young Jang, Hyo-Jong Kim, Byung-Ho Kim, Young Woon Chang, Rin Chang
Korean J Gastroenterol. 2010;56(1):39-44.    doi: 10.4166/kjg.2010.56.1.39.


Reference

1. Gold JS, Dematteo RP. combined surgical and molecular therapy: the gastrointestinal stromal tumor model. Ann Surg. 2006. 244:176–184.
2. Miettinen M, Lasota J. Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis. Arch Pathol Lab Med. 2006. 130:1466–1478.
3. van Oosterom AT, Judson IR, Verweij J, Stroobants S, Dumez H, Donato di Paola E, et al. Update of phase I study of imatinib (STI571) in advanced soft tissue sarcomas and gastrointestinal stromal tumors: a report of the EORTC Soft Tissue and Bone Sarcoma Group. Eur J Cancer. 2002. 38:S83–S87.
Article
4. Blanke CD, Rankin C, Demetri GD, Ryan CW, von Mehren M, Benjamin RS, 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. 26:626–632.
Article
5. Verweij J, Casali PG, Zalcberg J, LeCesne A, Reichardt P, Blay JY, et al. Progression-free survival in gastrointestinal stromal tumours with high-dose imatinib: randomised trial. Lancet. 2004. 364:1127–1134.
Article
6. Blanke CD, Demetri GD, von Mehren M, Heinrich MC, Eisenberg B, Fletcher JA, 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. 26:620–625.
7. Ballarini C, Intra M, Ceretti AP, Prestipino F, Bianchi FM, Sparacio F, et al. Gastrointestinal stromal tumors: a "benign" tumor with hepatic metastasis after 11 years. Tumori. 1998. 84:78–81.
Article
8. Miettinen M, El-Rifai W, H L Sobin L, Lasota J. Evaluation of malignancy and prognosis of gastrointestinal stromal tumors: a review. Hum Pathol. 2002. 33:478–483.
9. Tamborini E, Bonadiman L, Greco A, Albertini V, Negri T, Gronchi A, et al. A new mutation in the KIT ATP pocket causes acquired resistance to imatinib in a gastrointestinal stromal tumor patient. Gastroenterology. 2004. 127:294–299.
Article
10. Chen LL, Sabripour M, Andtbacka RH, Petel SR, Feig BW, Macapinlac HA, et al. Imatinib resistance in gastrointestinal stromal tumors. Curr Oncol Rep. 2005. 7:293–299.
Article
11. Debiec-Rychter M, Cools J, Dumez H, Sciot R, Stul M, Mentens N, et al. Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants. Gastroenterology. 2005. 128:270–279.
Article
12. Nilsson B, Bümming P, Meis-Kindblom JM, Odén A, Dortok A, Gustavsson B, et al. Gastrointestinal stromal tumors: the incidence, prevalence, clinical course, and prognostication in the preimatinib mesylate era--a population-based study in western Sweden. Cancer. 2005. 103:821–829.
Article
13. Tryggvason G, Gislason HG, Magnússon MK, Jónasson JG. Gastrointestinal stromal tumors in Iceland, 1990-2003: the icelandic GIST study, a population-based incidence and pathologic risk stratification study. Int J Cancer. 2005. 117:289–293.
Article
14. Morabito A, De Maio E, Di Maio M, Normanno N, Perrone F. Tyrosine kinase inhibitors of vascular endothelial growth factor receptors in clinical trials: current status and future directions. Oncologist. 2006. 11:753–764.
Article
15. Demetri GD, von Mehren M, Blanke CD, Van den Abbeele AD, Eisenberg B, Roberts PJ, et al. Efficacy and Safety of imatinib mesylate in advanced gastrointestinal stromal tumors. N Engl J Med. 2002. 347:472–480.
Article
16. Haller F, Detken S, Schulten HJ, Happel N, Gunawan B, Kuhlgatz J, et al. Surgical management after neoadjuvant imatinib therapy in gastrointestinal stromal tumours (GISTs) with respect to imatinib resistance caused by secondary KIT mutations. Ann Surg Oncol. 2007. 14:526–532.
Article
17. DeMatteo RP, Lewis JJ, Leung D, Mudan SS, Woodruff JM, Brennan MF. Two hundred gastrointestinal stromal tumors: recurrence patterns and prognostic factors for survival. Ann Surg. 2000. 231:51–58.
Full Text Links
  • YMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr