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Gastrointestinal Stromal Tumors

Gastrointestinal Stromal Tumors. Definition of Gastrointestinal Stromal Tumor . the most common mesenchymal malignancy of (GI) tract the diagnostic criteria for GIST remained controversial and somewhat confusing. Pathology Terms that Encompass the Spectrum of Gastrointestinal Stromal Tumors.

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Gastrointestinal Stromal Tumors

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  1. Gastrointestinal Stromal Tumors

  2. Definition of Gastrointestinal Stromal Tumor • the most common mesenchymal malignancy of (GI) tract • the diagnostic criteria for GIST remained controversial and somewhat confusing

  3. Pathology Terms that Encompass the Spectrum of Gastrointestinal Stromal Tumors • Gastrointestinal stromal tumor • Leiomyoblastoma • Gastrointestinal leiomyosarcoma • Gastrointestinal autonomic nerve tumor • Gastrointestinal pacemaker cell tumor • Plexosarcoma • Gastrointestinal neurofibrosarcoma

  4. KIT expression is noted in the vast majority (more than 95%) of GISTs, • KIT is not expressed by other smooth muscle tumors of the GI tract nor by other stromal tumors outside of the GI tract • The origin of the neoplastic cells of GIST remains a matter of active investigation

  5. the KIT protein serves as a transmembrane RTK; the CD117 antigen can be detected by immunohistochemical staining as a marker for the presence of the KIT protein

  6. Clinical Considerations • adults at a median age of 58 years • higher in men • (60% to 70%) stomach, (20% to 30%) small intestine, and fewer than 10% in the esophagus, colon, and rectum. GISTs can also occur in extraintestinal abdominopelvic sites such as the omentum, mesentery, or retroperitoneum.

  7. abdominal pain • abdominal mass, • nausea, vomiting, • anorexia • weight loss. • acute hemorrhage

  8. The vast majority of GIST metastases at presentation are intra-abdominal, either to the liver, omentum, or peritoneal cavity. • Metastatic spread to lymph nodes or to extra-abdominal sites via lymphatics is very rare

  9. Diagnostic Evaluation • CT • MRI • upper GI endoscopy • Ultrasonographically enhanced endoscopy

  10. an epithelioid (larger, rounder cells) or spindle cell histology. • expert pathologists can define a rare subset (fewer than 5%) of GISTs that fail to express CD117, and these are most likely to be driven by an alternative kinase such as PDGFRA • There are no definitive diagnostic criteria of CD117-GIST unless the tumor genotype analysis indicates a KIT or PDGFRA mutation characteristic of GIST

  11. DDX • soft tissue sarcomas Ewing's sarcoma and angiosarcoma • small cell lung cancers, • melanomas • desmoid tumors • seminomas, • ovarian carcinomas, • mastocytomas, • neuroblastomas, • adenoid cystic carcinomas, • subsets of lymphoma and acute myeloid leukemia.

  12. some contribution to prognosis • Other factors, such as the specific histologic subtype (epithelioid vs. spindle cell), the degree of cellular pleomorphism, and patient age, • Recurrence and survival rates have been reported to correlate with the location of the primary GIST lesion, with small bowel tumors showing a somewhat worse prognosis

  13. Diagnostic Imaging • PET FDG-PET imaging can detect lesions at least 1 cm • CT • MRI

  14. Management of Metastatic, Unresectable, or Recurrent Gastrointestinal Stromal Tumor • Cht: P-glycoprotein (the product of the multidrug resistance-1 [MDR-1] gene) and the multidrug resistance protein-1 MRP1 • RT:bleeding ,pain

  15. First Molecularly Targeted Kinase Inhibitor Therapy for Gastrointestinal Stromal Tumor: Imatinib Mesylate • FDA approved the use of imatinib for the treatment of metastatic or unresectable GIST • objective responses • control of symptoms • prolonging the survival

  16. FDA approval of imatinib for dermatofibrosarcoma protuberans

  17. toxicities • nausea, vomiting, and severe edema, • diarrhea • myalgia or musculoskeletal pain • skin rashes • headache • Myelotoxicity • Cardiotoxicity • hemorrhagic events • tachyphylaxis

  18. 18FDG-PET represents a useful diagnostic technique for very early assessment of response to imatinib therapy. • The optimal dose of imatinib for treatment of advanced GIST remains uncertain

  19. some marginal benefit might be obtained from modest dose escalation of imatinib in a subset of patients whose disease progresses despite continued dosing at lower therapeutic levels of imatinib

  20. The optimal duration of imatinib • continued dosing with imatinib as long as the disease is not progressive

  21. disease that is initially judged as unresectable may become amenable to surgical excision after a major response induced by imatinib therapy. Most centers recommend surgical resection for such patients because it is feared that residual GIST may develop secondary mutations that could result in clinical resistance to imatinib and progression of disease

  22. sunitinib definitely improved the progression-free survival of patients following imatinib failure due to resistance or intolerance

  23. Definitive expert surgery remains the mainstay of treatment for patients with localized, primary GIST

  24. Adjuvant Therapy to Improve Outcomes for Patients with Resected Early Stage • The standard of care after complete surgical resection of GIST has therefore been observation alone

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