gastrointestinal stromal tumours(gist)
DESCRIPTION
Gastrointestinal Stromal Tumours(GIST). INTRODUCTION :. Stromal or mesenchymal tumors of the GI tract are divided into two group s: 1. Those identical to tumors of the soft tissue arising in the rest of the body ( Lipomas, Schwannomas, Hemangiomas, Usual Leiomyomas, etc. ) - PowerPoint PPT PresentationTRANSCRIPT
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Gastrointestinal Stromal Tumours(GIST)
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INTRODUCTION :
• Stromal or mesenchymal tumors of the GI tract are divided into two groups:– 1. Those identical to tumors of the soft tissue arising in the
rest of the body (Lipomas, Schwannomas, Hemangiomas, Usual Leiomyomas, etc.)
– 2. Stromal tumors arising from the smooth muscle of the alimentary tract: GIST
• The term “GIST” was applied by Mazur and Clark in 1983 to define intra-abdominal tumors that were not carcinomas .
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EPIDEMIOLOGY
• Most common non epithelial benign neoplasm of the GI tract .
• GIST represents a form of sarcoma that comprises approx. 1% to 3% of all malignant GI tumors.
• GIST occurs predominantly in adults .
• The incidence has been slightly higher in men than women.
• Small asymptomatic GISTs are found at autopsy in more than 50 % of individuals over the age of 50
• GIST treatment trials estimate an annual incidence of 4,500 – 6,000 new cases
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MOLECULAR PATHOBIOLOGY GIST
• GIST represents a form of sarcoma.
• GISTs originally thought to derive from smooth muscle, but only rarely showed clear-cut features of complete muscle differentiation.
• Work in the 1990s: Some tumors classified as GIST were truly myogenic, some neural, others bidirectional and some had the ‘null’ phenotype
• Up to two-thirds were CD34 positive
• Unfortunately, Schwannomas and a proportion of true smooth muscle tumors were also CD 34 positive
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ENTER :Membrane (Receptor) Tyrosine Kinase
• PTKs are involved in cellular signaling pathways and regulate key cell functions such as proliferation, differentiation, anti-apoptotic signaling and neurite outgrowth.
• Unregulated activation of these enzymes can lead to various forms of cancer as well as benign proliferative conditions.
•Nishida T, Hirota S, Taniguchi M, et al: Familial gastrointestinal stromal tumours with germline mutation of the KIT gene
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GIST and C-kit
• The c-kit receptor is one of many membrane tyrosine kinase receptors involved in cellular signaling pathways.
• CD117 molecule (or antigen) is part of the c-kit receptor, a membrane tyrosine kinase.
• The c-kit receptor is a product of the c-kit or KIT protooncogene.
• The CD117 antigen is expressed by almost all GISTs in contrast to other spindle-cell tumors of the GI tract
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UNCONTROLLED KINASE ACTIVATION (THE MOLECULAR
ETIOLOGY)
• In normal cells activation of the of the c-kit tyrosine kinase requires the presence of an endogenous ligand (KIT ligand, c-kit ligand, or stem cell factor)
• Approx 80 % of GISTs have KIT protooncogene mutations that lead to activation of the c-kit receptor resulting in spontaneous receptor activation not requiring a ligand
• Observed both in sporadic and hereditary cases • A subset of GISTs lacking c-kit mutations have activating
mutations in the PGFRa gene (platelet derived growth factor receptor alpha), another tyrosine kinase
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GISTs are identified by:
• either c-kit immunoreactivity (detection of the CD117 antigen) or
• the presence of activating mutations in KIT or PDGFRa
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Are GISTs derived from ICCs?
• Interstitial cells of Cajal (ICC) form the interface between the autonomic innervation of the bowel wall and the smooth muscle itself.
• The KIT RTK plays essential roles in the development and maintenance of normal ICCs .
