New Developments in Targeted Therapy for Gastrointestinal Stromal Tumors
Oncology Briefings Vol. 7, No. 1
This activity is not sanctioned by, nor a part of, the 2009 Gastrointestinal Cancers Symposium.
Release Date: March 31, 2009
Expiration Date: March 31, 2010
Medical writer: Timothy Quill, PhD; Reviewed by: Jean-Yves Blay, MD, PhD
Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumor type of the gastrointestinal tract; approximately 6000 new cases are diagnosed in the United States each year. Activating mutations in the c-Kit receptor tyrosine kinase (TK) are the predominant cause of GIST, and the integration of TK-targeted agents into GIST treatment has markedly changed the management of these tumors. The use of TK inhibitors (TKIs) as therapy for GIST continues to evolve from treatment for metastatic disease to adjuvant therapy following surgical resection. Data on mutation status and efficacy that are relevant to the planning of an optimal personalized treatment course are emerging. Other novel agents under investigation are also expanding treatment options for patients with GIST.
The purpose of this activity is to inform physicians of new developments in the use of targeted therapies in patients with both resectable and unresectable GIST.
This activity is intended for medical oncologists involved in the care of patients with gastrointestinal stromal tumors (GIST). No specific skills or knowledge other than a basic training in oncology is required for successful participation in this activity.
Upon completion of this educational activity, you should be able to:
This online activity provides a maximum of 0.5 AMA PRA Category 1 Credit™.
You will be permitted 2 attempts to successfully complete the Posttest.
CME credit will be granted for only 1 form of participation, either online or via the printed publication.