Gastrointestinal stromal tumors (GISTs) belong to a group of cancers called soft tissue sarcomas. Sarcomas are a rare type of cancer that can occur in connective tissues, bones, muscles, fat, nerves, blood vessels, and cartilage. Sarcomas are derived from the general class of cells known as "mesenchymal cells". In contrast, most of the "common" cancers, such as lung cancer, skin cancer, and prostate cancer, are derived from a different type of cell, known as "epithelial cells", the cells which line the body's many surfaces. Why does this distinction matter? Because carcinomas and sarcomas behave very differently and are treated differently. Sarcomas are much less common than carcinomas. As a result, there are relatively few oncologists who specialize in treating sarcomas.

GIST often spreads from the original (primary) site to distant locations. If this happens, these tumors are called metastases (or simply, "mets"). If GIST tumors metastasize they usually travel to the liver, or the peritoneum. Metastases to the lymph-nodes and lungs are rare, but do occur. Metastases are usually harder to treat than primary tumors.

When GIST spreads to the liver, the liver tumors are GIST tumors, *not* liver cancer. GIST metastases in the liver are still derived from GIST cells and must be treated like GIST cells. Liver cancer is a completely different cancer that *starts* in the liver.

GIST tumors often grow quite large before they are discovered and primary tumors often produce few symptoms. Metastatic tumors can be quite numerous. GISTs are often discovered during emergency surgery for unexpected perforation of the gastrointestinal tract and consequent bleeding. When GIST tumors are first discovered, the most common symptoms are:

Although the term "GIST" was first used in 1983 (by Mazur and Clark), the 1998 discovery by Hirota that GIST tumors can contain mutations in the c-kit gene marked the beginning of a new understanding and reclassification of sarcomas of the GI tract. Prior to the year 2000, GISTs were previously classified as one of many types of soft tissue sarcoma (STS) including tumors of smooth-muscle origin (most commonly leiomyosarcoma, and also leiomyoma or leiomyoblastoma) and of neural-crest origin (eg, schwannoma, or nerve sheath tumor). Most tumors previously diagnosed as Gastrointestinal Autonomic Nerve Tumors (GANTs) are also now classified as GISTs and contain essentially the identical KIT mutations as GIST. What establishes GIST as a separate diagnoses from these other soft tissue sarcomas in not just the description of where the tumor is located, but also the additional factor that it is KIT (CD117-positive (although a small percentage of GISTs are KIT-negative). Most GIST patients are also CD34 positive and desmin negative.

The introduction of the drug Gleevec for the treatment of GIST has sparked a tremendous amount of interest and research. Gleevec is a molecularly targeted drug that is both more effective and has fewer side effects than traditional chemotherapy. This area of research is very fast moving so recent information is important. Because of this, we have tried to provide a date for key information provided. Such dates will appear in the text where appropriate and will be formatted similar to this: (date of comment: February, 2005). Also please check the " last modified" date at the bottom of each page.

"No one can take the place of an experienced GIST team of doctors. This may include a Pathologist, Oncologist, and a Surgeon. GIST is such a rare type of cancer that few doctors have much experience in treating it. The hospitals with top sarcoma treatment centers are likely to have more experience with GIST. This is especially true with the hospitals that conducted or are conducting clinical trials with Gleevec and Sutent (SU11248). They have seen many more GIST patients and are more familiar with their unique needs, with treatment options, managing side effects, monitoring considerations, and what to do if the initial treatment fails. "

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