• Ultrastructural and immunophenotypic features of both neuronal and smooth muscle differentiation (just like GISTs)
• It is postulated that GISTs originate from CD34 positive stem cells within the wall of the gut and differentiate toward the pacemaker cell phenotype (ICC)
• Malignant GISTs may represent dedifferentiated ICCs that maintain a CD34-positive stem cell phenotype
• Attractive hypothesis but still open to question
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LOCATION :
• Stomach – 50 percent
• Small bowel – 25 percent
• Colon/ Rectum– 10 percent
• Omentum/mesentery 7 – percent
• Esophagus – 5 percent
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CELLULAR MORPHOLOGY
• Three relatively distinctive types– Spindle cell type – 70 percent – Epithelioid type – 20 percent, more commonly c-
kit negative and found in omentum and mesentery – Mixed type – 10 percent Histologic type may be
of prognostic significance, worse with epitheloid
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HISTOPATHOLOGY
• Differential Diagnosis – H&E stain: Melanoma, leiomyoma/sarcoma, peripheral
nerve sheath tumor, desmoid – Histology difficult
– Immunophenotyping crucial • 95 % are positive for C-kit (CD117) • 60-70 % positive for CD34 • Negative for alpha-smooth muscle actin (SMA) (leiomyoma) • Negative for S100 protein (Schwannoma) • Negative for Desmin (desmoids)
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H&E stain C-kit(CD 117)
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Determinants of Malignant Determinants of Malignant Behavior Behavior
• Size: More than 3 cm in diameter(most malignant GISTs are larger than 10 cm at
diagnosis)
• Mitotic rate: > 25 mitoses per 50 high power fields
• Warning: Even very small lesions (< 2 cm) with a low mitotic rate occasionally metastasize
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Approach for defining Risk of Aggressive Behavior in Gastrointestinal
Stromal Tumors
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Metastasis
• GISTs behave differently than other soft tissue sarcomas: – GISTs frequently metastasize to the liver and
rarely to regional lymph nodes – GISTs virtually never metastasize to lungs whereas
this is the most common site of metastasis for leiomyosarcomas
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CLINICAL MANIFESTATIONS
• Mesenchymal tumors of the GI tract are often asymptomatic and discovered incidentally during endoscopic or barium studies.
• Overt GI bleeding — 40 percent • Abdominal mass — 40 percent • Abdominal pain — 20 percent
– The vast majority of GIST metastases at presentation are intra-abdominal, either with metastases to the liver, omentum, or peritoneal cavity .
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Diagnosis :
• CT scan – Leiomyomas: solid hypodense lesions – GISTs: typically enhance with IV contrast
• Endoscopy • Smoothly contoured submucosal mass, possible
central umbilication
• EUS • Hypoechoic mass arising from muscularis propria
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CT scan
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Endoscopy
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• PET scan and CT scans in a patient with a GIST metastatic to the liver, before (left) and after treatment with imatinib mesylate
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Management :
• European Consensus Conference Recommendations (Meeting in Lugano Mar 2004) pub in Ann Oncol. 2005 Apr;16(4):566-78.
• NCCN Sarcoma Guideline (GIST chapter) updated in 2005
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Imatinib (Gleevec) a Tyrosine Kinase Inhibitor
• Imatinib mesylate is a protein-tyrosine kinase inhibitor that inhibits the Bcr-Abl tyrosine kinase.
• Imatinib is also an inhibitor PDGF and c-kit, and inhibits PDGF- and SCF-mediated cellular events. In vitro, imatinib inhibits proliferation and induces apoptosis in (GIST) cells, which express an activating c-kit mutation
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Imatinib (Gleevec) a Tyrosine Kinase Inhibitor
• Imatinib (Gleevec) is very effective for CD114 positive GISTs
• It also has antitumor effficacy in tumors that lack KIT mutations but have alterations in the PDGF pathway
• Some PDGFRa mutations are imatinib-sensitive, others not therefore, patients with advanced tumors that are histologically c/w GIST should not be denied a trial of imatinib if they are c-kit negative.
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Management
PRIMARY, LOCALIZED DISEASE (EARLY-STAGE GIST)
• Surgery remains the mainstay of treatment for patients with primary localized GIST
• GIST lesions are highly vascularized and often exhibit a fragile pseudocapsule; therefore, surgeons should be careful to minimize the risk of tumor rupture.
• GIST rarely involves the locoregional lymph nodes. • Adjuvant Therapy :At present, it is unclear whether the
administration of imatinib in the postresection adjuvant setting would confer significant clinical benefits on patients.
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MANAGEMENT OF ADV. GIST
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MANAGEMENT OF UNRESECTABLE GIST :
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MANAGEMENT OF METASTATIC GIST :
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The incidental (asymptomatic) UGI subepithelial mass
• No firm clinical guidelines or consensus • Surface Endoscopy can establish a lipomatous nature of the
mass • If mass is > 1 cm referral for EUS, if < 1 cm repeat EGD in
one year, if stable probably no follow-up • If mass arises from muscle layer (4th EUS layer mass) and is
> 3 cm referral for surgery (likely GIST) • Clinical conundrum: The 1 - 3 cm mass • 4th layer mass should undergo EUS-FNA and c-kit staining • If a GIST is found discuss management strategies, esp.
surgery
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• If results are indeterminate or patient does not wish (or is not a candidate for) resection, endoscopic follow up
• Recommendations depend on the age of the patient, index of suspicion, etc.
• One reasonable strategy: EUS follow-up a year later and if lesion is stable for two consecutive follow-up periods, lengthening of the follow-up period.